Research associate jobs in Manchester, NH - 1,133 jobs

UII America, Inc., a subsidiary company of Shanghai United Imaging Intelligence Healthcare Co. Ltd. (UII), is building an organization of highly-motivated, talented and skillful AI experts and software developers to strengthen our R&D power and address the need of our innovative products in the USA market. United Imaging Intelligence (UII) is committed to providing AI solutions for medical devices, imaging, and diagnosis - to helping clients better understand and embrace AI. United Imaging Intelligence is led by two world-renown leaders in the AI industry. Together, they will lead UII in focusing on “empowerment” and “win-win.” UII empowers doctors and equipment in order for doctors and hospitals to win, for research institutions to win, and for third-party companies to win. UII America, Inc. is building a world-class research and development team in Boston, MA. We have immediate openings for LLM Research Interns with the following qualification requirements: [ Responsibilities ] Research and develop automated evaluation pipelines for Large Language Models (LLMs) in the medical domain, integrating clinical logic and bioinformatic standards; Implement and optimize evaluation frameworks using LLM/Agent-as-a-judge techniques and reward models to assess complex clinical reasoning capabilities; Conduct deep-dive analysis on model performance from both technical (NLP) and clinical perspectives, identifying failure modes and providing actionable insights for model alignment; Extend and improve the company's existing algorithms and evaluation libraries; Work closely with colleagues and management to develop company assets in NLP/LLM and Conversational AI; Be ambitious to lead the changes in future Healthcare with innovations. [ Qualifications ] Currently pursuing a PhD or Master's degree in Computer Science (AI/ML), Bioinformatics, Medical Informatics, Computational Biology, or a related quantitative/medical field; Strong interest in the intersection of AI and Healthcare, with the ability to bridge technical model evaluation and clinical domain knowledge; Strong programming skills with Python and familiarity with deep learning frameworks such as PyTorch; Understanding of the LLM life cycle, including data preparation and reinforcement learning (RLHF/RLAIF); Proven track record of publications in top-tier conferences and journals (e.g., NeurIPS, ICML, ACL, EMNLP, etc.) is a plus; Passion for applying AI to make a positive impact in the healthcare domain; Ability to develop practical solutions to challenging problems; Strong writing, communication, and cross-discipline collaboration skills

+++ SiPhox Health is redefining clinical immunoassay diagnostics by miniaturizing the analytical power of a central lab into an accessible, affordable, at-home platform. Our silicon-photonics architecture unites advanced biochemistry, microfluidics, and semiconductor-grade manufacturing to deliver precise, multiplexed biomarker quantification in minutes on a device the size of a coffee maker. We are building what we believe will become the first mass-market photonic blood analyzer, enabling continuous improvement in chronic disease management through frequent, high-quality testing. +++ The Opportunity +++ We are looking for a Senior Assay Development Scientist or Engineer who wants to build assays that have never been built on this kind of platform before. If you thrive on developing rigorous, quantitative immunoassays, including challenging free/competitive assays, and want your work to directly ship in a consumer device used by millions, this is one of the rarest opportunities in diagnostics today. This role sits at the center of platform innovation, contributing directly to analytical chemistry, surface chemistry, microfluidics, and silicon photonics integration. You will shape a growing assay menu that spans hormones, inflammatory markers, metabolic proteins, and future pediatric/specialty panels. +++ What You'll Do +++ Core Assay Development Develop quantitative sandwich and competitive immunoassays (including free hormone assays, displacement-driven formats, and low-abundance biomarkers) on a silicon-photonic resonance platform. Design, execute, and interpret experiments focused on: Binding kinetics & equilibrium optimization Surface functionalization strategies Competitive assay dynamic-range shaping Calibrator and control development (matrix selection, commutability) Assay precision, stability, robustness Analytical Performance & Validation Own assay verification and validation aligned with CLSI standards (EP05, EP06, EP07, EP09, EP10, EP17). Establish and demonstrate performance for: Analytical sensitivity & functional limit (LoB/LoD/LoQ) Linearity & reportable range (including hook effects, competitive assay inflection characterization) Repeatability, reproducibility, and nested CV analysis Interference and cross-reactivity studies Matrix equivalency & recovery studies Build calibration models for a novel platform (e.g., 4PL/5PL, competitive curve inversion, chip-specific normalization frameworks). Cross-Functional Integration Collaborate deeply with photonics, microfluidics, reader electronics, manufacturing, and product engineering teams to close the loop on real-world assay performance. Work with process development and chemistry groups to scale assays from prototype to production, enabling high-volume, chip-based manufacturing. Documentation & Execution Deliver high-clarity technical reports, protocols, V&V documentation, and design-history file content that meets IVD and FDA expectations. Present results across the company to inform design decisions and product milestones. +++ What We're Looking For +++ Technical Background PhD + 2 years, or MS + 6 years in biochemistry, chemical engineering, analytical chemistry, biophysics, bioengineering, or related fields. Expertise in immunoassay development (sandwich and competitive). Experience with free hormone assays is a major plus. Demonstrated ability to independently solve complex analytical and biochemical problems. Hands-on experience with complex analytical workflows, assay automation, and instrumentation. Strong understanding of calibration design, commutability, and control strategies. Familiarity with statistical analysis of assay performance, including mixed-model ANOVA, CV decomposition, and method-comparison frameworks. Regulatory & Platform Experience (Bonus) Experience with IVD development, ISO 13485, or 21 CFR 820. Experience with POC or novel-platform assay development. Knowledge of label-free sensors, waveguides, or photonic resonance systems. Experience with Python, R, or MATLAB for data analysis, curve fitting, and automation. Personal Traits Strong scientific intuition paired with rigorous data discipline. Thrives in a fast-paced, milestone-driven startup environment. Creative problem solver willing to challenge established assay paradigms. High integrity, willingness to own outcomes, and a collaborative mindset. +++ Why This Role Is Unique +++ Most assay developers spend their careers optimizing assays on platforms that already exist. At SiPhox, you will: Build the first generation of photonic immunoassays deployed in consumer health. Design assays whose constraints are shaped by semiconductor physics as much as biochemistry. Work on hard problems (free hormone assays, multiplexing, competitive equilibrium, small-volume matrices) where innovation, not incrementalism, wins. See your work ship in a product used at home by real people, not just research labs. If you want to work at the frontier of diagnostics (where photonics, biochemistry, and consumer health converge) we'd love to meet you.

