Chemist Jobs in Saugus, MA

Take a Look at Your Future with Quintara Biosciences · The mission of Quintara Biosciences is to provide integrated DNA services (DNA reading, writing, editing, and making) to the life science community by creating and delivering innovative translational technologies and platforms. · A path towards your most rewarding career.You will be challenged to work in a results-driven, fast-paced organization; you will work with passionate professionals who strive to develop innovative products and technologies that advance the life sciences; and you will excel in an environment of respect, integrity, and fair opportunities for growth. PRIMARY RESPONSIBILITIES ： · Beresponsible for the day-to-day work and management of the Oligonucleotideteams in Boston · Design and implement innovative strategies for the synthesis, purification, and scale-up of oligonucleotides · Utilize hands-on experience to optimize synthetic routes, purification methods, and bioconjugation protocols · Conduct analytical characterization using HPLC, LC-MS,and other analytical methods. · Complete the goals associated with specific oligonucleotide process optimization projects. · Develop solutions and providing recommendations as to the appropriate course of action to technical problems associated with the preparation of synthetic oligonucleotides. · Provides documentation and validation support in execution of synthesis and/or purification process changes. · Performs laboratory work and documentation in accordance with regulatory standards and company guidelines. · Mentor oligo team members, providing technical guidance and expertise in oligonucleotide chemistry EDUCATION AND EXPERIENCE： · Minimum of a Master Degree in Biochemistry, Chemistry, Molecular Biology or related discipline. · Minimum of 5 year of industrial or academic experience in the synthesis and purification of oligonucleotides. · Excellent understanding of the basic structure and function of DNA and RNA, including but not limited to advanced applications such as gene cloning, NGS preparation. SKILL REQUIREMENTS： - Competence & Skills · Experienced in high-throughput oligonucleotides synthesis, proficient in the operation of the 192&768 synthesizer, and carry out simple instrument troubleshooting and repair. · Proficient in multiple analytical and purification techniques for DNA/RNA oligonucleotidesto ensure that the purity and quality of oligonucleotides meeting experimental requirements. · Experienced in the application of LC-MS technology for accurate qualitative and quantitative analysis of nucleotides. · Knowledge of commonly used biomolecular analysis methods (e.g. qPCR, DNA sequencing) or relevant practical experience. · Knowledge of the downstream application of oligonucleotides, like gene synthesis, molecular cloning, NGS, etc. - Professional Attitude · Good scientific thinking and innovation ability, able to independently design experimental programs and promote project progress. · Good teamwork spirit, able to communicate effectively with other researchers and solve research problems together. · Strong willingness to learn and ability to quickly adapt to new technologies and methods. · Welcome challenge and extra responsibilities. · With clear career aspiration and willing to make impact to the environment · WORKING RELATIONSHIPS · Report to: Oligo Team Leader · Works with: you will be working with internal oligo team, as well as downstream gene synthesis, molecular cloning and NGS team at Boston

Outlier is the world's leading expert platform, connecting a network of over 100,000 contributors worldwide to improve AI models by providing expert human feedback. We partner with companies including OpenAI, Meta and Microsoft to enable advanced generative AI models to provide accurate responses and advanced reasoning capabilities. We are looking for advanced Chemistry experts to teach AI how to interpret and solve complex problems by: Evaluate AI-generated content for factual accuracy and relevance in Chemistry. Develop and answer Chemistry-related questions to refine AI understanding. Assess and rank AI responses based on scientific rigor. Required expertise and qualifications: Education: Master's degree or higher (PhD preferred) in Chemistry or a related field (can be currently enrolled) Research Experience: Strong preference for candidates with peer-reviewed publications, patents, conference presentations, research grants, or industry R&D contributions English Proficiency: Ability to read and write with minimal errors Bonus Skills: AI model training experience is not required but helpful Payment: Currently, pay rates for core project work by Chemistry experts range from $30 to $50 per hour USD but varies based on your geographic location (see note below) Opportunities for higher-paying research projects based on performance. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

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.

LNP Formulations - BS/MS in Chemistry, Chemical/Biochemical Engineering, Biochemistry, Pharmaceutical Sciences, or related discipline with 4+ years of industry experience - Direct experience with LNP synthesis, purification (TFF), characterization, and handling - Proficiency in analytical techniques such as DLS, zeta potential, UV-Vis and fluorescence spectrophotometry, and gel electrophoresis preferred - Experience with protein conjugation is preferred - Excellent verbal and written communication skills - Strong organizational skills - Manage multiple projects concurrently and collaborate across disciplines

