Chemist Jobs in Saco, ME

We are seeking a motivated and highly talented synthetic chemist at director level to join our Chemistry Excellence Department at Apeloa Pharma Solutions Co.. This position offers a leadership and hand-on opportunity to contribute to a variety of synthetic chemistry projects in a collaborative and fast-paced environment. The ideal candidate will have a deep understanding of organic chemistry, reaction mechanism and drug discovery process, and take a leading role in our medchem/synthetic chemistry team. He/she should have a track record of academic or industry accomplishments. His/Her project and team management experience will be preferred. Company Introduction Apeloa Pharmaceuticals Co., Ltd. is a publicly listed pharmaceutical company headquartered in Zhejiang, China, with over 7,000 employees worldwide. Apeloa provide drug substance and drug product development and manufacturing services to global clients through our state-of-the-art CDMO centers and GMP facilities. Apeloa Pharma Solutions Co. (APS), a wholly owned subsidiary of Apeloa Pharmaceuticals, locate in Billerica, MA. The Chemistry Excellence Department offers FTE and custom synthesis services and are develop multiple chemistry technology platforms in new modality areas to broad our chemistry support horizon. We are committed to fostering a collaborative and inclusive work environment and offer competitive compensation and benefits, including employment-based visa sponsorship for eligible candidates. Key Responsibilities · Lead MedChem/Synthetic chemistry team to execute customer project in a timely manner, and communicate effectively with customer for project update. · Contribute in an impactful manner to the synthetical route design and conduct hands-on organic synthesis laboratory work in need to support client projects. · Propose technology platform projects for internal synthetic technology development. · Present Apeloa platform to our customers and work closely with BDs to support business development. · Manager chemistry resource at Billerica and China sites with clear and open communication. · Active participation in recruitment, training, and development of scientific staff Qualifications: · PhD with >8 years of organic synthesis experience and track record of synthetical route design. · > 4 years of med-chem industrial experience and familiar with medicinal research process. · In-depth understanding of drug discovery process, including ADME/PK, physicochemical property optimization, computational chemistry, toxicology consideration. · Project and lab management experience at CRO or biotech company are preferred. · Synthetical and design experience at conjugate chemistry such as PROTAC/MGs and/or peptide/UAA areas are preferred. · Excellent communication and presentation skills are required. Apeloa is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.

CONTINUUS is looking for a local Analytical Chemisty co-op to join our team for six months beginning immediately. Co-ops work with the senior scientists to develop analytical methodologies and perform routine quantitative analyses of drug substances and drug products. Co-Ops perform hands-on laboratory work, data analysis, develop and maintain technical documentation, and are part of a multidisciplinary team solving unmet medical needs. Key responsibilities: Work within a cross-functional team and conduct data analyses to gain knowledge about process variables Plan and perform hands-on laboratory experiments using chromatographic analysis (HPLC, GC, dissolutions and Karl-Fischer Contribute and maintain detailed technical documentation (experimental plans, electronic notebook records, standard operating procedure, reports) Prepare literature review and team Power points as needed Other responsibilities: Occasionally asked to perform duties beyond formal job responsibilities. Educational requirements: Candidate for BS or MS in chemical engineering, chemistry, biochemistry, and pharmaceutical sciences. GPA of 3.5 or above preferred. Experience and skill requirements: Willingness to learn and take on responsibilities Team player in a fast-paced start-up environment Experience in research and development Knowledge or experience with any of the following is a plus: o Analytical instrumentation for small molecule identification and quantification o Wet chemistry o Scientific writing and notebook management o Organic chemistry