A leading cancer research institute in Chelsea is seeking a Scientific Officer or Higher Scientific Officer to conduct in vivo experiments aimed at optimizing vaccination approaches for treating cancers with homologous recombination defects. The ideal candidate will hold a current Home Office License, possess expertise in in vivo assays, and contribute to cutting-edge cancer research. This role offers a competitive salary, a supportive research environment, and opportunities for professional development. #J-18808-Ljbffr

Support raw materials of therapeutic proteins API Support creating liquid, powders, and acid and basis make sure to sample testing of the material Follow GDP and GMP environment Skills pH, Conductivity, sample prep, media prep, autoclaving, Specimen processing, Quality control, biology, Laboratory Top Skills Details pH,Conductivity,sample prep,media prep,autoclaving,Specimen processing Additional Skills & Qualifications Associate's Degree or BS life science 0-2 Experience working in a GMP environment Experience Level Entry Level Job Type & Location This is a Contract position based out of Portsmouth, NH. Pay and Benefits The pay range for this position is $23.25 - $23.25/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Portsmouth,NH. Application Deadline This position is anticipated to close on Feb 6, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Site: Mass General Brigham Incorporated Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. Job Summary The Research Compliance Associate is responsible for contributing to the overall success of the research compliance program at Mass General Brigham (MGB) as demonstrated by assisting with the development, oversight, and monitoring of research compliance functions through interpretation of MGB policy and local, state, and federal laws and regulations. The Research Compliance Associate should have a background in multiple research areas including, but not limited to, bench and laboratory research, animal research, human subjects research, international research activities, responsible conduct of research (RCR), research misconduct, research privacy, grants management, and controlled substances. The Research Compliance Associate will work under the direction of the Chief Research Compliance Officer and in collaboration with other departments within the research infrastructure. Qualifications Under the guidance of the Chief Research Compliance Officer, the Research Compliance Associate will have the following responsibilities: Assist with the development of an annual work plan based on risk assessment. Utilize metrics to measure program effectiveness. Assist with internal investigations and operational audits to assess risk of research related issues, identify potential research compliance vulnerabilities, and make recommendations to improve internal controls. Assist with education of the research community on research related topics to achieve compliance utilizing communication styles such as PowerPoint presentations, articles, website development, in-person training sessions, handouts, and infographics. Stay abreast of requirements and changes in the regulatory environment and assist with interpretation and distribution of emerging MGB policies as well as local, state, and federal laws and regulations as it relates to research compliance. Assist with evaluation of issues of non-compliance to include investigation, oversight, follow up, and resolution. Assist in the development and revision of written research policies, procedures, and guidelines. Assist in maintaining the research compliance webpage with relevant and up-to-date information in collaboration with the web development staff. Utilize tact and diplomacy to communicate, build rapport and foster strategic alliances within the research community. May represent Research Compliance at committee meetings. Contribute to MGB and the Office of Compliance initiatives to promote a positive work environment. Perform other related duties and responsibility as required. Education Bachelor's Degree required. Graduate degree in a healthcare field or law is preferred; related healthcare or legal experience considered in substitution Licenses and Credentials CHRC preferred Experience 3 years experience in project management in a complex organization required. 1-3 years experience in a research-related position, preferably in a research compliance role. Familiarity with current applicable local, state, and federal laws and regulations related to research activities. Knowledge, Skills and Abilities Proficient in using computer software applications such as Microsoft Excel, Word, PowerPoint, and Adobe. People Soft experience strongly preferred. Strong interpersonal and communication skills (oral and written), including public speaking to facilitate training sessions, and lead discussion groups. Ability to understand complex organizations; demonstrated political savvy. Strong project management skills Ability to work independently, with all levels, and within a strong team environment. Ability to manage multiple responsibilities, often under time pressures. Ability to function independently and effectively. Working Schedule Hybrid, depending on business needs. On average, onsite required 2 days per week. Additional Job Details (if