Chemist Jobs in Olean, NY

Join a Career That Moves You Forward - Travel with Siemens Healthineers Are you ready to take your career to the next level in a fast-paced, cutting-edge medical environment? Siemens Healthineers connects skilled professionals with full-time travel opportunities at top-tier partner hospitals across the U.S. These roles offer a chance to expand your expertise in cardiovascular procedures while working in state-of-the-art cath labs, delivering life-saving care to patients. Job Details: Schedule: 3x12: 0600-1830 Pay Package: $3169 weekly gross Benefit Eligible System Experience: Philips Azura Contract Length: 13 weeks About The Role: As a Travel Cath Lab Technologist, you will be a key part of a specialized cardiovascular team, assisting in diagnostic and interventional cardiac and vascular procedures. Your skills will support physicians in performing minimally invasive treatments that enhance patient outcomes. Key Responsibilities: Assist in cardiac catheterizations, angioplasties, stent placements, electrophysiology studies, and other interventional procedures. Operate fluoroscopy and other advanced imaging equipment to guide procedures with precision. Prepare and administer contrast media while monitoring patient responses. Maintain a sterile field and ensure adherence to safety protocols. Collaborate closely with physicians, nurses, and other medical professionals to optimize patient care. Why Join Us? Expert Training: Gain access to industry-leading education from Siemens Healthineers. Career Growth: Take advantage of professional development programs and opportunities to transition into other advanced imaging roles within a global healthcare leader. What We're Looking For: Education: Graduate of an accredited Radiologic Technology Experience: Minimum of 2 years of experience as a Cath Lab Technologist. Certifications: ARRT registered in Radiography (R) CPR and Basic Life Support (BLS) certification required. Skills: Strong proficiency in cath lab equipment, critical thinking, and excellent patient care. What You'll Gain: The opportunity to work with cutting-edge cardiovascular technology in a high-impact medical setting. A role where your expertise directly contributes to life-saving cardiac interventions and improved patient outcomes. #travel

We are seeking an experienced and innovative Food Product Development Scientist to lead the design and development low-acid aseptic products alongside our co-manufacturing partners. This role involves working on products from initial concept through commercialization, with a focus on delivering high-quality, consumer-centric solutions in the beverage industry. The ideal candidate will collaborate with cross-functional teams, including marketing, R&D, and manufacturing, to ensure successful product launches that align with business goals. Primary Purpose and Functions The Food Product Development Scientist will: Develop products from bench scale through production trial. Take ownership of all R&D aspects of product development pipelines, timelines, and project priorities. Ensure proper experimental designs, stability studies, and sensory protocols are implemented to create consumer-centric products. Collaborate with cross-functional teams to communicate project details and experimental results effectively. Support production runs at manufacturing sites and ensure seamless commercialization. Additionally, the person will work on processing or formulation related researches leading to potential new plant-based materials Essential Functions and Responsibilities Product Development and Commercialization: Lead the development of food, beverage, and dietary supplement products from concept to market launch. Conduct benchtop experiments, prototype development, and iterative testing to refine formulations. Develop and implement appropriate experimental designs, stability studies, and sensory tests to ensure product quality and consumer satisfaction. Knowledge of food safety principles and systems. Working knowledge of regulatory procedures and requirements including FDA, USDA, etc. Consumer-Centric Innovation: Utilize sensory protocols to ensure products meet consumer expectations. Ensure all products align with brand objectives and competitive market positioning. Cross-Functional Collaboration: Partner with marketing, brand teams, and other departments to align product development with business goals. Effectively communicate project timelines, experimental designs, and results to cross-functional teams. Collaborate with manufacturing teams to support production runs and troubleshoot any issues during commercialization. Continuous Improvement: Proactively identify problems and provide solutions to improve processes and product outcomes. Take opportunities to develop new skills and adapt to evolving roles within the organization. Research and Development Support on Steuben-GNS research and development effort in creating new plant-based ingredients. Knowledge, Skills, and Experience Education: Bachelor's or Master's Degree in Food Science or a related scientific field preferred. Experience: 0-2 years of experience in product development within the CPG, B2B, or dietary supplement industries. Technical Skills: Strong knowledge of product development for food, beverage, dietary supplements, or pharmaceutical products. Experience with sensory testing protocols and stage-gate processes. Proficient in experimental design, stability studies, and data analysis. Collaboration Skills: Proven ability to work with cross-functional teams and communicate effectively across departments. Competencies People Development: Open, curious, and willing to learn new skills. Takes initiative to develop individual competencies and align with evolving organizational roles. Business Planning: Understands key business operations that impact the team and role. Effectively manages time and priorities to meet project deadlines. Results Orientation: Delivers on commitments with a focus on quality and process. Supports team objectives beyond routine responsibilities. Problem Solving: Identifies problems proactively and provides actionable solutions. Continuously seeks opportunities for improvement within the scope of the role. Collaboration: Communicates effectively with team members, leadership, and internal customers. Open to feedback and fosters a collaborative work environment. Why Join Us? This is an exciting opportunity to shape the future of food and plant-based innovation. As a Food Product Development Scientist, you will play a critical role in creating high-quality, consumer-focused products that align with our mission of delivering excellence and driving business growth. If you are passionate about product development, consumer-driven innovation, and working in a dynamic, collaborative environment, we encourage you to apply!

About Us Imagine the innovation and expertise behind the world's leading cosmetic brands, brought to you by a distinguished Italian company with a legacy of excellence. Since 1972, Intercos Group has been at the forefront of color cosmetics, pencils, nail polish, skincare, and personal care products. We pride ourselves on being the only cosmetics manufacturer that combines top-tier quality and advanced technology with a global reach and a personalized touch. With 15 commercial offices and 15 production facilities across 12 countries, Intercos Group brings a local approach to a global stage. We continually set the standard for beauty, crafting exceptional product lines for brands worldwide. As one of the largest suppliers in the cosmetics industry, we are a leading force in the research, development, and production of beauty products, shaping the future of the industry with every season. Position Summary The Senior Chemist is responsible for all technical activities related to new/existing formulation, innovation and 1st production scale-up of new formulations in Congers, NY. Essential Functions Formulate and facilitate development of innovative colored cosmetic products, line extensions, and product improvements (i.e. Emulsion, Anhydrous, and Powder formulations). Leading a team of technicians/junior chemists to support with technical related activity Identify new/ improved formulation technologies and implement them to meet project needs, following different constraints (costs, regulatory, black lists, etc.) in collaboration with strategic marketing department. Interact with customers and provide technical support via oral, presentation and written venues. Work directly with clients in order to achieve the desired formulation when necessary. Proactively scan and research new concepts, materials, technical opportunities and partnerships. Interface with all departments throughout the company and interact with material suppliers. Monitor preliminary product stability for new/ existing formulations. Effectively manage projects and provide status reports to group leader/ manager. Execute all formula customization work in DEVEX and follow all SOP's with regards to development and formula creation. Ensure that all projects are done through the use of the BPM when communicating about projects and/or reporting results. To work with the Corporate Applied Research in order to standardize technical information and processes on a global basis for all new formulas. Work with Corporate Applied Research in the technical transfer arena of commercialized and non-commercialized formulations. Record and review all activity with the direct supervisor. Other duties as assigned. Job Qualifications Bachelor's Degree in Scientific Discipline, such as Chemistry, Biology, Physics, etc. 2-4 years in Cosmetic Formulation Cosmetic Formulation, color perception, raw material knowledge, regulatory knowledge, GLPs, GMPs, FDA guidelines Computer Skill (Word, Excel, SAP, Devex), Good Communication Skills, Math Skills, Professional, Courteous, Able to travel if needed 10% of the time Job Benefits Health Insurance: Comprehensive medical, dental, and vision coverage Retirement Plans: 401(k) plan, often with company matching Life Insurance: Coverage for employees in the event of death or disability Paid Time Off (PTO): Vacation days, sick leave, and personal days Holidays: Paid company holidays and floating holidays Professional Development: Training programs and opportunities for career advancement Performance Bonuses: Annual merit increase and/or bonus based on individual performance Company Events: Team-building activities, social events, and company outings Employee Assistance Programs (EAPs): Confidential counseling and support services for personal and professional issues. EEO Intercos Group is committed to creating a diverse and inclusive workplace where everyone is valued and respected. We believe that a wide range of perspectives and experiences enhances our innovation and success. We are an Equal Opportunity Employer and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or any other legally protected status. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to any of these characteristics. We are dedicated to providing a work environment that is free from discrimination and harassment and promotes equal opportunity for all.

