Chemist jobs in Rehoboth, MA - 236 jobs

Rangam is seeking candidates for a Direct Hire role as an Associate Scientist, Assay Development with our client, one of the world's largest pharmaceutical companies. Seeking candidates in Cambridge, MA or willing to relocate. Use Your Power for Purpose Client's purpose is to deliver breakthroughs that change patients' lives. At the core of fulfilling this purpose is Research and Development, where we translate advanced science and technologies into the therapies and vaccines that matter the most. You will be at the forefront of this mission, contributing to the discovery and development of innovative treatments that improve patients' lives. Client's BioMedicine Design (BMD) Assay Development group is seeking a highly motivated research associate to establish binding and functional assays and support hit-to-lead discovery of peptide and antibody-based therapeutics. The candidate will play a critical role in the design and execution of biochemical and of cell-based functional assays and high-throughput screening to support the BioMedicine Design portfolio. The candidate will be responsible for the development and execution of experiments using a variety of detection technologies including homogenous technology including HTRF, ELISA/DELFIA, FACS, imaging and cell-based functional assays focused on signaling, proliferation, or cytotoxicity. In addition, the candidate will analyze data, present results at internal meetings, and closely collaborate with project team members to develop strategies and identify lead molecules. We are looking for a creative, solution-oriented individual who enjoys the opportunity to explore new methods. What You Will Achieve In this role, you will: Develop assays to identify and characterize peptide, antibody and multispecific candidates to support programs across multiple therapeutic areas. Biochemical assay formats may include protein binding, competition and enzymatic cleavage assays. Cell based assays may include binding (FACS and ELISA), competition, cell signaling (NanoBiT, calcium flux, cAMP, phospho-protein HTRF/AlphaLISA, etc) and reporter gene assays using a variety of cell lines. Execute high-throughput screens using automated and semi-automated platforms and analyze results. Collaborate with project teams to establish screening strategies, interpret results, and make decisions to drive programs forward. Write protocols, maintain electronic lab notebook, and regularly review literature to maintain knowledge of scientific trends and new technologies. Here Is What You Need (Minimum Requirements): Bachelor's degree and 0-3 years of experience in molecular biology, biochemistry, cell biology or related discipline, along with a basic understanding of biologics drug discovery workflows. Demonstrated experience in assay development and troubleshooting with methods such as HTRF, ELISA/DELFIA, FACS, and cell-based functional assays focused on signaling, proliferation, or cytotoxicity. Demonstrated experience with plate-based assay formats and maintaining cell cultures is required. Track record of strong problem solving and organizational skills, attention to detail, and ability to multi-task. Strong written and oral communication skills Bonus Points If You Have (Preferred Requirements): Experience with Tecan or Beckman liquid handling platforms is preferred but not required. Experience with high content imaging and multiplex assay formats is preferred. Experience writing scripts to automate data processing or other coding experience is preferred. PHYSICAL/MENTAL REQUIREMENTS Requires work in BL2 laboratory environment with appropriate PPE Work Location Assignment: On Premise Last Day to Apply: January 22, 2026 The annual base salary for this position ranges from $60,200.00 to $97,500.00. In addition, this position is eligible for participation in client's Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with client's Matching Contributions and an additional client's Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at client's Candidate Site - U.S. Benefits | (uscandidates.my**benefits.com). Compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States. Relocation assistance may be available based on business needs and/or eligibility. To find out more about Rangam, and this role, click the apply button. Satnam Singh SA Technical Recruiter | Rangam Consultants, Inc M: ************** E: *****************| W: **************

Nextcea Inc. is a pharmaceutical services company that focuses on assessing drug efficacy and safety during late-stage drug development and clinical trials. We are currently seeking full-time Analytical Chemists to join our team. Qualified candidates will actively participate in LC-MS biomarker analysis at Nextcea. Successful applicants should hold an MS or PhD in Analytical Chemistry or a related field, along with relevant laboratory experience. While experience with LC-MS is preferred, it is not mandatory. We are seeking self-motivated candidates who are excellent team players and can effectively contribute to established laboratory procedures and protocols. Candidates should be able to work independently, demonstrate flexibility, and adapt to the challenges of pharmaceutical biomarker projects. At Nextcea, we value diversity and inclusion. We offer competitive compensation and benefits, including medical, vision, dental, and 401(k) plans, to all employees, regardless of their background or identity. Applicants are required to submit their resumes online via LinkedIn.