applicable) Remote Type Hybrid Work Location 399 Revolution Drive Scheduled Weekly Hours 40 Employee Type Regular Work Shift Day (United States of America) Pay Range - / Grade 6 At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package. EEO Statement: Mass General Brigham Incorporated is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran's Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at **************. Mass General Brigham Competency Framework At Mass General Brigham, our competency framework defines what effective leadership “looks like” by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Responsible for the execution and analysis of experiments and analytical procedures. • Displays an investigative or technological orientation in designing, executing and interpreting experiments and analytical procedures. • Investigates basic technical problems and performs routine scientific procedures and experiments under general supervision. • Plans and prioritizes concurrent experimental procedures. • Integrates, complies, and tabulates data and assists supervisor in the analysis and interpretation of the results. • May provide oral presentations on results to other department members. • Works under active supervision. • Follows established procedures. • Work is reviewed for soundness of technical judgment and overall adequacy and accuracy. • Contributes to the completion of milestones associated with specific projects. • Failure to achieve results or erroneous execution may cause delays in program schedules, and may result in the allocation of additional resources. • Frequent internal company contacts. Infrequent inter- departmental and outside constituent contacts on routine matters. Experience: • 0 to 3 years. Skills: • We seek a motivated, full-time employee to work on a collaborative team creating recombinant cell lines for the production of therapeutic proteins, in support of preclinical and clinical development programs The main responsibilities in this position will be expression vector construction, cell line generation, and cell culture analysis of selected cell lines. • Additional responsibilities will include managing work assignments and data analysis. • Attention to detail and good communication are required. • Experience in molecular cloning, cell line development, and/or flow cytometry. Qualifications • The candidate should have a B.S. degree in Biology, Bioengineering, or related field and a minimum of 1 year of molecular biology and/or mammalian cell culture laboratory experience. • Candidate must have excellent organizational skills and be able to work as part of a team. Additional Information For more information, Please contact Akriti Gupta ************** Morristown, NJ 07960

Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients' lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston's top workplaces for the past several years. For more information about our science, pipeline and people, please visit **************** or follow us on X (formerly Twitter) or LinkedIn. How we work: * PIONEER: We are courageous, resilient and rigorous in our mission to improve patients' lives through our revolutionary degrader medicines. * COLLABORATE: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine. * BELONG: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard. How you'll make an impact: We are seeking an energetic and talented scientist to support our internal compound management as part of the Protein Sciences and Lead Discovery (PSLD) team at Kymera. The ideal candidate will deliver on company compound requests and assist the Compound Manager in streamlining processes. This individual is a self-starter, driven, highly motivated, collaborative and looking to transform patients' lives through the development of novel therapeutics. * Process new samples into the internal compound inventory with accurate weighing and dissolution * Fulfill requests for assay-ready plates and powder/liquid aliquots for internal assays submitted through LIMS ordering system * Coordinate with lab scientists and chemists to order, receive, register, and store commercially available and bespoke compounds * Assist compound manager with other daily tasks as they arise Skills and experience you'll bring: * Bachelor's degree in Chemistry, Biology, Engineering, or related field; industry lab experience preferred * Ability to multitask and manage multiple requests * Detail-oriented and self-motivated mindset * Keen sense of organization * Ability to take direction and quickly execute on tasks * Strong communication, collaboration, and problem-solving skills * Aptitude for learning new software packages * Experience with Microsoft Office * Experience with compound management systems such as Hamilton, SPT Labtech, Azenta and/or laboratory automation such as tip-based and acoustic liquid handlers a plus Equal Employment Opportunity Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class. Compensation * Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay. * The anticipated base salary range for this role is $65,000 - $90,000, with eligibility for annual bonus, equity participation, and comprehensive benefits. * Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate's depth of experience and the capabilities they bring to the position.