Title: Research Associate Duration: 6 months+ Schedule: Monday-Friday, 8:30am-5pm, ** May need to work outside of standard hours sometimes (evenings/weekends) NOTES: Industry experience is preferred, Pharma experience is a plus. Life sciences degree (Biology, Biochemistry, Biotechnology, etc.) is required. MUST HAVE job-related tissue culture and metabolic assay experience; functional genomics (si RNA/CRISPR) experience a plus. MUST HAVES: 1) Experience in working with scientists to follow required protocols 2) Proficient at tissue culture and cell-based functional assays, with metabolic assays strongly preferred 3) Communication/Organization Purpose: To provide technical laboratory research support of projects focused on target validation using human in vitro models in metabolic functional assays such as Seahorse, lipolysis, and glucose uptake. Essential Functions: Work with scientists to conduct lab-based studies to support project efforts • Perform tissue culture work with human cell lines to develop and optimize workflows for in vitro target validation using mid-throughput (96-384 well plate) assays • Support project management efforts in standard operating procedure creation, sharing knowledge and skills, and fostering cross-functional teamwork • Engage in effective communication with colleagues within Client . Physical Requirements: No overnight travel required • Work with human cell lines and common molecular biology reagents in a laboratory environment that may include hazardous chemicals and blood borne pathogens • Functions may require some morning, evening, or weekend hours outside of standard business hours Qualifications • Bachelor's degree with 3-5 years of experience post-degree; relevant experience may be substituted as appropriate. Title is dependent on qualifications. • Tissue culture experience is required-including strong aseptic technique, BSL2 stewardship, and troubleshooting • Experience with cell-based screening systems and lab automation • Metabolic disease understanding is a plus • Experience with human primary cells (adipocyte, skeletal myoblasts) is a plus • Experience with automated laboratory equipment, complex machinery, and familiarity of high throughput data production principles are a plus • Ability to carry out complex protocols required • Experience in basic molecular biology techniques required • Experience working in a team environment required, industry (CRO, pharmaceutical, biotech) experience is preferred • Fluency in spoken and written English is a prerequisite for the role • Role requires proactive communication skills and cross-cultural understanding to interact within a global organization • Must be comfortable in asking for clarification and offering suggestions • Other desirable skills include: advanced cellular imaging and/or high throughput data collection skills, and ability to interpret interdisciplinary data • Must love to learn, be ambitious, and be determined to contribute to improving patients' well-being.

Nona Biosciences is seeking a highly skilled and experienced scientist to join our team in Natick, MA. The successful candidate will play a critical role in establishing antibody discovery and production capabilities in our US lab. The main responsibilities of this role include designing, producing, purifying, and analyzing antibodies to support all projects. The ideal candidate should have hands-on experience with CHO and 293 cell culture and transfection techniques, as well as expertise in antibody purification. Responsibilities Design and source DNA constructs used for antibody expression. Perform plasmid transfection in mammalian cells (CHO or HEK293) for antibody expression. Antibody or other biologics purification by the affinity chromatography. Characterize and quality control of purified antibodies using variety of analytical methods (SEC, SDS-PAGE, FACS etc.) Maintain a detailed and well-organized record of experiments in electronic notebook. Collaborate with other team members to support internal and external projects Help organize, maintain and supply the laboratory Requirements BS./M.S. in biochemistry, molecular biology, protein chemistry or related fields. 2+ years of hands-on experience with mammalian cell culture and recombinant mammalian protein expression, such as CHO and HEK293 cells. Experienced with protein purification techniques, such as affinity chromatography and SEC. Knowledge with protein characterization and quality control techniques, such as protein concentration measurement, SDS-PAGE, Western blot, and ELISA. Excellent organization/planning skills to meet deadlines and handle multiple tasks simultaneously Diligent, self-motivated, independent and strong sense of responsibility Good interpersonal skills for building relationships across functions internally and externally

The BTS Lab Analyst is responsible for providing technical support for IT systems in plant Quality Control (QC) and manufacturing operations. This role requires expertise in managing IT systems, ensuring compliance with data integrity policies, and supporting cybersecurity protocols. Key responsibilities include leading IT projects, managing system documentation, validating hardware and software, and providing technical support for QC and manufacturing applications. The ideal candidate will have experience with Acronis, CrowdStrike, Excel macros, PowerApps/Power BI, and lab instruments, along with strong communication, problem-solving, and project management skills. Must-Haves: 2+ years of IT QC System/Application Support experience. 3+ years of relevant IT experience. Bachelor's degree in Computer Science or related field. Strong communication and problem-solving skills. Key Responsibilities: Provide technical support for IT/BTS systems in plant Quality Control (QC) and manufacturing operations. Lead IT projects for QC and manufacturing systems. Ensure compliance with data integrity policies, regulatory requirements, and cybersecurity practices. Manage system documentation and validation/qualification of hardware and software. Support desktop/workstation and server applications for QC and manufacturing. Collaborate with cross-functional teams to deliver IT capabilities and provide technical leadership. Key Skills: Experience with Acronis, CrowdStrike (antivirus software), and patching systems. Strong knowledge of Excel macros and PowerApps/Power BI. Familiarity with IT QC systems and applications (e.g., Waters Empower, Sciex). Understanding of GMP standards and cybersecurity compliance. Experience with Lab instruments (e.g., Empower CE, Nexxus, Shimadzu). Proficiency in project management and ITIL/GAMP methodologies.

