Quality control analyst jobs in New Bedford, MA

Company Information: Tedor is a privately held pharmaceutical company a CDMO that develops drug product for both innovator and established companies. We are customer-focused oral solid dose CDMO with a strong track record of meeting aggressive development and commercialization timelines Over the past 20 years we have helped customers received many product approvals.We attribute this success to our company-wide focus on quality, customer service, and meeting timelines. Everything we do, and how we do it, is focused on helping our clients to achieve their product objectives. Position Summary: The role of the Quality Control Chemist is a vital role that is essential to manage and execute the quality testing that is required for drug substance on the commercial market. Quality Control Chemist will also be responsible for method validation and release & stability testing for clinical trial and commercial drug products; therefore, verifying all products and/or substances meet acceptable quality standards and that they are in accordance with the company's policies & procedures, FDA policies & procedures, and any applicable cGMP requirements. Additionally, ensuring compliance, accuracy, and timeliness of specified testing processes, environmental monitoring, data review, data analysis, and data trending of all raw materials, finished formulations, stability samples, client-based & company-based projects, method development, equipment calibrations/qualification and/or transfers, and cleaning study qualifications are all essential responsibilities. Quality Control Chemists are expected to collaborate with QC Analysts and Development Chemists while performing the QC Chemist position. This is a full-time, non-exempt position that includes a competitive salary, and strong benefits. The Quality Control Chemist will report Directly to the Quality Control Manager or Director. Position Description: Responsibilities Head the collaboration between QC and Developmental Chemists personnel but also cross department collaboration regarding drug product development, commercial operations, commercial manufacturing, Quality Assurance, and Analytical Development. Evaluation of QC laboratory operational execution and resources needed to preform tests. Generate, review and revise QC GMP documentation (SOPs, protocols, technical reports, specifications, etc.) as needed. Revise and manage technical transfer of methods from internal labs for raw material analysis, in-process testing, as well as API and Drug Product testing under supervision of the Director. Review and report all QC data and generate Certificates of Analysis. Monitor and trend QC data generated by internal and contract testing labs. Initiate ICH stability study protocols, execute and generate of interim reports. Manage, write, and review Out of Specification/Atypical results/Out of Trend investigations, deviations, and CAPAs. Investigate and troubleshoot method issues. Review relevant sections of regulatory filings. Monitor calibration schedule. Contact vendors. Schedule visits for PM/Calib and repairs. Assist vendors on site. Coordinate stability operation activities and ensure quality products and systems. Determine stability sample requirements, develop stability protocols and oversee execution of stability protocols. Monitor stability chambers and chart recorders on a daily basis to confirm environmental conditions for acceptance with established specifications. Prepare stability data graphs to estimate expiration dates and verify product shelf life. Evaluate stability trends and prepare reports. Equipment Qualification, including data integrity program. Position Type & Expected Hours of Work This is a full-time, non-exempt position requiring a minimum of 40 hours of work per week, Monday through Thursday and some in person Friday's.. Some responsibilities may require work outside of normal office hours. Work Environment Level 2: Office Environment and Laboratory Environment The work environment characteristics described here are representative of those a teammate encounters while performing the essential functions of this role and within the daily operations of a professional office environment. Reasonable accommodations may be made to enable employees with disabilities to perform essential functions. This job operates in a professional office environment, as well as the laboratory environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets, as well as standard laboratory equipment and instrumentation. An employee in this role will be exposed to standard hazards founds within a laboratory environment such as chemicals; bloodborne pathogens; fumes; select agents; confined spaces. Proper laboratory attire and safety gear such as protective eyewear; laboratory coat; appropriate gloves must be observed. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. This role requires standard physical demands within a standard office and laboratory environment where sustained periods of standing, sitting, or walking will be part of an employee's daily routine, whether they are at their desk or in the laboratory. While performing the duties of this role, an employee is regularly required to talk or hear; use hands or fingers to handle or feel; reach with arms; bend or stoop; climb stairs; crawl or crouch; kneel; push or pull; type on a keyboard; use a computer mouse. Lastly, an employee must be able to lift ten (10) pounds. Travel Limited travel is expected for this position. Required Education & Experience B.S. in Chemistry or Pharmaceutical Science, or other related discipline such as life sciences, drug product development. Five to Seven (3 - 5) years of work/laboratory experience in the pharmaceutical industry, Quality Control (QC). 3 + years of experience in a regulated manufacturing or QC laboratory environment of analytical methods for pharmaceutical products Experience in QC testing of pharmaceutical and/or biologic products in a GMP environment. Solid understanding of GMP compliance, Quality Control CMC requirements for ANDAs, and other regulatory filings Excellent interpersonal, verbal, and written communication skills Demonstrated collaborative skills and prior leadership roles or positions Comfortable in a fast-paced, small company environment, ability to adjust workload based upon changing priorities Technical knowledge Strong Microsoft Word, Excel, and Office skills Experience in contracting testing laboratories Preferred Experience & Experience BS in relevant life science, scientific, or engineering discipline Three to Five (3 - 5) years of work/laboratory experience in the pharmaceutical industry, Quality Control (QC). Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. All duties, responsibilities, and activities may be subject to change at any time with or without notice. EEO Statement: Tedor Pharma, Inc. is proud to be an Equal Employment Opportunity and Affirmative Action employer. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. We do not discriminated based upon race, religion, color, marital status, national origin, gender, sexual orientation, gender identity, gender expression, age, status as a protected veteran, ancestry, medical condition, pregnancy, genetic information, status as an individual with any mental and/or physical disabilities, or any other status protected under federal, state, or local law.

