Chemist Jobs in Powell, OH

The Senior Color Chemist is responsible for creating formulations to ensure our product matches our customers' color requirements for various applications. Responsibilities: Create Color Matches at a high level of quality and efficiency. Create formulations that meet customer specifications, cost parameters and manufacture capabilities at a high rate of efficiency. Perform and excel at multiple color matching techniques, coloring systems, & color solutions. Utilize strong knowledge and experience of formulating color and effects for multiple applications. Maintain accurate & legible records that align with Ampacet's ISO requirements, as well as good documentation practices (GDP). Be a mentor for other color chemists and assist in the development of the color chemists and color technicians. Interface with and support internal & external customers where applicable. Maintain lab and equipment in the highest standards for a clean working environment. Adhere to all safety rules and regulations according to quality and safety policies. Work at a high level of efficiency and productivity to support Ampacet service commitments. Provide support to Color Lab Sample Department on the processing & color corrections when applicable. Assisting Color Technicians as needed. Assist production/QC in color corrections Perform additional projects or tasks as assigned by Color Lab Supervisor Communicate effectively and proactively with Sales. Requirements: High School degree required. Higher education in a related discipline preferred, but years of experience will be considered in lieu of a college degree. Must have a minimum of 5 years' of colormatching for masterbatch experience, with a focus on rigid packaging. Experience formulating for engineered resins applications is a plus. Experience formulating for multiple applications, including but not limited to injection molding, blow molding, sheet extrusion, and thermoforming is required. Strong formulating background with engineering grade resins, as well as knowledge of multiple extrusion processes, blow molding and injection molding. Strong technical understanding and experience in all masterbatch formulating but with a specific focus on thermoplastics and engineered resins. Experience utilizing various coloring methods and chemistries including pigments, dyes, and special effect type raw materials is expected. Strong background in masterbatch as it relates to various color matching lab equipment types & processes, extrusion equipment, injection & blow molding Experience with X-Rite spectrophotometer and software. Must pass Farnsworth-Munsell Color Discretion Test Excellent Color Vision and discretion Proficiency in MS Office (Outlook, Word & Excel) Ability to work independently as well as on a team Excellent organizational and time management skills: ability to prioritize Able to communicate verbally and in writing with a high degree of professionalism. Ampacet is an Equal Employment Opportunity employer and will not discriminate against an applicant on the basis of age, sex, race, color, creed, religion, ethnicity, national origin, alienage or citizenship, disability, marital status, military or veteran status, or any other legally recognized protected basis under federal, state or local laws, regulations or ordinances.

Kelly Science has and Immediate opening for a Scientist III, QC Labs for our growing client near Columbus, OH Shift: 2nd Full-time Direct Hire Salary: $75,000-$100,000 DOE Your Role: As a Scientist III, QC Labs, you will play a pivotal role in ensuring the highest standards of quality and regulatory compliance. You'll be responsible for conducting sophisticated testing of raw materials, active pharmaceutical ingredients (APIs), and finished products to ensure they meet both customer requirements and regulatory standards. You'll also contribute to the continuous improvement of analytical methods and troubleshooting, working closely with a collaborative team in a fast-paced and ever-evolving environment. Key Responsibilities: Perform Analytical Testing: Conduct qualitative and quantitative chemical and physical testing for APIs, starting materials, packaging components, and finished products, ensuring accuracy and regulatory compliance. Ensure Regulatory Compliance: Maintain adherence to current DPs, SOPs, and cGMP regulations while performing testing and documenting results. Documentation & Reporting: Maintain clear, organized records in laboratory notebooks, worksheets, and documents. Author detailed technical reports to improve analytical methods. Investigative & Troubleshooting Work: Apply advanced analytical techniques to resolve complex issues, investigate discrepancies, and ensure proper use of laboratory equipment. Collaborate with Cross-Functional Teams: Act as a key player in meetings with stakeholders to discuss laboratory deviations, lead troubleshooting efforts, and provide guidance to junior scientists. Review & Approve Analytical Data: Ensure all analytical documentation and batch records are reviewed, validated, and released in accordance with company procedures and specifications. Desired Analytical Expertise: For APIs: Proficiency in UV, HPLC, GC, UPLC, KF, FTIR, Advanced Data Review, Lead Investigator, and Disposition (Packaging/Labeling). For Pharmaceutical Products: Expertise in HPLC, UPLC, Chromatographic Data Systems (Empower preferred), Laboratory Information Management Systems (LabWare preferred), and Advanced Data Review. Additional Desired Techniques: Experience with particle size analysis, ICP, AA, viscosity, XRD, GC, IC, droplet size distribution, FTIR, and microscopy. What You Bring to the Team: A BS in Chemistry (or related science field) with a minimum of 5 years of GMP pharmaceutical analytical chemistry experience, or 10 years of relevant experience with a high school diploma. Hands-on experience executing and evaluating analytical methods for APIs and pharmaceutical products, including both compendial and non-compendial testing. Expertise in advanced analytical techniques, method troubleshooting, and data review. Strong ability to work independently and as part of a team to manage multiple projects simultaneously in a fast-paced environment. Exceptional written and verbal communication skills, including the ability to organize and lead meetings with stakeholders to discuss lab deviations. A collaborative mindset with the ability to mentor junior scientists in laboratory techniques and best practices. What We Offer: Competitive Compensation: Annual performance bonus, commission, and share potential. Comprehensive Benefits: Health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits. Generous Time Off: Starting with 20 days PTO (prorated), additional days at milestone anniversaries, 3 personal days, and 11 company-paid holidays. Retirement & Savings: Auto-enrollment in a Hikma-sponsored 401(k) with a 100% match on the first 6% of eligible pay you contribute. Wellbeing & Employee Discounts: Access to our Wellbeing Rewards Program and employee discount offerings. Career Growth: Career advancement opportunities and access to tuition reimbursement to further your education. Family Support: Paid maternity and parental leave to support you during important life milestones. Why Join Us? We value your expertise and dedication. Here, your contributions matter. Join a company that prioritizes safety, quality, and growth. Together, we will innovate, improve, and make a lasting difference in the pharmaceutical industry. Ready to take your career to the next level? Apply now!

Main Responsibilities: • Data collection • Data tabulation • Product batching • Ingredient weighing • Sample collection • Sample submission • Lab analysis • pH and moisture analyses Skills: • Food Chemistry/Chemistry • Food Engineering • Microbiology • Basic Math and Science • Worked in a lab setting Education: Bachelor's degree in Food Science Additional: • Looking for 0-3 years experience. Analyzes verbal or statistical data to prepare reports and studies for use by professional workers in a variety of scientific areas. May be proficient in qualitative and/or quantitative lab methods. Includes all levels of education and experience.