Chemists - Join the Country Life team! Share our passion for natural health and pride in our company's commitment to excellence and quality. Our employees reflect our strong heritage and passion for success, delivering exceptional service and premium products. Each member of the Country Life team is dedicated, knowledgeable and driven for success. Country Life provides its employees with a work environment that is stimulating and supportive. We are committed to investing in our employees and believe that every employee is to be valued. Position Summary: Testing pharmaceuticals, vitamins and herbal products using HPLC, ICP, FTIT, NIR, UV-VIS and wet chemistry per USP, AOAC, FCC, BP (British Pharmacopeia) and internal procedures. Properly disposes of waste chemicals based on OSHA requirements. Position Scope: Handles approximately 15 - 35 analytical tests per week Position Responsibility: Works with lab instruments, e.g. HPLC, AA, PDA, RI detection methods, ICP and ICP-MS to perform analytical tests. Also works with chemicals and reagent solvents during the day. Records the raw data and results from scientific test results. Reports any lab instruments malfunction to Lab Manager. Prepares and files all Quality Control documents, e.g. Certificate of Analysis (COA) Deviations, Out of Specification (OOS) reports. Reviews testing and notebooks to prepare bulk product release. Conducts daily calibration of balances and Ph meter. Calibrates an expiration date for all product labels based on shelf life expectancy. Disposes of waste chemicals appropriately. Checks raw materials and finished product potencies. Proper disposal of expired raw materials, in-process and finished goods (final batches). Coordinates such activities with Safety Manager. Prepares samples for shipment to outside testing laboratory. Assists in the inventory of supplies and upkeep of laboratory and laboratory machinery. Preparation of purchase orders, receipt of supplies, and interfacing with other departments to expedite these functions. Chemist II: in additional to the above Qualification and maintenance of primary and secondary standards of raw material and finished products. Maintains R&D raw material inventory, laboratory notebooks, equipment logs and maintenance schedules. Prepares specification for raw materials and finished products. Conducts in process testing of manufactured samples. Conducts minor repairs of lab instruments and other apparatus. Supports the preparation, manufacture, evaluation and documentation of new or modified R&D in-process and finished products associated with Country Life formulations, e.g., tablets, capsules and powders. Writes detailed scientific instructions and lab procedures. Senior Chemist: in additional to the above Develops analytical methods and validations. Analyses, records and releases raw materials and conducts maintenance of raw material specifications. Maintains lab chemicals for consistency to standards (e.g. USP, GLP and OSHA). Performs analytical troubleshooting and updates SOPs, log books and lab solutions preparation book. Provides guidance and training for Chemists I and II. General Clean working space, desk, equipment/glassware and whole lab. Must wear Personal Protective Equipment (PPE) at all times as stipulated by SOPs. e.g. respirator, ear plugs, hair net, beard cover and lab coat. Lifting up to 20 lbs. may be required. Position requires considerable standing on lab floor. Maintains professional and technical knowledge by attending educational symposia; reviewing professional publications; establishing personal networks; participating in professional societies, etc. Satisfactory completion of appropriate corporate training as related to the position and/or department. Assures compliance by following Food and Drug Administration's Good Manufacturing Practices (FDA cGMPs / GLPs) as well as other regulatory standards as required by the department. Contributes to overall achievement by accomplishing related tasks and demonstrating characteristics that exemplify team building and support. The above is not intended to be an all-inclusive list of responsibilities. Other activities may be assigned as required by management. QUALIFICATIONS Experience and Skills: Chemist I will have one year Pharmaceutical laboratory or related experience as well as good mechanical aptitude. Training on specific laboratory equipment and instruments is preferred and may be provided if no work experience outside of classroom laboratory Chemist II will have three years of Pharmaceutical lab experience and good familiarity with HPLC, ICP and ICP-MS as well as good mechanical aptitude. Senior Chemist will have five years Pharmaceutical lab experience and strong experience with HPLC, ICP and ICP-MS as well as good mechanical aptitude. Good organizational skills. Good interpersonal skills. Excellent knowledge of PC software, MS Office, Word, Excel. Good written and verbal communication skills. Excellent Chemistry background as well as practical application of the technical knowledge. Excellent understanding and attitude towards cGMP and GLP, which will increase with job level.