We are seeking an enthusiastic Associate Synthetic Chemist to support the discovery of small molecules for next-generation 3D printing resins. You will work hands-on in the lab, executing syntheses of novel molecules, characterizing products, and exploring photochemical and photophysical structure-property relationships. This role is ideal for highly motivated early-career chemists who love synthesis and are excited to accelerate innovation through fast, iterative chemistry. You will be closely mentored by experienced synthetic chemists and will collaborate with analytical scientists and engineers developing our printing systems. Responsibilities Design, execute, and troubleshoot small molecule synthetic routes, with a focus on divergent or modular approaches to rapidly generate lead candidates. Purify products using chromatography and crystallization techniques. Characterize compounds via UPLC, NMR, UV/Vis and IR spectroscopy, and mass spectrometry. Work with cross-functional teammates to explore photochemical and photophysical structure-property relationships that drive 3D printing performance. Maintain excellent electronic lab notebook documentation. Contribute to management of chemical databases (e.g., commercial, proprietary, and virtual compound libraries). Minimum Qualifications Bachelor's degree in Chemistry or a closely related field with equivalent advanced chemistry coursework. ≥2 years of intensive organic synthesis laboratory experience (academic research and/or industrial roles). Experience with synthetic planning with chemical databases (e.g., SciFinder, Reaxys). Excellent command of synthetic and physical organic chemistry fundamentals. Experience with air-sensitive techniques (e.g., Schlenk line), purification (chromatography/crystallization), and data interpretation (NMR / LC-MS). Evidence of strong documentation and organizational skills, attention to detail, and the ability to manage multiple workflows efficiently. Evidence of strong collaboration and teamwork talents/skills. Ability to thrive in a fast-paced, collaborative R&D environment. Preferred Qualifications Command of the basics of photochemistry. Experience with heterocyclic and/or extended aromatic systems, especially those relevant to organic (opto)electronics. 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.

About Aura: Aura Biosciences is a clinical-stage biotechnology company focused on developing precision therapies for solid tumors that aim to preserve organ function. Our lead candidate, bel-sar (AU-011), is currently in late-stage development for primary choroidal melanoma and in early-stage development in other ocular oncology indications and bladder cancer. Aura Biosciences is headquartered in Boston, MA. Our mission is to grow as an innovative global oncology company that positively transforms the lives of patients. For more information, visit aurabiosciences.com. Follow us on X (formerly Twitter) @AuraBiosciences and visit us on LinkedIn. Position Summary: Aura Biosciences is seeking a highly motivated and detail-oriented QC Scientist to support method validation and routine QC operations for our innovative oncology therapeutics. This role is critical to ensuring the integrity and compliance of analytical methods used in the testing of drug substance and drug product across clinical stages. Key Responsibilities: Lead and execute method qualification and validation activities in alignment with ICH guidelines and GMP standards. Support and oversight of routine QC testing of plasmid, drug substance (DS) and drug product (DP), including release and stability studies. Collaborate with CMOs and CROs to ensure timely and compliant execution of analytical activities. Author and review technical documentation including validation plans, protocols, reports, SOPs, and CoAs. Manage validation timelines and proactively provide solutions to method challenges. Participate and lead investigations (OOT/OOS), CAPAs, and continuous improvement initiatives. Review and trend analytical data routinely for specification evaluation. Ensure compliance with internal quality systems and regulatory expectations. Contribute to cross-functional CMC discussions and provide technical input on overall analytical strategy. Key Skills Analytical Method Validation - Strong understanding of ICH Q2(R2), GMP principles including compendial methods and data integrity. Instrumentation Expertise - Proficiency in HPLC, UV-Vis, Empower, Bioassays, qPCR other analytical platforms and compendial methods. Collaboration - Effective communication with internal teams and prior experience managing external partners (CMOs/CROs) is preferred. Technical Writing - Skilled in drafting and reviewing protocols, reports, and SOPs. Problem Solving - Experience with OOS/OOT investigations and root cause analysis. Project Management - Ability to manage timelines and deliverables across multiple stakeholders. Regulatory Knowledge - Familiarity with FDA and EMA expectations for QC and validation. Attention to Detail - High level of accuracy in data review and documentation. Statistical analysis using JMP, Minitab or equivalent. Minimal travel is required to CMOs. Role is a hybrid role (minimum 3 days onsite). Minimum BS in Sciences with at least +5 years' experience or MS and 2+ years Salary & Benefit Information: Salary Range: $105,000/yr - $135,000/yr (Placement within the listed range depends on many factors including, but not limited to: geographic location, degree, years of experience, and internal company equity) Health insurance with FULL premium coverage 401K with company match Employee Stock Purchase Program (ESPP) Competitive paid time off (PTO) Company-paid short & long-term disability insurance and life insurance