Nutrition R&D Technician - Medical Device Industry Responsibilities: Collect and tabulate data for research projects Weigh ingredients and batch formulations Collect and submit samples for lab testing Perform pH and moisture analyses Skills: Knowledge of Food Science, Chemistry, or Microbiology Experience in a lab setting Strong analytical and math skills Requirements: Bachelor's degree in Food Science 0-3 years of experience 100% onsite role

Shift: Monday through Friday 8:00 am to 5:00 pm Experience with Prototype, science and lab equipment. Our Commitment to Safety Is Unconditional Contractor will support needs associated with Technical Insulation R&D Technology Development Project including the following: Sample preparation and testing of raw materials and trial prototype material Test method development supporting raw material and prototype material testing Support of safe work documentation for existing and new laboratory equipment Operation support of prototype equipment Responsibilities Include: Sample Preparation/Testing Prepare samples for laboratory and/or application testing Perform laboratory and/or application testing using learned knowledge of laboratory test methods to effectively test products Document testing results for communication with project team Prototype/Build/Operate Operate prototype equipment in support of development trials Work with project engineers/leaders to execute build needs for prototype or test equipment Minimum qualifications: Associates degree in science or engineering field Experience in a laboratory environment High school diploma and previous experience are acceptable Experience: Demonstration of safe work practices Comfortable operating lab equipment Use of computer and working knowledge of Microsoft Windows and Office Suite (Word, Excel, Outlook, and PowerPoint)

Job Posting End Date 04-08-2025 Please note the job posting will close on the day before the posting end date Chemists serve in support of power plants, energy delivery, and third party interests, performing a variety of independent, non-routine, and more complex quantitative analyses using sophisticated laboratory instrumentation. Performs, under direction, responsibilities which include, but are not limited to, the sampling techniques, preparation, and chemical analysis of environmental, industrial hygiene, and industrial/manufacturing samples. Demonstrates, under direction, the skills to evaluate analytical results and modify procedures within established limits based on sample matrix and quality control trends and the performance of analytical instruments, to schedule work based on current and anticipated workloads and deadlines, and to participate as an integral part of problem solving and process improvement teams as assigned Job Description ESSENTIAL JOB FUNCTIONS: 1) Essential Function: 1. Chemists perform daily operations for chemical analyses, adhere to policies and procedures, document daily operations and activities, and perform problem solving and decision making within the department. 2) Perform daily operations for chemical analyses: 1. Assists in the development of environmental, health, and safety policies for everyday tasks. 2. Performs routine analytical activities with minimal direction form higher level employees. 3. Uses scheduling techniques for work management. 4. Coordinates multiple analytical techniques and the work of technicians. 5. Analyzes asbestos by bulk analysis or fiber identification which is conducted by preparing material and viewed under a microscope using Polarized Light Microscopy (PLM). 6. Analyzes asbestos-airborne fiber count (NIOSH 7400). This analysis may include testing air samples for asbestos and other fibers by Phase Contrast Microscopy (PCM). 3) Adherence to policies and procedures: 1. Follows policies, practices, standards, and rules of the company and those regulations and procedures required by external agencies. 2. Understands and practices safe laboratory procedures. 3. Ensures work quantity and quality by requiring strict adherence to NIOSH methods and standard operating procedures for respirable crystalline silica, total and respirable dust, lead base paint, welding fumes, respirable metals, and hexavalent chromium. 4. Ensures work quantity and quality by requiring strict adherence to EPA (and EPA-approved) methods and standard operating procedures for chemical constituents in water, wastewater, waste, solid, oil, and process samples. 5. Ensures work quantity and quality by requiring strict adherence to ASTM (and ASTM-modified) or AEP-developed methods and standard operating procedures for chemical constituents, identification, and characterization of liquid, solid, organic, and airborne process samples. 6. Ensures work quantity and quality by requiring strict adherence to NIOSH methods, EPA (and EPA-approved) and ASTM (and ASTM-modified) standard operating procedures as appropriate. 4) Documents daily operations and activities: 1. Demonstrates ability to prepare and issue routine analytical reports, verbal and written skills for effective communication of analytical data and chemical information. 2. Develops, reviews, or presents routine technical reports clearly, concisely, and effectively. 3. Demonstrates ability to extrapolate beyond known facts to reach logical conclusions. 4. Prepares lab reports for submittal to customers and prepares reports on laboratory activities. 5. Provides basic training and guidance to lower level employees. Effectively trains other employees. 5) Problem solving and decision making within department: 1. Identifies and initiates solutions to routine problems which usually require additional definition or clarification before analysis can begin. 2. Demonstrates ability to identify problems that are beyond the normal routine. 3. Makes decisions, subject to review within established policies and procedures, concerning the validity of analytical test data. 4. Demonstrates proficiency in application and use of economic analysis techniques. 5. Initiates priority changes when analytical objectives are not met. MINIMUM REQUIREMENTS: Education requirements are listed below: Bachelor's degree in chemistry, related sciences, industrial hygiene, or engineering field. Work Experience requirement listed below: Minimum four years' experience in related field. Required License(s)/Certification(s) are listed below: Valid state driver's license. OTHER REQUIREMENTS: Physical demand level is Sedentary These are additional expectations for the job and could include specific work experience, license / certifications, preemployment testing, expectations about travel, shift work, etc. 1. Obtain license/certifications required if assigned to industrial hygiene analyses, but can be obtained after employment. 2. Actively seeks information to increase technical knowledge in additional areas of the laboratory. 3. Develop awareness of clients' needs in accordance with applicable standards. 4. Understand AEP's organizational structure and the specific roles and responsibilities of their individual organizational units. 5. Strong oral and written communication skills. 6. Organizational, planning, and analytical knowledge and experience. 7. Develop skills for improved decision making, for efficient organization of work to meet deadlines, and for effective troubleshooting of analytical procedures and instrumentation. 8. Demonstrate the highest standards of ethical behavior and support the Company's Corporate Compliance Policy and national standards. 9. Ability to work around hazardous chemical and potentially contaminated matrices. PHYSICAL DEMANDS: List physical demands required for this job, but not limited to. Compensation Data Compensation Grade: SP20-006 Compensation Range: $72,380.00-90,474.50 USD Hear about it first! Get job alerts by email. Log in to your Candidate Home Account today! If you don't have an account, you can create one. It is hereby reaffirmed that it is the policy of American Electric Power (AEP) to provide Equal Employment Opportunity in all respects of the employer-employee relationship including recruiting, hiring, upgrading and promotion, conditions and privileges of employment, company sponsored training programs, educational assistance, social and recreational programs, compensation, benefits, transfers, discipline, layoffs and termination of employment to all employees and applicants without discrimination because of race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, veteran or military status, disability, genetic information, or any other basis prohibited by applicable law. When required by law, we might record certain information or applicants for employment may be invited to voluntarily disclose protected characteristics.