Quality Control Analyst II Norton 45 per hour This is an onsite role in Norton, MA. First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training. Perform routine and non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies in accordance with SOPs Support weekend laboratory operations and maintain required training records Assist with laboratory equipment and inventory maintenance, including reagent and sample preparation Review data in a timely manner and serve as a qualified data reviewer Perform operational assignments such as raw material processing, environmental monitoring, and in-process testing Contribute to the creation and updating of controlled documents, including SOPs, work instructions, and test methods Follow internal policies, SOPs, and applicable regulatory standards (GMP, GLP, ICH) Participate in continuous improvement initiatives and cross-functional collaboration Support regulatory submissions, inspection readiness, and audits Qualifications Bachelor's degree in Chemistry, Biology, Biochemistry, or a related field 4-8 years of pharmaceutical or biotech experience in GMP QC or equivalent environments Experience with method transfer and implementation; understanding of method lifecycle management preferred Strong technical writing, data analysis, problem-solving, and organizational skills Excellent communication and teamwork abilities Proficiency in LabWare LIMS, Microsoft Excel, Word, and PowerPoint preferred

Industry: Pharmaceuticals Title: Quality Control Analyst II Duration: 11 months contract (+Possibility of extension) This is an onsite role in Norton, MA, with occasional responsibilities at other Client locations. Weekend coverage is required. First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training. Description: The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. This position enhances QC efficiency and effectiveness. Key Responsibilities' Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs. Support weekend lab operations and maintain training records. Assist in lab equipment and inventory maintenance, including reagent and sample prep. Review data timely and qualify as a data reviewer. Perform operational assignments (raw material processes, environmental monitoring, in-process testing). Contribute to updating controlled documents (SOPs, work instructions, test methods). Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH). Participate in continuous improvement initiatives and cross-functional collaboration. Support regulatory submissions, inspection readiness, and audits Qualifications: B.S. in chemistry, biology, biochemistry, or related field. 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent. Experience in method transfer/implementation; understanding of method lifecycle management preferred. Strong technical writing, data analysis, problem-solving, and organizational skills. Excellent communication and teamwork. Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred

Please send your updated resume to ****************** Quality Control Analyst II - Mansfield, MA area- Contract (Weekend Shift) Mansfield, MA area Contract - (Weekend Shift) Experienced in performing routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs. Support weekend lab operations and maintain training records. Assist in lab equipment and inventory maintenance, including reagent and sample prep Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the . All qualified applicants are welcome to apply Estimated Min Rate: $30.80 Estimated Max Rate: $44.00 What's In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh's network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh's extensive talent community that will provide you with access to Yoh's vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week) Health Savings Account (HSA) (for employees working 20+ hours per week) Life & Disability Insurance (for employees working 20+ hours per week) MetLife Voluntary Benefits Employee Assistance Program (EAP) 401K Retirement Savings Plan Direct Deposit & weekly epayroll Referral Bonus Programs Certification and training opportunities Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit ************************************************ to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh's hiring clients' preferences. To learn more about Yoh's privacy practices, please see our Candidate Privacy Notice: **********************************

A recognized pharma company is actively seeking a new Quality Control (QC) Analyst for a great entry-level position with their QC Bioassay group. In this role, the QC Analyst will be trained to perform cell-based bioassays, ELISAs, and other biological methods in a GMP-regulated setting, while also supporting external laboratory testing. Responsibilities: Learn and perform immunoassays (e.g., ELISA) and cell-based assays under supervision in a GMP environment to support product release and stability testing Assist in drafting and reviewing standard operating procedures (SOPs) and technical documents Support method transfer, qualification of critical reagents, and other assay-related activities Participate in the review and basic trending of QC data Assist with routine laboratory upkeep, including cell culture maintenance, instrument calibration, and inventory tracking Collaborate with internal teams and external partners as part of cross-functional project support Contribute to investigations and deviation reports under guidance Perform other duties, as needed Qualifications: Bachelor's Degree in Cell Biology, Molecular Biology, Biochemistry, or a related scientific field Familiarity with basic Lab techniques and Data Analysis methods Strong organizational, communication, and interpersonal skills Detail-oriented and eager to develop problem-solving skills in a regulated lab environment Enthusiasm for learning and the ability to work both independently and within a team Desired Skills: Academic or internship experience with Mammalian Cell Culture and/or ELISAs