Advancing medicine to save lives. Together. Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases. Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family-owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best-in-class solutions - together with our clients. Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability. As an independent family-owned company, we live by the motto: Many hands, many minds - ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together: advancing medicine to save lives. Duties and Responsibilities Laboratory role to support the qualification and validation of analytical methods for biologic drugs and process related impurities Primary focus on the execution of experiments to support the validation of molecular biology assays including but not limited to ELISAs for residual HCP, residual protein a, and relative potency assays as well as qPCR Work collaboratively within a group of scientists to perform analytical method development qualification or validation under cGMP in collaboration with the Quality Control unit Apply expertise in molecular biology, cell biology and/or immunochemistry to analytical development team across the lifecycle of the procedures Participate in the technology transfer of analytical methods into QC and analytical method qualification Method transfer, method validation, method development Review & revise SOPs and/or author reports, protocols & other documentation as appropriate Collaborate with other labs to prepare methods for transfer to the QC GMP labs Provide training and work direction for group members as required Qualifications Bachelor's Degree in chemistry or a biological science with minimum of 8+ years of related experience (or master's degree with 5+ years of experience) in a cGMP environment Experience utilizing Spectramax M5 or M2 plate readers and the associated Softmax GMP software required Strong understanding of molecular biology assays in support of the product quality testing for Biologics drug substances/drug products Experience with analytical characterization of biologics is expected Strong organizational, time management skills, and prioritize work schedule to meet deadlines Must be able to communicate effectively with managers, peers, and clients Must demonstrate effectiveness in ability to train others as needed Strong knowledge and expertise of quality requirements pertinent to pharmaceutical AD labs Strong working knowledge of laboratory safety including standard precautions associated with hazardous & biohazardous material handling Experience with drug substance, drug products, intermediates, as well as experience with monoclonal antibodies is desired Experience in other biophysical characterization methods CE (capillary electrophoresis), chromatography, SEC/RP/IEX-U(H) PLC, SDS-CGE, iCIEF, CIEX, Peptide mapping is a plus Computer skills to include full competence with Microsoft Word, Power Point & Excel Working Conditions Laboratory environment working with chemical reagents and analytical equipment Normal office working conditions: computer, phone, files, fax, copier Personal Protective Equipment must be worn as required Minimum travel required Physical Requirements Frequent lifting up to 10 lbs.; frequent standing/walking Manual and visual dexterity required to perform laboratory and computer tasks for prolonged periods PPE as required ____________________________________________________________________________ Base Pay Range $52/hr - $67/hr

Job Description Senior Scientist, Analytical Chemistry & Quality Control Salary: $100,000-$130,000 FLSA Status: Exempt We are on the search for a Senior Scientist to join our team at Pharmaron's manufacturing site in Coventry, RI. In this position, the Senior Scientist, Analytical will support process chemistry and manufacturing activities through analytical method development, optimization, validation, and transfer in compliance with all applicable guidelines. Primary Responsibilities: Develop, optimize and validate analytical methods that are GMP friendly based on quality-by-design and document formal protocols and reports. Participate in method transfer activities, including writing protocols and reports. Perform stability testing and data trending, as required. Review and Approval of Scientific Reports and SOPs. Manage analytical projects, coordinate analytical activities and ensure the project timelines are met. Implementing new analytical techniques and strategies to expand departmental capabilities. Solving multiple complex scientific problems. Ensuring adherence to GMP. Presenting and communicating clearly and effectively with clients. Experience and Education: PhD in Chemistry with 2 years of experience or MSc/BS in Chemistry or related field with 6 years of experience with the following instrumentation: HPLC, GC, NMR, FTIR, UV. Excellent communication skills, both verbal and written. Effective in managing multiple competing activities and delivering to timelines. Ability to work in a cross-functional environment. Working knowledge of cGLP/cGMP and applicable FDA, EMA, and ICH guidance preferred. High level of awareness of innovative technologies and ability to adapt to in-house needs. Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process. With over 21,000 employees and operations in the U.S., U.K., and China, Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China. Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. Our core cultural values are "Employees Number One" and "Clients Centered," setting Pharmaron apart from other organizations. Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package, including: Medical, Dental & Vision Insurance with significant employer contributions. Employer-funded Health Reimbursement Account. Healthcare & Dependent Care Flexible Spending Accounts. 100% Employer-paid Employee Life and AD&D Insurance. Short- and Long-Term Disability Insurance. 401(k) plan with generous employer match. Access to an Employee Assistance Program. Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences. #ED-L1

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.

- Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP - 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 - 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 Skills Hplc, Gmp, Karl Fisher, Particle size, icp, gc-ms, quality control, raw material, data entry, Wet chemistry, Analytical chemistry Top Skills Details Hplc,Gmp,Karl Fisher,Particle size,icp,gc-ms,quality control Additional Skills & Qualifications Frist Shift- General Shift: 8:30AM - 5:00PM Monday -Friday Level II Pay Rate- $5,000K-$82,500K Level III-$83,000-$90,000 They're hiring across levels (QC Chemist II & III). QC Chemist II should be between 2-3 years' experience in industry. Co-op experience in a cGMP pharmaceutical manufacturing setting is also acceptable especially for a level I. QC Chemist III should be at least 3-5 industry experience not academic experience. I'd prefer to focus on the Level II based on our previous experience with the hiring team and the level of expertise they desire. - Bachelor's degree (BS or BA), physical sciences required - Master's degree preferred - Minimum of 3-5+ years' experience. - 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. Experience Level Intermediate Level Job Type & Location This is a Permanent position based out of Fall River, MA. Pay and Benefits The pay range for this position is $65000.00 - $90000.00/yr. HealthVisionDental 401K Workplace Type This is a fully onsite position in Fall River,MA. Application Deadline This position is anticipated to close on Dec 15, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Since 2009, Info Way Solutions has earned a reputation as a full-service staffing firm that excels in a fast-paced marketplace. We have placed highly skilled professionals on a temporary, temporary-to-hire and direct-hire basis in the fields of accounting and finance, IT technology,office administration, marketing and design. Info Way Solutions is dedicated to providing you quality professionals with well-matched skills to your unique hiring requirements and workplace environment. We collaborate with customers to consistently and cost-effectively plan, execute and deliver high-quality services and results.Our consultants are seasoned professionals who build long-term,trusted relationships that bring about a high level of energy, integrity, experience and value to our client's work. Our superior client-consultant relationships and in-depth insight of services have resulted in significant repeated business with clients. In addition, we are partners with best-in-class technology vendors that enable us to best determine the most appropriate hardware, software and services to cater to any of our client's business needs. We have often collaborated with them to make optimal use of today's technology while also planning for the future. More than 50 customers - including mid-market leaders and many of the Fortune 500 Companies - rely on our expertise to leverage their investments. Job Description Responsible for cleaning\decontamination of returned product samples. After processing of samples, responsible for shipping samples to appropriate manufacturing location. Must be able to handle lifting of boxes on a daily basis. Will be responsible for lifting Biohazards shipping boxes with assistance from a second person to be placed on a designated cart; these boxes can weigh upwards of 55 pounds. Analyze samples using specific procedures and instrumentation. Maintain documentation. May provide assistance in troubleshooting results outside of predefined specifications. SUMMARY OF POSITION: The candidate will support the Post Market Vigilance Investigations team's activities for the Patient Monitoring and Recovery (PMR) Division. These activities include; assist in managing the receipt of incoming physical complaint product, conducting follow ups with accounts and/or International Subsidiaries to rectify discrepancies with product receipt, assisting in managing the process flow of complaint investigations, performing Device History Record Reviews, and performing root cause analysis on PMR Product customer returns to ensure high levels of quality, reliability, safety, and efficacy. Additional responsibilities include management of clinically applied medical device retains and associated paper records in accordance with Covidien Medtronic Record Retention Policies and support staffing needs. ESSENTIAL FUNCTIONS: • Assist PMV Investigations Coordinator with managing receipt of physical complaint product samples, in addition to corresponding with domestic and international accounts to rectify discrepancies in product receipt. • Assist in the coordination of sanitization of clinically applied medical device returns and shipment to respective Medtronic Manufacturing facilities, as well as coordinating the investigation process with internal Engineering and Quality groups. • Test and thoroughly evaluate clinically applied surgical medical devices of various degrees of complexity to determine root cause analysis within a closely monitored time frame. • Identifying the appropriate test method/regiment from existing Standard Operating Procedures for complaint sample evaluation, execute the method, and interpret the data (technical) for definitive root cause analysis determination. Test methods may include dimensional and/or tensile testing and interpretation of the technical data yielded in accordance with USP/EP/ASTM standards. • Replicate reported failure mode with bench top or in vivo test methods and document observations accordingly. • Initiate and distribute Corrective Action Requests to Manufacturing or Engineering Departments as needed. • Prepare technical investigation reports based on results of evaluation and/or review of the manufacturing plant reports to be documented in the QA (Quality Assurance) Department complaint database and incorporated into customer response letters. • Certification with OSHA's BloodBorne Pathogens Standard 29 CFR 1910.1030 and adherence to Corporate and Local Environmental Health and Safety Policies. MINIMUM REQUIREMENTS: Minimum Experience: 2 to 3 yrs • Academic or work experience in a laboratory or manufacturing environment. Experience with laboratory equipment or test equipment or manufacturing equipment highly desirable. • Experience with medical devices preferred but not required. Skills/Qualifications: • Must be proficient with MS Office (with emphasis on Excel and Word). • Critical independent thinking and timely follow up. • Time management skills. • Excellent written and verbal skills necessary. QD003425-001, Rev A ORGANIZATIONAL RELATIONSHIPS/SCOPE: • Quality Assurance • Manufacturing • Engineering • Research and Development • Regulatory Affairs • Legal • Marketing/Sales WORKING CONDITIONS: Biohazardous laboratory environment requiring use of personal protective equipment in accordance with CDC and OSHA regulations. Responsible for cleaning\decontamination of returned product samples. After processing of samples, responsible for shipping samples to appropriate manufacturing location. Must be able to handle lifting of boxes on a daily basis, some boxes weigh upwards of 50 pounds each. Must be able to handle lifting of boxes on a daily basis. Will be responsible for lifting Biohazards shipping boxes with assistance from a second person to be placed on a designated cart; these boxes can weigh upwards of 55 pounds. Analyze samples using specific procedures and instrumentation. Maintain documentation. May provide assistance in troubleshooting results outside of predefined specifications. Qualifications Education: BS Degree in a Science or Engineering discipline.

WHY WORK AT SILK TITLE CO. Silk Title Co. is a privately owned, fast-growing company which handles billions of dollars a year in real estate transactions for some of the nation's top fin-tech institutions. Our motto, Service at Scale, combines our technology, proprietary processes, and talented team to deliver title insurance, search, and settlement services across the nation. We recently completed the expansion of our office in Warwick, RI into a brand-new modern workspace and dedicated employee flex space and training room. We plan to bring on new hires as we continue our growth . Stuffy cover letters and fancy sounding resumes are not our thing. We want people with focused energy, solid work ethic and curious minds capable of absorbing everything we can teach about our business. Our employees are what make our company exceptional; we are a diverse team of problem solvers, QA experts, and business process gurus. We all depend on each other which is why everyone brings their A game each day. We work hard but also know how to incorporate some fun through team building challenges, staff meetings and an abundance of swag. Our workplace exemplifies our core values of quality, communication, experience, transparency, and respect. Other benefits include: Positive work environment where individual and team contributions are recognized and rewarded. Brand New Modern Workspace Dedicated Employee Flex Space and Training Room Tech focused environment Health Benefits Paid time off Employee Assistance Program 401k Pay range: $17-$21/hr., eligible for overtime. Business hours are 9am until 10pm THE POSITION: Recording/ Quality Control Specialist We are currently looking for top talent to fill our role of Recording/ Quality Control Specialist. The Recording/ Quality Control Specialist works as part of a team to ensure that all closing conditions, as laid out by the lender or their investor, are met after signing and that all transactions are disbursed timely as scheduled. ESSENTIAL RESPONSIBILITIES OF THE RECORDING/ QUALITY CONTROL SPECIALIST INCLUDE BUT ARE NOT LIMITED TO: Responsible for the daily workflow within the department and may include Reviewing, processing, or servicing of loan documentation Ensuring that all work has been completed and departmental deadlines have been met Responsible to understand and comply with bank policies and federal, state, and other governmental rules and regulations for multiple banks in multiple states Open packages, confirm contents, and distribute work based on what packages have arrived Responsible for quality control review of received packages Communicate and resolve any discrepancies on required documents Scan packages into Resware, confirm documents have been uploaded, and organize file per department standards Prepare and box original package for FedEx delivery to final destination Collaborate with the Funding department to ensure timely funding of completed packages Manage the Post-Closing inbox, ensuring to communicate with clients in a timely manner via telephone or email Review reporting and follow-up on files pending funding to ensure needed documents and corrections have been resolved Resolve any problems, issues or questions, both verbally and in writing, to ensure customer satisfaction and to maintain productive relationships with other bank departments. Participates in other duties as assigned. **The Recording Specialist must live within a commutable distance to the Warwick, RI office.**

