Chemist Jobs in Brockton, MA

Worcester, MA 6 month contract (Target PR: 30-36/hr · QC background · Documentation · Advance testing/CE-SDS, HPLC or ELISA experience · Empower or Softmax / PLA software experience is a plus · BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree and 2+ years of related work experience. We are currently seeking a Chemist II position in Quality Control to join our team. The Chemist II will perform laboratory testing within a fast-paced cGMP environment. Experience with capillary electrophoresis testing is required. Key Responsibilities Include: · Performs test methods validations for clinical and commercial projects. · Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements. · Understands, implements and maintains cGMP with respect to laboratory records, procedures and systems in accordance with procedural requirements. · Performs a multitude of laboratory techniques for which they are trained. · Accepts responsibility to complete assigned tasks within required timelines and works with others to accomplish business objectives. · Authors validation protocols and reports as well as corresponding test methods. · Support laboratory investigations in a timely manner. · Support a variety of testing techniques upon completion of training. Basic: · BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree and 2+ years of related work experience. · CE-SDS, HPLC or ELISA existing experience and troubleshooting experience · Empower or Softmax / PLA software experience Preferred: · Spectrophotometric concentration determination · Quality Control testing of phase III and commercial products · Experience with empower audit trail

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

We are currently seeking a Chemist I position in Quality Control to join our team. The Chemist I will perform general compendial testing of product and/or raw materials within a fast-paced cGMP environment. Additional responsibilities will include reagent preparation and routine equipment maintenance activities. Laboratory experience is required. Key Responsibilities Include: · Performs test methods as written to support product/material release. · Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements. · Understands, implements and maintains cGMP with respect to laboratory records, procedures and systems in accordance with procedural requirements. · Performs a multitude of laboratory techniques for which they are trained. · Accepts responsibility to complete assigned tasks within required timelines and works with others to accomplish business objectives. · Revises procedures as necessary and provides continuous improvement support for the department. · Support laboratory investigations in a timely manner. · Support a variety of testing techniques upon completion of training. Basic: · BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree and 1+ years of related work experience. · Solid understanding of cGMP and quality control and documentation requirements. Preferred: · Spectrophotometric concentration determination · Experience testing Appearance per USP, EP requirements · Quality Control testing of phase III and commercial products QC background Documentation Advance testing/CE-SDS, HPLC or ELISA experience Empower or Softmax / PLA software experience is a plus BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree and 2+ years of related work 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.”

Analytical Scientist Employment Type: Contract (12 Months) What You'll Do: Prepare and process both large and small molecule samples Operate LC systems (HPLC/UPLC, especially Waters instruments) Analyze data using Empower software Maintain thorough documentation in electronic lab notebooks (ELNs) Communicate progress and results with senior analysts Assist with troubleshooting and support method qualification/validation Work in a non-GxP lab environment initially What We're Looking For: 2-5 years of relevant industry experience Strong experience with HPLC/UPLC (Waters systems) Expertise in N-glycan analysis and GlycoWorks N-Glycan Kit Empower software and wet lab proficiency Excellent attention to detail and protocol adherence

** Candidates must be authorized to work in the U.S. without current or future visa sponsorship. Sponsorship is not available for this position. Are you a creative and results-driven lead chemist with a passion for developing innovative plastic formulations? Do you thrive in a fast-paced environment, collaborating with R&D, production, and customers to deliver high-performance plastic solutions? If so, we want to hear from you! Location: 30 minutes north of Worcester Why Join Us? Be part of a rapidly growing and innovative plastics manufacturer. Work on cutting-edge polymer formulations with industry-leading experts. Opportunity to make a direct impact on product development and customer success. Collaborative, fast-paced, and dynamic work environment. Key Responsibilities: Develop and optimize plastics formulations to meet customer requirements and improve first-pass acceptance rates. Manage multiple customer sample requests and ensure timely delivery within R&D lead times. Collaborate with operations and manufacturing to scale up new products and optimize production processes. Provide technical support to sales teams and customers, including product recommendations and troubleshooting. Maintain R&D records, formulations, and testing data while ensuring compliance with quality and environmental standards. What You Bring: 5+ years of hands-on experience in plastics or compounding formulation development, including processing and performance optimization. And the ability to take on progressively challenging responsibilities, with opportunities for professional growth and advancement within the organization. We will consider a manager-level candidate for this role. BS in Plastics, Materials Science, or related Ready to lead in a growing, innovation-focused environment? Join us and bring your expertise to a company rooted in quality, teamwork, and the future of plastics manufacturing. EOE Keywords : chemist, scientist, technical manager, chemical, polymer processing, resin handling, blending, extrusion operations, pelletizing systems, injection molding, thermoplastic materials, color, additives, plastics, advanced materials, engineered polymers, paint, coatings

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.