Advanced Patient Care: Laboratory Technologists Make It Possible Laboratory Technologist - Automated Lab (Chemistry) - Nights - Competitive Sign-On Bonus and New Rates At NewYork-Presbyterian/Columbia University Irving Medical Center, Laboratory Technologists are redefining the limits of science and medicine. We study some of the most complex and rarely seen medical conditions - with unmatched energy and expertise. You can help Make It Possible. Join a highly-skilled technical team of 48 Laboratory Technologists in our Chemistry area featuring Cobas 8000 series analyzers. Here you'll have an opportunity to work with nationally accredited colleagues and contribute to lifesaving results in an Ivy League affiliated Academic Medical Center environment. You will perform a variety of automated and manual tests and related duties to obtain data for use in diagnosis and treatment of disease, following established procedures. In state-of-the-art 24-hour facilities, you'll find real opportunities to maximize your time and training with complex & diverse caseloads working to the fullest capacity of your license. This position is Monday to Friday from 12:00am - 8:00am with alternate weekends and rotating holidays. Location is our Columbia campus in Upper Manhattan/Washington Heights. Competitive sign-on bonus up to $12K : New graduates eligible Experiential bonus commensurate with experience Additional bonus for night shift Shift differential Preferred Criteria Two years of experience in a clinical laboratory setting ASCP certification Required Criteria A Bachelor's degree in Medical Technology (or equivalent curriculum) New York State Clinical Laboratory Technologist licensure from the New York State Education department Join a healthcare system where employee engagement is at an all-time high. Here we foster a culture of respect, diversity, and inclusion. Enjoy comprehensive and competitive benefits that support you and your family in every aspect of life. Start your life-changing journey today. Please note that all roles require on-site presence (variable by role). Therefore, all employees should live within a commutable distance to NYP. NYP will not reimburse for travel expenses. __________________ 2024 “Great Place To Work Certified” 2024 “America's Best Large Employers” - Forbes 2024 “Best Places to Work in IT” - Computerworld 2023 “Best Employers for Women” - Forbes 2023 “Workplace Well-being Platinum Winner” - Aetna 2023 “America's Best-In-State Employers” - Forbes “Silver HCM Excellence Award for Learning & Development” - Brandon Hall Group NewYork-Presbyterian Hospital is an equal opportunity employer. Salary Range: $50.11-$62.33/Hourly It all begins with you. Our amazing compensation packages start with competitive base pay and include recognition for your experience, education, and licensure. Then we add our amazing benefits, countless opportunities for personal and professional growth and a dynamic environment that embraces every person. Join our team and discover where amazing works.

Title: Bioprocess Associate - Day Shift (6am-6pm) Duration: 06 months, with potential to extend Pay range: $20-21/hr Qualifications: Requirements: High school diploma Ability to adhere to written instruction, verify data, perform minor mathematics equations with instruction and accurately document results to perform work safely and compliantly Ability to collaborate with teammates to execute scheduled work safely and compliantly Strong communication skills Familiarity with common computer tools, such as web-based applications Possess a continuous improvement mindset, a desire to learn, and a drive to contribute to a culture of excellence and our mission of delivering benefits to patients worldwide Nice to Have: Mechanical aptitude Familiarity with general chemistry, microbiology, or clean room operations Prior manufacturing experience Prior experience with cGMP operations or aseptic technique Responsibilities: Job Type: Contract. This 6-month position starts ASAP. Schedule: Fixed shift schedule. 36 hours the first week, 48 hours the next week, alternating. DAY: 6AM - 6PM, NIGHT: 6 pm - 6 am. Must be willing to work scheduled holidays, weekends, and overtime. This is a DAY shift role. Position Overview: Work is performed in a biologics manufacturing environment with classified areas requiring clean hygiene, specified gowning, and personal protective equipment (PPE). This is not a lab position. This is an entry level position that will train for proficiency within assigned functional area(s). Biologics orientation and job function training will be provided. 100% Onsite. Primary Responsibilities: Set-up, operation, and cleaning of process equipment including manipulation of valves, hoses, clamps, piping, etc. Prepare buffers, media, and reagents up to 2000L Monitor process parameters and escalate abnormal conditions Maintain accurate documentation Sustain a clean and orderly work environment Achieve and maintain proficiency of above responsibilities through training This position includes physical demands which may involve bending, twisting, squatting, kneeling, climbing, or reaching as well as infrequent unassisted lifting (not to exceed 50lb) This role will require handling and working with hazardous materials such as caustic, acid and steam Dexian is a leading provider of staffing, IT, and workforce solutions with over 12,000 employees and 70 locations worldwide. As one of the largest IT staffing companies and the 2nd largest minority-owned staffing company in the U.S., Dexian was formed in 2023 through the merger of DISYS and Signature Consultants. Combining the best elements of its core companies, Dexian's platform connects talent, technology, and organizations to produce game-changing results that help everyone achieve their ambitions and goals. Dexian's brands include Dexian DISYS, Dexian Signature Consultants, Dexian Government Solutions, Dexian Talent Development and Dexian IT Solutions. Visit ******************* to learn more. Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status.

As a travel Cardiac Cath Lab Tech, you will assist physicians during cardiac catheterization procedures. Your role will involve operating equipment, monitoring patients, and ensuring optimal patient care in high-pressure settings. Responsibilities: • Set up and operate cardiac catheterization equipment • Monitor patient vitals during procedures • Assist in invasive diagnostic and therapeutic cardiac procedures • Maintain sterile fields and follow radiation safety protocols Qualifications: • ARRT certification • BLS certification • Minimum one (1) year of experience Benefits: • Medical, Dental and Vision Coverage • Health Savings Account • 401(k) Retirement Plan • Hospital Indemnity Insurance • Critical Illness Insurance • Accident Insurance • Referral bonuses Pay Information: • $3,498 per week* • *Estimated weekly pay packages are based on bill rates at the time this job was posted and include hourly wages as well as eligible reimbursements for meal and incidental expenses and housing. Bill rates can change frequently and without notice. Exact pay packages may vary based on guaranteed hours, distance being traveled, experience and other customizations available to travelers. About Premier Healthcare Professionals: Premier Healthcare Professionals (PHP) is a leading healthcare staffing company specializing in placing highly skilled healthcare professionals in a variety of settings, including hospitals, clinics, and long-term care facilities. With a personalized approach, PHP offers a wide range of flexible job opportunities across the country, allowing nurses and other healthcare professionals to choose assignments that fit their lifestyle and align with their career goals. Our dedicated support team ensures you're equipped with the tools and resources you need to succeed in each assignment, offering 24/7 support and a streamlined onboarding process. Whether you're looking to explore new locations or gain valuable clinical experience, PHP provides the flexibility and support to help you thrive in your healthcare career. Join a team that values your expertise and is committed to your success at every step. PandoLogic. Category:Healthcare, Keywords:Cardiology Technologist, Location:Penfield, NY-14526

Assists lab section supervisor in monitoring compliance of organization's Service Standards by POC end users Serves as back-up Supervisor for the POCT lab in the absence of the principal supervisor. Performs scheduling for end user training Trains new and current employees and oversees the technical performance of POC employees during orientation Offers continuing guidance and technical assistance to end users on POCT procedures and equipment. Completes certification, provides access and certifies operators in QML/GEM Website. Manages roster list of operators to comply with CAP, CLIA AND NYSDOH regulatory inspection. Assists with troubleshooting technical problems and takes remedial action to resolve the issues. Plans, organizes and schedules the training for expired certification of end users. Is knowledgeable about patient confidentiality requirements. Communicates POC problems with devices, reagents, and QC to the Lab supervisor, director and administration