JOIN THE TEAM! Under the supervision of our Operations Director, you will be trained to ensure all company standards are met and maintained at each individual location. We are looking for responsible individuals that: Will be reviewing daily store status reports Documenting and tracking store readiness per the given guidelines. Observing locations using video monitoring systems to ensure and report the given sales process are being followed. The individual must stay up-to date on all current sales promotions and processes. Requirements: High school diploma or general education degree (GED), required Ability to use video monitoring equipment Ability to interpret a variety of instructions furnished in written, oral or schedule form Ability to work on the internet, Spreadsheet, Presentation and Word Processing software Strong written and verbal communication skills Must have the ability to complete required applicable forms in English, which requires the ability to read and write in English. Ability to work well with others in fast paced, dynamic environment. Ability to be respectful, approachable and team oriented while building strong working relationships and a positive work environment. .

Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care. SUMMARY DESCRIPTION The Quality Control Inspector II will be responsible for performing quality inspections and testing according to established procedures. Inspection and testing activities will cover incoming, work-in-process, and finished goods. Selects random samples for tests at specified stages such as incoming or in production process, and tests products for variety of qualities, such as dimensions, performance, appearance, correct assembly, and other testing outputs. Records test data, applying statistical quality control procedures. Works collaboratively with Manufacturing, Engineering, Quality Assurance, and other functional experts to support all daily operational activities. Consults with management to resolve quality, production, and efficiency problems. Functions in conjunction with manager and functional experts on special department projects. Performs the essential duties and responsibilities listed in section below. ESSENTIAL DUTIES AND RESPONSIBILITIES To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Primary responsibilities are to: Perform chemical assay of solutions as well as general laboratory maintenance. Performs in-process and final inspection of all products for conformance to specifications. Maintains and records quality testing information as part of a DHR (Device History Record). Maintains work areas and equipment in a clean and orderly condition. Must be able to work in a Team environment, multi-task and communicate effectively. Inspection and testing of raw materials, intermediates and recording of test results. Maintains a working inventory of all components and archived materials and solutions. Assist as needed in test method validation, implementation, and execution. Provide database support, generate reports and analyze process data. Assist in Out of Specification (OOS) and non-conformance (NC) investigations. Assist in preparing for and participating in FDA audits, customer audits, etc. Demonstrate excellent organizational and time management skills. Demonstrated competency of MS Suite. Perform other duties as required. DESIRED MINIMUM QUALIFICATIONS Minimum required education and experience: High School Diploma or equivalent with 1+ years of experience in a medical device, pharmaceuticals, Quality/Regulatory Compliance, or other regulated industry. Familiarity with application of FDA and/or ISO quality standards in a government regulated industry. Moderate computer competence, including experience with database and Microsoft Office software to create reports, spreadsheets, analyze data and prepare presentations. Working knowledge of standard laboratory practices and safety. Ability to follow instructions precisely, recognize deviations, and recommend corrective action. Detail-oriented. TOOLS AND EQUIPMENT USED Calipers, rulers, dataloggers, standard office equipment (i.e. computers, phones, photocopiers, filing cabinets, other general office equipment). PHYSICAL REQUIREMENTS The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills required of position in order to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position. While undertaking the essential duties and responsibilities of the position, the employee must repeatedly sit, listen, speak and have the ability to move throughout all locations of the building. The employee is required to go to all areas of the company. The employee may be required to periodically lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. ADVERSE WORKING CONDITIONS The adverse working conditions listed in this section include, but are not limited to, those environmental conditions to which the employee may be exposed while undertaking the essential duties and responsibilities of this position. Adverse exposure may result from the handling of hazardous and bio-hazardous materials that include, but are not limited to, flammable and corrosive liquids, compressed gases, sharps, and medical wastes. SELECTION GUIDELINES Formal application, rating of education and experience; oral interview and reference check; job related tests may be required. DISCLAIMER The duties listed above are intended only as illustrations of the various types of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position. The job description does not constitute and employment agreement between the employer and employee and is subject to change by the employer as the needs of the employer and requirements of the job change. Salary Pay Range: $21.12 - $27.98 USD Hourly Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training. In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Additional Description for Pay Transparency: Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, Employees are eligible for the following ******************************************* Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status. This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices: EEO Is the Law | EOE including Disability/Protected Veterans Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at ***********************. Unsolicited Agency Submission Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate's name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails. Integra - Employer Branding from Integra LifeSciences on Vimeo