FL87, Inc. is a privately held, early-stage biotechnology company developing a novel approach to gene therapy that can address currently untreatable diseases. It was founded by Flagship Pioneering, an innovation enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Syros Pharmaceuticals (SYRS), Seres Therapeutics (NASDAQ:MCRB), Generate Biomedicines, Tessera Tx, Evelo Biosciences (EVLO), and Indigo Agriculture. The role We are seeking a motivated Research Associate / Senior Research Associate to support the development, preparation, and characterization of Lipid Nanoparticle (LNP) formulations. This role is highly hands-on and focused on formulating, screening, and analyzing LNPs to support discovery and development programs. The ideal candidate works well in a fast-paced, team-oriented environment and is eager to deepen their expertise in formulation science. Key responsibilities Prepare and formulate LNPs using established protocols and evolving methods Execute formulation experiments to support optimization and screening efforts Perform LNP characterization and analytics, including particle size, PDI, encapsulation efficiency, and stability testing Accurately document experimental procedures, results, and observations in laboratory records Analyze and summarize experimental data and communicate findings to project teams Collaborate closely with scientists across formulation, analytics, and biology functions Support routine laboratory operations, including reagent preparation, equipment upkeep, and inventory management Professional experience and qualifications BS or MS in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or a related field Hands-on experience with LNP formulations or lipid-based delivery systems Familiarity with LNP analytical techniques (e.g., DLS, encapsulation assays, basic stability studies) Strong attention to detail and ability to follow experimental protocols Ability to work effectively as part of a team in a fast-paced environment Good written and verbal communication skills What We Offer Opportunity to work at the forefront of LNP formulation innovation Collaborative, science-driven culture with high impact research Competitive compensation and benefits package ABOUT FLAGSHIP PIONEERING Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture. Flagship has been recognized twice on FORTUNE Change the World list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company annual list of the World Most Innovative Companies. Learn more about Flagship *********************************************************************************************** At Flagship, we accept impossible missions to enable bigger leaps. Our core values guide us through uncertainty and toward lasting impact. We are an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Recruitment & Staffing Agencies: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering's internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto. The salary range for this role is $65,000 - $93,500. Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. FL87 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL87's good faith estimate as of the date of publication and may be modified in the future.

Job Title: Quality Assurance Analyst / Pharma Manufacturing Duration: 12 months contract, extendable up to 18 months Note: Client has the right-to-hire you as a permanent employee at any time during or after the end of contract. You may participate in the company group medical insurance plan which includes dental and vision. Job Description: The Andover Site Operations Management group is looking for an individual to fill a Lead Investigator position within the Andover Site Investigations group. The Andover Site Investigation group is responsible for overseeing investigations for all GMP manufacturing suites in Andover, including both mammalian and bacterial based processes in support of commercial and clinical Drug Substance manufacture. The candidate will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. This position will report to the Manager of Investigations within the Site Operations Management Function. The candidate will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. The individual will be expected to develop collaborative relationships with the operational leadership and staff in each suite and the appropriate Quality and Functional Area representatives in order to facilitate investigations using continuous improvement techniques. The incumbent will be expected to have experience in the area of quality and compliance and a working knowledge of the appropriate regulations. Experience with and in depth understanding of cell culture and chromatography is highly desirable. They will be expected to assist in continually defining and improving the philosophy and justifications involved in investigations and to continually evolve to meet changing business needs. Additional responsibilities and expectations include: Have a fundamental understanding of the investigation process as it applies to manufacturing issues Have detailed understanding of the processes and systems involved in the manufacture of bio pharmaceutical. Be able to use that knowledge to investigate process deviations and atypical results and identify root cause Work with the appropriate people from both the quality and operational organizations develop a corrective action Ensure their investigations are conducted with a strict adherence to appropriate quality and compliance standards Exercise judgment in developing practices, techniques and evaluation criteria for obtaining results A BS or MS, preferably in a scientific or engineering discipline preferable. A minimum qualifications to BS + 4-6 yrs experience or MS + 2-4 yrs experience in a pharmaceutical and/or biological manufacturing operation with a strong technical background in a cGMP and Quality environment is required. Prior experience with investigations including conducting and writing investigations and in use of continuous improve methodology preferred. The incumbent must be a collaborative team player with strong coordination, facilitation and writing skills. Additional Information Anuj Mehta ************