Join a team recognized for leadership, innovation and diversity Join Honeywell as an Analytical Chemist who will lead new method development in a research environment. You will develop and guide method development for a variety of instrumentation including GPC, TGA, DSC, and other laboratory techniques. You will conduct research on identifying impurities and assay on a variety of analytes from small molecules to polymers. You will work with chemists and engineers from research to production phase to ensure product quality. You will be required to work closely with internal and external customers to meet deadlines. Follow all relevant safety and environmental rules and regulations. You will report directly to our R&D Manager and you'll work onsite out of our Buffalo, NY location. Key Responsibilities: * Develop methods to identify and characterize new molecules, mixtures, and polymers. * Write documentation for methods developed and transition methods from a small scale to a production environment. * Work with customers to meet needs in a fast-paced environment * Work on a variety of projects across multiple disciplines simultaneously BENEFITS OF WORKING FOR HONEYWELL In addition to a performance-driven salary, cutting-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer-subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays. For more information, The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates. COMPENSATION The annual base salary range for this position is $73,000 - $96,000. Please note that this salary information serves as a general guideline. Honeywell considers various factors when extending an offer, including but not limited to the scope and responsibilities of the position, the candidate's work experience, education and training, key skills, as well as market and business considerations. US PERSON REQUIREMENT Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. citizen, U.S. permanent resident, or have asylum or refugee status in the U.S. In October, 2024 Honeywell announced the spin-off of our Advanced Materials business to become a stand-alone publicly traded company, independent of Honeywell. Our intention is that this role, dedicated to the Advanced Materials business, will be a part of this future transaction when the separation occurs. YOU MUST HAVE * Master's degree in Analytical Chemistry, Chemistry, or Chemical Engineering * 3+ years of experience or a PhD in Chemistry * Work in a research environment * Experience in trace and bulk analysis WE VALUE * Preferred experience with GPC and thermal analysis * Method development skills * Excellent written communication including writing SOPs * Experience with cGMP, GLP or other regulatory compliance * Experience working within large groups of engineers and scientists * Excellent interpersonal and communication skills * Ability to ensure a high level of scientific rigor is applied to all projects * A passion for scientific curiosity and creativity * An open, honest, and team-oriented personality * Eagerness to get involved in hands-on work, with a positive attitude and desire to acquire new skills quickly * Experience in a fast-paced environment * Reliable and trustworthy with highest ethical standards * Experience with LIMS * Understanding of industry standards and security practices ABOUT HONEYWELL Honeywell International Inc. (Nasdaq: HON) invents and commercializes technologies that address some of the world's most critical demands around energy, safety, security, air travel, productivity, and global urbanization. We are a leading software-industrial company dedicated to introducing state-of-the-art technology solutions to improve efficiency, productivity, sustainability, and safety in high-growth businesses in broad-based, attractive industrial end markets. Our products and solutions enable a safer, more comfortable, and more productive world, enhancing the quality of life of people around the globe. THE BUSINESS UNIT As a global technology leader, Honeywell Energy & Sustainability Solutions (ESS) enables the energy evolution, provides solutions that reduce emissions, and delivers innovative sustainable materials to our customers across industries. Honeywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, care or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status. Additional Information * JOB ID: HRD256333 * Category: Engineering * Location: 20 Peabody St,Buffalo,New York,14210,United States * Exempt * Engineering (GLOBAL) Honeywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.

About Harry's Inc Harry's Inc. is building a modern CPG company by putting people first and delivering against real unmet consumer needs. The company's flagship brand - Harry's - was founded by Jeff Raider and Andy Katz-Mayfield in 2013. After successfully launching and scaling Harry's, Jeff and Andy saw an opportunity to bring their experience building Harry's to other CPG categories where the consumer has also been historically underserved. Harry's Inc. has grown significantly over the last ten years, and is now made up of four brands - Harry's, Flamingo, Lume, Mando - and Harry's Labs, the company's incubation and M&A engine. The company employs more than 900 people across the U.S., U.K. and Germany, and is the largest CPG company built in the last 20 years. At Harry's Inc, our mission is to Create Things People Like More - whether it's a product, an experience, or an internal tool, we believe in making the things around us better for our customers, and our team. Our mission extends beyond customers and team, to the community broadly. We believe that the best business models make a positive impact. That's why our brands donate year-round to nonprofit organizations that align with their social missions. At the end of the day, the key to our success is our amazing people. From chemists, mechanical engineers, CX associates, to creative directors, sourcing managers, and logistics specialists, the Harry's team is composed of some of the most brilliant, diverse, and humble people you'll ever meet. Our company is a place of inclusion, innovation, and deeply ingrained values. The Harry's Inc working model is in-office Tuesday, Wednesday, and Thursday. Our beautiful 70,000 square foot SoHo office is decked out with bagels on Wednesdays and lunch on Thursdays, and fully stocked kitchens with snacks, coffee, and drinks everyday. Can't forget the free products and the opportunity to have some meetings without Zoom! About the Team The R&D Soft Product Innovation Team at Harry's is responsible for all personal care category launches from concept to market. We are a team of researchers, developers, and formulators who are on a mission to create things people like more. As our brands continue to grow, the Soft Product Laboratory will be a key driver for both new product innovation and continuous improvement, raising the bar for product excellence. About the Role The Soft Product Formulation Chemist will support the global development of new products and enhance our existing personal care portfolio for the Harry's and Flamingo brands. In close collaboration with Product, Quality, and Sourcing teams, you'll help bring performance-driven, consumer-loved products to market while maintaining and improving our current formulations. We seek a hands-on, detail-oriented chemist with 2+ years of experience in personal care formulation. You'll thrive in our fast-paced, creative environment, where innovation, problem-solving, and cross-functional collaboration are key. What You'll Do: Develop and optimize formulations across skincare, bodycare, haircare, hairstyling, and suncare categories, balancing performance, aesthetics, cost, and timeline requirements. Identify opportunities to enhance existing formulas, including root-cause analysis, cost-saving initiatives, and technical transfers. Demonstrate creativity and resourcefulness in proactively identifying and proposing solutions to issues that may arise during product development or in transfer to manufacturing. Work closely with cross-functional teams and external partners to execute improvement strategies efficiently. Lead formulation testing, ensuring stability, compliance, and precise record-keeping. Manage raw material stocks, packaging inventory, and maintain traceability of formulation data. Support pilot runs and first production batches as needed. Stay ahead of scientific advancements, ingredient innovations, and market trends to drive innovation. Who You Are: Product Developer at Heart - Excited by new products, technologies, formats, and how they interact with one another to create the ultimate user experience, down to the last detail, have pride in the work and development of creating things. Creative Problem Solver - Energized by challenges and can't sleep until a solution is found. Lifelong Learner - Hunger for knowledge, admits when they don't know the answer and diligently works to find it. Proactive doer: Takes initiative, thrives in a “no task too small” environment with an eagerness to learn and address any issue that may arise. Execution-Focused - Gets things done, creates efficient systems for tracking, testing, and reporting. Results-Driven - Relentlessly committed to achieving goals while fostering strong internal and external relationships. Collaborative & Adaptable - Works well in cross-functional teams, embraces change, and pivots with shifting business needs. Communicative & Team-Oriented - You thrive on direct, honest, and constructive communication. Sense of Humor - We take our work seriously, but not ourselves too seriously! Requirements: Bachelor's degree in Chemistry, Biology, or a related science. 2+ years of formulation experience in cosmetics, personal care, or health & beauty. Experience in fast-paced product development, working with cross-functional teams, raw material suppliers, and third-party manufacturers. Strong analytical, organizational, and project management skills. Ability to juggle multiple projects and pivot as business needs evolve. Willingness to travel domestically and internationally as needed. Benefits and perks Medical, dental, and vision coverage 401k match Equity in Harry's Flexible time off and working hours Wellness and L&D stipends 4 weeks sabbatical after 5 years, 6 weeks after 10 years, and 8 weeks after 15 years Up to 20 weeks of pregnancy leave and up to 16 weeks of parental leave Fun IRL and virtual events including happy hours, team building events, and parties on our rooftop Free products from all of our brands Harry's is committed to bringing together individuals from different backgrounds and perspectives. We strive to create an inclusive environment where everyone can thrive, feel a sense of belonging, and do great work together. Harry's is an Equal Opportunity Employer, providing equal employment and advancement opportunities to all individuals. We recruit, hire and promote into all job levels the most qualified applicants without regard to race, color, creed, national origin, religion, sex (including pregnancy, childbirth and related medical conditions), parental status, age, disability, genetic information, citizenship status, veteran status, gender identity or expression, transgender status, sexual orientation, marital, family or partnership status, political affiliation or activities, military service, domestic violence victim status, arrest/conviction record, sexual or reproductive health decisions, caregiver status, credit history immigration status, unemployment status, traits historically associated with race, including but not limited to hair texture and protective hairstyles or any other status protected under applicable federal, state and local laws. Harry's commitment to providing equal employment opportunities extends to all aspects of employment, including job assignment, compensation, discipline and access to benefits and training. We respect the laws enforced by the EEOC and are dedicated to going above and beyond in fostering diversity across our company. We can't quantify all of the intangible things we think you'll love about working at Harry's, like the exciting challenges we tackle, the smart and humble team you'll get to work with, and our supportive and inclusive culture. That said, our salary ranges are based on paying competitively for our size and industry, and are one part of our total rewards package, which also includes a comprehensive set of benefits and our equity program. The base salary hiring range for this position is $90,800-$124,850, but the final compensation offer will ultimately be based on the candidate's location, skill level and experience.