Title: QC Specialist - Chemistry Employment Type: Contract Status: Accepting Candidates About the role This role supports Quality Control Chemistry operations by leading QC Sample Management activities across multiple lab functions. You will ensure compliant, on-time sample processing while partnering with digital and quality teams in a fast-paced cGMP environment. Shift: Wednesday-Saturday, 6:00 AM-4:00 PM. Key Responsibilities • Lead QC Sample Management operations supporting Chemistry, Microbiology, Bioassay, and Raw Materials • Oversee daily schedules to ensure compliant sample processing and documentation • Author and maintain SOPs, deviations, CAPAs, and change controls • Act as primary support for audit readiness and regulatory inspections • Partner with Digital teams to optimize LIMS (LabVantage) and data workflows • Manage CTU systems, investigations, and compliance issue resolution Qualifications • BA/BS with 3-5 years or MS with 1-3 years of cGMP Quality Control experience • Strong hands-on experience with QC Sample Management • Proficiency with LIMS and Veeva Quality Systems • Working knowledge of FDA, EU, and ICH regulations • Experience with gowning, aseptic technique, and lab safety practices • Proven people management and cross-functional leadership skills Compensation (MA Pay Transparency): • Estimated hourly range: $40-$45/hr (W-2) • Final rate within this range will be based on skills, experience, and interview results.

Responsibilities: • Perform environmental monitoring (EM) tasks for the aseptic environment, other controlled areas, and plant utility systems following specified instructions and techniques from Standard Operating Procedures (SOP), Training Material, and other GMP documents. • Incubate and enumerate microbial growth on EM plates. • Ensure all tasks are completed in a GMP compliant and safe manner. • Document all tasks within LIMS or standard laboratory paper documentation utilizing GDP principles. • Entry of information into logbooks as applicable for tasks per SOP. • Partner and communicate with operations, manufacturing, facilities, and other site departments as required for support of operations and GMP processes. • Actively participate in daily and weekly laboratory meetings. • Accurately complete task management tools and handover communications. • Perform general lab tasks including cleaning and equipment preparation. • Maintain training for all required tasks. • May assist in laboratory investigations with limited scope. Requirements: • Bachelor's degree with no experience, associate degree with 2+ years' experience, or High School Diploma [or Equivalent (GED)] with 4+ years' experience. • Good oral, written, and interpersonal communication skills. • Basic math skills and computer skills such as data entry, along with a high level of attention to detail. • A demonstrated ability to organize time independently, be able to perform several tasks concurrently (ability to multi-task) and be able to meet objectives in a team-oriented environment. • Must maintain aseptic qualifications Shift is Sunday - Wednesday, 10 hour days, after a 3 month training period of Monday - Friday, 8 hour days