Location: 150 Kerry Place, Norwood, MA, 02062 Would you like a new career where you get training and have an opportunity to advance? Do you want to stop working crazy hours and have some flexibility in your schedule? As a Field Manager / Quality Control / Trainer, you are a key team member in upholding our commitment to customer satisfaction and professionalism. With a career at Molly Maid, you will bring customers joy and relief, and reward yourself in the process. Ready to join a company and a team that will support you? Apply today - we're ready for you!Prior customer service, training, cleaning experience or equivalent experience with the ability to learn quickly is a must!This job is right for you if you are self-motivated, energetic, and enjoy helping people. You are driven to provide the highest level of customer service and satisfaction, and able to effectively manage a variety of situations on a day-to-day basis. We'll teach you everything you need to know about what makes Molly Maid unique including our proven cleaning process, highly trained programs, commercial grade equipment and supplies, and our unique culture. Once you've enjoyed training in the Molly Maid process, you'll provide support to the teams that will deliver exceptional service customers. Part-Time. No nights. No weekends. No holidays. Receive a guaranteed minimum wage of $18. 00 per hour, paid weekly. If you delight customers using our proven processes and reach weekly and monthly targets, EARN EVEN MORE with our attractive incentives!We provide:A stable and consistent working schedule Paid training on our proven systems that WOW customers. Come grow with us!A fun culture where success is celebrated as a team. Access to ongoing training. And… a COMPANY CAR during work hours so you don't have to put miles on yours (gas and insurance included) Branded and comfortable clothing Benefits & PayThe pay range for this position is from $18/hr and is dependent on your experience and ability to connect, mastery of our processes and ability to retain and grow both customers and employees with your leadership. As a Field Manager / Quality Control / Trainer, you will be responsible for:• Grow and retain customers and employees - Follow our process and training while being "YOU" and you'll please delight every customer and employee. Do this and we'll celebrate as a team and have fun in the process! • Communicate with customers and employees in a friendly, positive, and professional manner - Our team members love our customers, and you will too. Show them you care about their home, and you'll win. As our brand ambassador in the field, you train cleaning staff on our processes and quality. Coach our staff on quality feedback from customer communications and home visits. Celebrate their good work while connecting with them on how to improve and delight customers every time. • Perform quality checks - Coach our staff on quality feedback from customer communications and home visits. Celebrate their good work while connecting with them on how to improve and grow. Develop relationships to satisfy and retain customers. • Build our culture and team - Interview, hire, and train individuals that build our team's energy and culture. Embrace our culture of teamwork and let your positive attitude energize the team. • Kick off our day! - Connect with the teams and set them up for a successful day. Manage and monitor teams' performance. This job will be a great fit for you if…• You feel energized talking with customers in their home. • You enjoy improving professionally, learning about what makes Molly Maid unique, managing customer expectations and working with our cleaning teams to deliver an experience for our customers that they will recommend to their friends and family. • You take pride in your attention to detail and a job well done. • You like knowing that there's a process for providing great training and follow through. • You want to learn new things and work in a variety of environments while getting to know our customers. • You enjoy leading and training a team. • You enjoy developing relationships and following through on exceptional service. Job Requirements Minimum requirements to be considered for position. • Legally authorized to work in the United States• Are 18 years of age or older• Prior cleaning and supervisory experience or equivalent experience • Complete a background check • Valid Driver's License• You are available to work Monday through Friday, 8am to 2/3pmReady for a fresh start where you can be your best?If that's you, APPLY TODAY! ************ or email mollymaidcanton@mollymaid. com If you meet the requirements for this position, we will schedule you for an interview immediately. "You are applying to work for a franchise owner of Molly Maid. If hired, the franchise owner will be your only employer. Franchise owners are independent business owners who are solely responsible for their own wage and benefit programs that can vary among franchise owners. This job description is meant to describe the general nature and level of work being performed. "

& Purpose Allonnia's purpose is the pursuit of imaginative solutions to solve the world's toughest waste challenges through biology. Allonnia is leveraging the power of biotechnology and engineered systems to degrade or sequester pollutants and upcycle waste. Our ethos at Allonnia is to work in harmony with nature, combining biology and technology to fast forward time and bring Nature's future solutions to the present day. Through this collaboration we will unlock the potential in waste and enable a world where nothing is wasted. Allonnia is backed by Battelle, Ginkgo Bioworks, Viking Global, General Atlantic, EVOK and Cascade Investments. Mission of the Position The mission of the role is to 1) Advance the extraction and purification processes of mining ores through a multifaceted approach that includes use of biological and chemical solvents 2) perform lab experiments following SOPs and assisting with SOP optimization 3) operate and maintain laboratory instruments; record and manage data This is a full-time position that requires 100% time in the lab. This role is for Northeastern University students and will run from January-June 2026. Key Criteria/Requirements Preferred B.S or M.S. in chemistry, geology, chemical engineering or related field 0-2 years of Laboratory experience (college experience possible). Ability to follow standard operating procedures (SOPs) Strong analytical skills Excellent numerical skills Strong problem-solving skills Meticulous attention to detail and accuracy Experience with Microsoft Windows and Office tools Demonstrated ability to work independently as well as in team environment Excellent verbal and written communication skills Adaptable and able to work in a fast-paced environment Responsibilities & Measurable Accountabilities Perform a variety of laboratory experiments following SOPs and assist with SOP optimization Operate, maintain, and clean laboratory instruments and equipment Prepare buffers and media Knowledge of chemistry principles Comply with all safety standards Maintain a lab notebook; Record and manage data Communicate results, observations, and/or issues related to lab equipment, materials and experiments to supervisors Allonnia Core Values Purposeful Committing to work on the right things as individuals and as a company, making a difference every day Entrepreneurial Working with passion and curiosity to learn every day, creatively delivering results to the world Transparent Fostering a high trust environment that embraces constructive debate, achieving success together Key Competencies Analysis Skills Creativity Integrity Resourcefulness/Initiative Organization/Planning Listening Team Player Communications - Oral/Written Tenacity JOB CODE: 1000085

