Chemist Jobs in Seekonk, 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.

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.

Cambridge, MA (Onsite) Full-time Perm - Direct Hire PRIMARY RESPONSIBILITIES ： Be responsible for the day-to-day work and management of the Oligonucleotide teams 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 oligonucleotides to 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.

Job Title: Scientist - II Duration: 06+ Months Contract (Possible Extension) Pay Rate: $44.30.00/HR on W2 Contractor - Protein Analytics Client is a global health care leader with a diversified portfolio of prescription medicines, vaccines, and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where *** has codified its legacy for over a century. ***'s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Early Biologics Characterization - Boston of *** Research Laboratories (MRL) is seeking a contractor to execute on existing protein analytics workflows. Specifically, to perform intact MS, peptide mapping and other biophysical assays such as SEC, HIC, CE-SDS, DSF, DLS, Buffer Exchange. In this role you will build and then use a combination of skills to help with the biologics characterization workflow. Additional laboratory automation skills are desired but not required. This role will require an eagerness to learn and an ability to work with different teams and different equipment to operate a robust characterization platform. Your efforts will be a complement and core resource to existing capabilities and will serve to expand the team's ability to interrogate biologics diversity to identify optimal leads. You will have the opportunity to apply your enthusiasm and technical skills as a member of Discovery Biologics - Boston to support and help drive multidisciplinary biotherapeutic discovery programs. Responsibilities 1. Operate and maintain existing mass spectrometry platforms and implement new workflows for protein characterization 2. Perform LC-MS data analysis using various software and bioinformatic tools to elucidate the quality attributes of therapeutic proteins and other Client modalities. 3. Troubleshoot automation methods and devices to maintain optimal high throughput protein analyses 4. Generate frequent characterization summary reports. 5. Follow and improve Standard Operating Procedures for biologics characterization workflows. Quals-- • A minimum of a B.S in a relevant field (e.g. protein sciences, chemical or bioengineering, biochemistry or similar) with additional training being desirable. Experience: • BS with 6+ years of experience/MS with 4+years./PHD with 1-3years. • Industry experience is preferred. Required experience and skills: • Experience with mass spectrometry and other biophysical assays workflows and their inherent data management. • Knowledge and hands on experience in LC-MS based sample preparation for proteins • Strong problem solving and communication skills. • Ability to multitask, time management, and prioritize activities. Preferred experience and skills: • Experience with operating high resolution MS instruments such as Agilent Q-TOF, Thermo Orbitraps (e.g. QE+, QE-HF, Exploris 480) and liquid handling platforms such as Vanquish, Acquity UPLC. • Experience analyzing data with BioPharma finder, BioConfirm and other MS software is a plus • Experience with EMPOWER is a plus • ELN knowledge is desirable

-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

Associate investigator focusing on panel and wafer-level processing techniques, comfortable with exploring advanced/non-standard methods for unique applications Adept at hands-on lab work, creative thinking, problem solving in a unique and fast-paced laboratory environment Assume responsibility for execution of project workflows, such as laminations, coatings, lithography and cure techniques, as well as thermal and mechanical analysis. Key analytical techniques include CVS, HPLC, UPLC, GPC, % solids, titrations, potentiostatic measurements, surface tension, cloud point, densitometer, and rheometer. Proper documentation including new methods, method validation, batch data, management of change, etc. Support Research and Development of new additives and formulations used in electroplating and Polymeric / Dielectric products for the microelectronics industry. Help design and execute experiments, including operation of equipment and instrumentation for polymerization and electroplating of metals, electrochemistry, chromatography, optical microscopy, scanning electron microscopy, material, and mechanical testing, etc. Collect, analyze, and summarize data with appropriate documentation. Support Quality and Manufacturing for root cause investigations and customer complaints. Strict adherence to enhanced safety protocols and ability to work safely and participate in all group safety activities. Work safely in an R&D lab environment and hands-on experience needed. Qualifications B.S. or Associate degree in a technical or scientific field with industrial lab experience with clean room + wafer level processing methods & tools. 1-2 years hands-on industrial experience in semiconductor fab or similar environment Familiarity with material characterization, wafer-level metrology and/or thin film analysis Highly motivated and effective at working both individually and within team environment to accomplish tasks and project goals. Effective verbal and written communication skills in English along with strong attention to detail Understanding of analytical techniques used to characterize small organic molecules, polymers, and inorganic chemicals Strong data analysis skills; experience using JMP or other statistical tools is strongly preferred Demonstrated ability to work effectively with diverse teams Demonstrated ability to work safely with hazardous chemicals Demonstrated ability to follow a procedure and work with high degree of repeatability and attention to detail