Makro Scientific: Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific's proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations. Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent. Job Description Job ID : 43012 Location : Andover, MA Duration : 12 Months Job Title : Investigator Initiated Research (IIR) Associate The Andover Site Investigation group is responsible for overseeing investigations for all GMP manufacturing suites in Andover, including both mammalian and bacterial based processes in support of commercial and clinical Drug Substance manufacture. The candidate will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. This position will report to the Manager of Investigations within the Site Operations Management Function. Prior experience with investigations including conducting and writing investigations and in use of continuous improve methodology preferred. The incumbent must be a collaborative team player with strong coordination, facilitation and writing skills. The candidate will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. The incumbent will be expected to have experience in the area of quality and compliance and a working knowledge of the appropriate regulations. Experience with and in depth understanding of cell culture and chromatography is highly desirable. They will be expected to assist in continually defining and improving the philosophy and justifications involved in investigations and to continually evolve to meet changing business needs. Skills: Have a fundamental understanding of the investigation process as it applies to manufacturing issues Have detailed understanding of the processes and systems involved in the manufacture of bio pharmaceutical. Ensure their investigations are conducted with a strict adherence to appropriate quality and compliance standards Qualifications Experience required: 3-5 Years Education: BS or MS, preferably in a scientific or engineering discipline preferable. A minimum qualifications to BS + 4-6 yrs experience or MS + 2-4 yrs experience in a pharmaceutical and/or biological manufacturing operation with a strong technical background in a cGMP and Quality environment is required.

NO Agencies - Please Please keep in mind - salary range / pay is factored on years of direct work experience and education. The highly motivated Research Associate will support the development and execution of MALDI imaging workflows to advance research in rare diseases, mitochondrial biology, oncology, neurology, and related therapeutic areas. This role is hands-on and focused on tissue handling, sample preparation, slide processing, and assisting with MALDI-MSI data acquisition. The Research Associate will help generate high-quality spatial omics data that contribute to biomarker discovery and mechanistic insights across multiple internal programs. ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform routine sample preparation for MALDI imaging, including tissue cryosectioning, slide preparation, matrix application, and on-tissue treatments. Assist with MALDI-MSI data acquisition, including instrument setup, calibration, sample acquisition monitoring, and documentation. Support qualitative and quantitative MALDI imaging studies by preparing samples, organizing datasets, and performing basic data quality checks. Work collaboratively with scientists in oncology, neurology, and analytical chemistry to help execute imaging workflows and maintain consistency across internal studies. Maintain laboratory supplies, equipment logs, and adherence to SOPs to ensure high-quality imaging data generation. Present experimental updates or data summaries to project teams when needed. Perform other duties as assigned. QUALIFICATIONS: Requires a B.S. (0-2 years of experience) or M.S. (with 0-1 years of experience) Biochemistry, Neuroscience, Biomedical Engineering, or related field with 1-2 years of prior laboratory experience required. Hands-on experience with tissue handling, cryosectioning, histological workflows, or mass spectrometry sample preparation is strongly preferred. Familiarity with MALDI mass spectrometry, imaging techniques, or matrix application methods is a plus. Experience working with large datasets, imaging data, or data integration tools is preferred (e.g., spatial omics platforms, visualization tools, or basic scripting). Foundational understanding of metabolic pathways, lipidomics, or small-molecule analysis relevant to oncology and neurology is advantageous but not required. Ability to follow detailed SOPs, manage samples carefully, and document experiments accurately. Strong teamwork, communication, and organizational skills. Demonstrated ability to learn new techniques, troubleshoot basic lab procedures, and contribute to a fast-paced research environment.