Work Schedule Second Shift (Afternoons) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials Job Description Sr. Quality Control Technician Location: Plainville, MA Schedule/Hours: M-F 8-4:430 * Shift will transition to Wed-Sat 2nd Shift (1:00PM-11:30PM) Thermo Fisher Scientific's Viral Vector Services (VVS) is a fast-growing gene therapy CDMO looking for skilled individuals to improve processes and products for clients. As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Location/Division Specific Information: At Viral Vector Services (VVS) a division of Thermo Fisher Scientific, we deliver from process development through commercial supply, we offer the expertise and resources necessary to help clients deliver innovative gene therapies. Placed in the forefront of our leading and ground breaking Cell and Gene Therapy business, our mission is to enable clients to cure genetic, rare, and otherwise untreatable diseases. How Will You Make an Impact? The Senior Quality Control Technician offers advanced QC support for sample control and routine maintenance activities, ensuring compliance with lab documentation systems. This role upholds stringent control of sample traceability to internal and external QC labs and is instrumental in training junior associates. A Day in the Life: Provide QC support for sample control and routine maintenance activities. Ensure compliance of lab documentation systems. Maintain critical control of sample traceability to internal and external QC labs. Train junior associates. Perform inspections and sampling of incoming materials, including bulk liquids and cell banks, and review and disposition of raw materials. Support general laboratory functions such as ordering and stocking supplies, maintaining chemical retain inventory, and managing hazardous waste disposal. Assist with drafting and revising material specifications, standard operating procedures (SOPs), and other department documentation. Lead or assist in deviation investigations to ensure timely closure. Lead new equipment initiation and preventative maintenance tasks. Education: High school diploma or equivalent education required. Experience: Required: Minimum of 2 years of work experience in QA or QC or related field Preferred: Experience in a cGMP environment. Knowledge, Skills, Abilities: High ethical standards - will not compromise quality requirements. Advanced documentation, communication, and digital literacy. Extensive experience with aseptic technique required. Advanced proficiency in using standard computer programs such as MS Excel, Word, and Access. Physical Requirements / Work Environment Frequently required to stand, sit, use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. Occasionally required to walk, climb, balance, stoop, kneel, crouch, or crawl. Must frequently lift and/or move up to 10 pounds with or without accommodation. Specific vision abilities required by this job include close vision and the ability to adjust focus. Required to wear Personal Protective Equipment (PPE). Daily computer use. May include working with dry ice, liquid nitrogen cryogenics, hazardous and infectious agents, as well as marked changes in temperature. Flexibility to be reassigned to other business unit locations within Massachusetts as business needs dictate. What We Offer Compensation Competitive Hourly Pay Rate Additional shift differential for 2nd shift and 3rd shift positions! Annual performance-based bonus Annual merit performance-based increase Excellent Benefits Benefits & Total Rewards | Thermo Fisher Scientific Medical, Dental, & Vision benefits-effective Day 1 Paid Time Off & Designated Paid Holidays Retirement Savings Plan Tuition Reimbursement Employee Referral Bonus Career Advancement Opportunities Compensation and Benefits The hourly pay range estimated for this position based in Massachusetts is $21.82-$36.36. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: *****************************************************

Senior Scientist, Analytical Chemistry & Quality Control Salary: $100,000-$130,000 FLSA Status: Exempt We are on the search for a Senior Scientist to join our team at Pharmaron's manufacturing site in Coventry, RI. In this position, the Senior Scientist, Analytical will support process chemistry and manufacturing activities through analytical method development, optimization, validation, and transfer in compliance with all applicable guidelines. Primary Responsibilities: Develop, optimize and validate analytical methods that are GMP friendly based on quality-by-design and document formal protocols and reports. Participate in method transfer activities, including writing protocols and reports. Perform stability testing and data trending, as required. Review and Approval of Scientific Reports and SOPs. Manage analytical projects, coordinate analytical activities and ensure the project timelines are met. Implementing new analytical techniques and strategies to expand departmental capabilities. Solving multiple complex scientific problems. Ensuring adherence to GMP. Presenting and communicating clearly and effectively with clients. Experience and Education: PhD in Chemistry with 2 years of experience or MSc/BS in Chemistry or related field with 6 years of experience with the following instrumentation: HPLC, GC, NMR, FTIR, UV. Excellent communication skills, both verbal and written. Effective in managing multiple competing activities and delivering to timelines. Ability to work in a cross-functional environment. Working knowledge of cGLP/cGMP and applicable FDA, EMA, and ICH guidance preferred. High level of awareness of innovative technologies and ability to adapt to in-house needs. Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process. With over 21,000 employees and operations in the U.S., U.K., and China, Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China. Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. Our core cultural values are "Employees Number One" and "Clients Centered," setting Pharmaron apart from other organizations. Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package, including: Medical, Dental & Vision Insurance with significant employer contributions. Employer-funded Health Reimbursement Account. Healthcare & Dependent Care Flexible Spending Accounts. 100% Employer-paid Employee Life and AD&D Insurance. Short- and Long-Term Disability Insurance. 401(k) plan with generous employer match. Access to an Employee Assistance Program. Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences. #ED-L1

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.