Title: Quality Control, Stability Status: 6-12 month contract QC Contractor Stability provides oversight for GMP stability programs, supporting management of stability studies, including but not limited to data review and reporting, and vendor oversight. The successful candidate will provide support in Analytical Development, Quality Control, Manufacturing, CMC, Validation, and Quality Systems. Responsibilities Support systems for stability programs including tracking and trending of stability data, generation of protocols and reports, support test methods, specifications and quality records for GMP Stability program Data entry into stability LIMS systems Generate stability reports from LIMS to support routine reporting of stability data Perform routine trending of stability data to support shelf-life of GMP products Verify and maintain the integrity of data used in assessments Qualifications: BS in a scientific area with 7+ years experience in Quality Control in pharma/biotech Experience supporting Quality Control and/or product stability functions Experience with LIMS Working knowledge of statistical tools, methodologies, and related software, experience with JMP a plus Knowledge of quality systems and domestic and international regulatory requirements Proven ability to manage projects and work with cross-functional teams comprised of internal and/or external contacts, including CTLs

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

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 The QC Analyst II, Flow Cytometry & Molecular Team, will be executing analytical method transfers to Quality Control, optimize and troubleshoot assays for improvement. He/she will be responsible for authoring Standard Operating Procedures (SOPs) and Test Methods. He/she will be executing various quality control methods, analyzing data, and reporting data. He/she will assist in the implementation of new assay methodologies and the associated instrumentation. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. This position is highly visible in the organization and requires the ability to interface with multiple groups, and the ability to assess method suitability, interpret results, perform tasks independently, and troubleshoot. HOW YOU WILL MAKE AN IMPACT • Perform routine and non-routine quality control testing on in-process samples and finished products. • Operate and maintain laboratory equipment and instruments, ensuring proper calibration and adherence to cGMP Compliance. • Provide support for method transfers/qualification/validation and stability testing. • Support analytical equipment installation and qualification • Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner. • Review all data in accordance with applicable procedures and cGMP requirements. • Author, review, and/or approve SOPs, Test Methods, and other procedures required to operate a QC laboratory. • Participate in internal and external audits, inspections, investigations, change controls and CAPAs • Contribute to continuous improvement initiatives, identifying opportunities for efficiency gains and process optimization within the quality control function. • Anticipate and troubleshoot problems. Communicate effectively with management regarding task completion, roadblocks, and needs. • Become a qualified trainer on assigned assays and deliver training to analysts, documenting training per procedural and cGMP requirements. • Work independently in a high-paced team environment, meet deadlines, and prioritize work from multiple projects. • Communicate effectively with cross-functional peers, and department management. WHAT YOU WILL BRING • Bachelor's Degree in scientific discipline. • 3+ years of relevant experience in cGMP Quality Control Laboratory. • Hands-on experience with various analytical techniques such as flow cytometry, qPCR, dPCR, ELISAs, cell-based assays, and scientific knowledge in the characterization and transfer of analytical methods. • Hands-on experience with Raw Material sampling or system management is a plus. • Experience with rapid microbiological methods is a plus (e.g. mycoplasma) • Knowledge of cGMP/ICH/FDA regulations. • Ability to independently prioritize/manage activities. • Ability to prioritize objectives from multiple projects and adhere to scheduled timelines while maintaining flexibility and attention to detail. • Proficient in MS Office applications and information technologies that support documentation and data management systems. • Strong troubleshooting, problem-solving skills, oral and written skills. • Ability to multi-task and interact with multiple groups in a team-oriented environment. 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.

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

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

Associate Quality Control with GMP Experience (Onsite Job in West Greenwich, RI) Terms: Contract W2 Duration : 11 Months Contract (Will Get Extended for Long) Description: ***100% onsite***** RI Shift is Sat, Sun, Mon, Tue 6:45 AM- 5:15 PM*** 11 months duration with possible extension. Ideal candidate: Understands the importance of GMP and the why behind a regulated industry. More lab experience than just academic experience Degree in Scientific field. lab Experience. Must have experience working within a team in a lab setting. Bachelor's Degree