About AIRCO AIRCO is a world leader in carbon conversion technology, paving the way to global energy security by transforming CO₂ into a valuable resource. Its proprietary AIRMADE™ Technology is an adaptable platform that allows any industry to efficiently produce high-demand, fully-formulated synthetic fuels from waste CO₂ and hydrogen. The company has commercial partnerships with airlines including JetBlue and Virgin Atlantic, amongst others, and has been awarded multiple government contracts, including with NASA and the United States Department of Defense's Defense Innovation Unit. The company has received industry recognition through awards such as Time Best Inventions, Inc. Best in Business, Fast Company World Changing Ideas, and the XPrize for Carbon Removal. AIRCO's many accolades include winning the prestigious Green Chemistry Challenge Award from the Environmental Protection Agency in October 2023, an award given to organizations that reinvent processes to reduce the generation of hazardous substances and byproducts. AIRCO was also recently declared a winner for the World Economic Forum UpLink Sustainable Aviation Challenge, which accelerates the development of promising technology pathways that enable widespread uptake of SAF. The Position We are looking for an Analytical Chemist to join our team. This person will report directly to our Senior Analytical Chemist. The ideal candidate will have rich experience in operating and maintaining Gas Chromatography (GC), Gas Chromatography-Mass Spectrometry (GCMS), and Liquid Chromatography (LC) instruments, as well as developing analytical methods using these techniques. The Analytical Chemist will play a key role in our analytical chemistry laboratory, supporting research and development efforts, conducting quantitative analysis, and ensuring high-quality control of analytical data. The candidate should have experience with Chemstation and Chromeleon, and ideal industry experience in chemical, oil and gas, pharmaceutical, or environmental sectors. This role will be based in Brooklyn, New York. What you get to do Operate, maintain, and troubleshoot GC, GCMS, and LC instruments. In-depth knowledge of Chemstation and Chromeleon software, ensuring optimal performance and reliability. Perform routine and non-routine sample analysis using GC, GCMS techniques, interpret data, and prepare analytical reports with high attention to detail and accuracy. Develop and validate analytical methods for the quantitative analysis of samples using GC, GCMS techniques, following established protocols and industry standards. Conduct sample preparation techniques, including extraction, derivatization, and purification, as necessary for analysis. Collaborate with other team members to ensure timely delivery of analytical results, and effectively communicate any deviations or issues encountered during analysis. Assist in the maintenance of laboratory equipment, including calibration, troubleshooting, and documentation of instrument performance. Follow all safety protocols and maintain a clean and organized laboratory environment. What you bring to AIR COMPANY Bachelor's in Analytical Chemistry or related field and 1- 3 years of experience in operating and maintaining GC, GCMS instruments, and developing analytical methods using these techniques. Strong understanding of the principles of analytical chemistry, quantitative analysis, and quality control. Proficiency in interpreting and analyzing complex analytical data, and preparing detailed analytical reports. Experience with Chemstation, Openlab, Chromeleon, Empower software for instrument control, data acquisition, and data analysis. Familiarity with relevant industry standards, regulations, and guidelines. Ideal industry experience in chemical, pharmaceutical, or environmental sectors. Excellent problem-solving skills, with the ability to troubleshoot and resolve instrument issues. Ability to work independently and in a team-oriented environment. Strong communication skills, both written and verbal. Ability to prioritize and manage multiple tasks effectively. Attention to detail and accuracy in all aspects of work. Bonus Points Master's degree Salary Range: $ $65,000 - $80,000 The approximate annual base compensation range and benefits listed above may vary based on the applicant's experience, skills, abilities, and relevant industry expertise. At Air Company we value employees for their unique perspectives. We are an inclusive Equal Employment Opportunity employer. We consider applicants without regard to gender, gender identity, sexual orientation, race, ethnicity, disabled or veteran status, or any other characteristic protected by federal, state or local laws. Don't meet every single requirement? Studies have shown that women, marginalized genders and people of color are less likely to apply to jobs unless they meet every single qualification. At AIR COMPANY we are dedicated to building a diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't align perfectly with every qualification in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles Working at Air Company In addition to standard medical and dental benefits, that kick in Day 1, we are: A people-first, climate solutions company driven to move society to a more sustainable future A unified team of climate optimists with an exceptional and diverse range of backgrounds Committed to fostering collaboration with a team that believes in the power of science and that business can be used as a force for good… We also provide: Comprehensive Health Benefits Full coverage for employee base premiums on health, dental, and vision insurance. 70% coverage for spouse and dependent base premiums. Choose between base plans or enhanced options to fit your needs. Health Savings & Flexibility Access company-sponsored HSA and FSA accounts to save on healthcare and dependent care expenses. Income Protection & Insurance Company-paid Short-Term Disability insurance. Optional Long-Term Disability and Life Insurance plans. Time Off & Leave Flexible and generous paid time off, including national holidays and sick leave. Paid family leave to support you during important life moments. Retirement Savings Tax-deferred 401(k) plan with a 3% company match to help you invest in your future. Commuter Benefits Pre-tax savings on transit and parking, plus monthly company contributions. Additional Perks Ancillary benefits through Sequoia, including pet insurance and financial wellness programs. Employee wellness program to support your well-being. Sponsored team events and diversity, equity, and inclusion (DEI) initiatives. Weekly catered lunch every Wednesday.

