Chemist Jobs in Pocono, PA

Job Title: Chemist II An industry leading pharmaceutical manufacturing firm is seeking a Chemist II to conduct routine laboratory testing for raw materials, stability, and finished pharmaceutical products in a high-throughput quality control lab. Key tests include HPLC, assays, dissolution, and Karl Fischer (KF) analysis. Key Responsibilities: Perform analytical testing on raw materials, in-process materials, stability samples, and finished products according to test methods, SOPs, or USP procedures. Conduct wet chemistry tests per USP compendia, including assays, preservative content, LOD, ROI, water content, and identification tests. Perform complex chemistry testing, including related substances/impurities, residual solvents, dissolution, disintegration, heavy metals, etc. Operate analytical instruments such as HPLC, GC, KF titrators, FT-IR, UV/Vis spectrophotometer, and others during routine testing. Assist in preparing technical documentation, including test methods, SOPs, analytical reports, and change controls. Troubleshoot technical issues with guidance from the group leader. Review laboratory data and assist in investigations. Train lab personnel as needed and ensure compliance with GMP, GLP, and EHS standards. Report deviations and assist in corrective actions to ensure data integrity. Comply with DEA and site requirements for handling and disposing of controlled substances. Requirements: Bachelor's/Master's degree in Chemistry, Pharmaceutical Sciences, or related field with 4-7 years of pharmaceutical lab experience. Strong knowledge of solid dosage forms and testing methods (HPLC, assays, dissolution, KF). Experience with Empower chromatography software is a plus. Excellent communication skills and ability to work in a team. Proficient in general computer applications (Word, Excel, databases). Commitment to safety and environmental standards. Physical Requirements: Sedentary role; occasional light lifting (up to 10 lbs) and walking. Requires close visual acuity for data analysis, inspection, and measurement. Use of company-approved PAPR as needed. This role offers an opportunity to work in a dynamic laboratory environment supporting the production of specialty pharmaceutical products.

FedChem, Inc., a subsidiary of FPC International, Inc. is seeking a motivated, technically savvy, and strong problem solver to join our team. In this role, the Jr. Research Chemist is responsible for the participation, testing, and development of Kolate products. This position will develop an in-depth understanding of FedChem's products and their chemistries, as well as proficiency in testing chemical raw materials, intermediate products, and finished goods. Our Culture: Entrepreneurial, family-friendly, and great work-life balance. New ideas are encouraged. Definitely an opportunity to make an impact! Very collaborative environment. Location: 275 Keystone Dr., Bethlehem, PA (in-office) Work Schedule: Day shift (M-F, 8 hours/day) Team Dynamics: On a team with other key contributors - Research Chemists, Operations & Sales. The Ideal Candidate will have: Experience in basic lab instrumentation, solid documentation skills and ability to work and communicate well at all levels within the organization. Benefits: We're a small company but have all the 'big company' benefits to offer including a 401k match, medical, dental, vision, long & short term disability, life insurance, accidental, etc. We have 10 paid holidays that start immediately and a generous PTO plan that is based off years of service. We believe in investing in employee growth and as such offer a very generous tuition reimbursement program, online learning, coaching and other trainings as it relates to the role. What you'll be doing: Conducts experiments under the guidance of senior researchers. Maintains accurate and detailed records of experimental procedures and results. Collaborates with cross-functional teams to support research projects and contribute to problem-solving efforts. Assists in the evaluation of new and existing products and customer formulations for performance, cost and efficiency. Stays current on relevant scientific literature and developments in the field. Learns and performs proprietary and standard methods of physical testing and chemical analyses. Participates in onsite activities such as ISO, Safety Programs, special projects, assisting with training, etc. Background you'll need: Must have a Bachelor's degree in Chemistry or a closely related field. Must have a minimum of one to three (1-3) years of experience in a chemical laboratory setting. Experience in GC, FTIR, Flashpoint tester, Refractometer, Karl Fischer analyzer, Particle Size analyzer and wet chemistry methods. FedChem, Inc. offers benefits, competitive salary, bonus potential, generous vacation, paid holidays, and 401K benefits. FedChem, Inc. is an equal opportunity employer. FedChem, LLC. is a global leader in the production of aluminum organic-based products for use in the grease, ink and other industries? The quality of our Manalox ink gellants and Kolate grease products has helped establish FedChem, LLC. as a leading provider of aluminum organic-based solutions for the chemical industry. Headquartered in Bethlehem, PA, FedChem, LLC. is a wholly owned subsidiary of FPC International, Inc. Find out more at our parent company website: ************************ Why apply to this role: Ability to have a great work/life balance and make an impact with a collaborative team. We encourage employee growth and welcome new ideas as we're an entrepreneurial company!

Primary Duties & Responsibilities Performs tasks related to wafer inspection and characterization in accordance with instructions from the R&D Team. These tasks include cleaning and inspection of wafers, running metrology tools for wafer surface and defect characterization. Monitors, collects and reports data from several advanced characterization and metrology tools, participates in gauge R&R exercises, performs basic data analysis under the guidance of engineers. Maintains accurate records in accordance with procedures. Participates in the maintenance of metrology equipment. Participates in troubleshooting of equipment, identifies causes and participates in in-house equipment repairs. Supports inventories of spare parts and materials. Keeps materials and work areas organized and clean. Supports the development and evolution of operating procedures and assists in training Participates in FMEA activities. Follows all health, safety, environmental and ergonomic requirements, regulations and procedures Education & Experience Associates Degree or Bachelor's degree in an engineering or science discipline is desirable. Hands-on experience in a technical field Exposure to a technological process, equipment maintenance, measurements and data collection are desirable Computer literate. Experience with Microsoft Word, Excel, Outlook, PowerPoint, Email and Internet. Skills Must be technically inclined with good mechanical skills. Must be well organized and able to perform several tasks in parallel. Must be computer-literate to operate computer-controlled equipment and make data entry. Ability to communicate well ITAR compliance requirement: Individual must be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3). Working Conditions Normal working hour 9-5; however, must be prepared to work flexible hours, evenings and weekends if needed, as a part of R&D work schedule. Physical Requirements Ability to work in a Cleanroom environment Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. 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. If you need assistance or an accommodation due to a disability, you may contact us at ****************************** .