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.

Seeking a Chemist II position in Quality Control to join our team. The Chemist II will perform laboratory testing within a fast-paced cGMP environment. Experience with capillary electrophoresis testing is required. Responsibilities: Performs test methods validations for clinical and commercial projects. Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements. Understands, implements and maintains cGMP with respect to laboratory records, procedures and systems in accordance with procedural requirements. Performs a multitude of laboratory techniques for which they are trained. Accepts responsibility to complete assigned tasks within required timelines and works with others to accomplish business objectives. Authors validation protocols and reports as well as corresponding test methods. Support laboratory investigations in a timely manner. Support a variety of testing techniques upon completion of training Experience: 2+ years of related work experience. Skills: QC background Documentation Advance testing/CE-SDS, HPLC or ELISA experience Empower or Softmax / PLA software experience is a plus Education: BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree. Ravi Sharma Recruiter Scientific and Clinical Division **************** ********************************** 10 Exchange Place, Jersey City, NJ 07302, USA 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.

WHO WE ARE Strand Research is a biotechnology startup dedicated to developing and optimizing novel molecules for consumer applications, with a primary focus on hair. Positioned at the crossroads of science and beauty, our mission is to address the most significant challenges in hair care faced by consumers today. We are committed to innovation driven by rigorous data and relentless pursuit of efficacy, creating solutions that will set new industry standards and redefine what is possible in hair care. Our lab is based in Kendall Square and we have secured substantial funding, providing us with several years of runway to bring groundbreaking ingredients to market. We are at a stage of rapid growth, and looking for results-driven, high octane, resourceful individuals who thrive in a fast-paced, high intensity environment. THE OPPORTUNITY We're looking to hire an experienced Formulation Scientist to join as our first cosmetic formulation R&D lead. In this role, you will be responsible for taking novel ingredients from the bench and translating them into innovative new topical haircare products. This individual will: Lead the development of formulations based on product briefs, formed in partnership with Strand Research scientists and leadership Interface with external raw material, ingredient and equipment suppliers to set up cosmetic formulation capabilities for in-house formulation development Define formulation parameters and target properties of formulas based on market insights and benchmarks Manage process for development and iteration of formulations (samples batching, process documentation, maintaining records, revisions based on feedback). Perform or coordinate testing to ensure efficacy, safety, and stability of final products (including but not limited to thermal stability, preservative efficacy, shelf-life, impurity, compatibility testing, etc.). Follow good laboratory practices while maintaining detailed and accurate records of samples, analyses, ingredients, and results, demonstrating traceability and repeatability through organized documentation and reporting. Maintain product ingredient lists and final specifications Assist in formulation hand-off to product development or external manufacturer teams Stay apprised of beauty and wellness market trends, as well as formulation techniques, ingredients, and regulations to inform new product formulation and development WHO YOU ARE Experienced formulator with at least 3-4 years of industry experience in a hands-on role (cosmetics, personal care products, etc.). Knowledge of surfactant and emulsion systems is a must. B.S. or higher in cosmetic science or related fields is preferred. Experienced in using mixers, homogenizers, viscometers, and pH meters Experienced in maintaining a formulation software or database required (formula breakdown and entry of raw materials, including CAS, INCI, and cost information) Strong understanding of the beauty and wellness customer and a proven ability to translate consumer needs into novel products. Independent problem solver with strong initiative in solving ambiguous problems Strong project management and organizational skills, and experience with Google Workspace Very hard worker with a high level of accountability. You hold yourself to high standards but also expect those around you to ask well.. You believe good enough never really is good enough. You want to always improve, both personally and professionally. You are adaptable and a team player, willing to go the extra mile and jump in on ad hoc tasks to support the overall company growth. ADDITIONAL INFORMATION This position is hiring for an immediate start This position is in-office 5 days a week in our Cambridge, Massachusetts office