Are you looking to power the next leap in the exciting world of advanced electronics? Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At Qnity, we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. We are seeking a hands-on, self-motivated Analytical Chemist to support New Product Development (NPD) and commercial product support across the ACP portfolio; ranging from metallization/plating chemistries to advanced packaging polymers and formulated materials. This role will lead development, implementation, and continuous improvement of analytical and characterization methods for specially synthesized raw materials (small molecules through complex polymers) and finished products, partnering closely with cross-functional stakeholders (DE, NPD, Manufacturing, Quality, and Technical Service) to enable scale-up, specifications, and customer support. Key responsibilities * Analytical method development & execution: Develop, optimize, and run analytical/characterization methods for raw materials, intermediates, and formulated products supporting NPD milestones and commercial needs. * Core techniques: Apply techniques such as CVS, HPLC/UPLC, GPC, % solids, titrations, potentiostatic measurements, surface tension, cloud point, densitometry, and rheology (and related wet/physical methods). * Other techniques relevant: ICP-OES/ICP-MS for metals/impurities, UV-Vis, FTIR, NMR, IC, TOC, DSC/TGA, particle size/zeta potential, SEM/EDS * Method validation, transfer, and sustainment: Author/maintain methods, validation protocols/reports, and ensure robust method transfer to R&D and Manufacturing as needed. * Data integrity & documentation: Maintain high-quality written documentation (methods, validation, batch/lot data packages, change control / MOC) and ensure traceable, audit-ready records. * Troubleshooting & investigations: Support root-cause investigations, out-of-spec troubleshooting, and customer complaint response in collaboration with Quality/Manufacturing. * Statistical/data analysis: Use statistical tools to analyze method performance, capability, trends, and investigation data (DOE, GR&R, SPC as applicable). * Safety & teamwork: Work safely with hazardous chemicals in a collaborative, fast-paced lab environment; communicate clearly in both informal updates and formal presentations. Required qualifications * Education: B.S. in Chemistry, Biology, Chemical Engineering, Materials Science, or related field. * Experience: 3-5 years of hands-on experience in analytical chemistry supporting R&D/NPD, development engineering, manufacturing, or quality environments. (Experience characterizing small molecules, polymers, and/or inorganic/metal-containing chemistries is strongly valued.) * Demonstrated ability to follow procedures with high repeatability, strong attention to detail, and commitment to safe lab practices. * Strong written and verbal communication skills; able to translate data into clear technical conclusions and recommendations. * Strong data analysis capability; JMP/Minitab (or similar) preferred. Preferred qualifications * Demonstrated success developing/validating new analytical methods and supporting method transfer. * Experience supporting semiconductor materials (e.g., plating baths, photoresists, dielectrics, silicones, packaging polymers) and working across interdisciplinary teams. * Six Sigma (Green/Black Belt) or demonstrated experience applying structured problem-solving tools. Join our Talent Community to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered 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. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information. Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page. We use Artificial Intelligence (AI) to enhance our recruitment process.

**Are you looking to power the next leap in the exciting world of advanced electronics?** Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At **Qnity** , we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. We are seeking a hands-on, self-motivated Analytical Chemist to support New Product Development (NPD) and commercial product support across the ACP portfolio; ranging from metallization/plating chemistries to advanced packaging polymers and formulated materials. This role will lead development, implementation, and continuous improvement of analytical and characterization methods for specially synthesized raw materials (small molecules through complex polymers) and finished products, partnering closely with cross-functional stakeholders (DE, NPD, Manufacturing, Quality, and Technical Service) to enable scale-up, specifications, and customer support. **Key responsibilities** + Analytical method development & execution: Develop, optimize, and run analytical/characterization methods for raw materials, intermediates, and formulated products supporting NPD milestones and commercial needs. + Core techniques: Apply techniques such as CVS, HPLC/UPLC, GPC, % solids, titrations, potentiostatic measurements, surface tension, cloud point, densitometry, and rheology (and related wet/physical methods). + Other techniques relevant: ICP-OES/ICP-MS for metals/impurities, UV-Vis, FTIR, NMR, IC, TOC, DSC/TGA, particle size/zeta potential, SEM/EDS + Method validation, transfer, and sustainment: Author/maintain methods, validation protocols/reports, and ensure robust method transfer to R&D and Manufacturing as needed. + Data integrity & documentation: Maintain high-quality written documentation (methods, validation, batch/lot data packages, change control / MOC) and ensure traceable, audit-ready records. + Troubleshooting & investigations: Support root-cause investigations, out-of-spec troubleshooting, and customer complaint response in collaboration with Quality/Manufacturing. + Statistical/data analysis: Use statistical tools to analyze method performance, capability, trends, and investigation data (DOE, GR&R, SPC as applicable). + Safety & teamwork: Work safely with hazardous chemicals in a collaborative, fast-paced lab environment; communicate clearly in both informal updates and formal presentations. **Required qualifications** + Education: B.S. in Chemistry, Biology, Chemical Engineering, Materials Science, or related field. + Experience: 3-5 years of hands-on experience in analytical chemistry supporting R&D/NPD, development engineering, manufacturing, or quality environments. (Experience characterizing small molecules, polymers, and/or inorganic/metal-containing chemistries is strongly valued.) + Demonstrated ability to follow procedures with high repeatability, strong attention to detail, and commitment to safe lab practices. + Strong written and verbal communication skills; able to translate data into clear technical conclusions and recommendations. + Strong data analysis capability; JMP/Minitab (or similar) preferred. **Preferred qualifications** + Demonstrated success developing/validating new analytical methods and supporting method transfer. + Experience supporting semiconductor materials (e.g., plating baths, photoresists, dielectrics, silicones, packaging polymers) and working across interdisciplinary teams. + Six Sigma (Green/Black Belt) or demonstrated experience applying structured problem-solving tools. Join our Talent Community (*************************************************************** to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered 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. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information (**************************************************** . Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page (*************************************************************************** . **We use Artificial Intelligence (AI) to enhance our recruitment process.** The Pay range for this role is $67,200.00 - $105,600.00 Annual **How Base Pay is Determined:** Qnity has job leveling frameworks that help organize roles based on progressive levels of responsibility, proficiency and qualifications. Each role has an associated pay range (or an established pay rate for some roles) based on the competitive market in each country where we operate. Each individual's pay is based on a variety of factors, including their role and the associated pay range for that role, their geographic location (i.e., country, state, metropolitan area), as well as their skills, experience, education and certifications, and performance.