About Us: Founded more than 15 years ago and headquartered in Chicago, the DV Group of financial services firms has grown to more than 450 people operating throughout North America and in Europe. Since spinning out of a large brokerage firm in 2016, DV Trading has rapidly scaled as an independent proprietary trading firm utilizing its own capital, trading strategies, and risk management methodologies to provide liquidity to worldwide financial markets and hedging opportunities to commodity producers and users. Now, DV group affiliates include two broker dealers, a cryptocurrency market making firm, and a bourgeoning investment adviser. DV Energy is a rapidly growing division that specializes in trading crude oil, refined products, natural gas, and related energy markets across US, Europe, and Asia. Our proprietary risk management and trading methodologies along with a strong ability to adapt to changing conditions has allowed DV Energy to grow into one of the largest financial participants within the global energy complex. Responsibilities: Develop in-house trading strategies, used by both discretionary and quantitative traders. Conduct quantitative research on market microstructure, applying knowledge to improve trading algorithm and identify market anomalies. Collaborate with cross-functional teams, including portfolio managers and researchers, to design and implement solutions for the trading strategies. End-to-end development, including alpha idea generation, data processing, strategy backtesting, optimization, and production implementation. Maintain and improve portfolio trading in a production environment. Contribute to the analysis framework for scalable research. Requirements: BS, MS or PhD in mathematics, statistics, machine learning, computer science, engineering, quantitative finance, or economics. A minimum of 3 years of experience in trade execution development or research for futures or cash equities. Proficiency in programming languages such as Python or C++. Fluency in data science practices, e.g., feature engineering. Experience with machine learning is a plus. Experience with signal blending and portfolio construction. Highly motivated, willing to take ownership of his/her work. Collaborative mindset with strong independent research abilities. Commitment to the highest ethical standards. Annual compensation range $150-200K base + discretionary bonus. DV is not accepting unsolicited resumes from search firms. Only search firms with valid, written agreements with DV should submit resumes in response to DV's posted positions. All resumes submitted by search firms to DV via e-mail, the Internet, personal delivery, facsimile, or any other method without a valid written agreement shall be deemed the sole property of DV, and no fee will be paid in the event the candidate is hired by DV. DV is proud to be an equal opportunity employer and committed to creating an inclusive environment for all employees.