Do you want to take responsibility and make a difference with your work? With your expertise, we can achieve great goals together. We are WACKER - Reliable. Determined. Ambitious. As one of the world's most research-intensive chemical companies, we've been making countless products that are an integral part of your everyday life possible for over 100 years. From vegan food to resource-efficient buildings to solar cells, we develop sustainable solutions that change the future. To strengthen our team in Allentown, we are looking for you as a(n) Sr. Polymer Synthesis Chemist - Emulsion Polymerization. This is Us: You know us. You just didn't know it. WACKER is a global chemical manufacturer that prides itself on "Creating Tomorrow's Solutions". WACKER materials are so versatile and adaptable, they have virtually unlimited applications just about anywhere imaginable, making WACKER an integral part of daily life. Whether it's protecting buildings from the elements, a tube of toothpaste, a cell phone, airbags, or cosmetics, people from all over the world come into contact each day with our products and achievements. We are looking for capable, innovative, and enthusiastic achievers to join our team and grow with us. We are currently seeking a Sr. Polymer Synthesis Chemist - Emulsion Polymerization at the site in Allentown, PA. What you will do: The Sr. Polymer Synthesis Chemist - Emulsion Polymerization will develop new products and technologies that enable both growth as well as strengthen and defend the existing business position. In addition, this role will leverage core technology to develop offerings that provide long term performance and/or economic advantage in the marketplace, as well as serve as the dispersion chemistry expert for the purposes of safety, plant operation, raw material strategy, quality, and regulatory. The Sr. Polymer Synthesis Chemist - Emulsion Polymerization will also provide training for junior scientists/engineers, sales, purchasing, and manufacturing personnel, share knowledge of analytical chemistry related to dispersions to ensure that adequate analytical capabilities and methods exist to support research and manufacturing, especially related to product quality, and develop and maintain intellectual property to strengthen the overall business position. Lastly, this role will monitor industry technology trends to understand competitive positions, identify future opportunities where core technologies can be leveraged to create sustainable market advantage, supervise the staff and operation of the research laboratories, and ensure the safe operation of the laboratories as well as maximize the impact of technology has on meeting the overall objectives of the business. * Develop new products and technologies via planning and execution of projects and analysis and interpretation of data. * Provide manufacturing support to improve plant safety, quality, efficiency, etc. * Supervise and train technical staff and coordinate efforts to achieve objectives in an optimal fashion. * Maintain the excellent safety performance of the research labs, as well as provide chemistry related safety input to manufacturing. * Establish intellectual asset protection for the products and technologies developed and keep current on IP developments both internally and with competitors What we need from you: * Master's degree in chemistry, polymer science, material science or engineering. PhD preferred. * Minimum of 5 years relevant experience. * Detailed knowledge of polymer chemistry (including both polymerization and structure property aspects of the science) is necessary. * Knowledge of the raw materials used to manufacture dispersions (from both a chemistry and economic perspective) is needed. * Understanding of the various end use markets served, as well as knowledge of the industry. * Knowledge of analytical chemistry in general and as it specifically relates to polymer chemistry is needed * Understanding of regulatory matters that impact R&D, manufacturing and the end use markets served is also required. * Knowledge of the practice of intellectual property protection is necessary. * The ability to translate an idea into a viable commercial product is essential. * The ability to communicate effectively with a wide range of individuals, both on the technical side as well as the commercial side, is necessary. * The ability to effectively supervise and train exempt and non-exempt staff is preferred. * Ability to travel (possibly some international) less than 10% of the time. What do we offer? WACKER is an equal opportunity employer committed to diversity, equity, inclusion, and sustainability. We are innovators, researchers, and pioneers and we believe that our individual differences are our collective strength. We foster an inclusive environment that promotes individuality, celebrates diversity, and builds cohesive teams. Together, we create exceptional value for our employees, our customers, and our communities by creating a culture of inclusion and equity that enables, empowers, and values our diverse contributions. WACKER strives to reward its employees in a fair and equitable manner. Our Total Rewards Package considers employee wellbeing and is comprised of compensation, benefits, work-life balance, performance & recognition, and career development. * Compensation and Incentive plans * Medical, Dental, and Vision Insurance effective day 1 * Paid Time Off in addition to personal days and holidays * Paid parental leave * Wellbeing fund * Flexible hybrid work arrangements * 401(k) with company match * Education Assistance Program * Career development and advancement opportunities * Support for Community Involvement We are looking forward to your online application at *************** Reference Code: 29156 #IND123 #LI-KM1 The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. A minimum requirement for this US-based position is the ability to work legally in the United States on a permanent unrestricted basis. Visa sponsorship is not available for this position, including for any type of US permanent residency (e.g., for a green card). WACKER is proud to be an Equal Opportunity/Affirmative Action Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class.