Chemist II Pay Rate: $65,100 - $86,800 Multiple factors, including Individual experience, skills and abilities will determine where an employee is ultimately placed in the pay range. Variable pay may provide additional opportunities for financial awards. This job is eligible to participate in IP's annual and long-term incentive plans. Category/Shift: Salaried Full-Time Physical Location: 13307 Industrial Parkway Marysville, OH 43040 The Job You Will Perform: The Chemist II position is in the International Paper ink lab, which is part of the Enhanced Graphics division within the Custom Packaging and Display group. IP Ink supplies water based flexographic printing inks and related services to corrugated packaging converters, bag manufacturers, and other flexographic printers within International Paper and to external customers. The ink lab provides color matching, technical service, formulation, and research and development services to our customers in order to help them produce high quality packaging products. The Chemist II reports to the Lab Manager. * Responsible for product improvement, new product development, raw material evaluation and other lab functions as necessary * Coordinate and plan projects with Lab Manager and Chemist III * Conduct applicable lab testing, maintain project files and reports * Maintain a Laboratory Notebook * Maintains test chemical inventory. * Operate all laboratory testing equipment. * Identify proper vehicle system for given application. * Identify/recognize a customer's environmental restrictions and formulate accordingly. * Make proper anilox selection per machine requirements. * Provide color match and customer service support as needed * Conducts Chemical Approval process for new items * Schedules and participates in field-testing for new and/or improved products. May involve offsite travel * Responsible for specific manufacturing and R&D laboratory instrument maintenance and/or repair. * Participates in training and continuing education activities related to the job * Creates procedures and related SOP's for manufacturing and R&D. * Completes all required tasks and responsibilities while adhering to Specialty Products Safety Standards. * Initiates and implements cost saving projects. * All other duties assigned. * Participates in IPs ongoing 5S program * Generate best color match within cost constraints. * Works directly with vendors on R&D and complaint resolution. The Qualifications, Skills and Knowledge You Will Bring: * 4-year degree in Chemistry or related discipline, and 2+ years' experience in ink formulation/testing or related industry is preferred. * Industry related experience is desirable: Ink, paint, printing, or coatings. * Ability to travel up to 25%. * Previous experience with color or color matching and knowledge of industrial batch process and equipment is desired. * Strong technical/customer support skills. You will be required to work closely with sales, technical service and our customer base in a wide array of situations * Proficient in Microsoft Office applications (Word, Excel) * Ability to self-start, remain calm in stressful situations, and have a positive outlook are beneficial to this position. * Proficiency with Batchmaster Enterprise * Ability to communicate well verbally, and across electronic platforms such as e-mail, text, and instant messaging The Benefits You Will Enjoy: International Paper offers a benefits package that includes health, welfare and retirement plans including Medical, Dental, Life insurance, Flexible Spending Accounts, Short-term and Long-term Disability, 401(k), Company-funded retirement contributions, Paid Time Off, Education & Development (including Tuition Reimbursement), Student Loan Repayment Assistance, and Voluntary Benefits including insurance for home, auto, vision and pets. The Career You Will Build: Sales and Leadership training, promotional opportunities within a global company The Impact You Will Make: We continue to build a better future for people, the planet, and our company! IP has been a good steward of sustainable practices across communities around the world for more than 125 years. Join our team and you'll see why our team members say they're Proud to be IP. The Culture You Will Experience: International Paper promotes employee well-being by providing safe, caring and inclusive workplaces. We have team members all around the world with diverse backgrounds, experiences, and perspectives. These are our strengths. We are committed to creating a culture where all individuals are respected, valued, engaged and have an opportunity to do their best work every day. We invite you to bring your uniqueness, creativity, talents, experiences, and safety mindset to be a part of our increasingly inclusive and diverse culture. The Company You Will Join: International Paper (NYSE: IP) is a global producer of sustainable packaging, pulp and other fiber-based products, and one of the world's largest recyclers. Headquartered in Memphis, Tenn., we employ approximately 39,000 colleagues globally who are committed to creating what's next. We serve customers worldwide, with manufacturing operations in North America, Latin America, North Africa and Europe. Net sales for 2023 were $18.9 billion. Additional information can be found by visiting internationalpaper.com. International Paper is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. International Paper complies with federal and state disability laws and makes reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact reasonable.accommodations@ipaper.com or ************** Share this job: Location: Marysville, OH, US, 43040 Category: Technology Date: Mar 26, 2025 If you are not finding suitable opportunities, please click below to join our talent community! Join Our Community Nearest Major Market: Columbus Nearest Secondary Market: Dublin

Currently hiring a Mid-Level Chemist for a Chemical Laboratory in Central, OH. An ideal candidate will have 3 to 5 years of experience as a Chemist and have used analytical equipment such as LECO, XRF, AA, ICP, Mass Spectrometers. INTERESTED CANDIDATES CAN SEND THERE UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA TO SET UP A PHONE INTERVIEW AT ************** This position is a 2nd shift M-F with Flexible start times. Can also be a 4-10 schedule on 2nd shift! The Chemist measures production samples and prepares new methods and procedures in the analytical laboratory. The Chemist works to keep a clean work area and ensures all safety protocols are followed. Responsibilities * Measure samples utilizing equipment such as LECO gas analysis, X-Ray Fluorescence (XRF), Atomic Absorption (AA), Inductively Coupled Plasma (ICP) emission, and Glow Discharge Mass Spectrometry (GDMS). * Measure surface roughness using an Interferometer. * Measure resistivity using a four-point probe. * Measure the density of solid materials using the wet density apparatus. * Prepare analytical samples in the analytical laboratory. * Develop new methods and procedures. * Work with equipment technical support teams to troubleshoot equipment problems. * Understand and adhere to all safety requirements, communicate identified risks to leadership, and assist in resolution. * Complete all 5S standards to maintain a safe, organized, and efficient work environment. * Maintain regular and reliable attendance. * Contribute to company culture through alignment with company values and code of conduct, maintain a positive attitude, display enthusiasm for assigned tasks, and communicate effectively and professionally with team members. * Perform other related duties as assigned. Essential Skills * Bachelor's degree in chemistry or related field or equivalent experience. * 3-5 years of industry experience. * Experience with analytical equipment such as LECO, XRF, AA, ICP, Mass Spectrometers or equivalent. * Proficiency with computers and ability to learn new software packages. * Attention to detail, strong organizational skills, and ability to manage own work schedule. * Willingness to work with acids, solvents, compressed gases, and liquid nitrogen. * Ability to communicate well with people inside and outside the immediate work area. Pay and Benefits The pay range for this position is $30.00 - $40.00 Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Grove City,OH. Application Deadline This position will be accepting applications until Feb 7, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Position: Full-Time Total Rewards: Benefits/Incentive Information If you've worn a pair of glasses, we've already met. We are a global leader in the design, manufacture, and distribution of ophthalmic lenses, frames, and sunglasses. We offer our industry stakeholders in over 150 countries access to a global platform of high-quality vision care products such as the Essilor brand, with Varilux, Crizal, Eyezen, Stellest and Transitions, iconic brands that consumers love such as Ray-Ban, Oakley, Persol and Oliver Peoples, as well as a network that offers consumers high-quality vision care and best-in-class shopping experiences such as Sunglass Hut, LensCrafters, and Target Optical, and leading e-commerce platforms. Our unique business model and relentless pursuit of operational excellence ensures that consumers everywhere have access to products. Balancing speed, efficiency and proximity, the Company manages a global supply chain with cutting-edge technology, based on centralization for frames and on a capillary network for lens finishing and prescription laboratories. In our dynamic environment, fueled by technology and innovation, our people have the space to pioneer new solutions. Join our global community of over 200,000 dedicated employees around the world in driving the transformation of the eyewear and eyecare industry. Discover more by following us on LinkedIn! GENERAL FUNCTION Entry-level role in the kilogram-scale manufacture of specialty chemicals, including dyes and dye intermediates for use by both internal and external customers. MAJOR DUTIES AND RESPONSIBILITIES Specialty chemical production on kilogram scales Chemical apparatus set-up, reactor loading (solvents, raw materials) and unloading Chemical process monitoring and control Product purification (crystallization, chromatography, rotary evaporation, solvent recovery) Spectroscopy (ultraviolet, visible, infrared) Quality control Record keeping (Laboratory notebooks, Certificates of Analysis) Reporting (Standard Operating Procedures, Production reports) Compliance with safety and environmental regulations (OSHA, EPA) and internal practices BASIC QUALIFICATIONS Bachelor's degree in chemistry, chemical engineering, or related field Certifications: None required University research experience Familiarity in handling chemicals and chemical equipment Familiarity with running analytical instruments including GC, UV/Vis spectrometers Familiarity with Microsoft Office applications Excellent oral and written communication skills PREFERRED QUALIFICATIONS Bachelor's degree, Organic Chemistry with 1-2 years of industrial experience Experience in handling chemicals and chemical equipment on kilogram scales Experience in maintaining spectrometers and interpreting spectra Experience with maintaining analytical instruments including GC, UV/Vis spectroscopy Familiarity with SciFinder and SAP Employee pay is determined by multiple factors, including geography, experience, qualifications, skills and local minimum wage requirements. In addition, you may also be offered a competitive bonus and/or commission plan, which complements a first-class total rewards package. Benefits may include health care, retirement savings, paid time off/vacation, and various employee discounts. Upon request and consistent with applicable laws, EssilorLuxottica will provide reasonable accommodations to individuals with disabilities who need assistance in the application and hiring process. To request a reasonable accommodation, please call the EssilorLuxottica SpeakUp Hotline at ************ (be sure to provide your name and contact information so that we may follow up in a timely manner) or email ********************************. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, national origin, social origin, social condition, being perceived as a victim of domestic violence, sexual aggression or stalking, religion, age, disability, sexual orientation, gender identity or expression, citizenship, ancestry, veteran or military status, marital status, pregnancy (including unlawful discrimination on the basis of a legally protected pregnancy or maternity leave), genetic information or any other characteristics protected by law. Native Americans in the US receive preference in accordance with Tribal Law. .job Title{ display:none !important; } Nearest Major Market: Columbus Job Segment: Supply Chain, Social Media, Supply, Ophthalmic, Operations, Marketing, Healthcare