Rochester Midland Corporation, a leading manufacturer and global supplier of specialty chemicals is searching for an experienced R&D Formulation Chemist for its Food & Beverage division located in Rochester, NY. The R&D Formulation Chemist is responsible for developing new products and improving existing formulations for the company's product line. This role involves research, experimentation and testing to create formulations that meet quality standards and regulatory requirements. The R&D Formulation Chemist collaborates closely with product line managers, quality assurance and production to ensure formulations align with customer needs, company goals and industry trends. Job Functions * Develops and optimizes formulations for new products * Creates product prototypes and samples * Improves or modifies existing formulations to enhance performance, stability, cost-effectiveness or customer needs * Analyzes product performance and stability, identifying and troubleshooting formulation issues as needed * Conducts laboratory tests, stability studies and evaluations on formulations to ensure they meet company standards * Prepares technical reports and documentation on formulation methods, procedures and results. * Assists with managing field trials, pilot studies and panel tests * Assists with scale-up from development to production quantities * Enters new product formulas into Vicinity Manufacturing Software * Provides input to the QA Laboratory Manager to develop Statistically Valid, Customer Driven QA Specifications * Collaborate with EH&S teams to ensure products meet regulatory and safety requirements * Advises product line manager of compatible packaging options for formulations * Research new ingredients, raw materials, and technologies to incorporate into formulations * Perform market and competitor analysis to identify potential areas for formula innovation and advancement * Documents all research, testing and formulation processes accurately * Provides experimental direction and mentoring to junior staff members EDUCATION/ SPECIAL LICENSES OR CERTIFICATION: * Bachelor's or Master's degree in Chemistry Experience: * 10 years experience as a Senior or Principal Formulation Development Chemist in formulation development, preference for experience in food cleaning and sanitation industries Skills: * Strong understanding of organic and inorganics chemistry, laboratory practices and formulation techniques * Experience with analytical methods such as HPLC, GC, IR or other laboratory instrumentation is preferred * Awareness of potential hazards and proper handling of chemicals and materials in the lab Competencies: * Technical Expertise * Innovation and Creativity * Attention to detail * Analytical and Critical Thinking * Project management * Collaboration * Problem Solving Physical Requirements/ Working Conditions: 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. Sit or stand for extended periods of time * Visual acuity necessary to utilize a computer monitor throughout the course of a normal workday * Ability to perform repetitive keyboarding activities and operate general office equipment. * Extra hours and some travel may be required SAFETY RESPONSIBILITIES: Employee shall be familiar and comply with all safety policies and procedures of the company. We're an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. We articulated our 2022 winning aspiration to double the number of patients we serve and hence, double the impact we create as a global pharmaceutical company. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division. We at Cipla are inspired by our purpose of 'Caring for Life' and strive to extend this philosophy to our associates and their families. We are looking for talented individuals to grow their careers while growing our business. About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited. Scope The scope (content and statements) of this is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent of this job description is to be representative of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position satisfactorily and in accordance with the established performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual assigned basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role. InvaGen pharmaceuticals is looking for talent in the following areas at our manufacturing site in Central Islip, NY. Purpose The job of the "Chemist" is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes-specific testing group. The role may be further modified based upon individual education, training, experience, or a combination of all three. Generally, modifier designation with respect to experience for Chemist are as follows. However, combination of education, training, and special skills will determine the assignment of Level to a specific individual: Level 1:0 to 3 years Level 2:3 to 5 years Level 3:5 to 10 years Senior:more than 10 years Level 2 or above is strongly preferred. These are full-time positions, and shift timings are from 8:30 AM to 5:00 PM. A second shift of 1:00 PM - 9:30 PM is avaliable as well. Summary of Responsibilities: * Conduct routine testing or other analysis in a specific group or department setting. * Conduct advanced testing and/or critical testing, as required. * Operate specialized equipment or conduct specialized skill testing. * Participate in investigation activities. * Ensure compliance to all data integrity and cGMP practices, procedures, and expect ensuring compliance with all good documentation practices. * Other duties and responsibilities as assigned by the Head of the Department or Section Head Educational, Skills & Experience Requirements and Preferences: * Bachelor's degree (BS or BA), physical sciences preferred. * Must have current Good Manufacturing Practices (cGMP) Good LaboratoryPractice(GLP) knowledge. * Working knowledge of raw materials and finished product testing and instruments and techniques such as GC, High-Performance Liquid Chromatography (HPLC), Karl Fischer (KF), Dissolution,Particle Size and ICP. * Familarity with Chromatography systems is required,Enpower is a plus. * Proficiently speak, communicate, and understand (read and write) scientific work in English. * Have excellent organization, learning and teaching skills required to work in teams. * Ability to understand and analyse complex data sets and must have working knowledge of Microsoft Office programs and other scientific based software. * Experience in Oral Solidsis a plus. * Effective interpersonal relationship skills and the ability to work individually and as a part a team. * Must be a detail-oriented self-starter, demonstrate initiative and possess a positive professional attitude towards work. * Must have strong organization and communication skills (written, verbal, and presentation). Physical Requirements: * Work standing or walking unassisted for 75% or greater of an 8-hour period. * Unassisted lifting up-to 10 kg, may be required. * Able to wear appropriate personal protective equipment at all times, when required. * Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period. Locations: Central Islip, New York, Hauppauge, New York. EEO Statement: Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify patients' lives to as many people as possible. With 30 years of technological expertise, we position ourselves as a world leader in sterile single dose with 10 sites on 4 continents and more than 2000 employees. Since 2013, our site Unither Manufacturing LLC. based in Rochester (NY), specializes in the manufacture of Blow-Fill-Seal, Liquid Stick-Packs, Pharmaceutical bottles, Tablets and Capsules. It has more than 280 employees. Your role Reporting to the Stability Supervisor, JOB SUMMARY: Performs routine analyses of materials, drug substances and drug products following cGMPs. May support analytical method development & validation, and analytical troubleshooting under technical supervision. Assists with maintaining lab quality systems. ESSENTIAL DUTIES / RESPONSIBILITIES: Completed Analyses (40%) Performs, interprets, evaluates, and records routine and some non-routine analytical lab tests of materials, drug substances and drug products following CGMPs. Execute protocols, experiments as written. Maintains instruments and equipment. Sets up instruments and conducts sample tests. Performs routine calibration of instrumentation. Ensures an adequate supply of test materials are available to perform daily testing. Maintains and updates training records in a timely manner. Safe, Compliant, Efficient Labs (30%) Supports lab systems as assigned and maintains laboratory in compliance with SOPs, cGMPs, HS&E requirements, and FDA, DEA, USP, EP, and OSHA regulations. Problems Identified (30%) Identifies and communicates actual and potential problems. May support/provide input for investigations, troubleshooting, and method development/validation with supervision. Writes basic investigations with supervision. Your profile REQUIRED EDUCATION: Associate's Degree (Bachelor's preferred) in Chemistry or related science QUALIFICATIONS/EXPERIENCE: A.A.S. with 2+ yrs. or B.S. with 0+ yrs. experience in chemistry or related science discipline. SPECIFIC SKILLS: Experience with laboratory analytical techniques preferred. Experience in a cGMP environment a plus. Familiarity in 2 or more following areas: HPLC, GC, UV-VIS, FTIR, dissolution. Experience in written notebook documentation practices a plus. Write basic investigations with supervision. Computer Skills: Basic Outlook skills as evidenced by creating and sending messages, working with address books, message handling, creating and using personal folders, scheduling appointments, working with meeting requests and managing tasks. Basic Microsoft Word skills as evidenced by the ability to produce basic business letters and simple tables and charts; as well as check spelling, set tabs, change page orientation, sort, save, open and organize electronic files. Basic Excel skills as evidenced by the ability to use workbooks, create simple formulas, insert and delete data, create and edit charts, filter and sort lists, and format data. Familiarity with LIMS and instrument operating software desirable. PHYSICAL REQUIREMENTS/ENVIRONMENT: (List the details of the environment within/under which work is performed and physical requirements for this position.) Must demonstrate visual acuity, color recognition, finger dexterity. The ability to read, write and communicate in English. Work responsibilities involve chemical and biological agents that have assigned biological and chemical hazards. Sitting approximately 50% of day and standing approximately 50% of day. Work responsibilities may involve repetitive use of the hands through keyboarding, simple grasping and fine manipulation. Occasional lifting of up to 35 pounds. Normal office environment and occasional controlled environment work that may require removal of jewelry and cosmetics. Occasionally subjected to weekend, holiday and irregular hours. Compensation range 21.64 - 26.44 USD * The referenced compensation range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations. Learn more about us: We are a dynamic company driven by a spirit of victory and are therefore pursuing strong growth while maintaining a close relationship with our customers and employees. Our culture is based on 5 values: Respect, Responsibility, Trust, Courage and Innovation. We are committed to bringing these values to life with our employees by granting them a high degree of autonomy in the exercise of their profession and by encouraging their initiatives. We are committed to providing them with working conditions and atmosphere that is conducive to their development and the expression of their potential. We propose you to integrate a site that values the meaning of work and that entrusts our employees with a high level of responsibility. Join us and make a difference!

Why Endo? We want the best and brightest people at Endo to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward. Our shared values of Integrity & Quality, Innovation, Drive, Collaboration and Empathy guide our team and enable us to deliver upon our vision of helping everyone we serve live their best life. Summary The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. Job Description Scope of Authority - span of control (work unit, site, department, division, etc.), monetary value of budget/spend authority ( capital, operating, etc.), P&L responsibility, etc. Typically supports one Par business, at a single site Key Accountabilities - key outcomes/deliverables, the major responsibilities, and % of time Accountability Responsibilities % of Time Analysis & Testing * Conducts laboratory analyses: finished product testing, stability testing, raw material testing, cleaning verification testing and manufacturing in-process testing. Typical activities may include buffer/solution preparation, standard preparation and operating analytical instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc. * Uses laboratory software for analyses * May review and approve laboratory test data and documentation for completeness and compliance * Is alert to and detects abnormalities during performances of tests and reviews * May perform lab methods transfer and participate in method validation/verification studies 65% Lab Equipment * Provides general laboratory support such as routine instrument cleaning/preventative maintenance/calibration, sample receiving, chemical inventory, document filing and housekeeping * Cleans lab working surfaces and dispose of any excess chemicals, solutions, solvents, etc. in the special waste containers for each class of waste chemicals * Learns to troubleshoot instrument/chromatography problems 20% Investigations * With guidance, participates in OOS/OOT/NOE and other investigations * Elevates questionable sample results, OOS, and aberrant results immediately to Supervisor and recommends a course of action * May draft, edit and review SOPs and laboratory investigations 10% Training * Maintains assigned training records current and in-compliance * Actively assumes/demonstrates responsibility in training others in good documentation practice, practical lab skills, and chemical theories, methodologies and procedures 5% Compliance * Performs assigned work in a timely and safe manner conforming to regulatory, company and compendiaI requirements within pharmaceutical manufacturing setting * Document accurately data generated in notebooks/worksheets/LIMS in compliance with SOPs * Follows internal processes related to controlled substances continuous Safety * Follows EH&S procedures to ensure a safe work environment * Follows all applicable safety and standards guidelines, such as SOPs, cGMP, DEA regulations good documentation practice and/or MSDS continuous Total 100% Qualifications Education & Experience Minimal acceptable level of education, work experience and certifications required for the job * Bachelor of Science Degree in chemistry, chemical engineering or related field with 2+ years' relevant analytical laboratory experience OR * Master's Degree in above disciplines with 1+ years' relevant analytical lab experience preferred Knowledge Proficiency in a body of information required for the job e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc. * Demonstrated proficiency with various laboratory techniques/instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc. * Working knowledge of applicable safety and standards guidelines, such as SOP, cGMP, GLP, DEA regulations and/or MSDS * Has demonstrated competence in conducting chemical analyses * Good knowledge of wet chemistry techniques * In-depth working knowledge of laboratory software and chromatographic software (e.g. Waters Empower, Agilent ChemStation and Sotax WinSotax) * Competency in Microsoft Office Suite Skills & Abilities Often referred to as "competencies", leadership attributes, skills, abilities or behaviors that may be enterprise, functional or job specific e.g. coaching, negotiation, calibration, technical writing etc. * Ability to display and analyze data in a logical manner * Good verbal and written communication skills as well as good computer skills * Attention to details and accurate record keeping * Establish and maintain cooperative working relationships with others * Solid organizational skills * Ability to train less senior staff and develop laboratory skills and ability * Ability to take initiative, set priorities and follow through on assignments Physical Requirements Physical & mental requirements e.g. lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc. * Extended periods of sitting, standing, walking, reaching, climbing/balancing, kneeling/crouching/crawling, looking at monitor for extended periods, moderate noise levels and potential business travel. Work is in an FDA and DEA-regulated pharma lab environment with risk of exposure to various chemicals * Must occasionally lift and/or move up to 15-25 lbs. * Ability to wear personal protective equipment, including respirators, gloves, etc. * Specific visions abilities are required by this job include close vision and color vision * Ability to occasionally tolerate significant differences in temperature and/or humidity for short periods Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required. EEO Statement: At Endo, we firmly believe in the principles of equal employment opportunity and strive to create an atmosphere where all employees, regardless of their race, color, creed, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability (including pregnancy), age, or military or veteran status, feel valued, respected, and empowered. Our commitment to EEO extends to every aspect of employment, including recruitment, hiring, training, promotions, compensation, benefits, transfers, terminations, and all other employment practices. We are dedicated to ensuring that all employment decisions are based on qualifications, skills, and merit.