Job Title: Production / Process Chemist Reports To: Director of Quality Control & Product Development Department: Production (Reaction Distillation) Summary: Plans the production, monitors the progress, and troubleshoots the processes associated with the Reaction Distillation area. In conjunction, oversees the process development and small-scale production with support from a Lab Technician. Duties and Responsibilities include the following. Other duties may be assigned. In conjunction with the Planning Department, recommend and in turn schedule the production for all products that are manufactured via chemical Reactions and / or Distillation in the designated equipment. Supported by an analytical and quality team, monitor the progress of the reactions and / or distillation to ensure the process meets the quality and timeliness of the established standards. Utilizing the support of an Established Process Development team, develop processes that will improve on established products and in conjunction with our commercial team, In coordination with the Commercial Team, assists in the development of processes for new products and supervises the progress of these processes with the Process Development Team. Evaluates production batches against established product standards and specifications and modifies as needed. Directs, coordinates, and advises production personnel coordinating all three shifts accordingly in the course of scheduling the production, monitoring the progress of the processes, and making the necessary adjustments conditions as needed. Coordinate's production activities between all three (3) shifts. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Experience in a chemical processing environment including: interacting with production personnel; developing and troubleshooting chemical processes; an awareness of safety protocols while working with chemicals under various conditions (pressure and temperature) Must have the ability to multi-task and work in a fast-paced environment. Education/Experience: Bachelor's degree in Chemistry or related field such as Chemical Engineering from a four-year college or university is required. 5 to 10 years of experience is preferred, however, all candidates with strong mechanical aptitude, a solid background in Chemistry and relevant experience will be considered. Language Ability: Demonstrated ability to make successful presentations to individuals and/or groups at all levels of an organization. Excellent written and verbal communication skills. Ability to deal effectively with a variety of individuals at all organizational levels. Ability to read, analyze and interpret general business periodicals, professional journals, technical procedures or government regulations. Ability to write reports, business correspondence and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers and the general public. Math Ability: Candidate must be able to calculate reaction stoichiometric quantities, percent yields and interpret GC plots to determine the reaction status or nature of reaction purity. Reasoning Ability: Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Computer Skills: To perform this job successfully, an individual should have basic computer skills and knowledge of how to use Office 365, develop spreadsheets, and ERP and Planning Systems, , inventory software and contact management systems. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly exposed to fumes or airborne particles. The employee is frequently exposed to work near moving mechanical parts and chemicals pertinent to the processes and may be occasionally exposed to allergens. The noise level in the work environment is usually moderate. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use hands; reach with hands and arms and talk or hear. The employee is frequently required to stand; walk and sit. The employee is occasionally required to climb stairs balance and stoop, kneel, crouch, or crawl.

Job Title: Entry-Level ChemistJob Description We are seeking an Entry-Level Chemist to join our dynamic team. You will be a key contributor within the laboratory, focusing on safety, maintenance, operation, and quality assurance. This role involves preparing and analyzing samples and solutions, performing sample preparation for metals analysis, and maintaining laboratory equipment and supplies. This is an excellent opportunity for a recent chemistry graduate to grow and develop their skills in a supportive and innovative environment. Responsibilities + Work under immediate supervision. + Contribute to laboratory safety, maintenance, operation, and quality assurance. + Ensure the lab is stocked with appropriate chemicals and supplies. + Prepare samples and solutions, including volumetric and gravimetric solutions. + Accurately prepare samples, standards, and solutions for analysis, including basic and advanced sample extractions. + Perform sample preparation for metals analysis using acid digestion and microwave-assisted digestion. + Prepare samples and titration units for various titration methods. + Set up, adjust, and operate basic laboratory equipment following defined methods in support of projects within the trace metals and titrations laboratories. + Perform general lab housekeeping, including analytical waste disposal, cleaning glassware, and ordering supplies as needed. Essential Skills + Bachelor's degree in chemistry, biochemistry, general sciences, or chemical engineering. + Experience with HPLC, wet chemistry, ion chromatography, or ICP. + Experience in research and analysis, lab techniques, mass spectrometry, or GCMS. Additional Skills & Qualifications + Experience as a chemist, ideally with a year of hands-on experience. + Strong analytical and problem-solving skills. + Ability to work independently and as part of a team. + Willingness to ask questions and continuously learn and grow as a scientist. Work Environment The company fosters a culture of continuous learning and growth. The role is located in the west part of Allentown, and you will be part of a team of about 40 employees. The work schedule is Monday to Friday, with flexible hours between 7:00 am - 4:00 pm, 8:00 am - 5:00 pm, or 9:00 am - 6:00 pm. This is a first-shift position in a supportive environment that encourages development and innovation. Pay and Benefits The pay range for this position is $24.00 - $28.00/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 ALLENTOWN,PA. Application Deadline This position is anticipated to close on Apr 25, 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.

About Us Queens Carbon's mission is to build a sustainable future by eliminating deep-rooted CO2 emissions in industrial manufacturing and beyond. Backed by Breakthrough Energy Fellows, we're developing a novel process that dramatically reduces the energy needed to extract and capture CO2 from carbonate minerals. This low energy solution for carbonate processing creates a commercially viable path for widespread carbon capture projects and carbon neutral cement production. At scale, this technology will enable gigaton-scale reductions in industrial CO2 emissions via avoidance and capture routes. Our team is united behind the idea that preventing climate change is the single most important task of this generation. If you are excited about cutting edge science, saving the environment, and want to have fun while doing it, join us! Position Overview As a Lab Technician at Queens Carbon, you will operate testing machinery and lab testing equipment to characterize the physical properties and performance of materials that are used in cement manufacturing and the performance of products made using Queens Carbon's processes. The process includes following procedures for sample preparation according to either ASTM standards or Queens Carbon specific standard operating procedures. The technician is also tasked with maintaining the testing equipment to ensure it is operating according to either manufacturer's specifications or according to required standardized testing requirements. Lab Technicians have direct contact with Scientists and Engineers by reporting the results of testing or reporting observations of specimen performance. Roles and Responsibilities Manage material testing workflow from sample submission through testing completion. Accurately record testing results via database management. Follow SOPs to operate and maintain laboratory testing equipment and machinery. Import testing data to graphing programs for analysis by R&D team. Manage inventory of lab consumables. Work with the lab team to brainstorm improvements to our technology. Comply with all Health, Safety and Environmental policies and procedures. Requirements The job is performed in a hands-on work environment. The employee must have the ability to sit, stand, walk and lift 35 pounds unassisted or more than 35 pounds assisted. The employee must be able to communicate well in both verbal and written means and use fine motor skills to operate a computer, make measurements and control equipment/machinery. At least 1 year of research experience in an academic or industrial setting. Bachelor's Degree in Engineering or Applied Science disciplines Ability to work full time and in person at our lab in Pine Brook NJ. Strong problem-solving skills, the ability to learn quickly, and the propensity to tackle new problems. A great team-focused attitude, and a willingness to teach and learn from others. A desire to save the planet, and an interest in becoming a part of the growing group of climate change innovators. These requirements are not set in cement, so if you're passionate about this role and think you'd be a great fit, please reach out! Benefits and Salary A competitive salary Equity in the company Insurance options including health, dental, vision, life, and 401k. A friendly time-off policy that encourages a healthy work-life balance. Company-wide hiking retreat on Earth Day Cool company swag :) We're Committed to Diversity Queens Carbon is committed to building a diverse team and is home to an inclusive culture. We are an equal opportunity employer, and we strive to include a variety of voices in our team that can provide different perspectives. We do not discriminate based on race, religion, ethnicity, gender, sexuality, disability status, age, or veteran status.