Job Title: R&D Chemist Department: Research & Development Last Reviewed: February 2025 Meridian Adhesives Group is a rapidly growing, full service global adhesive solutions provider, specializing in adhesive technologies used in electronics, industrial, and infrastructure applications. Fueled by a series of strategic acquisitions since its formation in 2018, we have established ourselves as an adhesive technology leader for a broad, global, blue-chip customer base comprised of OEMs, distributors, and industrial clients with an expanding global footprint. Guided by our core values-Safety & Sustainability, Respect, Integrity, Accountability, and Teamwork-we are driven to make a meaningful impact in everything we do. When you join Meridian, you become part of a dynamic team that values diverse perspectives, fosters professional growth, and encourages bold ideas. We're committed to creating a supportive environment where you can thrive, grow, contribute to groundbreaking projects, and help shape the future of our industry. Meridian Adhesives Group does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. Summary The Chemist will play a key role in the formulation, development, and testing of adhesive materials. Reporting to the R&D Manager, this position involves hands-on research, product development, and laboratory testing to support the company's innovative efforts and market-driven solutions. The Chemist will collaborate closely with cross-functional teams, ensuring new products meet technical requirements, performance expectations, and regulatory standards. Salary Range & Benefits $70,000 - $75,000 + 10% annual performance bonus target Health, dental, and vision insurance. 401(k) matching plan. Flexible spending account. Health savings account. Life, short-term and long-term disability insurance. Parental leave. Referral program. Paid time off. Paid holidays. Duties & Responsibilities Conduct research and development of new adhesive formulations and product enhancements. Perform laboratory testing to evaluate material properties, product performance, and stability. Analyze and interpret data, documenting results and preparing technical reports. Support scale-up and commercialization of new products, working closely with manufacturing and quality teams. Maintain an in-depth understanding of raw materials, formulation chemistry, and application methods. Collaborate with sales and technical teams to provide customer support, including troubleshooting and recommendations. Ensure compliance with safety, quality, and regulatory standards in laboratory operations. Maintain laboratory equipment, coordinate maintenance, and ensure proper documentation of experiments and findings. Stay up to date on industry trends, new technologies, and competitive products. Skills & Abilities Strong analytical and problem-solving skills with attention to detail. Hands-on experience with formulation, testing, and analytical instrumentation. Ability to interpret technical data and translate findings into actionable solutions. Excellent communication skills, both written and verbal, with the ability to work collaboratively. Strong organizational and time management skills, with the ability to manage multiple projects. Knowledge of regulatory requirements and testing protocols relevant to adhesives and electronic materials. Occasional travel to customer sites. Education & Experience Bachelor's degree in Chemistry, Chemical Engineering, or a related technical field. 2-5 years of experience in formulation chemistry, R&D, or a similar role. Experience with adhesives, coatings, or polymer-based products is highly preferred. Proficiency in MS Office (Excel, Word, PowerPoint, Outlook). Physical Requirements Prolonged periods of sitting at a desk and working on a computer. Additionally, prolonged periods of standing and working at a lab bench. Must be able to lift up to 15 pounds at times. The company is an Equal Opportunity Employer, drug free workplace, and complies with ADA regulations as applicable.