Are you looking to power the next leap in the exciting world of advanced electronics? Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At Qnity, we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. We are seeking a hands-on, self-motivated Analytical Chemist to support New Product Development (NPD) and commercial product support across the ACP portfolio; ranging from metallization/plating chemistries to advanced packaging polymers and formulated materials. This role will lead development, implementation, and continuous improvement of analytical and characterization methods for specially synthesized raw materials (small molecules through complex polymers) and finished products, partnering closely with cross-functional stakeholders (DE, NPD, Manufacturing, Quality, and Technical Service) to enable scale-up, specifications, and customer support. Key responsibilities Analytical method development & execution: Develop, optimize, and run analytical/characterization methods for raw materials, intermediates, and formulated products supporting NPD milestones and commercial needs. Core techniques: Apply techniques such as CVS, HPLC/UPLC, GPC, % solids, titrations, potentiostatic measurements, surface tension, cloud point, densitometry, and rheology (and related wet/physical methods). Other techniques relevant: ICP-OES/ICP-MS for metals/impurities, UV-Vis, FTIR, NMR, IC, TOC, DSC/TGA, particle size/zeta potential, SEM/EDS Method validation, transfer, and sustainment: Author/maintain methods, validation protocols/reports, and ensure robust method transfer to R&D and Manufacturing as needed. Data integrity & documentation: Maintain high-quality written documentation (methods, validation, batch/lot data packages, change control / MOC) and ensure traceable, audit-ready records. Troubleshooting & investigations: Support root-cause investigations, out-of-spec troubleshooting, and customer complaint response in collaboration with Quality/Manufacturing. Statistical/data analysis: Use statistical tools to analyze method performance, capability, trends, and investigation data (DOE, GR&R, SPC as applicable). Safety & teamwork: Work safely with hazardous chemicals in a collaborative, fast-paced lab environment; communicate clearly in both informal updates and formal presentations. Required qualifications Education: B.S. in Chemistry, Biology, Chemical Engineering, Materials Science, or related field. Experience: 3-5 years of hands-on experience in analytical chemistry supporting R&D/NPD, development engineering, manufacturing, or quality environments. (Experience characterizing small molecules, polymers, and/or inorganic/metal-containing chemistries is strongly valued.) Demonstrated ability to follow procedures with high repeatability, strong attention to detail, and commitment to safe lab practices. Strong written and verbal communication skills; able to translate data into clear technical conclusions and recommendations. Strong data analysis capability; JMP/Minitab (or similar) preferred. Preferred qualifications Demonstrated success developing/validating new analytical methods and supporting method transfer. Experience supporting semiconductor materials (e.g., plating baths, photoresists, dielectrics, silicones, packaging polymers) and working across interdisciplinary teams. Six Sigma (Green/Black Belt) or demonstrated experience applying structured problem-solving tools. Join our Talent Community to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered 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. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information. Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page. We use Artificial Intelligence (AI) to enhance our recruitment process.