Primary Duties & Responsibilities * Performs tasks related to wafer inspection and characterization in accordance with instructions from the R&D Team. These tasks include cleaning and inspection of wafers, running metrology tools for wafer surface and defect characterization. * Monitors, collects and reports data from several advanced characterization and metrology tools, participates in gauge R&R exercises, performs basic data analysis under the guidance of engineers. Maintains accurate records in accordance with procedures. * Participates in the maintenance of metrology equipment. Participates in troubleshooting of equipment, identifies causes and participates in in-house equipment repairs. * Supports inventories of spare parts and materials. Keeps materials and work areas organized and clean. * Supports the development and evolution of operating procedures and assists in training * Participates in FMEA activities. * Follows all health, safety, environmental and ergonomic requirements, regulations and procedures Education & Experience * Associates Degree or Bachelor's degree in an engineering or science discipline is desirable. * Hands-on experience in a technical field * Exposure to a technological process, equipment maintenance, measurements and data collection are desirable * Computer literate. Experience with Microsoft Word, Excel, Outlook, PowerPoint, Email and Internet. Skills * Must be technically inclined with good mechanical skills. * Must be well organized and able to perform several tasks in parallel. * Must be computer-literate to operate computer-controlled equipment and make data entry. * Ability to communicate well * ITAR compliance requirement: Individual must be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3). Working Conditions Normal working hour 9-5; however, must be prepared to work flexible hours, evenings and weekends if needed, as a part of R&D work schedule. Physical Requirements Ability to work in a Cleanroom environment Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. 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. If you need assistance or an accommodation due to a disability, you may contact us at ******************************.

Business: Critical Care Department: Quality Control Schedule: 7:00pm-7:30am Perform testing on in-process material, bulk drug substance, finished drug product, and stabilities in support of production, packing release, R&D and regulatory filings. Key Stakeholders: Internal Cross Functional teams in Plant, Teamwork Key Stakeholders: External Auditor Reporting Structure Directly reports to Quality Control Lab Supervisor Essential Duties and Responsibilities * Perform analytical testing and release of in-process material, bulk drug substance, finished drug product, and stability sample * Sampling, inspection and testing of raw materials and packaging components upon receipt * This includes proper documentation of all work according to cGMP * Responsible for Sampling of Bulk API and Bulk drums (API and Raw material) for analysis by QC * Perform Calibration and minor troubleshooting on select laboratory equipment including GC, UV/Vis, IR, Potentiometer, Refractometer, Karl Fischer, Density meter and ICP/MS (with appropriate training) * Perform minor maintenance on GC equipment when necessary * Perform daily general duties in a proper functioning QC lab like: Balance checks, glassware washing, gas cylinder changes, temperature record checks, verify inventory supplies etc * Assist other chemists in completing quality laboratory investigations in response to out of specification, apparent failure or questionable results or in response to a lab deviation * Peer Review of raw data of initial analyst in order to release material in a timely fashion * Assist Lab Coordinator with Stability put-ups or take-outs when necessary due to large volume of samples Key Competencies (knowledge, skills and abilities every person must possess to be successful) * Critical Thinking - using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems * Excellent customer service skills and professional demeanor at all times to interface effectively with all internal and external customers * Excellent verbal and written communication skills * Creative and able to present various solutions * Energetic, enthusiastic and motivational disposition * Maintain confidentiality * Coaching skills Education / Experience * Bachelor's Degree in Science or Associates Degree * 3+ plus years of experience * Understand chemical processes and reactions * Awareness on cGMP, quality and safety norms and requirements * Usage of technology tools such as SAP, MS office, Ensur, Openlab, LabX General Oversight and Direction: Receives moderate to limited supervision working from objectives set by Manager. Employee organizes and carries out most assignments in accordance with standard practices, instructions or previous training. Employee handles some situations independently. Equal Employment Opportunity Piramal Critical Care is committed to Equal Employment Opportunity. It is the policy of the Company to encourage and support equal employment opportunity for all associates and applicants without regard to age, sex, race, color, ancestry, religious creed, national origin, pregnancy, physical or mental disability, medical condition, marital status, political affiliation, sexual orientation, disabled veteran or Vietnam Era Veteran Status. Americans with Disabilities Act Applicants as well as employees who are, or become, disabled must be able to perform the essential job functions either unaided or with reasonable accommodation. The organization shall determine reasonable accommodation on a case-by-case basis in accordance with applicable law. Employee Job Responsibilities You are expected to follow all policies, procedures and guidelines, conducting yourself in ways that protect the interests and safety of all employees and the company.