Job Title: QC Scientist Responsibilities: Perform aseptic cell therapy operations including cell expansion, harvesting, and cryopreservation in a GMP cleanroom environment. Support gene therapy production processes including viral vector preparation, transduction, and purification steps under sterile conditions. Conduct microbiological testing such as environmental monitoring, bioburden, and endotoxin testing to ensure aseptic integrity. Execute Quality Control assays related to cell viability, identity, sterility, and gene expression analysis. Maintain and review detailed batch records, SOPs, and QC documentation in compliance with pharmaceutical quality standards. Collaborate with cross-functional teams including Manufacturing, QC, QA, and Microbiology to troubleshoot and maintain compliance throughout the process lifecycle.

Engineering Technician in R&D for a medical device client. Troubleshoot and resolve issues that occur with products on the product lines. Work with sales, marketing and R&D engineering to build prototype assemblies using internal resources and outside vendors. Construct fixtures for the test and development of new and upgraded product. Assist in the design of tests and perform feasibility testing of new product designs. Write and/or contribute to ECOs for the implementation of designs and changes. Specify and order parts & equipment in support of day-to-day functions. Work cooperatively with Manufacturing Engineering to aid in the development and construction of new fixtures and to specify new equipment. Microscope or magnification expertise a must. Education/Experience: AS plus minimum 3 years' experience in an engineering environment or equivalent Medical device experience preferred Ability to read and interpret mechanical and electrical drawings and BOMs. Experience using basic meters, oscilloscopes, and hand tools Bilingual English/Spanish preferred but not required Ability to assemble and troubleshoot micro-assemblies under magnification Must be able to work in a team environment SolidWorks CAD experience a plus Full time opportunity

Our Life Sciences client is hiring a Senior Analyst I, Quality Control Chemistry on a one-year contract basis near Boston, MA. The Senior Analyst will specifically support the gene therapy program and will also work on data trending, invalid assays investigations, quality events (investigations, deviations, Change control, CAPAs). Responsibilities Execute analytical test methods to support product release and stability of AAV products using different analytical techniques (e.g. HPLC, LCMS, AUC, UV, CE-SDS, compendia methods like Osmolality, pH, Sub visible particulates and Appearance) Review and approval of cGMP analytical data for release and stability testing from chemistry analytical test methods Supports and leads QC Chemistry laboratory operations (ex. Instrument qualification and maintenance. Housekeeping, qualify critical reagents, etc). Author and support quality events; Change controls, Deviation, CAPA, OOS Investigation, as needed. Write, prepare, and present technical data, technical reports, and standard operating procedures (SOPs), Method transfer/ validation protocol, Method transfer/ validation report for internal and external methods. Method Transfer / Validation of QC chemistry methods at internal and external laboratory. Model leadership behaviors and mentor/train junior staff The job responsibilities may change as needed to support activities relevant to the clinical phase. Qualifications: Experience working in the cGMP QC lab of the pharmaceutical or biopharmaceutical industry is a must. BS/MS Analytical Chemistry, Biochemistry, Biophysics, or a related discipline with at least 5 years of experience working in a cGMP environment. Experience analyzing nucleic acids, virus capsids, antibodies, and/or other biologics materials using HPLC/UPLC, LCMS, AUC, UV- Vis, CE-SDS is strongly preferred. Experience working with external contract labs (CMOs, CROs) is a plus. Strong collaboration and team-working skills. Strong communication, interpersonal and organizational skills. Proven ability to work independently and effectively plan and organize work activities and prioritize task completion to meet schedules and deadlines.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description The successful candidate will be responsible for conducting various analytical tests and experiments, interpreting results, and recording findings in a detailed and accurate manner. The Analytical Lab Technician will work in a general chemistry laboratory environment and will play a critical role in supporting the company's client-based testing needs and objectives. Key Responsibilities: Perform a wide range of analytical tests and experiments using various techniques and equipment (ICP-OES, HDXRF, GC/MS, LC/MS, UV-Vis, FT-IR) Analyze and interpret data and present results in a clear and concise manner. Record and maintain accurate and detailed laboratory records, including test methods, results, and conclusions. Maintain and troubleshoot laboratory equipment and perform routine maintenance and calibration. Participate in the development and validation of new analytical methods. Collaborate with other team members to ensure that all projects are completed on time and to the required quality standards. Adhere to strict laboratory safety procedures and regulations. Qualifications Associates or Bachelors Degree in Chemistry or related Science with at least 5 years of experience. Continuing Technical Education Pursue Technical Training through Agilent and/or other technical training resources both in person and online in order to maintain proficiency with instrumentation and to facilitate current testing methods improvements. Additional Information Schedule: Monday - Friday - 8:30AM to 5:00PM What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Consumer Product Testing is a Disabled and Veteran Equal Employment Opportunity employer. PandoLogic. Keywords: Laboratory Technician, Location: Norwood, MA - 02062 , PL: 597425076