Your Impact at Lila Lila Sciences is seeking a highly skilled Research Associate specializing in Protein Purification and Characterization to run a high-throughput protein purification and characterization platform. In this role, you will operate Lila's Scientific Super intelligence platform by leveraging your expertise in protein analytics, collaborating with cross-functional teams, and applying your analytical and data analysis skills. What You'll Be Building Operate and maintain automated workcells to enable high-throughput protein purification and characterization, spanning diverse protein classes including enzymes and binders. Partner closely with automation engineers and cross-functional scientists to troubleshoot, develop, and continuously improve experimental workflows. Own the analysis, interpretation, and communication of QC data generated by automated platforms, ensuring data quality and reliability. Contribute to workflow optimization by identifying opportunities to improve efficiency, robustness, and scalability of protein purification and analytical methods. Stay current with advances in protein purification technologies, laboratory automation, and analytical techniques, and proactively apply relevant innovations to the platform. What You'll Need to Succeed Bachelor's degree in Biochemistry, Biophysics, Molecular Biology, Bioengineering, or a related field, with 0-3 years of relevant industry experience. Hands-on experience with bead-based purification systems and/or protein characterization techniques such as CE-SDS, colorimetric assays, or biolayer interferometry (BLI). Strong analytical and problem-solving skills, with meticulous attention to detail and data integrity. Experience working with laboratory automation and high-throughput screening platforms. Experience with coding and data analysis (e.g., Python, R, or similar) and interest in automating experimental workflows is a strong plus. Bonus Points For Protein Purification Protein Characteristics Operate Liquid handlers About Lila Lila Sciences is the world's first scientific superintelligence platform and autonomous lab for life, chemistry, and materials science. We are pioneering a new age of boundless discovery by building the capabilities to apply AI to every aspect of the scientific method. We are introducing scientific superintelligence to solve humankind's greatest challenges, enabling scientists to bring forth solutions in human health, climate, and sustainability at a pace and scale never experienced before. Learn more about this mission at *********** If this sounds like an environment you'd love to work in, even if you only have some of the experience listed below, we encourage you to apply. Compensation We expect the base salary for this role to fall between $72,000 -$94,000 USD per year, along with bonus potential and generous early equity. The final offer will reflect your unique background, expertise, and impact. We're All In Lila Sciences is committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Information you provide during your application process will be handled in accordance with our Candidate Privacy Policy. A Note to Agencies Lila Sciences does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Lila Sciences or its employees is strictly prohibited unless contacted directly by Lila Science's internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Lila Sciences, and Lila Sciences will not owe any referral or other fees with respect thereto.