Business: Critical Care Department: Quality Control Schedule: 7:00pm-7:30am Perform testing on in-process material, bulk drug substance, finished drug product, and stabilities in support of production, packing release, R&D and regulatory filings. Key Stakeholders: Internal Cross Functional teams in Plant, Teamwork Key Stakeholders: External Auditor Reporting Structure Directly reports to Quality Control Lab Supervisor Essential Duties and Responsibilities Perform analytical testing and release of in-process material, bulk drug substance, finished drug product, and stability sample Sampling, inspection and testing of raw materials and packaging components upon receipt This includes proper documentation of all work according to cGMP Responsible for Sampling of Bulk API and Bulk drums (API and Raw material) for analysis by QC Perform Calibration and minor troubleshooting on select laboratory equipment including GC, UV/Vis, IR, Potentiometer, Refractometer, Karl Fischer, Density meter and ICP/MS (with appropriate training) Perform minor maintenance on GC equipment when necessary Perform daily general duties in a proper functioning QC lab like: Balance checks, glassware washing, gas cylinder changes, temperature record checks, verify inventory supplies etc Assist other chemists in completing quality laboratory investigations in response to out of specification, apparent failure or questionable results or in response to a lab deviation Peer Review of raw data of initial analyst in order to release material in a timely fashion Assist Lab Coordinator with Stability put-ups or take-outs when necessary due to large volume of samples Key Competencies (knowledge, skills and abilities every person must possess to be successful) Critical Thinking - using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems Excellent customer service skills and professional demeanor at all times to interface effectively with all internal and external customers Excellent verbal and written communication skills Creative and able to present various solutions Energetic, enthusiastic and motivational disposition Maintain confidentiality Coaching skills Education / Experience Bachelor's Degree in Science or Associates Degree 3+ plus years of experience Understand chemical processes and reactions Awareness on cGMP, quality and safety norms and requirements Usage of technology tools such as SAP, MS office, Ensur, Openlab, LabX General Oversight and Direction: Receives moderate to limited supervision working from objectives set by Manager. Employee organizes and carries out most assignments in accordance with standard practices, instructions or previous training. Employee handles some situations independently. Equal Employment Opportunity Piramal Critical Care is committed to Equal Employment Opportunity. It is the policy of the Company to encourage and support equal employment opportunity for all associates and applicants without regard to age, sex, race, color, ancestry, religious creed, national origin, pregnancy, physical or mental disability, medical condition, marital status, political affiliation, sexual orientation, disabled veteran or Vietnam Era Veteran Status. Americans with Disabilities Act Applicants as well as employees who are, or become, disabled must be able to perform the essential job functions either unaided or with reasonable accommodation. The organization shall determine reasonable accommodation on a case-by-case basis in accordance with applicable law. Employee Job Responsibilities You are expected to follow all policies, procedures and guidelines, conducting yourself in ways that protect the interests and safety of all employees and the company.

Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Pathogen Lab Analyst to join our growing team! Job Summary: Perform analytical and microbiological testing of food products, ingredients, and environmentals. The position performs the application and evaluation of approved microbiological techniques and methodologies. Essential Responsibilities: * Accurately perform and read test results and notify Laboratory Management of deviations * Prepare and analyze samples for indicator organisms, pathogens, and chemistries * Apply aseptic/microbiological techniques in daily workload * Report inventory and expendable supplies/materials needed for testing requirements * Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control * Assist in quality duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc. * Pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements * Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends * Perform all activities in a neat, safe, hygienic, and efficient manner * Share information in an open and timely manner * Assisting with managing priorities and schedule such that individual goals as well as team goals are achieved with encouraged participation in the Food Safety Net Services Team * Responsible for the safety of oneself and others working within their area Supervision: * This job does has no supervisory responsibilities. Education & Experience: * Associate degree in Life Science or related field with two or more years of laboratory experience, preferred * Two or more years of experience in a commercial food-testing or analytical laboratory * Or equivalent combination of education and experience * Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures * Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures * Broad knowledge of concepts, practices, and procedures of a food testing laboratory * Ability to travel when necessary Physical Demands/Work Environment: * Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components * Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens * Noise level varies from quiet to loud * Temperature varies from hot to cold * Interactive and fast-paced team oriented tasks * Overnight Travel is required at the discretion of management * Occasionally lift and/or move up to 25 pounds * Color vision and depth perception Benefits: * Progressive 401k Retirement Savings Plan * Employer Paid Short- Term and Long-Term Disability, and Life Insurance * Group Medical * Tuition Reimbursement * Flexible Spending Accounts * Dental * Paid Holidays and Time Off Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status. 2 Overnight Schedules: * Mon-Fri, 11pm-7:30am * Tue-Sat, 11pm-7:30am

The Chemical Manufacturing Technician I will run all chemical manufacturing processes in compliance with all associated quality systems. Packs and ships all products. Maintains processes in their validated or compliant state. $22/HR. - Shift 3 days on , 3 days off - 8am-8pm •Reads and follows written and electronic batch records •Ability to record data in accordance with Good Manufacturing Practices (GMP) •Operates Powered Industrial Vehicles to move product, as needed •Handles lab equipment to monitor product dryness using lab moisture balance •Cleans reactors, filters and other process related equipment, process rooms, general cleaning •Records appropriate steps on batch record and associated documents •Understands and complies with quality regulations as they relate to job responsibilities •Complies with good housekeeping and safety rules •Understands various process pumps •Operates various process pumps •Troubleshoots process related equipment- type of equipment is dependent on operator level •Shovels product from bin into dryer feed hopper •Scoops product from drums and weighs amounts •Rolls drums onto and off from skids •Accurately weighs material on scales during final packaging in accordance with packaging documentation. •Monitors in-process batches with regard to temperature, clarity, volume, etc. •Documents value points per SOP •Takes bags off skids and empties contents into reactor •Changes cartridges on various filters •Continuous Processes •Frequent Respirator use •Other duties may be assigned as deemed appropriate by management IND1