QC Chemist II & III - Pharmaceutical Manufacturing (Relocation Offered!) Ready to take your analytical skills to the next level? Join a leading pharmaceutical team where precision, innovation, and quality drive everything we do. We're hiring QC Chemists (Levels II & III) to perform critical testing and ensure compliance in a dynamic cGMP environment. What You'll Do: + Perform routine and advanced testing using cutting-edge instruments such as HPLC, GC, ICP, Karl Fischer, and Particle Size Analyzers. + Conduct raw material testing and release activities to maintain product integrity. + Lead investigations and troubleshoot complex analytical challenges. + Operate specialized equipment and perform critical testing to support manufacturing and quality goals. + Ensure strict compliance with cGMP, data integrity, and good documentation practices. + Collaborate with cross-functional teams and contribute to continuous improvement initiatives. What We're Looking For: + Bachelor's degree in Physical Sciences (Chemistry preferred); Master's degree is a plus. + QC Chemist II: 2-3 years of industry experience (Co-op experience in cGMP setting considered). + QC Chemist III: 3-5+ years of industry experience. + Strong knowledge of analytical chemistry techniques and instrumentation. + Excellent organizational skills and ability to analyze complex data sets. + Proficiency in English (written and verbal) and Microsoft Office tools. Why Join Us? + Competitive salary: + Level II: $75,000-$82,500 + Level III: $83,000-$90,000 + Relocation assistance available - we'll help you make the move! + Work in a state-of-the-art cGMP pharmaceutical environment. + Opportunity for career growth and skill development in a collaborative team setting. + General shift: Monday-Friday, 8:30 AM - 5:00 PM. If you're ready to advance your career and contribute to life-changing therapies, apply today and be part of something impactful! Job Type & Location This is a Permanent position based out of Fall River, MA. Pay and Benefits The pay range for this position is $65000.00 - $90000.00/yr. HealthVisionDental 401K Workplace Type This is a fully onsite position in Fall River,MA. Application Deadline This position is anticipated to close on Dec 12, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Job Description Position: QC Scientist/Sr. Scientist (3rd shift, working hours: 11 pm- 7am), Quality Control & Analytical FLSA Status: Exempt We are on the search for a 3rd shift QC Scientist to join our QC team at Pharmaron's manufacturing site in Coventry, RI. In this position, the Scientist will support manufacturing and process chemistry activities through analytical method verification, optimization and sample testing in compliance with all applicable guidelines. Primary Responsibilities: Sample raw materials and conduct QC testing of raw materials, intermediates, API, IPC and cleaning verification samples following established procedures. Document and report results of all experiments in a timely-manner consistent with department practices and governing procedures, as applicable. Participate in method transfer or validation activities, including executing the protocols and preparing the reports. Review experimental data, notebooks, and instrument qualification protocols / reports. Write, revise, develop, and evaluate SOPs. Maintain good laboratory practices and GMP in compliance with safety and environmental requirements. Ability to work successfully in both a team/matrix environment as well as independently. Report lab event or deviation and participate in the investigation. Ensure high quality in QC and analytical work and accurately document all necessary and relevant information in a clear concise manner as per cGMPs. Provide training to other team members on instrument and testing method. Participate, support and facilitate site audits as directed and required. Perform other related assignments and duties as required and assigned. Experience and Education: BS in Chemistry with 3+ years of experience or MSc in Chemistry with 1+ year of experience. Have experience of using the following instrumentation: HPLC, GC, FTIR and KF. Ability to perform routine QC work independently or with less guidance. Excellent communication skills, both verbal and written. Effective in managing multiple competing activities and delivering to timelines. Ability to work in a cross-functional environment. Working knowledge of cGLP/cGMP and applicable FDA, EMA, and ICH guidance preferred. Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process. With over 21,000 employees and operations in the U.S., U.K., and China, Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China. Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. Our core cultural values are "Employees Number One" and "Clients Centered," setting Pharmaron apart from other organizations. Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package, including: Medical, Dental & Vision Insurance with significant employer contributions. Employer-funded Health Reimbursement Account. Healthcare & Dependent Care Flexible Spending Accounts. 100% Employer-paid Employee Life and AD&D Insurance. Short- and Long-Term Disability Insurance. 401(k) plan with generous employer match. Access to an Employee Assistance Program. Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences. #IL-14

Job Title: Quality Control (QC) Chemist FLSA Classification: Full-Time, Exempt Professional Work Hours: General Shift: 8 AM - 5 PM (may vary based on business needs) Reports To: Quality Control Manager Pay Range: $65,000 - 90,000 (Annually) InvaGen pharmaceuticals is looking for talent in the following areas at our manufacturing site in Fall River, MA. 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. 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. * Ensures QC Analysts receive proper training. * Attends meetings to keep informed of manufacturing priorities. * Ensures that safety standards are maintained. * 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), in Chemistry, Biology, Pharmaceutical Sciences, or related field, and a preferred 1-year experience in the pharmaceutical or biotechnology industries preferred. * Must have current Good Manufacturing Practices (cGMP) * Good Laboratory Practice (GLP) knowledge Professional and Behavioral Competencies * Proficiently speak, communicate, and understand (read and write) scientific work in English. * Have excellent organization, learning and teaching skills required to work in teams. * You enjoy working in a fast-paced environment and are flexible to changing requirements. * 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. * Lead Investigation activities * Familiarity with Chromatography systems is required, Empower is a plus. * Ability to understand and analyse complex data sets and must have working knowledge of Microsoft Office programs and other scientific based software. * Experience in Inhalation products (MDI) is 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). * 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 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: Fall River, Massachusetts 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.