Pay is approximate. Please apply for your personal pay package! Join the Plexsum Team for this exciting assignment! Profession/Specialty: Med Lab Tech - Laboratory City/State: Coudersport, PA Shift: 5x8 Evenings Assignment Length: 13 Weeks Apply and Log in at plexsum.com to see more jobs and pay! Benefits - We’ve got you covered! Your success is our priority, and that includes your health and wellness both on and off the clock. We want you to thrive in mind, body, and spirit, and rest well in knowing that we’ve got your back with an affordable, comprehensive benefits package. As a Plexsum employee, you will enjoy: Most lucrative pay in the industry. As a traveler you will receive private housing or a generous lodging stipend. 401k Plan – Helping you get ahead! Your financial health is an important piece of your overall well-being. Concerned with your quality of life, we match the first 3% of your contributions at 100%, and also match your next 2% of contributions at 50%. Plus, all employer match contributions are 100% vested immediately. That’s just how much we care to help you achieve your retirement goals! National Healthcare Insurance. We care about your health and overall well-being, and realize everyone’s needs are different. That is why we offer you a national healthcare insurance that includes prescription coverage. We back our commitment to you by making a generous contribution to your coverage to keep your premiums affordable. Plexsum paid $15000 life insurance. Yep, that’s right! Imagine the peace of mind in knowing that life insurance is in place should the unthinkable happen. We provide a $15000 life insurance policy at NO COST TO YOU when you work a full time assignment. We understand that everyone’s needs are different. We offer voluntary insurance coverage so that you can choose the plans that are right for you: Dental Insurance to help maintain healthy smiles and better overall health. Exams and cleanings 2 in any 12 month period. Vision Insurance with eye exams that can detect other health conditions. Well recognized VSP carrier. Basic and Voluntary Life Insurance to protect your family if something happens to you. Short-Term Disability Insurance that pays a portion of your income if a covered disability prohibits you from working. Long-Term Disability Insurance to protect your savings when you can’t work for an extended time. Critical Illness Insurance for help if you are diagnosed with a covered illness. Accident Insurance that provides a range of benefits for covered accidental injuries. JOIN US TODAY!

This is not a real job. But it would involve controlling for quality.

Are you a self-driven person looking to advance your career as a high-impact player on a team? If so, we have an exciting challenge for you and your future! At HP Hood LLC, we celebrate our differences. Our diversity of people, backgrounds, experiences, thoughts and perspectives are fostered to create an inclusive work environment. We are at our best when we respect and value each other - One Team One Company! Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration that fosters a strong employee engagement, teamwork, safety and wellness. We offer a competitive benefits package that includes health, dental, vision, wellness programs, employee discounts, 401k matches, tuition reimbursement, ongoing development, advancement opportunities and more. This position is also eligible for our bonus program. Founded in 1846, today HP Hood is one of the largest and most trusted food and beverage manufacturers in the United States. Our portfolio of national and super-regional brands and licensed products includes Hood, Heluva Good, Lactaid, Blue Diamond Almond Breeze, Planet Oat and more. Position Summary Perform routine bacteriological and chemical testing of dairy products to ensure all company and regulatory standards are met. Position Responsibility Hold valid NYSAM licenses to perform required tests (Milk Receiver, Appendix N, and DMC) Perform chemical, bacteriological, and organoleptic analysis of raw, in-process, and finished products. Obtain samples for testing from silos, tanks and production lines Generation of processing batch tickets from computerized system Preparation of lab testing materials/supplies Maintain a professional relationship with production and maintenance personnel. Instruct, and train present and future laboratory technicians as needed. Maintain, review, and distribute quality control reports as requested by QA Manager. Calibration of laboratory equipment to assure proper testing. Review of lab procedures and policies Assist in the samplings and shipment of monthly customer, sales, and regulatory samples. Accept, suggest, and assist in the assignment and performance of special projects. Be active in the development and enforcement of Lab Safety practices Attend trade organization meetings and training sessions as deemed appropriate by the Q.C. Manager. Support SQF by maintaining food safety through completing job tasks and maintaining the area in a sanitary manner. Maintain all documented information as per SQF requirements. Work overtime, as needed, which will require an obligation from you to fulfill. Carry out additional duties assigned by the Lab QC Manager or Supervisor. Understand and follow all safety procedures, always wear proper PPE, and never put yourself or other employees in harm's way. Report food safety problems to personnel with authority to initiate action. Pick up work area before leaving at the end of shift. Adapt to new technology as it comes into the department. Job Requirements Posses a minimum of a 2 year degree in a Dairy Science or other related field or previous laboratory experience. Basic English/Math skills. Must be physically fit without any medical restrictions to perform job duties that will be required. Able to meet all safety compliance standards. For applicants in NY State, this job pays $20.32 per hour to start, 10% increase after six months, and another 10% increase at 1 year of active employment