A well-funded and highly innovative start up from Third Rock Ventures is emerging out of stealth with a syndicate of marquee investors and is seeking a talented Scientist/Associate Scientist (AS) to join the Biology-In vivo pharmacology team. The Scientist/AS will support the in vivo pharmacology team for discovery-stage pipeline program(s) focused on antibody-driven diseases. The role will work collaboratively with the Biology team lead(s) to contribute to lead characterization and development candidate selection. The Scientist/AS will aid in the management of both external and internal in vivo pharmacology studies and contribute to the growth of internal in vivo capabilities. The ideal candidate is an experienced lab-based biologist with a background in immunology and biologics drug discovery. Responsibilities: Design and carry out in vivo biology experiments that support preclinical drug discovery including PK/PD analysis, mechanism of action studies, and disease modeling Aid in expanding our internal in vivo pharmacology capabilities at a shared vivarium space, including animal handling, dosing, sample collection/processing Independently develop and execute quantitative assays for the analysis/characterization of ex vivo samples (ELISA, flow cytometry, etc.) Work collaboratively with peer team leads to advance program(s) to IND Proactively review literature to bring in newest scientific findings, ideas, and methods/technologies for discovery research Manage out-sourced CRO-based workflows, including study design and data analysis Required qualifications and experience: PhD with 0-3 years or a Bachelors with 8+ years or Masters with 6+years in relevant scientific area, such as immunology, cell/molecular biology with Experience in the design and execution of in vivo studies (experience assessing pharmacokinetics/pharmacodynamics of biologics preferred) Experience with ex vivo sample analysis and data interpretation (ELISA, immunophenotyping) Capacity to work within a dynamic matrix environment, with strong contributions to project strategy and execution Excellent communication, presentation, and inter-personal skills; superb organizational and problem-solving skills

ABOUT THE COMPANY At QurAlis, we are neuro pioneers on a quest to cure. We work with a relentless pursuit of knowledge, a precise attention to craft, and an optimistic mindset to discover and develop effective precision medicines that will alter the trajectory of amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), and other neurodegenerative diseases. Founded by an internationally recognized team of neurodegenerative biologists from Harvard Medical School and Harvard University, QurAlis is a clinical-stage biotechnology company advancing a pipeline with therapeutic candidates that target specific components of ALS and FTD pathology and defined patient populations based on both disease-causing genetic mutation(s) and clinical biomarkers. Summary of Position QurAlis is seeking a highly motivated Discovery Scientist to support and execute its cutting-edge screening and discovery efforts. The Discovery Scientist will work closely with the QurAlis scientific and management teams to perform studies in a high quality and scientifically rigorous fashion. Primary Job Responsibilities: Design and implement discovery plans and oversee the execution Analyze data, interpret results, identify problems, and develop creative troubleshooting plans Management of contract research studies and research associates Proactively review the scientific literature to identify and share new scientific findings, ideas, and methods with other scientists at QurAlis Discover ALS disease related phenotypes using patient derived iPSC cell types Initiate and perform efficacy and mechanism of action studies to advance therapeutic programs Independently plan and execute experiments, and contribute high level scientific neurodegeneration pathways expertise Must have scheduling flexibility to enable weekend and holiday work rotations Present research findings internally and externally at scientific meetings/conferences Minimum Qualifications Required A PhD in cell biology, biochemistry, neuroscience, or a related field 3-5 years relevant experience in academic and/or industry (biotech or pharma) settings including experience in neurodegenerative disease mechanisms, disease modeling, drug discovery and antisense oligonucleotides (ASO). Proven track record of scientific excellence as evidenced by high impact, peer reviewed publications Proactive, willingness to contribute to bench work in the lab Ability to work independently and collaboratively in cross-functional teams Strong organizational skills, work ethic, and high-level motivation Capacity to be highly productive in a dynamic and fast-paced work environment Excellent oral, written and interpersonal communication skills Authorized to work legally in the United States Additional Qualifications Desired Hands-on experience culturing induced pluripotent stem cells or neurons Drug discovery experience in target validation and/or mechanism of action studies High content imaging assay development and analysis Expertise in RNA metabolism, novel RNA detection assay design mRNA and protein quantitation techniques

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

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.