PolyJoule, an MIT spinoff based in Boston, is pioneering conductive polymer battery technology using non-metallic, rare-earth-free polymer supply chains. We develop ultra-safe, sustainable, long-life, low-cost battery energy storage systems. Job Description PolyJoule has an available full-time position in the field of Electrochemistry and Cell Engineering. Candidates should hold a degree in chemistry, chemical engineering, electrochemistry, materials science, or a related field, with hands-on experience in electrochemical cell and battery testing and construction. This position requires both independent and collaborative work, focusing on experimental design, process optimization, and high throughput testing and analysis. The role is based in Billerica, MA, and requires in-person attendance. Responsibilities Participate in the full battery development process, including material synthesis, characterization, cell fabrication (pouch), and electrochemical performance testing. Design and optimize electrochemical cells, including analyzing anode, cathode, and electrolyte formulations. Conduct cell testing using off-the-shelf and custom hardware/software systems for energy storage analysis. Collaborate with R&D chemists to improve chemical engineering techniques and material synthesis. Optimize electrode formulations and test new materials. Evaluate binders and conductive additives for optimal electrode quality. Assess additives to ensure appropriate slurry properties (consistency, viscosity, homogeneity) for manufacturing. Fabricate electrodes. Fabricate cells manually and with automated equipment. Use Python to develop data collection and analysis tools. Work with vendors and suppliers to select, source, and evaluate raw materials. Contribute to other tasks and projects supporting the team. Qualifications B.S. or M.S. in chemistry, chemical engineering, electrochemistry, materials science, or a related field. 1+ years of experience in battery chemistry, including cathode, anode, electrolyte materials, and/or battery cell testing. Strong foundation in non-aqueous electrochemistry, organic chemistry, solid-state chemistry, interfacial chemistry, or corrosion science. Experience with Li-ion batteries, including experimental skills in material and cell characterization (e.g., battery cyclers, glove boxes, EIS). Strong understanding of battery chemical processes and mechanisms from formation to end of life. Familiarity with electrochemical characterization techniques, including cyclic voltammetry, potentiometry, constant current/potential methods, galvanostatic charge-discharge, and electrochemical impedance spectroscopy. In-depth understanding of electrochemical transport phenomena and battery testing protocols. Proficiency in Microsoft Excel and modeling tools (Python) for quantitative data analysis and visualization. A passion for working in a dynamic startup environment with a focus on critical thinking and innovative problem-solving. Strong attention to detail, problem-solving, organizational, documentation, communication, and presentation skills. Excellent verbal and written communication skills. Ability to analyze and draw conclusions from large datasets. Ability to integrate solutions into the product development cycle. Experience with spectroscopy and other quality control techniques is a plus. PolyJoule offers an exciting opportunity to work on groundbreaking battery technology in a dynamic, innovative environment. We are committed to building a diverse and inclusive team where everyone feels valued and respected.

Immunology R&D organization is expanding its early discovery team at the Cambridge Research Center (CRC) in Cambridge, MA. We are seeking a highly motivated contractor/Scientist III to join the Tissue Homeostasis team. Immune‐mediated inflammatory diseases (IMIDs) pose a high burden on the healthcare system worldwide. Long term remission from IMIDs represents an unmet need. Current therapeutic options that target the stromal compartments are limited, thus highlighting the urgent need to identify and validate novel stromal targets. At Tissue Homeostasis, we aim at deciphering the molecular mechanisms that perpetuate chronic inflammation across different tissues, with the ultimate goal to develop transformative therapeutics that can achieve IMID remission. In particular, we focus on understanding the stromal cell biology in the context of chronic inflammation and tissue damage/pathology. Key questions include but not limited to 1) how stromal cells communicate with immune cells to maintain homeostatic states of tissues; 2) how dysregulation of cell-cell and cell-extracellular matrix (ECM) interactions may contribute to inflammatory disorders; and 3) how key signaling aspects of tissue biology in health and IMIDs can be recapitulated in multi-cellular coculture systems or complex in vitro systems. As a contractor/Scientist III, the candidate will participate in target validation and assay development efforts with a focus on dissecting the molecular mechanisms underlying stromal inflammation. This is a hands-on and lab-based role requiring significant cell biology and immunology expertise, the ability to critically assess literature knowledge, and design experiments to support target validation and platform building processes in the Tissue Homeostasis team. Key Responsibilities: As member of the Tissue Homeostasis team, work with the company's Disease Discovery Teams (DDTs) and Genomics Research Center (GRC) team members to design and execute in vitro cell biology and mechanism of action experiments to advance target validation and assay platform development efforts in using immune cells and stromal cells. Perform mammalian cell culture of primary and transformed cells. Develop immune-stromal cell co-culture systems (e.g. Myeloid cells-fibroblast) to dissect signal transduction in cell-cell interactions with disease relevant cues Perform qPCR analysis, flow cytometry, and Western Blotting analysis. Perform cell-based assay with human primary cells and human cell lines (AlphaLISA, ELISA, HTRF, and proliferation assays). Utilize technical knowledge and experience to effectively troubleshoot and optimize assays. Maintaining laboratory notebooks to the required company standard. Communicating results to internal meetings. Interpret findings and effectively present scientific data, concepts, and recommendations to various internal audiences. Compile and review technical reports, protocols, manuscripts, and other key documents. Requirements: Ability to work in a fast-paced environment and delivery results in a timely and agile manner. Ability to work independently and collaboratively with cross-functional teams. Willing to learn new techniques and develop new assays as needed Extensive cell biology and immunology experience, proficiency in working with human primary cells and immortalized cell lines. Experience with co-culture systems or complex in invitro systems with primary human cells Demonstrated knowledge and experience of key cell biology assays and techniques. Genetic manipulation of human cells using sh RNA/si RNA/CRISPR tools. Proficiency in molecular biology skills such as qPCR analysis, flow cytometry, and Western Blotting analysis. Trouble-shooter able to adapt ideas and experiments to achieve key project objectives and adhere to timelines. Excellent communication of complex scientific ideas (written and verbal) and interpersonal skills. Strong organizational skills required, in particular good time management skills. Inclusive, open-minded, collaborative, and forward-thinking. Desired: Background in cell biology of inflammation or Immunology Excellent oral and written communication, analytical, and computer skills. Qualification: Current or perspective BS/MS/PHD students in Biotechnology, Immunology, Molecular Biology, Cell Biology or Microbiology- 5 + years' experience EEO: “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”