Title : Quality Control Analyst Duration: 12 Months Pay Range : $35.00/ Hr to $ 40.00/ Hour on W2 The Quality Control Operations (QCO) Analyst III Contractor plays a crucial role in supporting the department's efforts to maintain the highest standards of quality and compliance from development through to commercialization. In addition to executing routine and non-routine testing in support of development through commercial programs, the Analyst III will also participate in data trending, investigations, and laboratory operations. This position will also play a role in method transfers, method qualification/validation, verification, and implementation. By ensuring these critical activities are executed with precision, the Analyst III significantly contributes to routine laboratory operations, thereby enhancing the overall efficiency and effectiveness of the QC functions. Key Responsibilities: • Perform routine and non-routine analytical and/or microbiological assays to support raw materials, in-process samples, product release, and stability studies, following established SOPs • Support a continuous operational schedule by supporting weekend laboratory operations (Analytical, Microbiology, Raw Materials). • Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the department's commitment to meeting project timelines and quality metrics • Assist in the maintenance of laboratory equipment and inventory, including the preparation of reagents and samples to ensure smooth laboratory operations • Ensure data are reviewed timely; qualify as a data reviewer to ensure timely and efficient data availability. • Perform role-specific operational assignments (e.g., raw material processes including SAP transactions, environmental monitoring, in-process testing). • Contribute to the revision and updating of controlled documents, including SOPs, work instructions, and test methods, to ensure continuous improvement and compliance with current industry standards and regulatory requirements • Adhere to internal standards, policies, and SOPs, as well as regulatory and industry standards (e.g., GMP, GLP, ICH guidelines) to maintain the highest levels of quality and compliance. • Actively participate in continuous improvement efforts by identifying and suggesting enhancements to methods and laboratory processes, particularly those related to efficiency and reliability. • Collaborate with QC and cross-functional teams to ensure seamless quality control operations and to support the collective Alnylam goals • Pursue ongoing training and development to deepen expertise in QC testing techniques, TOQ operations, and regulatory compliance. • May assist in preparing technical documentation for regulatory submissions by performing data verification, ensuring accuracy and compliance with regulatory standards. • Participate in inspection readiness activities as well as supporting onsite audits and inspections, as needed. • Actively participate in continuous improvement initiatives aimed at enhancing QC processes and procedures, increasing laboratory efficiency and effectiveness. • Collaborate with other organizational functions including CMC Development, Manufacturing, Manufacturing Technical Services, Materials Management, and Quality Assurance to ensure alignment with overall business goals. Qualifications: • B.S. in chemistry, biology, or biochemistry, or related scientific field; • Pharmaceutical/Biotech industry experience with 4 years in a GMP Quality Control function or equivalent, relevant industry experience • Experience in method transfer and/or analytical method implementation; solid understanding of method lifecycle management and phase-appropriate approach is desirable • Demonstrated technical writing skills, with preference for technical writing of investigations • Proficient in data analysis and interpretation, with excellent attention to detail to inform decision-making • Solid problem-solving skills and experience in conducting investigations and implementing CAPA • Strong organizational skills with the ability to manage multiple tasks simultaneously and autonomously • Excellent communication and teamwork abilities, capable of working effectively in a collaborative environment • Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred

Industry: Pharmaceuticals Title: Quality Control Analyst III Duration: 08 months contract (+Chances of extension) 2 openings - 1 Micro QC, 1 Chemistry QC This position is onsite and will be primarily located in Norton, MA, with potential occasional responsibilities at other client locations. The role requires flexibility for weekend coverage to support a continuous operational schedule. This is a first shift position Friday-Monday (4 x 10 hours), but will require an initial period of Monday-Friday work to accommodate training. Overview The Quality Control Operations (QCO) Analyst III Contractor plays a crucial role in supporting the department's efforts to maintain the highest standards of quality and compliance from development through to commercialization. In addition to executing routine and non-routine testing in support of development through commercial programs, the Analyst III will also participate in data trending, investigations, and laboratory operations. This position will also play a role in method transfers, method qualification/validation, verification, and implementation. By ensuring these critical activities are executed with precision, the Analyst III significantly contributes to routine laboratory operations, thereby enhancing the overall efficiency and effectiveness of the QC functions. Key Responsibilities (including but not limited to): • Perform routine and non-routine analytical and/or microbiological assays to support raw materials, in-process samples, product release, and stability studies, following established SOPs • Support a continuous operational schedule by supporting weekend laboratory operations (Analytical, Microbiology, Raw Materials). • Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the department's commitment to meeting project timelines and quality metrics • Assist in the maintenance of laboratory equipment and inventory, including the preparation of reagents and samples to ensure smooth laboratory operations • Ensure data are reviewed timely; qualify as a data reviewer to ensure timely and efficient data availability. • Perform role-specific operational assignments (e.g., raw material processes including SAP transactions, environmental monitoring, in-process testing, etc.). • Contribute to the revision and updating of controlled documents, including SOPs, work instructions, and test methods, to ensure continuous improvement and compliance with current industry standards and regulatory requirements • Adhere to internal standards, policies, and SOPs, as well as regulatory and industry standards (e.g., GMP, GLP, ICH guidelines) to maintain the highest levels of quality and compliance. • Actively participate in continuous improvement efforts by identifying and suggesting enhancements to methods and laboratory processes, particularly those related to efficiency and reliability. • Collaborate with QC and cross-functional teams to ensure seamless quality control operations and to support the collective company goals • Pursue ongoing training and development to deepen expertise in QC testing techniques, TOQ operations, and regulatory compliance. • May assist in preparing technical documentation for regulatory submissions by performing data verification, ensuring accuracy and compliance with regulatory standards. • Participate in inspection readiness activities as well as supporting onsite audits and inspections, as needed. • Actively participate in continuous improvement initiatives aimed at enhancing QC processes and procedures, increasing laboratory efficiency and effectiveness. • Collaborate with other organizational functions including CMC Development, Manufacturing, Manufacturing Technical Services, Materials Management, and Quality Assurance to ensure alignment with overall business goals. Qualifications • B.S. in chemistry, biology, or biochemistry, or related scientific field; • Pharmaceutical/Biotech industry experience with 4 years in a GMP Quality Control function or equivalent, relevant industry experience • Experience in method transfer and/or analytical method implementation; solid understanding of method lifecycle management and phase-appropriate approach is desirable • Demonstrated technical writing skills, with preference for technical writing of investigations • Proficient in data analysis and interpretation, with excellent attention to detail to inform decision-making • Solid problem-solving skills and experience in conducting investigations and implementing CAPA • Strong organizational skills with the ability to manage multiple tasks simultaneously and autonomously • Excellent communication and teamwork abilities, capable of working effectively in a collaborative environment • Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred

Job Title: QC Analyst Duration: 12 months with possibility of extension Hourly contract Position (W2 only) Note: Experience required with A280, CE-SDS, ic IEF, ELISA, SoloVPE, qPCR Job Description: The Quality Control Technical Transfer Analyst 3 will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. Also participate in quality testing for customer in-process, final product testing and stability studies when needed. Applies job skills and company's policies and procedures to complete a variety of tasks of increased scope. Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. Applies job skills and company's policies and procedures to complete a variety of tasks. Running test samples for In-Process, Lot Release and Stability studies. Running test samples for (but not limited to) investigations, transfers and validations. Reviewing assays Training others Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods Projects - such as method transfers, new instruments, method qualifications Use of Microsoft Suites (Word, Excel, PowerPoint) Use of Laboratory computer systems Potential previous use of GMP Quality Systems such as: TrackWise, LIMS Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. Apply Data Integrity principles in all aspects of work, in compliance with client DI policies, guidelines and procedures. Perform other duties as assigned. Associate's degree Microbiology, Biochemistry or Related Science Fields Strong ability to speak publicly. Strong ability to interpret data both alone and with guidance. Perform assigned, complex and/or varied tasks. Prioritization and problem solving. Comprehend and follow instructions. Direct, control and plan tasks/projects. Brainstorming Strong ability to communicate in both written and verbal format . Exercises judgment within defined procedures and practices to determine appropriate action. Self-motivated team player Completes assignments on-time and accurately Displays commitment to quality and performs job functions to the best of his/her ability Relate to others in a team setting. Maintain positive attitude in a team environment. Timeliness in completing assigned tasks. Works entire assigned shift, including arriving on time