At SES AI, base pay is one part of our total compensation package and is determined within a range. The base pay range for this role is between $50,000 and $120,000. SES AI considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and skills. What We Offer Company paid Health and Dental insurance (ability to add dependents) Global travel insurance for employees traveling while on business Company sponsored retirement plan with 100% vesting and up to 5% match. Life and AD&D Insurance Employee Assistance Program Six Paid Holidays, and one floating holiday per a quarter equivalent to 4 per calendar year 10 accrued vacation days per calendar year that increases with tenure. Bonus + Equity, based on position and eligibility requirements Note: SES AI benefit, compensation, and employee stock programs are subject to eligibility requirements and other terms of the applicable plan or program. About SES AI: SES AI Corp. (NYSE: SES) is powering the future of global electric transportation on land and in the air with the world's most advanced Li-Metal batteries. SES AI is the first battery company in the world to accelerate its pace of innovation by utilizing superintelligent AI across the spectrum of its business, from research and development; materials sourcing; cell design; engineering and manufacturing; to battery health and safety monitoring. Founded in 2012, SES AI is an Li-Metal battery developer and manufacturer headquartered in Boston and with operations in Singapore, Shanghai, and Seoul. Learn more at SES.AI Position Scope SES has an immediate opening for an Associate Chemist. The right person will be passionate about mobile energy storage and have the knowledge and skills to extract insights and explore opportunities for improvements from our large cell testing data. The Associate Chemist will report to the Director and Head of Chemistry and will assist in Synthetic Chemistry experiments. This position will be based in Woburn, MA, and cannot be done remotely. Responsibilities Perform a variety of routine laboratory tasks and carry out chemistry synthesis under supervision, in support of the conduct of normal laboratory operations. Adhere to all safety and Good Laboratory Practice regulations as well as company policies. Must be able to execute Standard Operating Procedures and be able to keep detailed, organized records and complete the required documentation for the associated tests. Must be able to effectively use balances, meters, pumps, stir plates, funnels, pipets, burets, heating plates, fume hoods, and other standard laboratory equipment. Must be able to execute various glassware-cleaning procedures used in the laboratory and be able to work with moisture-sensitive solvents, organic compounds, acids, bases. Must understand and execute appropriate disposal of liquid and solid wastes and able to perform duties with a respirator on an as-needed basis and be able to understand basic chemistry in the laboratory. Work in the chemistry lab closely with chemistry supervisor and perform and optimize established synthetic methods. Electrolyte preparation, maintain and improve the safety and organization of your designated lab area. Perform tasks according to work instructions and standard operating procedures. Requirements Bachelor's degree or master's degree in chemistry or affiliated majors Knowledge of chemistry principles and methods with the ability to interpret results and an ability to communicate effectively. Good problem-solving skills, the ability to think out of the box, and be able to follow the product development processes. Experience with synthetic chemistry research is strongly preferred. Strong communication and quantitative skills. A good team player. Lab experience is a plus.

Analytical Chemist I Woburn, MA Verdox, Inc. is dedicated to reversing climate change through the development and deployment of advanced technology. The company's proprietary electro-swing process, developed at MIT, enables carbon dioxide and other acid gasses to be captured with up to 80% less energy and 70% less cost than conventional approaches. Verdox is backed by institutional investors and based in Boston. Verdox does not and shall not discriminate in employment on the basis of race, color, religion (creed), gender, gender expression, age, national origin (ancestry), disability, marital status, sexual orientation, or military status. To apply, send your CV to ************************* and reference the position "Analytical Chemist I" Key Responsibilities Verdox seeks an Analytical Chemist I to join our team. This position reports to the Analytical Chemistry Manager. Responsibilities * Collaborate with a team of analytical chemists to characterize redox-active small molecules using spectroscopy (e.g. UV-Vis, stopped-flow UV-Vis, IR, fluorimetry, NMR), electrochemistry (e.g. cyclic voltammetry, chronoamperometry, chronopotentiometry), and similar techniques * Generate samples for analysis using both wet lab and electrochemical (e.g. bulk electrolysis) techniques * Study molecular degradation pathways under device-relevant conditions * Organize and maintain collated datasets on redox-active molecules * Quantitatively analyze experimental data * Communicate results to cross-functional teams via both written and verbal presentations Skills, Knowledge and Expertise The candidate must have the following required qualifications: * Bachelor's degree in Chemistry, Chemical Engineering, or equivalent * Minimum 2 years of hands-on laboratory work experience * Hands-on experience with wet lab techniques and electronic/vibrational spectroscopy * Understanding of organic chemistry theory and experimental techniques * Understanding of analytical chemistry principles and techniques such as titration, calibration and method validation * Experience using Excel or (preferred) MATLAB/Python (or equivalent) * Ability to work in cross-functional teams * Strong oral and written communication skills * High attention to detail in experimentation, analysis, and presentation of results * Comfortable working in an evolutionary and dynamic startup environment A preference will be shown to candidates with the following qualifications and prior experience: * Experience performing quantitative analysis using MATLAB/Python (or equivalent) * Experience with air-free laboratory techniques, glove box use, etc. * Laboratory experience in electrochemical characterization of molecules, materials, and/or electrochemical cells Benefits We believe in taking care of our team so they can do their best work. Here's what you can expect when you join us: * Comprehensive Health Coverage - Medical, dental, and vision insurance to keep you and your family healthy * 401(k) Plan - Save for the future * Paid Time Off - Enjoy 3 weeks of PTO to recharge and reset * Unlimited Sick Leave - Take the time you need to rest and recover, no questions asked * Paid Holidays - 11 company holidays, plus 1 floating holiday for a day that's meaningful to you * Supportive Culture - We prioritize work-life balance, flexibility, and employee well-being

Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space. Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity. ANALYTICAL CHEMIST II Position Summary: Ocular Therapeutix is seeking an analytical chemist to support Pharmaceutical Development activities. This role will be responsible for laboratory testing to chemically and physically characterize the company's lead sustained release hydrogel-based intravitreal implant drug product in support of commercial scale-up activities. Principal Duties and Responsibilities include the following: Support Pharmaceutical Development activities to characterize the chemical and physical properties of implant prototypes generated during implant production scale-up studies. Perform analytical chemistry testing and data analysis using standard laboratory techniques and instrumentation (assay, purity, solubility, stability, dissolution). Support method development and testing internally and interface with contract analytical testing labs. Implement appropriate characterization methods to understand and anticipate drug product, API, and polymer-related physicochemical properties. Design and support implant scale-up studies for drug products, APIs, and polymers. Analyze, summarize, and present data to group and cross-functional project teams. Collaborate with a multidisciplinary team of chemists, engineers, and scientists to gather knowledge, identify gaps, design relevant experiments, transfer methods, and document information at appropriate project intervals. Support calibration and maintenance of analytical equipment as necessary. Follow good documentation practices (maintaining contemporaneous records, laboratory notebooks, equipment logbooks, forms, etc.). Qualification Requirements: Degree in Chemistry, Pharmaceutics, Biochemistry, or related scientific discipline. MS or BS with 2+ years of relevant drug product analytical development experience desired. Prior analytical chemistry working experience in either quality or R&D groups in the pharmaceutical and/or biotechnology industry. Experience with HPLC/UPLC, GPC, LC-MS, Empower software. Experience with additional characterization techniques is a plus (UV-Vis, DSC, TGA, DVS, SEM/EDS, FT-IR, XRPD). Experience with polymer characterization is ideal. Excellent problem-solving, organizational, and communication skills. Experience and knowledge in analytical and bioanalytical chemistry, including common practices and techniques. Knowledge of safe laboratory practices. An understanding of GXP analytical operations and ICH/FDA guidelines is a plus. A collaborative, hard-working, team player passionate about science who can effectively work in a dynamic, cross-functional team environment. Ocular Therapeutix is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws regarding nondiscrimination. Ocular Therapeutix provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, or status as a veteran. For information on how Ocular Therapeutix collects, stores, and utilizes candidate information please see our privacy policy found at **************************************

6 Month Contract (May extend or convert to permanent) $35.30/hour - $44.30/hour W2 Must haves: Large molecules experience (Antibodies) LC-MS experience ELN knowledge is desirable Job Description: In this role you will build and then use a combination of skills to help with the biologics characterization workflow. Additional laboratory automation skills are desired but not required. This role will require an eagerness to learn and an ability to work with different teams and different equipment to operate a robust characterization platform. Your efforts will be a complement and core resource to existing capabilities and will serve to expand the team's ability to interrogate biologics diversity to identify optimal leads. Responsibilities: Operate and maintain existing mass spectrometry platforms and implement new workflows for protein characterization. Perform LC-MS data analysis using various software and bioinformatic tools to elucidate the quality attributes of therapeutic proteins and other novel modalities. Troubleshoot automation methods and devices to maintain optimal high throughput protein analyses. Generate frequent characterization summary reports. Follow and improve Standard Operating Procedures for biologics characterization workflows. Required Skills/Background: BS in a relevant field (e.g. protein sciences, chemical or bioengineering, biochemistry or similar) with 6+ years of experience OR MS in a relevant field (e.g. protein sciences, chemical or bioengineering, biochemistry or similar) with 4+years OR PHD in a relevant field (e.g. protein sciences, chemical or bioengineering, biochemistry or similar) with 1-3years. Experience with mass spectrometry and other biophysical assays workflows and their inherent data management. Knowledge and hands on experience in LC-MS based sample preparation for proteins Strong problem solving and communication skills. Ability to multitask, time management, and prioritize activities. Preferred Skills/Background: Industry experience is preferred. Experience with operating high resolution MS instruments such as Agilent Q-TOF, Thermo Orbitraps (e.g. QE+, QE-HF, Exploris 480) and liquid handling platforms such as Vanquish, Acquity UPLC. Experience analyzing data with BioPharma finder, BioConfirm and other MS software is a plus Experience with EMPOWER is a plus ELN knowledge is desirable

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.

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.