Battelle delivers when others can't. We conduct research and development, manage national laboratories, design and manufacture products and deliver critical services for our clients-whether they are a multi-national corporation, a small start-up or a government agency. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. **Job Summary** Battelle's Life Science Research is currently seeking candidates for a full time, permanent position as a **Bio-Analytical Chemist** in the Chemistry Technical Center (CTC). This position is located in **Columbus, OH.** Join our CTC Team as a Chemist, where you'll collaborate with interdisciplinary teams to conduct experiments, analyze data, and drive scientific discovery. The ideal candidate will have a strong background in analytical chemistry, proficiency in analytical instrumentation, and a passion for scientific inquiry. Your work will support our mission to protect and promote human health through advanced toxicological sciences. By upholding the highest standards of scientific integrity, you'll contribute to identifying hazardous substances and evaluating their effects on human health. This role supports research that safeguards public health, aligning with Battelle's mission to apply science and technology to solve complex global challenges. **Responsibilities** + **Sample Preparation** : + Prepare samples for analysis using techniques such as extraction, digestion, filtration, and dilution. + Ensure sample integrity and homogeneity by isolating target analytes from complex matrices. + **Analytical Testing and Data Analysis** + Perform analytical testing and characterization using HPLC, GC, GCMSD, UV-Vis, LC/MS/MS, and ICP-MS. + Determine chemical composition, identify impurities, and assess product quality. + Analyze experimental data and interpret results using scientific principles and statistical analysis. + Draw conclusions to support research findings, troubleshoot issues, and guide decision-making. + **Technical Reporting:** + Prepare technical reports and document experimental procedures, results, and conclusions. + Ensure compliance with regulatory requirements, industry standards, and internal protocols. + **Instrument Maintenance:** + Maintain analytical instruments by performing routine maintenance and troubleshooting malfunctions. + Calibrate instruments according to manufacturer specifications to ensure accuracy and reliability. + Evaluate instrument performance and monitor quality control parameters. + Implement corrective actions to address deviations and maintain analytical accuracy and precision. + **Method Development and Optimization:** + Develop and validate analytical and bioanalytical methods for qualitative and quantitative analysis. + Support research and development projects and ensure compliance with regulatory standards. + Optimize experimental conditions, instrument parameters, and data acquisition protocols. + Enhance method sensitivity, accuracy, precision, and robustness for specific applications. + **Quality Control, Compliance and Safety:** + Perform quality control of data as required. + Ensure compliance with laboratory safety procedures, GLP, and regulatory requirements (e.g., FDA, EPA, ISO). + Maintain data integrity, sample traceability, and laboratory accreditation. + **SOP Management:** + Review and update Standard Operating Procedures (SOPs). + Ensure all documentation is accurate and complete. **Key Qualifications** + Minimum requirement of bachelor's degree in chemistry with 2-5 year's experience. + Proficient in standard wet chemistry sample extraction and cleanup techniques. + Proven experience with operation, calibration, and maintenance of various analytical instruments and interpretation of data (Sciex LC/MS, GC-MSD, HPLC, ICP, ICP/MS, Watson, Analyst, Masshunter,). + Problem solving skills based on understanding of raw data. + QC experience + Proficient in Microsoft Office suite and experienced in electronic data review + U.S Citizen **Benefits: Live an Extraordinary Life** We care about your well-being, not just on the job. Battelle offers comprehensive and competitive benefits to help you live your best life. + **Balance life through a compressed work schedule** : Most of our team follows a flexible, compressed work schedule that allows for every other Friday off-giving you a dedicated day to accomplish things in your personal life without using vacation time. + **Enjoy enhanced work flexibility, including a hybrid arrangement:** You have options for where and when you work. Our Together with Flexibility model allows you to work 60% in-office and 40% remote, with Monday and Tuesday as common in-office days, dependent on team and position needs. + **Take time to recharge** : You get paid time off to support work-life balance and keep motivated. + **Prioritize wellness** : Stay healthy with medical, dental, and vision coverage with wellness incentives and benefits plus a variety of optional supplemental benefits. + **Better together** : Coverage for partners, gender-affirming care and health support, and family formation support. + **Build your financial future** : Build financial stability with an industry-leading 401(k) retirement savings plan. For most employees, we put in 5 percent whether you contribute or not, and match your contributions on top of that. + **Advance your education** : Tuition assistance is available to pursue higher education. **A Work Environment Where You Succeed** For brilliant minds in science, technology, engineering and business operations, Battelle is the place to do the greatest good by solving humanity's most pressing challenges and creating a safer, healthier and more secure world. You will have the opportunity to thrive in a culture that inspires you to: + Apply your talent to challenging and meaningful projects + Receive select funding to pursue ideas in scientific and technological discovery + Collaborate with world-class experts in an inclusive environment + Nurture and develop the next generation of scientific leaders + Give back to and improve our communities **Vaccinations & Safety Protocols** _Battelle may require employees, based on job duties, work location, and/or its clients' requirements to follow certain safety protocols and to be vaccinated against a variety of viruses, bacteria, and diseases as a condition of employment and continued employment and to provide documentation that they are fully vaccinated. If applicable, Battelle will provide reasonable accommodations based on a qualified disability or medical condition through the Americans with Disabilities Act or the Rehabilitation Act or for a sincerely held religious belief under Title VII of the Civil Rights Act of 1964 (and related state laws)._ _Battelle is an equal opportunity employer. We provide employment and opportunities for advancement, compensation, training, and growth according to individual merit, without regard to race, color, religion, sex (including pregnancy), national origin, sexual orientation, gender identity or expression, marital status, age, genetic information, disability, veteran-status veteran or military status, or any other characteristic protected under applicable Federal, state, or local law. Our goal is for each staff member to have the opportunity to grow to the limits of their abilities and to achieve personal and organizational objectives. We will support positive programs for equal treatment of all staff and full utilization of all qualified employees at all levels within Battelle._ The above statements are intended to describe the nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, activities and skills required of staff members. **No statement herein is intended to imply any authorities to commit Battelle unless special written permission is granted by Battelle's Legal Department.** For more information about our other openings, please visit ************************

KDC is a network of best-in-class custom formulators and manufacturers of color cosmetics, skincare, haircare, bath & body, fragrance, deodorant, home, health, industrial, and auto care products. KDC delivers high-touch innovation, operational excellence, and speed to market to well-known and emerging beauty, personal, and specialty companies from coast to coast. KDC has its head office in Longueuil, Québec. In addition, KDC has 10 operating facilities located throughout North America. Altogether, the company employs nearly 4,800 talented and dedicated employees in North America. About us: Kdc/one is currently hiring at our Groveport, Ohio location. As part of the kdc/one network, we are the leading best-in-class producer of beauty and personal care products! Our Groveport location is accessible with an easy commute located on RT. 33/Hamilton Rd. We offer excellent opportunities with competitive wages from entry level, semi and skilled trade positions. We have opportunities for advancement at all of our sites and are excited to have you join the kdc/one Team! General Information: The QC Chemist is responsible for the evaluation and testing of all incoming raw materials, in-process bulk, finished bulk and packaged products in accordance with all applicable standard operating procedures (SOP) and work instructions (WI). What are we looking for? * BS in chemistry or related sciences knowledge * Strong experience using various laboratory equipment and aseptic sampling techniques * SAP experience strongly preferred. * Strong English communication (both written and oral), interpersonal, and organizational skills. Benefits Include: * Competitive Wages/Salary * Health/Vision/Dental/401k/bonus potential! * 11 Paid Holidays * Paid Vacation Days * Immediate openings This position is responsible for: * Inspects, samples and tests all incoming raw materials from tanker delivery, and bulk chemical tanks, and RO water, in both a lab and warehouse environment. Manages results to ensure specifications are met according to company and customer requirements. * Prepares Certificate of Analysis (CofA) for product test results and completes product releases in the SAP system. * Conducts testing and standardization in-process bulk, finished bulk, and packaged products; and with preparing necessary reagents and equipment (such GC, HPLC, FTIR) required to complete the quality control analysis. * Assists QC management with investigations of Out of Specification (OOS) results, which may require retesting and/or resampling product. * Reviews bulk product testing results to ensure any required adjustments to the bulk are within specification, and submits recommended adjustments and corrective measures to the QC management team. * Maintains customer standards and requirements for chemicals and finished goods. * Provides recommendations to improve lab operations and assists with writing or updating departmental SOPs and WIs. * Maintains appropriate records associated with OOS or non-conformance results for bulk product and finished goods. * Assembles and calibrates scientific testing and laboratory instruments. * Performs all work in a manner that is consistent with the company's quality system and FDA good manufacturing practices, includes maintaining a clean, contaminant-free and orderly work area at all times. * Follows, promotes and enforces KDC's safety and environmental policies, practices and procedures. * Performs other duties as assigned. KDC-ONE is an equal opportunity employer and does not discriminate on the basis of race, religion, color, national origin, age, sex, gender, disability or any other characteristic protected by law. I understand that employment with KDC-ONE Company is at-will, meaning that I or KDC-ONE Company may terminate my employment at any time, or for any reason consistent with applicable state or federal law. I understand that KDC-One requires the successful completion of a drug and/or alcohol test as a condition of employment. Other details * Pay Type Hourly * Employment Indicator Indirect Apply Now * kdc/one Groveport, 4400 South Hamilton Rd, Groveport, Ohio, United States of America