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers . If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post. Job Description Chemical Technician II - Allentown, PA Intertek, a leading provider of quality and safety solutions to many of the world's top-recognized brands and companies, is actively seeking a Chemical Technician to join our Chemicals & Pharmaceuticals team in Allentown, PA. This is a fantastic opportunity to grow a versatile career in Analytical chemistry. Intertek's Chemical & Pharmaceuticals team brings quality and safety to life through regulatory guidance and supply chain assurance to support your unique pharmaceutical or biopharmaceutical outsourcing requirements. Over the last 20 years, our network of laboratories and regulatory experts have provided high quality custom pharmaceutical services ensuring Total Quality Assurance for some of the world's largest and most innovative pharmaceutical companies. Intertek is continually innovating and evolving to reduce risk for consumers, brands and organizations in every sector and industry around the world. We go beyond Testing, Inspection and Certification of products: we are a Total Quality Assurance Provider to industries worldwide. Our Purpose: Bringing quality, safety, and sustainability to life. What are we looking for? The Chemical Technician is responsible for supporting Scientists in our analytical laboratory. You will assist with performing and documenting procedures used to test polymers, materials, oils and other chemical compositions using modern analytical instrumentation. Salary & Benefits Information Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons. In addition to competitive compensation packages, when working with Intertek you can expect benefits including medical, dental, vision, life, disability, 401(k) with company match, generous vacation / sick time (PTO), tuition reimbursement and more. What you'll do: Prepares samples, standards and solutions Sets up, adjusts, operates and calibrates basic laboratory equipment and instruments Performs standard lab analyses under direct supervision Prepares and documents test results in lab records, including notebooks, audit trails, standardized forms, and other documentation Performs work in compliance with current procedures and regulations Performs general laboratory housekeeping duties This position outline is a general guideline and does not represent all encompassing details. The position assumes that the incumbent has both the mental and physical requirements to carry out the above defined duties. Additional Qualifications/Responsibilities Minimum Requirements & Qualifications: BA/BS Chemistry, Biology or related scientific degree 0-2 years of related industry experience in an analytical laboratory Preferred Qualifications: Related experience in ICP, ICP/MS, Ion Chromatography, Wet Chemistry

Chemical Technician II - Allentown, PA Intertek, a leading provider of quality and safety solutions to many of the world's top-recognized brands and companies, is actively seeking a Chemical Technician to join our Chemicals & Pharmaceuticals team in Allentown, PA. This is a fantastic opportunity to grow a versatile career in Analytical chemistry. Intertek's Chemical & Pharmaceuticals team brings quality and safety to life through regulatory guidance and supply chain assurance to support your unique pharmaceutical or biopharmaceutical outsourcing requirements. Over the last 20 years, our network of laboratories and regulatory experts have provided high quality custom pharmaceutical services ensuring Total Quality Assurance for some of the world's largest and most innovative pharmaceutical companies. Intertek is continually innovating and evolving to reduce risk for consumers, brands and organizations in every sector and industry around the world. We go beyond Testing, Inspection and Certification of products: we are a Total Quality Assurance Provider to industries worldwide. Our Purpose: Bringing quality, safety, and sustainability to life. What are we looking for? The Chemical Technician is responsible for supporting Scientists in our analytical laboratory. You will assist with performing and documenting procedures used to test polymers, materials, oils and other chemical compositions using modern analytical instrumentation. Salary & Benefits Information Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons. In addition to competitive compensation packages, when working with Intertek you can expect benefits including medical, dental, vision, life, disability, 401(k) with company match, generous vacation / sick time (PTO), tuition reimbursement and more. What you'll do: * Prepares samples, standards and solutions * Sets up, adjusts, operates and calibrates basic laboratory equipment and instruments * Performs standard lab analyses under direct supervision * Prepares and documents test results in lab records, including notebooks, audit trails, standardized forms, and other documentation * Performs work in compliance with current procedures and regulations * Performs general laboratory housekeeping duties This position outline is a general guideline and does not represent all encompassing details. The position assumes that the incumbent has both the mental and physical requirements to carry out the above defined duties. Minimum Requirements & Qualifications: * BA/BS Chemistry, Biology or related scientific degree * 0-2 years of related industry experience in an analytical laboratory Preferred Qualifications: * Related experience in ICP, ICP/MS, Ion Chromatography, Wet Chemistry Intertek: Total Quality. Assured. Intertek is a world leader in the Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts. With passion, pace, and precision we work to exceed our customers' expectations, while engaging with our employees to be 10X in their performance and professional growth. Intertek is a drug-free workplace. As a condition of employment, certain positions may be required to pass a pre-employment drug test based on the type of work that will be performed. We Value Diversity Intertek's network of phenomenal people are our greatest assets, and the diversity they bring fuels our success. Intertek is an Equal Employment Opportunity Employer that values inclusion and diversity. We take affirmative action to ensure all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected characteristics. For individuals with disabilities who would like to request accommodation, or who need assistance applying, please email ******************* or call ************** (option #5) to speak with a member of the HR Department. #LI-JC1