Job Title: Chemist - Stability Testing - Quality Control FLSA Classification: Full-Time Work Hours: 8 AM - 5 PM (May vary based on business needs) Salary: $75,000 - $105,000 (DOE) Benefits: Bi-Weekly Pay, Paid Time Off, Health Insurance Benefits start on day 1 (Medical, Dental, Vision), Disability Insurance, Shift Differential, Overtime, 401K Match, company sponsored events, career advancement, training, etc. Cipla is seeking a Stability QC Chemist who will provide support to the Quality Control Department in drug quality assessments under the influence of environmental factors. The general duties and responsibilities of the job include but are not limited to the following: 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 Working knowledge of raw materials testing and release Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP Lead investigation activities. Ensure compliance to all data integrity and cGMP practices, procedures, and expect Ensure compliance with all good documentation practices. Other duties and responsibilities as assigned by the Head of the Department or Section Head Education and Experience Bachelor's degree (BS or BA), physical sciences preferred Proficiently speak English as a first or second language Have at least 3 years' experience with formulations stability testing. Proficiently 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 analyze complex data sets. Working knowledge of Microsoft Office programs and other scientific based software. Experience in Inhalation products (MDI) is a plus Must be authorized to work permanently in the United States Must be able to work on-site Working conditions This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. Physical requirements Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to10 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. GLOBAL COMPANY Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. GLOBAL COMPANY Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. CIPLA Fall River (INVAGEN PHARMACEUTICALS, INC.) 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 metered dose inhaler (MDI). The company was founded in 2003 and is based in Central Islip and 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 job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic 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.

Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at ***************** Astellas is announcing a Computational Chemist Lead opportunity at their Astellas Innovation Management (AIM) site in Cambridge, MA. Purpose: This role supports drug discovery efforts by applying advanced computational chemistry techniques to design and optimize small-molecule therapeutics. The position requires close collaboration with internal teams and external CROs to accelerate candidate selection and improve research productivity. The successful candidate will lead strategy across multiple programs and shapes the computational chemistry platform/standards in Innovation Lab, working closely with global teams. As Computational Chemist, you will be expected to contribute across multiple therapeutic areas and drug discovery efforts across various modalities including small molecules, proteins, bifunctional degraders, and biologics. Essential Job Responsibilities: Computational Drug Design: Apply molecular modeling, docking, molecular dynamics, homology modeling, and structure-based design to guide compound optimization Use cheminformatics and machine learning tools to analyze SAR, ADME/Tox profiles, and predict compound behavior. Develop generative models, reinforcement learning pipelines, and predictive analytics for compound design and optimization Curate chemical libraries, manage data pipelines, and support SAR/ADME analysis Can make recommendations on compound progression, integrate new platforms and tools and can make Go/No-Go decisions on compound progression, setting project goals and defining plans Drug Design & Synthesis: Design novel compounds based on ADME and SAR principles; optimize lead molecules for potency, selectivity, and pharmacokinetics. Data Analysis & Reporting: Analyze large datasets from simulations and experimental data with scientific rigor; interpret computational results and prepare detailed research reports and present findings internally and externally to technical and non-technical audiences. Cross-functional Collaboration: Work closely with medicinal chemistry, biology, pharmacology, protein science, and preclinical teams to ensure drug candidates meet efficacy and safety standards. Participate in program-related meetings and contribute strategic insight Intellectual Property: Identify and protect IP through patent filings and strategic documentation. Ensure accurate documentation of compound synthesis and project data Foster a collaborative, transparent, and creative team environment that drives innovation and invention. Close partnership with colleagues in Japan is expected. Technology Integration: Explore and apply cutting-edge technologies and global scientific trends to enhance research capabilities Stay current with scientific literature and emerging technologies Manage team priorities and resources in alignment with the company's overall I-Lab strategy and objectives CRO Management Oversee computational chemistry execution at CROs, including troubleshooting and performance enhancement Evaluate and onboard new CROs to improve cost-efficiency and research quality Maintain weekly communication and productivity tracking with CRO teams