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details We are building a new chemistry lab to test the products in our packaging. This Quality Control (QC) Chemist II role will be creating the required documentation needed for the lab in preparation for initiating in-house testing. This QC Chemist II will focus on method development and validation testing, as required, of products repackaged at AHP. The QC Chemist II will also assist in troubleshooting methods and OOS investigations for the chemistry lab. As time allows they will also assist in stability and release testing, as necessary, and work closely with other departments within the Quality Unit to ensure drug product meets all standards. * Ensure stability and release testing activities are compliant with FDA, DEA, other regulatory body requirements as applicable. Ensure compliance with local and corporate policies and procedures. * Perform method development and validation testing for AHP repackaged products. * Perform troubleshooting and assist with OOS investigations. * Perform stability and release testing for drug products in accordance with compendial and global requirements, as applicable. * Develop, revise, and review standard operating procedures (SOPs), work instructions (WIs), and test method documents to ensure compliance with applicable compendia and regulations. * Assist in the support of manufacturing operations including process validation, environmental monitoring, and utilities as applicable. * Perform review and release of stability and release tests for compliance to SOPs and regulatory requirements and ensure data is reported accurately. * Prepare lab reports as required. * Assist with root cause investigations for quality incidents related to chemical analysis for stability and release tests. * Maintain Quality System records and ensure completeness and accuracy. * Coordinate with department management to identify and implement compliant process improvements. * Clarify regulations, policies, and procedures to internal teams as applicable. * Coordinates with departmental leaders to develop appropriate corrective actions resulting from investigations, internal audits, and facility inspections. * Conduct follow-up checks on the effectiveness of corrective actions Performs other duties to support Quality Systems and Regulatory Affairs department as assigned. Education: * Bachelor's degree in chemistry or related field required. Experience: * Five or more years' experience within a pharmaceutical manufacturing (cGMP) laboratory environment. * Should have a working knowledge of pharmaceutical manufacturing requirements, Quality System principles (Documentation, Training, Investigations/CAPA, Change Control, etc), and global Quality Control regulations. * Should have method development and validation experience. * Experience with MasterControl or other electronic quality management system preferred. Skills & Knowledge: * Good oral, written, communication, and interpersonal skills. * Ability to develop and maintain cooperative working relationships with others. * Effectively interfaces with multiple levels of associates within the organization, including management and plant associates. * Ability to work independently. * Ability to handle a variety of tasks simultaneously. * Attention to detail. * Familiarity with concepts of electronic documentation management systems (EDMS). Work Environment: * The work environment characteristics described here are representative of those an associate may encounter while performing the essential functions of this job. * Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: * General pharmaceutical laboratory, production, and warehouse facility. The noise level in the facility is moderate. Physical & Mental Requirements: The physical demands described here are representative of those that must be met by an associate to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: * Physical activity requiring reaching, bending, kneeling, stooping, lifting, finger dexterity, grasping, feeling, repetitive motions, talking and hearing. * Ability to lift up to 50 lbs. * Visual requirement is for close vision, distance vision, peripheral vision and ability to adjust focus. * Associate is required to stand, walk (or otherwise be mobile). * Ability to deal with stressful situations as they arise. What Cencora offers We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members' ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more. For details, visit ************************************** Full time Equal Employment Opportunity Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law. The company's continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory. Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call ************ or email ****************. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned Affiliated Companies Affiliated Companies: AmerisourceBergen Drug Corporation

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details We are building a new chemistry lab to test the products in our packaging. This Quality Control (QC) Chemist II role will be creating the required documentation needed for the lab in preparation for initiating in-house testing. This QC Chemist II will focus on method development and validation testing, as required, of products repackaged at AHP. The QC Chemist II will also assist in troubleshooting methods and OOS investigations for the chemistry lab. As time allows they will also assist in stability and release testing, as necessary, and work closely with other departments within the Quality Unit to ensure drug product meets all standards. Ensure stability and release testing activities are compliant with FDA, DEA, other regulatory body requirements as applicable. Ensure compliance with local and corporate policies and procedures. Perform method development and validation testing for AHP repackaged products. Perform troubleshooting and assist with OOS investigations. Perform stability and release testing for drug products in accordance with compendial and global requirements, as applicable. Develop, revise, and review standard operating procedures (SOPs), work instructions (WIs), and test method documents to ensure compliance with applicable compendia and regulations. Assist in the support of manufacturing operations including process validation, environmental monitoring, and utilities as applicable. Perform review and release of stability and release tests for compliance to SOPs and regulatory requirements and ensure data is reported accurately. Prepare lab reports as required. Assist with root cause investigations for quality incidents related to chemical analysis for stability and release tests. Maintain Quality System records and ensure completeness and accuracy. Coordinate with department management to identify and implement compliant process improvements. Clarify regulations, policies, and procedures to internal teams as applicable. Coordinates with departmental leaders to develop appropriate corrective actions resulting from investigations, internal audits, and facility inspections. Conduct follow-up checks on the effectiveness of corrective actions Performs other duties to support Quality Systems and Regulatory Affairs department as assigned. Education: Bachelor's degree in chemistry or related field required. Experience: Five or more years' experience within a pharmaceutical manufacturing (cGMP) laboratory environment. Should have a working knowledge of pharmaceutical manufacturing requirements, Quality System principles (Documentation, Training, Investigations/CAPA, Change Control, etc), and global Quality Control regulations. Should have method development and validation experience. Experience with MasterControl or other electronic quality management system preferred. Skills & Knowledge: Good oral, written, communication, and interpersonal skills. Ability to develop and maintain cooperative working relationships with others. Effectively interfaces with multiple levels of associates within the organization, including management and plant associates. Ability to work independently. Ability to handle a variety of tasks simultaneously. Attention to detail. Familiarity with concepts of electronic documentation management systems (EDMS). Work Environment: The work environment characteristics described here are representative of those an associate may encounter while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: General pharmaceutical laboratory, production, and warehouse facility. The noise level in the facility is moderate. Physical & Mental Requirements: The physical demands described here are representative of those that must be met by an associate to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: Physical activity requiring reaching, bending, kneeling, stooping, lifting, finger dexterity, grasping, feeling, repetitive motions, talking and hearing. Ability to lift up to 50 lbs. Visual requirement is for close vision, distance vision, peripheral vision and ability to adjust focus. Associate is required to stand, walk (or otherwise be mobile). Ability to deal with stressful situations as they arise. What Cencora offers We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members' ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more. For details, visit ************************************** Full time Equal Employment Opportunity Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law. The company's continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory. Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call ************ or email ****************. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned Affiliated CompaniesAffiliated Companies: AmerisourceBergen Drug Corporation

