Chemist Jobs in Lawrence, 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

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

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.

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.

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

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

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

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.

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

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

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

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.

The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA Sciences. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. PRIMARY DUTIES AND RESPONSIBILITIES · Prepares and analyzes products to determine chemical and physical properties. · Under close supervision confers with chemists and other client personnel regarding research, procedures performed, related results and prepares reports. · Under close supervision will be trained to become proficient at assigned tasks in order to become subject matter experts. · Performs routine data generation and problem solving with a minimal rework. · Works under close supervision to ensure all work performed is performed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration. · Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies. · Performs system maintenance and calibrations to ensure equipment is operating with specified requirements. · Learns proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules. · Documents work in a clear and organized manner. · Follows all safety rules and regulations and conducts periodic safety audits. · Follows all cGMP rules and regulations. REQUIREMENTS & QUALIFICATIONS Qualification include a Bachelor's degree in Chemistry or a related science discipline is required with 0-2 years of related experience. Knowledge of cGMPs and related compliance regulations and guidances is preferred. MINIMUM SKILLS REQUIREMENTS · Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently. · A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel. · Must have excellent organizational, verbal communication and technical documentation skills. · Solid computer skills. · Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples. · Must be a team player with integrity and concern for the quality of Company products, services and staff members.

Job Details Experienced Zink Holdings Massachusetts - Billerica, MA Full Time 4 Year Degree None 10 hour shifts on a routine basis ManufacturingDescription Senior Analytical Chemist Zink Holdings, located at 37 Manning Drive, Billerica, MA is looking for a Senior Analytical Chemist to join our team as a Senior Scientist. Purpose: Provide broad routine and non-routine analytical support to R&D and manufacturing. Integrate analytical information from disparate sources to reach understanding of materials and processes. Provide analytical expertise to other development chemists and formulators. Provide analytical expertise to manufacturing. Interface with R&D and manufacturing chemists to determine specifications for raw materials and internal intermediates. Interface with and assist suppliers in dealing with quality problems. Provide analytical expertise to supply chain sourcing and substitute materials. Provide analytical expertise in health, safety, environmental, sustainability and regulatory compliance issues. Maintain existing analytical capability and recommend additional capabilities. Maintain systematic analytical record keeping. Train and mentor other analytical personnel. Interface with third party analytical service labs for analytical needs outside of company capabilities. Perform other lab, technical and administrative tasks as assigned. Qualifications Requirements: MS/PhD analytical chemistry or related discipline; 5 years industrial experience. Excellent understanding of and prior experience with liquid and gas chromatographic techniques, including GC-MS and LC-MS. Excellent understanding of and prior experience with thermal characterization techniques. Excellent understanding of and prior experience with quantitative analytical method development. Excellent written and oral communication skills. Excellent computer skills for systematic data analysis and presentation. Excellent understanding of statistical methods for data analysis and experiment planning. Detail oriented but able to understand the big picture. Excellent interpersonal skills. Ability to work independently. Ability to work on the milligram scale with "good hands”. Functional Skills: Works independently to plan and coordinate technical activities. Works collaboratively with other staff, suppliers and customers. Collects, correlates and interprets data from multiple sources. Works safely and mindfully of health and environmental issues. Other Valued Skills: Experience supporting R&D, scale-up, pilot and manufacturing for coating operations and small molecule organic synthesis. Experience in negotiating vendor specifications. Experience in wet chemistry analytical techniques. Experience in physical characterization of materials. Experience in microscopy and microtomy. For immediate consideration, please send your resume to **********************

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

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: ***************

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 **************************************

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $23.20 - $31.90 By joining the Bio-Techne team you will have an impact on future cutting-edge research. Bio-Techne, and all of its brands, provides tools for researchers in Life Sciences and Clinical Diagnostics. Bio-Techne's Diagnostic Reagents Division has been providing essential products to the in vitro diagnostics industry for over 40 years. We supply quality controls and reagents for clinical laboratory and point-of-care testing, along with custom products to other companies serving the IVD market. Position Summary: The primary responsibilities of the Manufacturing Chemist are to execute formulations and perform in-process testing on customer specific formulations using Good Laboratory Practices and cGMP. In this role you will execute formulation activities independently and under the direction of senior chemists. The Manufacturing Chemist will be responsible for identifying manufacturing issues and effectively communicating those issues to management. The working hours for this role are 6am-2:30pm at our facility in Devens, MA. Principle Responsibilities: Prepare products using approved procedures and keep details and accurate records. Prepare production equipment for formulation operations per outlined procedures in accordance with SOPs and cGMP. Perform in process analysis and determine adjustments to bring analytes into specification. Write or modify procedures and assist in process optimization to meet department formulation needs and cGMP compliance. Perform processing steps including centrifugation, autoclaving, and filtering. Perform daily QC calibrations and testing on laboratory instruments and balances. Maintain inventory of chemicals and testing supplies and identify shortages or expiring raw materials. Work with R&D and QC to resolve issues with formulations prior to manufacture. Report formulations within ERP system and document control software. Use Non-Conforming Material Reports to identify and remove defective material or product from the inventory system. Perform laboratory and equipment cleaning. Understand and train on safety requirements in working with biologicals and hazardous chemicals. Analyze data, draw conclusions and make decisions for next steps on assigned projects. Perform other duties as required. Qualifications: BS or BA degree in Biology, Chemistry or related science discipline. 1-3 years' experience in biologic formulation or biologic buffers in a GMP environment is desired. Must have good math skills, manual dexterity and possess a basic mechanical aptitude. The ability to work as part of a team, be reliable, multitask, and execute manufacturing goals is required Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.