Quality Control Analyst III - Contract - Norton MA Proclinical is seeking a dedicated Quality Control Analyst III to support the department's commitment to maintaining high standards of quality and compliance from development through commercialization. Primary Responsibilities: This role will be involved in routine and non-routine testing, data trending, investigations, and laboratory operations. This position requires flexibility for weekend coverage and is primarily based onsite in Norton, MA. Skills & Requirements: Degree in chemistry, biology, biochemistry, or related scientific field. Experience in a GMP Quality Control function within the pharmaceutical/biotech industry. Knowledge of method transfer and analytical method implementation. Strong technical writing skills, particularly for investigations. Proficient in data analysis and interpretation with attention to detail. Problem-solving skills and experience in conducting investigations and implementing CAPA. Strong organizational skills and ability to manage multiple tasks. Excellent communication and teamwork abilities. Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred. The Quality Control Analyst's responsibilities will be: Conduct routine and non-routine analytical and microbiological assays for raw materials, in-process samples, product release, and stability studies. Support weekend laboratory operations to maintain a continuous operational schedule. Maintain training records, adhere to testing schedules, and ensure timely completion of assignments. Assist in maintaining laboratory equipment and inventory, including reagent and sample preparation. Review data promptly and qualify as a data reviewer for efficient data availability. Perform operational assignments such as raw material processes and environmental monitoring. Contribute to revising and updating controlled documents to ensure compliance with industry standards. Adhere to internal and regulatory standards to maintain quality and compliance. Participate in continuous improvement efforts to enhance laboratory processes. Collaborate with QC and cross-functional teams to support seamless operations. Pursue ongoing training to deepen expertise in QC testing techniques and regulatory compliance. Assist in preparing technical documentation for regulatory submissions. Participate in inspection readiness activities and support audits and inspections. Collaborate with other organizational functions to align with business goals. If you are having difficulty in applying or if you have any questions, please contact Anderson Maldonado at a.maldonado@proclinical.com Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.

-Pay: 41hr -10 month contract The role requires flexibility for weekend coverage to support a continuous operational schedule. This is a first shift position Friday-Monday (4 x 10 hours), but will require an initial period of Monday-Friday work to accommodate training. The Quality Control Operations (QCO) Analyst III Contractor plays a crucial role in supporting the department's efforts to maintain the highest standards of quality and compliance from development through to commercialization. In addition to executing routine and non-routine testing in support of development through commercial programs, the Analyst III will also participate in data trending, investigations, and laboratory operations. This position will also play a role in method transfers, method qualification/validation, verification, and implementation. By ensuring these critical activities are executed with precision, the Analyst III significantly contributes to routine laboratory operations, thereby enhancing the overall efficiency and effectiveness of the QC functions. Key Responsibilities (including but not limited to): • Perform routine and non-routine analytical and/or microbiological assays to support raw materials, in-process samples, product release, and stability studies, following established SOPs • Support a continuous operational schedule by supporting weekend laboratory operations (Analytical, Microbiology, Raw Materials). • Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the department's commitment to meeting project timelines and quality metrics • Assist in the maintenance of laboratory equipment and inventory, including the preparation of reagents and samples to ensure smooth laboratory operations • Ensure data are reviewed timely; qualify as a data reviewer to ensure timely and efficient data availability. • Perform role-specific operational assignments (e.g., raw material processes including SAP transactions, environmental monitoring, in-process testing, etc.). • Contribute to the revision and updating of controlled documents, including SOPs, work instructions, and test methods, to ensure continuous improvement and compliance with current industry standards and regulatory requirements • Adhere to internal standards, policies, and SOPs, as well as regulatory and industry standards (e.g., GMP, GLP, ICH guidelines) to maintain the highest levels of quality and compliance. • Actively participate in continuous improvement efforts by identifying and suggesting enhancements to methods and laboratory processes, particularly those related to efficiency and reliability. • Collaborate with QC and cross-functional teams to ensure seamless quality control operations and to support the collective goals • Pursue ongoing training and development to deepen expertise in QC testing techniques, TOQ operations, and regulatory compliance. • May assist in preparing technical documentation for regulatory submissions by performing data verification, ensuring accuracy and compliance with regulatory standards. • Participate in inspection readiness activities as well as supporting onsite audits and inspections, as needed. • Actively participate in continuous improvement initiatives aimed at enhancing QC processes and procedures, increasing laboratory efficiency and effectiveness. • Collaborate with other organizational functions including CMC Development, Manufacturing, Manufacturing Technical Services, Materials Management, and Quality Assurance to ensure alignment with overall business goals. Qualifications: • B.S. in chemistry, biology, or biochemistry, or related scientific field; • Pharmaceutical/Biotech industry experience with 4 years in a GMP Quality Control function or equivalent, relevant industry experience • Experience in method transfer and/or analytical method implementation; solid understanding of method lifecycle management and phase-appropriate approach is desirable • Demonstrated technical writing skills, with preference for technical writing of investigations • Proficient in data analysis and interpretation, with excellent attention to detail to inform decision-making • Solid problem-solving skills and experience in conducting investigations and implementing CAPA • Strong organizational skills with the ability to manage multiple tasks simultaneously and autonomously • Excellent communication and teamwork abilities, capable of working effectively in a collaborative environment • Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred

6-12 Month Contract-to-Hire *Must be local to Worcester, Massachusetts, United States Job Description Responsible for the provision of technical support for all IT/BTS (Business Technology Solutions) systems, activities, development, and administration of plant Quality Control (QC) and IT systems as well as similar scope on manufacturing operations Supports all hands-on projects that affect the lab and manufacturing IT infrastructure, systems, security, workstations, support, and IT standards. Responsibilities: Work on Company IT QC systems and application projects. Work on Company IT manufacturing systems and application projects. Is responsible for the implementation and rollout of new IT systems. Lead Company IT QC systems and application projects. Lead Company IT manufacturing systems and application projects. Ensure system documentation and computerized systems compliance with Data Integrity policies and regulatory requirements. Collaborate with BTS IAI (Infrastructure Architecture Innovation) to maintain oversight over Company network infrastructure pertaining to the site. Is responsible for ensuring the maximum availability of IT equipment and systems to support the business. Participate in continuous improvement by identification and implementation of cost saving opportunities within the IT area. Is the site subject matter expert (SME) for plant IT systems. Continually building knowledge of the business while keeping current with new technologies. Collaborate closely with other site functions on cross-functional projects and, responsible for delivering IT capabilities and support to site projects. Liaise with IT Contractors/Consultants and ensure compliance with contractor management site policies. Support of QC desktop/workstation and server applications. Support of manufacturing desktop/workstation and server applications. Training of employees on relevant applications. Validation / Qualification of hardware and software as required by Company policies and SOPs. Is responsible for data backup and administration / maintenance of the plant QC & manufacturing systems. Protect Company from cyber risk on QC equipment and site assets, adhering to cyber security procedures and practices of Company. Is responsible for patching of the plant QC systems. Is responsible for patching of the plant manufacturing IT systems. Participation in cross functional teams and initiatives across the site. Adheres to and supports all EHS standards, procedures, and policies. Provide technical leadership on IT to functional areas and collaborates with key stakeholders. Qualifications: Bachelor's degree: Degree level qualification in computer science or equivalent relevant discipline or respective proven expertise and experience Cognitive/Business Skills: Requires a high level of attention to detail and mental concentration to always ensure accuracy and total compliance with procedures. Requires proven problem-solving skills and the ability to adapt to new requirements. Must be results driven striving to meet all targets and metric standards as set by site/department and division leaders. Requires innovative thinking, where new and untested solutions are proposed, demonstrated, and implemented on a regular basis. Requires total commitment to quality and always maintaining a high standard of work. Always demonstrates the highest levels of integrity and a strong work ethic. Strong communication skills, both verbal and written, are required for the execution of this role. Strong interpersonal skills are required. Supports the principles of Perfect Performance. Apply advanced technical knowledge and experience to the solution of a broad array of technical problems. Job/Technical Skills 2 years plus in IT QC System / Application Support (essential) 3 years plus of relevant IT experience (Essential) ITIL (Desirable) GAMP (Desirable) Project Management must Waters Empower (Desirable) Familiarity with Acronis, CrowdStrike installs and maintenance as well as Lab instruments-Empower CE, SOloVPE, SHimatsu,Nexxus, BCS and others Microsoft O365 PowerApps / PowerBi Very strong knowledge on excel macros and powerapps Familiarity with Sciex,Biotek,Waters,Plate freezers You Will Receive The Following Benefits: Medical & Dental Insurance Health Savings Account (HSA) 401(k) Paid Sick Time Leave Pre-tax Commuter Benefit Applicants must be currently authorized to work in the United States on a full-time basis now and in the future. Motion Recruitment provides IT Staffing Solutions (Contract, Contract-to-Hire, and Direct Hire) in major North American markets. Our unique expertise in today's highest-demand tech