Akkodis is seeking a Scientific III for a 12-month contract with a client. Title: Scientific III Contract: 12 months Contract Pay Rate: $75/hr to $79/hr (The rate may be negotiable based on experience, education, geographic location, and other factors.) cell culture and reactor experience within the scope of spike protein production (COVID). Lab experience: Aseptic Techniques, Reactor Experience, and Cell Culture or Bacterial Experience. 90% in the lab - sampling, harvesting and analyzing. 100% onsite Plus - experience with writing protocols and reports. Function as a member of vaccine development laboratories. Execute bioreactor studies for process development and process improvement studies. Author protocols and reports. Primarily bench-scale lab work with some administrative work. Follow company safety procedures and compliances. Lead investigations to resolve problems and to identify root causes. Will be required to work with glass and stainless steel reactors and be comfortable with manual labor. Familiarity with ascetic techniques is a must, familiarity with bioreactors is a plus. Meet project requirements and timelines. Basic Qualifications: Work experience in an cell culture or bacterial laboratory or Bachelor's or Master's Degree/Graduate Degree in Science (e.g. Biology, Biochemistry or Chemistry). Ph.D.'s with research experience are welcome to apply. Good communication skills (verbal and written), math skills, and general computer skills. Experience writing and revising documents (e.g. testing methods, protocols, reports). Experience utilizing Microsoft Word, Excel, and Outlook (MS 2010). Experience participating in teams and collaborative work environments. Preferred Qualifications: 2 L to 10 L Glass Reactor and/or 200 L SUB Experience. General experience with rHA and rS proteins. Equal Opportunity Employer/Veterans/Disabled Benefit offerings include medical, dental, vision, term life insurance, short-term disability insurance, additional voluntary benefits, commuter benefits, and a 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility criteria. Disclaimer: These benefit offerings do not apply to client-recruited jobs and jobs that are direct hires to a client. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit ****************************************** The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: · The California Fair Chance Act · Los Angeles City Fair Chance Ordinance · Los Angeles County Fair Chance Ordinance for Employers · San Francisco Fair Chance Ordinance

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

Support Research and Development of new additives and formulations used in electroplating products for the electronics industry Polymer synthesis and characterization Help design and execute experiments involving equipment and instrumentation for electroplating of metals, electrochemistry, chromatography, microscopy, X-ray diffraction, material and mechanical testing, and additive synthesis. Handle and mix plating bath components and additive solutions at both small and intermediate scales Collect, analyze, and summarize data with appropriate documentation Strict adherence to enhanced safety protocols and ability to work safely and participate in all group safety activities Required Qualifications Bachelor's degree in chemistry or related discipline Demonstrated ability to handle wet chemistry and operate standard chemical and analytical instrumentation and equipment. Highly motivated and effective at working both individually and within team environment to accomplish tasks and project goals Preferred Requirements Organic, inorganic, materials chemist Experience with polymer synthesis Experience with plating bath formulation, electrochemistry, or electrodeposition. Experience with analytical techniques including X-ray Diffraction (XRD), cyclic voltammetry, and NMR. Strong knowledge and demonstrated use of statistics and design of experiments (DOE) principles. Thanks