Work Schedule: D Crew- Night Shift Opening The Quality Control Technician is responsible for inspecting and testing raw materials and finished products to ensure they meet required levels of quality and industry regulations. This position performs quality tests, inspection checks, and communicates test results to their Quality Supervisor. Essential Functions/Key Deliverables Take measurements and samples according to the control/sampling plan (e.g., lacquer weights and distribution, visual can inspection, bar code and QR code inspection, abrasion testing, mobility testing, etc.) Conduct tests using high-tech measurement equipment (Torus, Versatile, Sencon) and interface with quality control reporting system Monitoring and testing of critical control points (CCPs) Monitor the quality of products on the line and at specific production stages and provide support and feedback to production team members Provide final approval for finished goods Contain out-of-spec finished goods per containment guidelines and report to supervisor Create and analyze quality reports Communicate quality status and progress to all team members Collaborate with all plant teams and areas to ensure the highest quality Ensure compliance with BRCGS Understanding of HARA Perform any other duty reasonable corresponding with the role Knowledge/Skills/Experience Specific vision abilities required include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus High attention to detail Ability to communicate with and influence others Ability drive for root cause identification and corrective actions Ability to run reports and analyze data Familiarity with basic and sophisticated measurement devices Proficient in Microsoft Office Products CAN DO attitude, ability to work in a highly collaborative team environment, and a desire to WIN Physical Demands N (Not Applicable) Activity is not applicable to this position. O (Occasionally) Position requires this activity up to 33% of the time (0 - 2.5+ hrs/day) F (Frequently) Position requires this activity from 33% - 66% of the time (2.5 - 5.5+ hrs/day) C (Constantly) Position requires this activity more than 66% of the time (5.5+ hrs/day) Lift/Carry 10 lbs or less F 11-25 lbs O 25-50+ lb- O Push/Pull 10 lbs or less F 11-25 lbs O 25-50+ lb- O Stand C Walk C Sit O Manually Manipulate O Reach Outward O Reach Above Shoulder O Climb O Crawl O Squat or Kneel O Bend O Other Physical Requirements Vision (Near, Distance, Color, Peripheral, Depth) Sense of Sound - Ability to understand conversational speaking Sense of Touch Ability to wear Personal Protective Equipment (PPE) - per safety guidelines Mobility to cover expansive manufacturing environment Work Environment Ability to work in an environment that can become very hot (temperature) depending on the weather. Reasonable Accommodations Statement To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. If you are a current CANPACK employee, please apply through your Workday account. CANPACK Group is an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, age, sex, sexual orientation, gender identity, national origin, disability, or any other characteristic protected by law or not related to job requirements, unless such distinction is required by law.

Work Schedule: D Crew- Night Shift Opening The Quality Control Technician is responsible for inspecting and testing raw materials and finished products to ensure they meet required levels of quality and industry regulations. This position performs quality tests, inspection checks, and communicates test results to their Quality Supervisor. Essential Functions/Key Deliverables Take measurements and samples according to the control/sampling plan (e.g., lacquer weights and distribution, visual can inspection, bar code and QR code inspection, abrasion testing, mobility testing, etc.) Conduct tests using high-tech measurement equipment (Torus, Versatile, Sencon) and interface with quality control reporting system Monitoring and testing of critical control points (CCPs) Monitor the quality of products on the line and at specific production stages and provide support and feedback to production team members Provide final approval for finished goods Contain out-of-spec finished goods per containment guidelines and report to supervisor Create and analyze quality reports Communicate quality status and progress to all team members Collaborate with all plant teams and areas to ensure the highest quality Ensure compliance with BRCGS Understanding of HARA Perform any other duty reasonable corresponding with the role Knowledge/Skills/Experience Specific vision abilities required include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus High attention to detail Ability to communicate with and influence others Ability drive for root cause identification and corrective actions Ability to run reports and analyze data Familiarity with basic and sophisticated measurement devices Proficient in Microsoft Office Products CAN DO attitude, ability to work in a highly collaborative team environment, and a desire to WIN Physical Demands N (Not Applicable) Activity is not applicable to this position. O (Occasionally) Position requires this activity up to 33% of the time (0 - 2.5+ hrs/day) F (Frequently) Position requires this activity from 33% - 66% of the time (2.5 - 5.5+ hrs/day) C (Constantly) Position requires this activity more than 66% of the time (5.5+ hrs/day) Lift/Carry 10 lbs or less F 11-25 lbs O 25-50+ lb- O Push/Pull 10 lbs or less F 11-25 lbs O 25-50+ lb- O Stand C Walk C Sit O Manually Manipulate O Reach Outward O Reach Above Shoulder O Climb O Crawl O Squat or Kneel O Bend O Other Physical Requirements Vision (Near, Distance, Color, Peripheral, Depth) Sense of Sound - Ability to understand conversational speaking Sense of Touch Ability to wear Personal Protective Equipment (PPE) - per safety guidelines Mobility to cover expansive manufacturing environment Work Environment Ability to work in an environment that can become very hot (temperature) depending on the weather. Reasonable Accommodations Statement To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. If you are a current CANPACK employee, please apply through your Workday account. CANPACK Group is an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, age, sex, sexual orientation, gender identity, national origin, disability, or any other characteristic protected by law or not related to job requirements, unless such distinction is required by law.

Replies within 24 hours Needs to make sure that products being produced meet the expectations of the consumer. They examine jobs to make sure they meet quality expectations then assess the final product after production. Their role is to establish an acceptable variation range for jobs and identify when something fails to meet those requirements. Responsible for monitoring and ensuring that each stage of production is followed by all the necessary procedures and each product coming out of the production process. Document the results of their inspections and make recommendations on how to prevent common errors. Responsible for ensuring the quality control of all printing and sign products as well as packaging and shipment/delivery of all products. Responsible for checking in all vended products and ensuring they are ready for delivery or shipment. Duties and Responsibilities ● Must have attention to detail on quality and packaging for all outgoing shipments. ● Must be very organized while maintaining the ability to multitask. ● Coordinate with shipping companies like FedEx, UPS and others and ensure timely delivery. ● Work effectively with the center manager and sales team for quality delivery and escalations. ● The job requires repetitive lifting of sometimes heavy boxes. ● Must be a team player, dependable and have a good work ethic. ● Good written and verbal communication skills ● Excellent problem-solving and analytical skills ● Keen attention to detail ● Basic computer and math skills to calibrate and measure specifications ● Ability to use measuring devices like scales and tape measures ● In-depth understanding of company standards ● Understanding of target market and consumer needs ● Documentation and reporting skills ● Teamwork and collaboration ● Comfortable standing or walking for long periods of time Some cross training into bindery or other areas of the company will be required at times if another teammate is out. Experience Entry Level Job Full time Print Smith, Shipleap and Microsoft Office knowledge is a huge plus. Compensation: $15.00 per hour At AlphaGraphics, we offer careers for everyone! Whether you are just starting out, looking for that next great growth opportunity, or seeking a change, we have exciting roles to suit you. We pride ourselves on our training programs in management, sales, operations, print, signs, design, and marketing. Join us with or without experience, and we will succeed together as a team! We invite EVERYONE to apply! *AlphaGraphics centers (locations) are independently owned and operated. The posted positions are offered by individual franchisees who interview, hire, manage and pay the employees hired for positions in a specific local location (center) through their specific business.