WHO WE ARE RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change people's lives. Collaborative, dedicated, and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilizing ground-breaking science. THE ROSLINCT WAY Here at RoslinCT, our team can contribute to the development of revolutionary treatments. We live every day by our core values: Partner Focus, One Team, Personal Growth, Integrity, Innovation, and Trust and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work-life balance. Our people are the key to our success. At RoslinCT we focus on developing our corporate culture, people's development, growth, and the ability to impact patients. ACCELERATING YOUR FUTURE · Author, review, approval, and final authorization of microbiology methods (test results and records, test methods, equipment records) and ensuring adherence to regulatory agency requirements, Client standards, policies, SOPs for cell therapy products and experience with EU Annex requirements. · Execute procedures for microbiology methods in support of method lifecycle activities including method transfer, qualification, validation, compendial verification, and performance monitoring. · Support microbiology equipment installation and qualification, ensuring 21 CFR Part 11 compliance. · Participate as microbiology method subject matter expert (SME) in investigations, OOS, deviation, change controls, and CAPAs to support cGMP operations. · Provide support to QC Operations as method SME: develop training approach, training documents and provide training for new methods. · Perform non-routine/routine QC testing for in process samples, product testing, stability testing, or raw material testing as needed. · Work collaboratively with cross functional departments including but not limited to QC Technical Services, Quality Assurance, and Program Management. · Ability to prepare technical data and present to senior leadership. WHAT YOU WILL BRING · Bachelor's degree in Biology (Microbiology) · 4+ years of microbiology laboratory experience with rapid microbiological methods is a plus (rapid sterility, endotoxin, gram stain). · Experience in a cGMP QC laboratory environment performing environmental monitoring, contamination control and investigation writing. · Excellent/Effective written and verbal communications skills. · Prepare technical data and present to senior leadership. · Escalate issues professionally and on a timely basis. OUR COMMITMENT All RoslinCT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. RoslinCT is proud to be an equal opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics.

Cambridge Isotope Laboratories, Inc. (CIL) is searching for an Associate Formulations Chemist within the Environmental Standards group based onsite in our Andover, MA facility. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Associate Formulations Chemist will work closely with a team of chemists to develop and optimize formulations that meet the stringent requirements of our customers in pharmaceuticals, diagnostics, and other high-tech industries. This role encompasses hands-on laboratory work and collaborative research to ensure the successful execution of projects. The team may also assist with the formulations for CIL's neonatal screening and metabolomics applications, using batch records and technical records as dictated by business needs. The work will be carried out in compliance with cGMP and/or ISO quality systems. Responsibilities Perform documentation and data entry following detailed standard operating procedures (SOPs), in accordance with Quality System requirements, with close supervision Prepare single component solutions for the environmental standards product line Maintain accurate and detailed laboratory records, ensuring compliance with SOPs and safety protocols Regularly monitor, organize, and maintain the laboratory inventory to ensure that all supplies and equipment are adequately stocked and readily accessible Manage multiple projects simultaneously under tight deadlines Provide support to other laboratory staff as necessary Requirements Bachelor's degree in Chemistry or related discipline, or relevant equivalent experience 0-2 years of experience working within a laboratory environment Must possess familiarity with standard laboratory equipment Strong problem-solving skills and the ability to interpret complex data is required A high attention to detail and strong organizational skills is essential Excellent written, verbal and interpersonal communication skills Benefits CIL and CIS offer a competitive salary and comprehensive benefits including generous paid time off, Long Term Incentives, 6% matching 401K plan and health insurance with no in-network deductible. Cambridge Isotope Laboratories is an Equal Opportunity Employer. Learn more about us on our website: *************** About Us: Cambridge Isotope Laboratories, Inc. (CIL) is the world's leading producer of stable isotopes and stable isotope-labeled compounds. With approximately 750 employees and laboratories in four countries, CIL specializes in the process of labeling biochemical and organic compounds with highly enriched, stable (nonradioactive) isotopes of carbon, hydrogen, nitrogen and oxygen. Our chemists substitute common atoms (e.g., 1H, 12C, 14N, 16O) with rare, highly valued isotopes (e.g., 2H or D, 13C, 15N, 18O) so that the final product can be readily measured or traced using mass spectrometry (MS) or nuclear magnetic resonance (NMR). CIL's products are utilized in laboratories, medical, government and academic research centers and health care facilities worldwide. We are proud that CIL products have contributed to medical advancements in cancer research, new-drug development, environmental analysis, and medical diagnostic research. In the past decade, as the fields of proteomics and metabolomics have developed as leading techniques for determining biomarkers for disease presence, progression and the monitoring of therapeutic response, CIL has worked closely with industry leaders and researchers to provide the stable isotope-labeled tools needed for improved quantitation and qualification of complex biological systems. After decades of research, stable isotopes have found their place in an ever expanding commercial scale applications in pharmaceuticals, semiconductors, flat panel displays as well as other high technology fields specifically with deuterium oxide (D2O) and deuterium gases. Pharmaceutical companies have begun to investigate deuteration of molecules that may provide advantages over their existing nondeuterated counterparts. In addition, increasing research into the potential medical advantages of new deuterated drugs is also occurring. In high technology, deuterated organic molecules and deuterium gas are commonly used in the manufacturing of microelectronics and OLEDs, which contribute to the increased lifetime of the devices. Learn more about us on our website: ***************