• Isolation & characterization of human blood cells. • Contractor will request donor samples, isolate cells from human or monkey peripheral blood, set up cultures with isolated cells, perform cell stimulation or differentiation by test compounds, harvest cells and supernatants, prepare these samples for further analysis; run ELISA tests to study effector function of compounds; analyze and present the data generated by these experiments. Top skill requirements: • Primary cell isolation and culture. • ELISA. • Flow cytometry highly preferred. • Basic lab techniques, pipetting samples, dealing with cells, cleanliness. • Enthusiastic. Education and experience: • BS or MS & 3-5 years of biochemistry lab experience. Work environment: • 100 % Lab, benchwork. About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Recruiter Details: Name: Shivangi Email: ********************************* Internal Id: 25-35946

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

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 ： · Execute the daily operations for gene synthesis and cloning workflows, ensuring timelines, quality, and efficiency are met. · Build and optimize protocols for cloning and gene synthesis to improve accuracy, turnaround time, and scalability. · Identify areas of improvement in processes and implement innovative solutions for workflow optimization. · Collect and analyze data to monitor operational performance and identify potential bottlenecks. · Collaborate with R&D, production, and quality assurance teams to ensure seamless integration of new technologies. · Assist in the onboarding, training, and management of team members. · Other tasks assigned by the manager, including strategic projects and cross-department collaborations. EDUCATION AND EXPERIENCE： · Ph.D., Master's, or Bachelor's degree in Molecular Biology, Biotechnology, Biochemistry, or a related field. · Minimum of 5 years of relevant experience in gene synthesis, cloning, or related workflows, with at least 2 years in a leadership or managerial role. SKILL REQUIREMENTS： - Competence & Skills · Must have the working experiences in a CRO company. · Strong understanding of molecular cloning techniques, including PCR, restriction digestion, plasmid purification, Gibson assembly, Golden Gate assembly, and restriction-ligation cloning. · Technical knowledge of gene synthesis, cloning and plasmid production processes. · Ability to troubleshoot and optimize complex workflows in a fast-paced environment. · Excellent organizational and analytical skills with the ability to handle multiple projects simultaneously. - Professional Attitude · Proactive, with a positive attitude and a strong drive to achieve operational excellence. · Strong willingness to innovate and embrace challenges to improve existing systems. · Welcome feedback and demonstrate resilience in problem-solving. · Clear career aspiration to grow within the field of DNA technologies and operational management. WORKING RELATIONSHIPS · Report to: Director, Patrick Zhang · Works with: Internal R&D team, production staff, business stakeholders, and cross-departmental colleagues.

The successful candidate will have outstanding expertise in mouse handling and mouse procedures. They will be responsible for managing mouse colonies, performing project-specific in vivo experiments, intravenous injections of hematopoietic stem cells in humanized murine models, retro-orbital and submandibular blood collection, and blood cell FACS analyses and in vivo imaging. This is a collaborative role that will be partnering with other team members to assist with project-specific- in vivo experiments as well as other needs across the process development function. Role and Responsibilities: Hands-on role with a commitment to designing, conducting and analyzing in vivo studies to assess engraftment of hematopoietic stem cells Execute pluripotent stem cell culture and differentiation into hematopoietic stem cells to support process development, optimization, and characterization Document experimental procedures and results according to established guidelines; Perform statistical analysis of experimental data Collaborate effectively within departmental teams, engage in team discussions to resolve issues, and lead projects with a fully integrated team to facilitate successful outcomes Prior experience in bioreactor-based process development for iPSC-derived cell therapies is highly desirable Qualifications: Advanced degree (M.S. or Ph.D.) in molecular biology or pharmacology, with at least 2 years of industry experience is required Experience working with human induced pluripotent stem cells (iPSC), hematopoietic stem cells (HSC), and/or immune cell biology; including scale-up processes utilizing bioreactors such as PBS vertical wheel, Rotea counterflow centrifuge is required Proficiency with in-vivo techniques including animal handling, intra-bone and intravenous transplants, blood collection and tissue dissection Experience in standard processing techniques including flow cytometry, molecular biology assays such as CFUs, immunological assays, and aseptic cell culture technique is required Experience with experiment design tools such as FlowJo and practical knowledge of statistical analysis is required Strong organizational, analytical, problem-solving, root-cause-analysis, and trouble-shooting skills are required