Business: Critical Care Department: Quality Control Schedule: 7:00pm-7:30am Perform testing on in-process material, bulk drug substance, finished drug product, and stabilities in support of production, packing release, R&D and regulatory filings. Key Stakeholders: Internal Cross Functional teams in Plant, Teamwork Key Stakeholders: External Auditor Reporting Structure Directly reports to Quality Control Lab Supervisor Essential Duties and Responsibilities Perform analytical testing and release of in-process material, bulk drug substance, finished drug product, and stability sample Sampling, inspection and testing of raw materials and packaging components upon receipt This includes proper documentation of all work according to cGMP Responsible for Sampling of Bulk API and Bulk drums (API and Raw material) for analysis by QC Perform Calibration and minor troubleshooting on select laboratory equipment including GC, UV/Vis, IR, Potentiometer, Refractometer, Karl Fischer, Density meter and ICP/MS (with appropriate training) Perform minor maintenance on GC equipment when necessary Perform daily general duties in a proper functioning QC lab like: Balance checks, glassware washing, gas cylinder changes, temperature record checks, verify inventory supplies etc Assist other chemists in completing quality laboratory investigations in response to out of specification, apparent failure or questionable results or in response to a lab deviation Peer Review of raw data of initial analyst in order to release material in a timely fashion Assist Lab Coordinator with Stability put-ups or take-outs when necessary due to large volume of samples Key Competencies (knowledge, skills and abilities every person must possess to be successful) Critical Thinking - using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems Excellent customer service skills and professional demeanor at all times to interface effectively with all internal and external customers Excellent verbal and written communication skills Creative and able to present various solutions Energetic, enthusiastic and motivational disposition Maintain confidentiality Coaching skills Education / Experience Bachelor's Degree in Science or Associates Degree 3+ plus years of experience Understand chemical processes and reactions Awareness on cGMP, quality and safety norms and requirements Usage of technology tools such as SAP, MS office, Ensur, Openlab, LabX General Oversight and Direction: Receives moderate to limited supervision working from objectives set by Manager. Employee organizes and carries out most assignments in accordance with standard practices, instructions or previous training. Employee handles some situations independently. Equal Employment Opportunity Piramal Critical Care is committed to Equal Employment Opportunity. It is the policy of the Company to encourage and support equal employment opportunity for all associates and applicants without regard to age, sex, race, color, ancestry, religious creed, national origin, pregnancy, physical or mental disability, medical condition, marital status, political affiliation, sexual orientation, disabled veteran or Vietnam Era Veteran Status. Americans with Disabilities Act Applicants as well as employees who are, or become, disabled must be able to perform the essential job functions either unaided or with reasonable accommodation. The organization shall determine reasonable accommodation on a case-by-case basis in accordance with applicable law. Employee Job Responsibilities You are expected to follow all policies, procedures and guidelines, conducting yourself in ways that protect the interests and safety of all employees and the company.

We are seeking an Entry-Level Chemist to join our dynamic team. You will be a key contributor within the laboratory, focusing on safety, maintenance, operation, and quality assurance. This role involves preparing and analyzing samples and solutions, performing sample preparation for metals analysis, and maintaining laboratory equipment and supplies. This is an excellent opportunity for a recent chemistry graduate to grow and develop their skills in a supportive and innovative environment. Responsibilities * Work under immediate supervision. * Contribute to laboratory safety, maintenance, operation, and quality assurance. * Ensure the lab is stocked with appropriate chemicals and supplies. * Prepare samples and solutions, including volumetric and gravimetric solutions. * Accurately prepare samples, standards, and solutions for analysis, including basic and advanced sample extractions. * Perform sample preparation for metals analysis using acid digestion and microwave-assisted digestion. * Prepare samples and titration units for various titration methods. * Set up, adjust, and operate basic laboratory equipment following defined methods in support of projects within the trace metals and titrations laboratories. * Perform general lab housekeeping, including analytical waste disposal, cleaning glassware, and ordering supplies as needed. Essential Skills * Bachelor's degree in chemistry, biochemistry, general sciences, or chemical engineering. * Experience with HPLC, wet chemistry, ion chromatography, or ICP. * Experience in research and analysis, lab techniques, mass spectrometry, or GCMS. Additional Skills & Qualifications * Experience as a chemist, ideally with a year of hands-on experience. * Strong analytical and problem-solving skills. * Ability to work independently and as part of a team. * Willingness to ask questions and continuously learn and grow as a scientist. Work Environment The company fosters a culture of continuous learning and growth. The role is located in the west part of Allentown, and you will be part of a team of about 40 employees. The work schedule is Monday to Friday, with flexible hours between 7:00 am - 4:00 pm, 8:00 am - 5:00 pm, or 9:00 am - 6:00 pm. This is a first-shift position in a supportive environment that encourages development and innovation. Pay and Benefits The pay range for this position is $24.00 - $28.00/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 ALLENTOWN,PA. Application Deadline This position is anticipated to close on Apr 25, 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.