Job Title: Quality Control (QC) Chemist (Metrology) FLSA Classification: Full-Time, Exempt Professional Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs) Reports To: Quality Control Manager Salary Range: $75,400 - $93,600 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, a combination of education, training, and special skills will determine the assignment of Level to a specific individual: 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 job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic 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. Duties and Responsibilities The general duties and responsibilities of the "Chemist" include but are not limited to the following: * Calibration and preventive maintenance of instruments. * Communications with vendors for installation, qualification and maintenance. * 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 * Working knowledge of raw materials testing and release * Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP * Lead investigation activities. * Ensure compliance to all data integrity and cGMP practices, procedures, and expect * Ensure compliance with all good documentation practices. * Other duties and responsibilities as assigned by the Head of the Department or Section Head Education and Experience: * Bachelor's degree (BS or BA), physical sciences preferred * Proficiently speak English as a first or second language * Proficiently 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 analyze complex data sets. * Working knowledge of Microsoft Office programs and other scientific based software. * Experience in Inhalation products (MDI) is a plus Working conditions This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or required. Physical requirements * Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to10 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. Professional and Behavioral Competencies * Must be willing to work in a pharmaceutical packaging setting. * Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday. * Must be willing to work some weekends based on business needs as required by management. * No remote work available * No employment sponsorship or work visas. GLOBAL COMPANY Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.) 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 Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited. 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.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description JobDescription: Skills: Must be detail-orientedand able to work with a high volume of documents in a fast-paced environment.Be highly organized and process-oriented. PreferredQualifications: Additional Information Best Regards, Sneha Shrivastava***********

Piper Health & Sciences is seeking a full-time iPSC Production Scientist to join a growing organization's Bio/Engineering Production team onsite at their Massachusetts location. The ideal candidate will have a strong biology background and hands-on experience in iPSC stem cell culture, differentiation, and QC within a pharmaceutical or biotech environment. Responsibilities of the iPSC Production Scientist Include: * Full-time onsite schedule: Monday-Friday, 9:00 AM - 5:00 PM * Lead and support iPSC production and related lab activities * Perform hands-on stem cell culture and differentiation * Execute QC-related tasks in accordance with SOPs * Maintain accurate lab documentation and records * Support Bio/Engineering Production workflows * Follow all safety, GMP, and GLP standards Qualifications of the iPSC Production Scientist Include: * Biology degree is strongly preferred (Biomedical Engineering degrees are NOT a fit) * Proven hands-on experience with: * iPSC cell culture * Stem cell differentiation * Quality Control (QC) processes * Pharmaceutical or biotech industry experience preferred Compensation of the iPSC Production Scientist Includes: * Salary Range: $83,200.00 - $114,000.00 per year (equivalent to $40.00 - $55.00 per hour), based on experience and certifications. * Comprehensive Benefits: CIGNA Medical, Dental, Vision; 401k through ADP and sick leave as required by law. * Ability to work with a well renowned and growing organization that has a robust pipeline and quality culture. This job opens for applications on 1/12/2026. Applications for this job will be accepted for at least 30 days from the posting date. #LI-AW1 #LI-ONSITE keywords: Scientist, iPSC Production, stem cell culture, induced pluripotent stem cells, cell differentiation, quality control, QC, laboratory scientist, cell biology, biotechnology, pharmaceutical production, bioengineering, GMP, GLP, SOP compliance, tissue engineering, regenerative medicine, bioprocessing, cell therapy, stem cell research, lab operations, onsite scientist, Medford MA jobs, contract scientist, PhD biology, master's biology, postdoctoral research, biotech scientist, pharma scientist, cell culture specialist, stem cell specialist, iPSC scientist, QC scientist, bio production scientist, laboratory techniques, cell-based assays, biotech careers, pharma careers, stem cell manufacturing, cell culture workflows, life sciences jobs, biopharma jobs, laboratory compliance, scientific documentation, biotech industry experience, pharmaceutical industry experience, cell line development, research scientist, production scientist, laboratory QC, stem cell differentiation protocols, cell culture maintenance, full-time onsite scientist, bioengineering production team, regenerative biology, tissue culture, cell therapy manufacturing, biotechnology research, pharmaceutical QC, biomanufacturing, cell biology techniques, stem cell QC testing, scientific method, laboratory safety standards, GMP compliance, GLP compliance, biotech contract role, scientist contract position, iPSC culturing, stem cell production, biotech Medford MA, pharma Medford MA, scientific careers, laboratory scientist jobs, cell therapy scientist, bioprocess scientist, QC laboratory scientist, stem cell lab work, biotech production workflows, pharmaceutical production workflows, life sciences contract jobs, biotech contract scientist, pharma contract scientist.