Simcere is seeking a highly motivated, creative, and collaborative Scientist/Senior Scientist to join our Target Discovery Group. In this role, you will have a specific focus on fibroblast cell biology to uncover and validate novel therapeutic targets in autoimmune diseases-especially in areas such as rheumatoid arthritis, idiopathic pulmonary fibrosis, and systemic sclerosis (scleroderma). Your work will directly shape our future pipeline and involve cross-functional collaborations, from early-stage drug discovery through IND submission. Key Responsibilities Fibroblast Biology & Disease Modeling Develop and execute cutting-edge experiments focused on fibroblast cell biology in the context of autoimmune diseases, including rheumatoid arthritis, idiopathic pulmonary fibrosis, and systemic sclerosis. Identify novel molecular targets related to fibroblast pathobiology and inflammation, contributing to target validation and mechanistic studies. Collaborate with the in vivo pharmacology team to develop disease-relevant animal models for evaluating the efficacy of drug leads. Target Screening & Validation Conduct cell-based screenings of potential targets using various molecular biology techniques (e.g., cloning, CRISPR, RNAi, RNA-seq). Implement genomic, protein, and cell-based assays to confirm discoveries and elucidate mechanisms of action. Experimental Design & Data Analysis Independently design experiments, analyze results, and communicate findings to internal stakeholders. Maintain thorough documentation and ensure data integrity. Cross-functional Collaboration Partner with research, development, and other teams to translate early discoveries into viable therapeutic strategies. Serve as a scientific resource within the organization, sharing expertise on fibroblast biology and autoimmune pathology and support BD team for evaluating potential collaboration opportunities in the relevant fields. Scientific Leadership Supervise Associate Scientist(s), providing mentorship and fostering a collaborative lab environment. Keep abreast of the latest scientific and technological advancements in fibroblast biology and autoimmune research. Qualifications & Experience Education PhD in Molecular and Cellular Biology, Immunology, Cancer Biology, Biochemistry, Genetics, or a related field, with a minimum of 2 years of relevant postdoctoral or industry experience. Technical Expertise Demonstrated proficiency in molecular biology (e.g., cloning, transfection, transduction, qPCR, CRISPR, RNAi, RNA-seq, Western blot). Hands-on experience with pooled libraries (CRISPR, sh RNA) for high-throughput screening. Solid background in cell culture techniques (including primary human T cells, myeloid cells, and/or fibroblasts) under both normoxic and hypoxic conditions. Skilled in various cell-based assays (flow cytometry, proliferation, cytotoxicity); experience in imaging platforms (e.g., immunofluorescence microscopy, Incucyte) is a plus. Disease-Focused Background Research experience in fibroblast pathobiology and/or autoimmune disease models-especially in rheumatoid arthritis, idiopathic pulmonary fibrosis, or systemic sclerosis-is highly preferred. Familiarity with generating and characterizing Cancer-Associated Fibroblasts (CAF) and/or other fibrotic models is a plus. Track Record History of success in target identification/validation, supported by peer-reviewed publications or patents. Soft Skills Excellent communication and organizational skills, with the ability to juggle multiple projects and lead junior scientists effectively.

Codify Therapeutics is an innovative startup committed to leveraging alternative splicing to discover transformational medicines. Our mission is to develop groundbreaking treatments that address unmet medical needs and improve the lives of patients. Leveraging cutting-edge technologies from world-renowned scientific founders, Codify is dedicated to pushing the boundaries of cancer research and treatment. Job Description As a Scientist at Codify Therapeutics, you will play a key role in our growing organization, both to meet R&D needs and to drive projects in the Platform and Target Discovery group. This position offers a unique opportunity to collaborate with cross-functional teams and be a part of the early scientific team building a new and exciting therapeutic modality. Responsibilities Design and perform cell-based models and develop assays for new therapeutic target discovery Techniques may include CRISPR and/or lentivirus based genetic manipulation, and the development of fluorescent or luminescent reporters Design and execute experiments for therapeutic target and hit identification using a combination of molecular, cellular, genetics, and functional genomics skills Techniques may include mammalian cell culture, RT-PCR, qPCR, Western blot, flow analysis, cellular assays (viability, death, dose response), and genetic perturbation using ASOs, si RNAs, sh RNAs, CRISPR Design and execute high throughput screens, as well as downstream data analysis Execute experiments and analysis diligently to yield meaningful results - Interpret data thoughtfully - Identify potential pitfalls and obstacles and overcome them - Communicate with clarity on timelines and research plans Collaborate with cross functional teams and support training of junior researchers Other research skills: Data analysis and visualization - Maintain clear and detailed electronic notebook - Communicate findings and results at internal meetings Qualifications PhD degree in biology, molecular biology, genomics, or related science and relevant research experience Experience with experimental or computational research in functional genomics or RNA biology is a plus, as well as experience with MPRA or CRISPR screens and AmpliconSeq analysis