Parallel Squared Technology Institute (PTI) is a non-profit research institute aiming to catalyze a leap in protein analysis technology and use it to explore new biological frontiers. PTI supports open research and educational opportunities supporting rapid career development for scientists, engineers, and mathematicians. Why? Protein dysfunctions directly cause many diseases, such as Alzheimer's disease. Yet, proteins remain understudied because of technological hurdles. How? To resolve these limitations, PTI will develop mass tags enabling a new framework for multiplexed protein analysis by mass spectrometry towards achieving 100-fold increase in throughput. Scientists at and collaborating with the institute will use these gains to directly investigate disease mechanisms and resolve problems that have proven intractable for decades. Our proof of principle technology and strategies are outlined at: parallelsq.org. PTI's new approach requires synergy between a diverse team of chemists, machine learning engineers, biologists, and mass spectrometrists. Alzheimer's disease and aging will be among the first focuses of this technology-driven research organization. New career opportunities Members of PTI will be supported with industry-level resources to lead research projects and disseminate their discoveries and innovations to the broader biomedical community through frequent publications, presentations, and submissions to public data portals. Summary of PositionWe are looking for either a Research Associate or Senior Research Associate who is interested in mass spectrometry. This person will be working on maintaining MS instruments for running multitudes of samples for a variety of projects in addition to other responsibilities. In order to be seriously considered for this position, we require a cover letter as part of the candidate's application.Responsibilities You will learn how to set up, operate and maintain mass spectrometers from multiple major vendors. Protein sample preparation. Inventory management for reagents and samples. Analyze experimental data and interpret results for internal and public presentation. Preparation of lab reagents and media. Required Qualifications Bachelor's degree in Chemistry, Biology, or related field. Advanced degrees or >2 years of experience will be considered for Senior RA position. Basic proficiency with biochemistry techniques or chemistry techniques. Demonstrated enthusiasm and interest in analytical chemistry. High level of initiative and flexibility, excellent communication and teamwork skills. Attention to detail. Good time management. Preferred Qualifications Familiarity with analytical techniques, mass spectrometry preferred. Familiarity with liquid chromatography. Protein and peptide sample preparation and purification methods. Who Will Love This Job You are passionate about science and technology and are eager to work in a team environment. You love learning new techniques, new technologies, and new concepts. You want an environment that will support your future plans as a scientist or engineer. You are committed to open science ideas and want to see your work disseminated broadly. We Offer An opportunity to change the world and work with some of the smartest and the most talented experts from different fields. Excellent medical, dental, and vision insurance with many $0 premium options for you and your family with several national and regional providers. Most employees have more than 20 plan options to choose from. Company-paid group life, AD&D, long- and short-term disability insurance 15 days PTO + 10 sick days per year 18 company holidays + your birthday off $5,000 per year educational reimbursement Up to 16 weeks paid parental leave Industry competitive salary We aim to help fill a structural gap in today's R&D system. We enable fundamental research that requires unusual levels of scale and coordination yet is not rapidly monetizable by industry. We're bringing together top talent from academia, industry, and startups to build a new model for innovative R&D. As an incubator within the Schmidt Futures Network, we identify high-impact scientific or technical research and development opportunities, ultimately defining and launching these projects as Focused Research Organizations. We are an Equal Employment Opportunity employer that proudly pursues and hires a diverse workforce. We do not make hiring or employment decisions on the basis of race, color, religion or religious belief, ethnic or national origin, nationality, sex, gender, gender-identity, sexual orientation, disability, age, military or veteran status, or any other characteristic protected by applicable local, state, or federal law or company policy. We strive for a healthy and safe workplace and strictly prohibit harassment of any kind.We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Torus Therapeutics is a new biotech company founded by Atlas Venture that is developing transformative gene therapies for severe genetic and rare diseases. Torus Therapeutics uses a unique and proprietary platform that is differentiated from current viral and mRNA gene therapy approaches. Join Torus' dynamic and growing team as we build the product platform to bring much-needed therapies to patients. Job Description Torus seeks a highly-motivated research associate contractor to support daily operations in the molecular biology laboratory. The successful candidate would report directly to the Senior Scientist, Platform Development and will assist in the development of Torus's overall platform technology. Primary Responsibilities include: Perform experiments supporting novel gene therapy platform Develop and execute analytical methods for the evaluation of novel constructs Execute analytical studies to evaluate gene expression Design, develop and organize novel libraries of gene therapeutics Conduct small-scale purifications to support process development Assist in the generation and review of protocols and reports Prepare, evaluate, and present data internally to cross functional teams Qualifications B.S. in Biology, Biochemistry, Molecular Biology or related discipline 1-3 years of relevant lab experience is ideal Experienced with molecular biology techniques (Western blot, qPCR, cloning) Primary laboratory presence (≥50%) required Strong communication, interpersonal and organizational skills Must have excellent attention to details Strong collaboration and team-working skills Candidate must be able to work independently and organize activities Additional Information We look forward to receiving your application! All your information will be kept confidential according to EEO guidelines. Please no agencies at this time.

Job DescriptionScismic is supporting the growth of a Cambridge, MA biotech startup that is pioneering mRNA-modulating therapies to cure a broad range of genetic diseases. The company is exploring the use of its novel platforms in neurological disorders, heart disease, and muscular dystrophies. Position summary: As an expert scientist in cellular neurobiology, you will be responsible for establishing cellular assays to demonstrate in vitro proof of concept for company tRNA therapeutic leads and characterize the cellular activity and downstream disease-relevant biology to help prioritize candidates for in vivo studies. Key responsibilities for this position include: Establish in vitro disease models in relevant cell types including primary neurons and glia isolated from transgenic animal models and patient-derived iPSC lines. Design, troubleshoot, and execute cell-based assays in human and rodent cell lines to characterize the efficacy and safety of company's novel tRNA therapeutic leads. Understand mechanism of action of lead candidates and establish assays and endpoints relevant to downstream target and disease biology. Conduct literature searches; communicate understanding in internal forums and with external collaborators and partners. Minimum qualifications: A BS/MS in Neurobiology, Molecular/Cellular Biology, physiology, or a related discipline. Extensive hands-on experience with a variety of molecular, cellular and/or physiological techniques (isolating rodent neurons and establishing primary neuronal cultures, neurite outgrowth, qPCR, western blotting, microscopy, calcium imaging, synaptic imaging, multi-electrode arrays, human IPS/ES cell culture, etc). Prior experience using AAV/lentivirus in primary or iPSC-derived neurons is highly desirable. Ability to master new concepts and technologies quickly and run experiments independently. Scientifically rigorous, highly organized, with excellent oral and written communication skills. Ability to work independently as well as collaborate with colleagues and effectively prioritize and manage multiple tasks in a fluid, fast-paced work environment Title commensurate with level of experience. We are accepting applications to build a pipeline of potential candidates for future opportunities. If your qualifications align with our requirements, we will contact you once the hiring process begins. Thank you for your interest in this role.