We are seeking a passionate PhD-level synthetic chemist to drive the discovery of small molecules for next-generation 3D printing resins. This position involves rapid exploration of chemical space through organic synthesis to develop photochemical and photophysical structure-property relationships. This role will be particularly appealing to chemists with a passion for both synthetic and physical organic chemistry. Our process uses a small amount of each lead candidate, so synthetic creativity is not limited by the scalability concerns that usually narrow the available chemical space in materials applications. Responsibilities Design, execute, and troubleshoot small molecule synthetic routes, with a focus on divergent or modular approaches to rapidly generate lead candidates. Characterize lead candidates via UPLC, NMR, UV/Vis and IR spectroscopy, and mass spectrometry. Contribute to the development of high-throughput analytical capabilities, small molecule databases, and virtual libraries. Work with cross-functional teammates to explore photochemical and photophysical structure-property relationships that drive 3D printing performance. Mentor junior scientists. Maintain excellent electronic lab notebook documentation. Minimum Qualifications PhD in Organic Chemistry or BS in Chemistry and 5+ years of experience in a small molecule discovery role. Strong expertise in both synthetic and physical organic chemistry, demonstrated through publications and other activities. Significant experience designing and executing multi-step synthetic routes. Extensive experience with modern computing and data analysis tools relevant to synthetic chemistry. Excellent communication, organizational, and time management skills. Demonstrated ability to independently drive an idea from conception to project completion. Evidence of strong collaboration and teamwork talents/skills. Strong publication record, both as lead author and as contributor to other projects. Preferred Qualifications Expertise in photochemistry and/or radical chemistry. Significant experience with synthesis of heterocyclic and/or extended aromatic systems, especially those relevant to organic (opto)electronics. Experience with cheminformatics and/or computational chemistry tools (e.g. DFT) relevant to the production of structure-property relationships. Benefits We offer competitive compensation packages in our VC-backed startup. Benefits include a full suite of offerings covering medical, dental, vision and 401k plan. Beautiful setting looking out over a river and seaport; outdoor seating and picnic areas. Highly collaborative work environment. Additional Information Travel: Occasional travel may be required from time to time Location: Boston, Massachusetts We value diversity in our company and are an Equal Opportunity Employer.

Job Title: QC Chemist II FLSA Classification: Full-Time, Exempt Professional Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs) Reports To: Quality Control Manager Salary Range: $72,800 - $93,600 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, a combination of education, training, and special skills will determine the assignment of Level to a specific individual: Duties and Responsibilities The general duties and responsibilities of the "Chemist" include but are not limited to the following: • Calibration and preventive maintenance of instruments. • Communications with vendors for installation, qualification and maintenance. • 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 • Working knowledge of raw materials testing and release • Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP • Lead investigation activities. • Ensure compliance to all data integrity and cGMP practices, procedures, and expect • Ensure compliance with all good documentation practices. • Other duties and responsibilities as assigned by the Head of the Department or Section Head Education and Experience • Bachelor's degree (BS or BA), physical sciences preferred • Proficiently speak English as a first or second language • Proficiently 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 analyze complex data sets. • Working knowledge of Microsoft Office programs and other scientific based software. • Experience in Inhalation products (MDI) is a plus Working conditions This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or required. Physical requirements • Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to10 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. Professional and Behavioral Competencies • Must be willing to work in a pharmaceutical packaging setting. • Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday. • Must be willing to work some weekends based on business needs as required by management. • No remote work available • No employment sponsorship or work visas. GLOBAL COMPANY Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.) 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 Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited. 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.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description JobDescription: Skills: Must be detail-orientedand able to work with a high volume of documents in a fast-paced environment.Be highly organized and process-oriented. PreferredQualifications: Additional Information Best Regards, Sneha Shrivastava ***********