Transcendia is a leader in custom engineered materials for critical product components in a wide range of markets and applications. The company provides deep material science expertise, outstanding customer service through broad geographic coverage and trusted product reliability. Job Summary: Provides support to R&D activities by conducting a wide range of physical and chemical testing on materials, assisting with product development activities, and providing support for product regulatory management. Job Duties: * Performs research activities in a a laboratory environment to aid in the planning, designing, and conducting of experiments. * Conducts routine maintenance and safety checks on lab equipment to ensure working order * Collects, prepares, and tests samples and records measurements or observations. * Conducts specialized tests and evaluations of materials and packaging samples in support of departmental activities including, but not limited to the following: * Tensile tests (seal strength, elongation, tensile strength, yield strength) * Material chemical characterization (FTIR) * Optical Microscopy skills * Tear resistance, impact/puncture strength * Heat seal and other package strength characterizations * May be responsible for cleaning, disinfecting, and maintaining cleanrooms and equipment. * Provides support as needed for plant and pilot line trials * Works with Supply Chain function and suppliers to maintain product regulatory data * Maintains confidentiality on development projects, tests, products, and equipment * Prepares test reports and maintains files and records * Other duties as assigned Job Qualifications: * High school diploma or general education degree (GED), plus two to four years of related experience and/or training; technical/science Associates, Bachelor's degree or technical school preferred * Up to three years experience in a manufacturing setting, * Manufacturing Lab Tech experience preferred * Proficient in Excel and Word * Must have organizational skills with an ability to prioritize and multi-task * Must possess good problem-solving skills * Ability to interact in a professional manner with employees and vendors * Ability to communicate effectively both verbally and in writing * Must be dedicated to continuous improvement * Willingness to work as team member or independently Transcendia is an equal opportunity employer and will consider all candidates for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We're looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas: Physical and Emotional Wellness Financial Wellness Support for Caregivers For a full list of our comprehensive benefits, see our website: ******************************* The Importance of the Role This is an exciting opportunity for a highly motivated and creative individual to work in a key drug discovery group in our research organization, and play a central role in applying and managing immunology and assay development studies. The successful candidate will work in the lab conducting immuno-assays to support the advancement of Gene Therapy. The candidate will closely with cross-functional teams, such as research scientific leads, research and lab operations, and program management. The individual will be responsible for creation of project plans, identifying and tracking critical path/activities, risks, contingencies, and alternatives and communicating routinely with cross-functional teams. The individual will oversee project teams in support of in-process and final project characterization, they will act as an immunogenicity SME for methods conducted internally and externally at contract research organizations. The successful candidate will manage the immunology department to support immunology research and capabilities for technological advancements. The Opportunity to Make a Difference Serve as subject matter expert on gene therapy pre-clinical development for existing and new programs. Conduct immunology assays and laboratory activities to support clinical trials and R&D studies. Conduct laboratory activities in Sarepta in-house laboratory, interacts with research, translational biology and bioanalytical groups. Ownership of a new or ongoing immunology assay to help drive pre-clinical development through stage gates and key milestones to support regulatory and clinical development. Serve as study director for clinical and non-clinical testing studies Author scientific method validation plan, testing study and validation reports Maintains compliant laboratory records, consistently and accurately documents all laboratory activities in laboratory notebooks and internal technical reports. Work in cross-functional manner to design and plan pre-clinical GT studies in collaboration with other research group and other key stakeholders. Author development reports and powerpoint slide decks, study protocols, and pre-clinical study reports to communicate ongoing activities internally and externally. Perform other related duties incidental to the work described. More about You Ph.D. with 0-3 years experience in biology or related, immunology preferred Hands-on experience with immunological techniques including ELISA, ELISpot assay, MSD, and Flow cytometry. Prior experience with human samples (PBMC) is a plus. Ability to plan and carry out experiments independently with strict adherence to laboratory methods and SOPs. Demonstrates proficient written and oral communication and presentation skills and a documented ability to troubleshoot technical issues. Experience with statistical and computer productivity software (i.e. Word, Excel, Outlook, etc.). Desire to work in a high-functioning, collaborative team Desire to work in a dynamic, fast-paced team environment and to make a difference in the lives of people through our innovative medicines Recognized by former peers, colleagues, managers and direct reports for attributes congruent with Sarepta Values: Drive, Excellence, Resilience, Teamwork, Innovation and Compassion Due to the nature of work, schedule includes occasional evening and weekend hours. What Now? We're always looking for solution-oriented, critical thinkers. So, if you're comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply. #LI-Onsite#LI-TG1This position requires work on site at one of Sarepta's facilities in the United States.The targeted salary range for this position is $95,200 - $119,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta's compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity.Candidates must be authorized to work in the U.S.Sarepta Therapeutics offers a competitive compensation and benefit package.Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.

Job Posting End Date 04-08-2025 Please note the job posting will close on the day before the posting end date Chemists serve in support of power plants, energy delivery, and third party interests, performing a variety of independent, non-routine, and more complex quantitative analyses using sophisticated laboratory instrumentation. Performs, under direction, responsibilities which include, but are not limited to, the sampling techniques, preparation, and chemical analysis of environmental, industrial hygiene, and industrial/manufacturing samples. Demonstrates, under direction, the skills to evaluate analytical results and modify procedures within established limits based on sample matrix and quality control trends and the performance of analytical instruments, to schedule work based on current and anticipated workloads and deadlines, and to participate as an integral part of problem solving and process improvement teams as assigned Job Description ESSENTIAL JOB FUNCTIONS: 1) Essential Function: 1. Chemists perform daily operations for chemical analyses, adhere to policies and procedures, document daily operations and activities, and perform problem solving and decision making within the department. 2) Perform daily operations for chemical analyses: 1. Assists in the development of environmental, health, and safety policies for everyday tasks. 2. Performs routine analytical activities with minimal direction form higher level employees. 3. Uses scheduling techniques for work management. 4. Coordinates multiple analytical techniques and the work of technicians. 5. Analyzes asbestos by bulk analysis or fiber identification which is conducted by preparing material and viewed under a microscope using Polarized Light Microscopy (PLM). 6. Analyzes asbestos-airborne fiber count (NIOSH 7400). This analysis may include testing air samples for asbestos and other fibers by Phase Contrast Microscopy (PCM). 3) Adherence to policies and procedures: 1. Follows policies, practices, standards, and rules of the company and those regulations and procedures required by external agencies. 2. Understands and practices safe laboratory procedures. 3. Ensures work quantity and quality by requiring strict adherence to NIOSH methods and standard operating procedures for respirable crystalline silica, total and respirable dust, lead base paint, welding fumes, respirable metals, and hexavalent chromium. 4. Ensures work quantity and quality by requiring strict adherence to EPA (and EPA-approved) methods and standard operating procedures for chemical constituents in water, wastewater, waste, solid, oil, and process samples. 5. Ensures work quantity and quality by requiring strict adherence to ASTM (and ASTM-modified) or AEP-developed methods and standard operating procedures for chemical constituents, identification, and characterization of liquid, solid, organic, and airborne process samples. 6. Ensures work quantity and quality by requiring strict adherence to NIOSH methods, EPA (and EPA-approved) and ASTM (and ASTM-modified) standard operating procedures as appropriate. 4) Documents daily operations and activities: 1. Demonstrates ability to prepare and issue routine analytical reports, verbal and written skills for effective communication of analytical data and chemical information. 2. Develops, reviews, or presents routine technical reports clearly, concisely, and effectively. 3. Demonstrates ability to extrapolate beyond known facts to reach logical conclusions. 4. Prepares lab reports for submittal to customers and prepares reports on laboratory activities. 5. Provides basic training and guidance to lower level employees. Effectively trains other employees. 5) Problem solving and decision making within department: 1. Identifies and initiates solutions to routine problems which usually require additional definition or clarification before analysis can begin. 2. Demonstrates ability to identify problems that are beyond the normal routine. 3. Makes decisions, subject to review within established policies and procedures, concerning the validity of analytical test data. 4. Demonstrates proficiency in application and use of economic analysis techniques. 5. Initiates priority changes when analytical objectives are not met. MINIMUM REQUIREMENTS: Education requirements are listed below: Bachelor's degree in chemistry, related sciences, industrial hygiene, or engineering field. Work Experience requirement listed below: Minimum four years' experience in related field. Required License(s)/Certification(s) are listed below: Valid state driver's license. OTHER REQUIREMENTS: Physical demand level is Sedentary These are additional expectations for the job and could include specific work experience, license / certifications, preemployment testing, expectations about travel, shift work, etc. 1. Obtain license/certifications required if assigned to industrial hygiene analyses, but can be obtained after employment. 2. Actively seeks information to increase technical knowledge in additional areas of the laboratory. 3. Develop awareness of clients' needs in accordance with applicable standards. 4. Understand AEP's organizational structure and the specific roles and responsibilities of their individual organizational units. 5. Strong oral and written communication skills. 6. Organizational, planning, and analytical knowledge and experience. 7. Develop skills for improved decision making, for efficient organization of work to meet deadlines, and for effective troubleshooting of analytical procedures and instrumentation. 8. Demonstrate the highest standards of ethical behavior and support the Company's Corporate Compliance Policy and national standards. 9. Ability to work around hazardous chemical and potentially contaminated matrices. PHYSICAL DEMANDS: List physical demands required for this job, but not limited to. Compensation Data Compensation Grade: SP20-006 Compensation Range: $72,380.00-90,474.50 USD It is hereby reaffirmed that it is the policy of American Electric Power (AEP) to provide Equal Employment Opportunity in all respects of the employer-employee relationship including recruiting, hiring, upgrading and promotion, conditions and privileges of employment, company sponsored training programs, educational assistance, social and recreational programs, compensation, benefits, transfers, discipline, layoffs and termination of employment to all employees and applicants without discrimination because of race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, veteran or military status, disability, genetic information, or any other basis prohibited by applicable law. When required by law, we might record certain information or applicants for employment may be invited to voluntarily disclose protected characteristics.