BS in Food Science/Engineering/related science or engineering field Internship in related field or applicable food processing technology and statistical process experience. MS/PhD in Food Science/Engineering/related science or engineering field Knowledgeable about food chemistry, sensory, microbiology, food packaging systems and food engineering. Product development experience. Problem solving skills. Ability to work with cross-functional teams at multi levels within the organization. Excellent interpersonal, communication skills. Accept feedback. Flexible and resilient. 1. Conduct research including new product research and the development of foods. 2. Develop new and improved methods and systems for food processing, production, quality control and packaging. 3. Work in pilot plant and support production scale ups and commercializations. 4. Field customer requests both internal and external to satisfy project needs from a conceptual phase through commercialization and troubleshooting. • Participate in ideation/brainstorming • Develop gold standards while working with Culinary and subject matter experts (SMEs) • Match competitive products • Formulation Optimization • Concept to Commercialization • Execute internal processes • Ability to understand and troubleshoot customer processes 5. Be a strong part of customer facing team to deliver solutions that will “Nourish and Delight” our customers. 6. Coordinate customer calls with sales/culinary representatives through presentations both technical and culinary based. 7. Work with cross functional groups to optimize the strengths of Kerry and deliver the best Taste and Nutrition experience for our customers 8. Develop and protect Intellectual Property by documenting research notes. 9. Study methods to improve quality of foods such as flavor, color, texture, nutritional value, convenience, or physical, chemical, and microbiological composition of foods 10. Complete project requests within the time frame required by the customer. 11. Employ efficient time management 12. Assist customers with technical issues that may arise. 13. Travel to Kerry production plants and to customers. 14. Must be able to taste and smell chemicals, flavors and food products. 15. Must be able to stand for long periods of time in a laboratory setting and lift 50 pounds. 16. Excellent verbal and written communication skills. 17. Must work well in teams.

Job Title: Laboratory Technician Onsite Requirements: Active Security Clearance Flexibility with Shift Availability and Off-Hours Support Laboratory Experience Job Description: This is a 1-year contract. At the end of the period of time, the operations team will be reviewing the requirement for 24/7 operations. Probability for extension will be determined in that time. Responsibilities include but are not limited to: Monitor sensor telemetry and execute daily procedures to ensure safe operation of payloads. Identify and respond to system anomalies, coordinating with appropriate personnel for spacecraft recovery. Achieve and maintain operational proficiency, leveraging mission unique software to complete daily tasks. Communicate with the Factory Support Center (FSC), Engineering, Development, Integration, and Sustainment (EDIS), Mission, Space Operations Command (SpOC), and Space Systems Command (SSC) concerning ongoing operations and/or anomalies. Maintain operations logs and conduct handover procedures in accordance with prescribed Tactics Techniques and Procedures. Support FSC and EDIS in performing maintenance activities, troubleshooting procedures, and implementation of prescribed anomaly resolutions. Must Have: Demonstrated track record of successful critical mission execution on a tight timeline. High degree of proficiency with Microsoft Outlook, Word, Excel, and PowerPoint. Experience following and executing formal operating and safety procedures. Demonstrated ability and confidence to make sound decisions. Self-motivation, strong communication skills, ability to work within a team. Nice to Have: Familiarization with space domain awareness concepts and operations is desirable. Experience supporting operational missions/programs preferred. Skill Matrix: Must Have Experience: Currently holds a Secret Clearance (OR a higher clearance) Executing formal operating and safety procedures: 2 years Track record of successful critical mission execution on a tight timeline: 2 years Software Tools: Microsoft Office Suite (Word, Excel, PowerPoint, Visio, Outlook): 2 years Currently holds a Top Secret/SCI clearance **Due to the nature of the work, a United States Government Clearance is required to be eligible for the position**

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

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.

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

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