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

The Company Pando is an AI-driven synthetic biology company revolutionizing enzyme engineering for the pharmaceutical manufacturing and diagnostics industry. Our ultra-high-throughput screening platform screens 1000-fold more enzymes 75% faster and 80% cheaper than traditional methods. This empowers our AI models to efficiently optimize enzymes across multiple properties, delivering high-performing, industrial-grade enzymes that create and capture new market value. The Role We are seeking a creative and motivated scientist to assist in day-to-day lab operations, experiment planning, and completing diverse projects. You will do molecular biology (PCR, cloning, etc), strain engineering, high-throughput screening, and HPLC method development. The ideal candidate will be comfortable working with 96-well plate workflows and have experience in cell culture, analytical chemistry, bioanalytical methods, or related fields. The ideal candidate should feel comfortable working on diverse projects in a fast-paced company. Key Responsibilities: Run molecular biology experiments including PCR, qPCR, DNA purification, plasmid assembly, and transformation of E. coli . Build and screen protein libraries using high throughput screens (e.g., enzyme activity assays, HPLC for quantification of small molecules) Design, run, and debug standard molecular biology and protein engineering experimental workflows. Develop and optimize HPLC methods for quantifying small molecules in enzymatic reactions. Implement and run high-throughput 96-well plate HPLC workflows. Analyze chromatographic data to assess enzyme activity and method quality. Troubleshoot an Agilent HPLC system to ensure reproducible data generation. Developing SOPs for protein purification and quality control of new enzymes, running existing purification, and Q.C. SOPs. Document and report findings clearly for internal teams and external stakeholders. Qualifications: We recognize that not all candidates may meet the entire list below. We're eager to train the right candidates for this role and encourage those who meet at least two-thirds of the criteria to apply. Notes on applying: Within the application, please plan to answer a few simple questions and attach your resume. A bachelor's degree with 2+ years of relevant work experience A graduate degree (Master, PhD) in Biology, Biomedical Engineering, Bioengineering, Molecular Biology, Cell Biology, or related fields. Understand the differences between a startup and a larger corporation, and embrace the fast-paced, entrepreneurial environment. Hands-on experience in molecular cloning, strain engineering, protein production, and general biochemistry. Familiarity with high-throughput screening techniques. Experience with HPLC method development, particularly for small-molecule analysis. Comfortable and familiar with using an electronic laboratory notebook (ELN) for documentation. Industry experience in biocatalysis, enzyme engineering, or pharmaceuticals is a plus but not required. Open to candidates with a range of experience, from recent graduates with strong analytical skills to seasoned professionals. Responsibilities will be proportional to experience. Nice to have: Experience expressing and purifying enzymes from E. coli, Picha, and/or Cell Free Protein Synthesis (CFPS) Experience taking working HPLC methods and reducing their runtime to increase throughput. Strong background in analytical chemistry, biochemistry, or a related field. Ability to troubleshoot HPLC instruments and optimize separations. Experience with data analysis tools for chromatographic data processing. Benefits Competitive compensation. Comprehensive benefits package including medical, dental & vision coverage, etc 401(k) program A dynamic early-stage work environment and highly interdisciplinary, talented, and collaborative team. Professional growth opportunities through mentoring, training, immersion in cross-functional projects, and opportunities to learn and try new things. Why Join Us? Be at the cutting edge of AI-driven enzyme engineering and biocatalysis. A collaborative and dynamic environment focused on scientific innovation. Simply fun. If you're passionate about revolutionizing enzyme-driven biocatalysis, we'd love to hear from you! It is the policy of Pando Bioscience, Inc. to provide equal employment opportunity for all applicants and employees. The Company does not unlawfully discriminate on the basis of race, religion, creed, color, national origin, ancestry, physical and/or mental disability, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, transgender status, pregnancy, marital status, age, sexual orientation, and military or veteran status, or any other basis protected by law. It also prohibits unlawful discrimination and harassment based on the perception that anyone has any of those characteristics or is associated with a person who has or is perceived as having any of those characteristics. Pando does not accept unsolicited resumes from any source other than directly from potential candidates. Any resumes submitted by a staffing agency in the absence of a current executed contract will automatically become Pando's property and no recruiting fees or other obligations will be owed in the event of a potential hiring.

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

Job Title: Laboratory Technician 1 Duration: 12 Months Job Type: Contract Work Type: Onsite Shift Timings: 7:30am - 4:00pm Pay Rate: $24.50-24.50/hr TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. The below client is with one of our client which is a leading global medical technology company. It offers a wide range of diagnostic imaging and laboratory diagnostics, as well as advanced therapies and digital health services. Its solutions span from prevention and early detection to diagnosis, treatment, and follow-up care, empowering healthcare providers worldwide. Job Description: This is a role well suited to an ambitious professional, looking for the next step in their career. As a Laboratory Technician , you will be responsible for: Performance of MFG formulation protocols Data Review, batch record review Knowledge of Microsoft Office Foster Team Environment Calibration and Maintenance of Lab Equipment Lab Duties as required Basic Understanding of SAP Knowledge of and compliance with ISO, GMP, QSR Demonstrates a basic knowledge of professional principles and skills. Effectively uses fundamental concepts, practices, and procedures of particular area of specialization. Contacts are primarily with immediate manager and others in the group. Requirements: This position may suit you best if you are familiar with what is below, and would like to do develop your career with Client Previous experience working in a cGMP manufacturing environment a plus. Required skills to have for the success of this role: BS/BA in related discipline, or advanced degree, where required, or equivalent combination of education and experience. 0-2 years of lab experience Excellent organization and time management skills Excellent laboratory technique Ability to lift up to 50 pounds Ability to work individually and in a team setting. Must pass a Drug Enforcement Agency (DEA) background check. TekWissen Group is an equal opportunity employer supporting workforce diversity.

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**

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.