** Chemist II **Pay Rate** : $65,100 - $86,800 _Multiple factors, including Individual experience, skills and abilities will determine where an employee is ultimately placed in the pay range. Variable pay may provide additional opportunities for financial awards. This job is eligible to participate in IP's annual and long-term incentive plans._ **Category/Shift** : Salaried Full-Time **Physical Location:** 13307 Industrial Parkway Marysville, OH 43040 **The Job You Will Perform:** The Chemist II position is in the International Paper ink lab, which is part of the Enhanced Graphics division within the Custom Packaging and Display group. IP Ink supplies water based flexographic printing inks and related services to corrugated packaging converters, bag manufacturers, and other flexographic printers within International Paper and to external customers. The ink lab provides color matching, technical service, formulation, and research and development services to our customers in order to help them produce high quality packaging products. The Chemist II reports to the Lab Manager. + Responsible for product improvement, new product development, raw material evaluation and other lab functions as necessary + Coordinate and plan projects with Lab Manager and Chemist III + Conduct applicable lab testing, maintain project files and reports + Maintain a Laboratory Notebook + Maintains test chemical inventory. + Operate all laboratory testing equipment. + Identify proper vehicle system for given application. + Identify/recognize a customer's environmental restrictions and formulate accordingly. + Make proper anilox selection per machine requirements. + Provide color match and customer service support as needed + Conducts Chemical Approval process for new items + Schedules and participates in field-testing for new and/or improved products. May involve offsite travel + Responsible for specific manufacturing and R&D laboratory instrument maintenance and/or repair. + Participates in training and continuing education activities related to the job + Creates procedures and related SOP's for manufacturing and R&D. + Completes all required tasks and responsibilities while adhering to Specialty Products Safety Standards. + Initiates and implements cost saving projects. + All other duties assigned. + Participates in IPs ongoing 5S program + Generate best color match within cost constraints. + Works directly with vendors on R&D and complaint resolution. **The Qualifications, Skills and Knowledge You Will Bring:** + 4-year degree in Chemistry or related discipline, and 2+ years' experience in ink formulation/testing or related industry is preferred. + Industry related experience is desirable: Ink, paint, printing, or coatings. + Ability to travel up to 25%. + Previous experience with color or color matching and knowledge of industrial batch process and equipment is desired. + Strong technical/customer support skills. You will be required to work closely with sales, technical service and our customer base in a wide array of situations + Proficient in Microsoft Office applications (Word, Excel) + Ability to self-start, remain calm in stressful situations, and have a positive outlook are beneficial to this position. + Proficiency with Batchmaster Enterprise + Ability to communicate well verbally, and across electronic platforms such as e-mail, text, and instant messaging **The Benefits You Will Enjoy:** International Paper offers a benefits package that includes health, welfare and retirement plans including Medical, Dental, Life insurance, Flexible Spending Accounts, Short-term and Long-term Disability, 401(k), Company-funded retirement contributions, Paid Time Off, Education & Development (including Tuition Reimbursement), Student Loan Repayment Assistance, and Voluntary Benefits including insurance for home, auto, vision and pets. **The Career You Will Build:** Sales and Leadership training, promotional opportunities within a global company **The Impact You Will Make:** We continue to build a better future for people, the planet, and our company! IP has been a good steward of sustainable practices across communities around the world for more than 125 years. Join our team and you'll see why our team members say they're **Proud to be IP** . **The Culture You Will Experience:** International Paper promotes employee well-being by providing safe, caring and inclusive workplaces. We have team members all around the world with diverse backgrounds, experiences, and perspectives. These are our strengths. We are committed to creating a culture where all individuals are respected, valued, engaged and have an opportunity to do their best work every day. We invite you to bring your uniqueness, creativity, talents, experiences, and safety mindset to be a part of our increasingly inclusive and diverse culture. **The Company You Will Join:** International Paper (NYSE: IP) is a global producer of sustainable packaging, pulp and other fiber-based products, and one of the world's largest recyclers. Headquartered in Memphis, Tenn., we employ approximately 39,000 colleagues globally who are committed to creating what's next. We serve customers worldwide, with manufacturing operations in North America, Latin America, North Africa and Europe. Net sales for 2023 were $18.9 billion. Additional information can be found by visiting internationalpaper.com. _International Paper is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law._ _International Paper complies with federal and state disability laws and makes reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact_ _reasonable.accommodations@ipaper.com_ _or **************_ Share this job: Location: Marysville, OH, US, 43040 Category: Technology Date: Mar 26, 2025 If you are not finding suitable opportunities, please click below to join our talent community!

INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT ************** TO SET UP A PHONE INTERVIEW!Job Description: + Role Focus: Sample preparation, test preparation and execution, data analysis, and project support. + Methods Used: Optical and scanning electron microscopy, electron backscatter diffraction (EBSD), X-ray diffraction, hardness, tensile/yield strength testing, and Keyence image analysis. Responsibilities: + Prepare samples by dissecting sputtering targets, sawing, cutting, and polishing. + Perform laboratory testing, including microscope analysis, chemical testing, and physical testing (hardness, tensile, strength). + Conduct X-ray diffractions. + Set up equipment, assemblies, and experiments. + Collect data per work instructions or experimental plans. + Prepare reports with data and analysis. + Maintain a safe and clean work environment. Must Have Qualifications: + Education: Bachelor's degree in Chemistry, Materials Science, or a similar field. Candidates with an Associate's Degree and relevant experience may also be considered. + Experience: Industry experience is a PLUS! Pay and Benefits The pay range for this position is $20.00 - $23.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision- Critical Illness, Accident, and Hospital- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available- Life Insurance (Voluntary Life & AD&D for the employee and dependents)- Short and long-term disability- Health Spending Account (HSA)- Transportation benefits- Employee Assistance Program- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Grove City,OH. Application Deadline This position is anticipated to close on Apr 14, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.