Job Description Work closely with Scientists to evaluate antibodies, proteins, small molecules, and drugs by in vitro cell-based assays including cytotoxicity assays, flow cytometry, functional assays, and molecular biology assays, including ELISA, WB, ect. Job will involve maintaining cell lines, setting up and developing in vitro assays, working closely with in vivo team to supply cells and then receive ex vivo samples and analyzing assays with harvested blood serum/tissue, and maintaining a lab notebook. Powered by JazzHR YmFHsmtNfV

Job Description Biocytogen is a comprehensive research and discovery service provider for biotech and pharmaceutical industry and academic institutions. Its service platform integrates preclinical studies with innovative animal models, CRISPR-based gene editing, and animal supplies, with the current focus on immuno-oncology and oncology. We are looking for a highly motivated research associate with the ability to work both independently and in a collaborative manner. Biocytogen is a fast-growing company and has an abundance of opportunities available for you to grow your career. Biocytogen is committed to nurturing junior scientists to progress within our organization, providing a supportive environment for career advancement. This opportunity is ideal for individuals who can recognize and seize learning opportunities. Job Responsibilities: ● Perform preclinical pharmacology studies in rodents. Tasks include drug administration via multiple routes (IV, IP, SC, PO etc), blood and tissue collection, and tumor volume measurement. Experience with small animal surgery is a plus. ● Communicate and coordinate with other scientists on a project team to draft, finalize, and implement study protocols. Follow protocols and independently execute tasks. ● Collect and record data. Prepare summaries of experimental procedures and results and present data in team meetings. ● Develop, perform, interpret, and troubleshoot a broad range of in vitro assays including immune cell profiling, cytokine profiling, functional assays using primary cells, as well as cytotoxicity/apoptosis assays using primary and/or cultured cells. ● Innovate and expand our assay portfolio by identifying, evaluating, and implementing new assay technologies through literature research, academic collaborations, and adaptation from other groups within the company. Requirements ● Bachelor's or Master's degree with 1-3 years of academic or industry research experience. Demonstrated experience in small animal handling and pharmacology is highly preferred. ● Experience with small animal handling, drug administration, and blood and tissue collection is preferred. ● Experience in cell biology, biochemistry, and/or molecular biology, in particular assay development and execution, is required. This includes cell-based assays, tissue culture, biochemical assay technologies, and protein and RNA expression analysis. ● Experience with cell culture and in vitro assays is desirable. ● Experience in primary immune cell-based assays is strongly preferred. ● Experience in flow cytometry (FACS) analysis is preferred. ● Demonstrate ability for quality execution, attention to detail, and proficiency in multi-tasking in a fast-paced environment. ● Collaborative team player. Be flexible and prioritize tasks based on team and company goals. ● Communicate effectively at all levels, within teams, with internal and external collaborators. ● Strong organizational skills. Maintain research data and records with the highest integrity. ● Ability to multitask in a fast-paced environment. Benefits Medical Insurance Dental Insurance Vision Insurance Health Reimbursement Accounts Life and AD&D Insurance Short & Long Term Disability Insurance 401K with Company Match Paid Time Off Paid Sick Days & Holidays BIOCYTOGEN is an Equal Opportunity Employer. Employment opportunities at BIOCYTOGEN BOSTON CORP are based upon one's qualifications and capabilities to perform the essential functions of a particular job. All employment opportunities are provided without regard to race, color religion, sex, national origin, ancestry, age, sexual orientation, gender identity and expression, veteran status, military status, disability, mental illness, genetic information, or any other characteristic protected by law. This Equal Employment Opportunity policy governs all aspects of employment, including, but not limited to, recruitment, hiring, selection, job assignment, promotions, transfers, compensation, discipline, termination, layoff, access to benefits and training, and all other conditions and privileges of employment.

Kula Bio is at the forefront of sustainable agriculture, providing pioneering nitrogen solutions that empower farmers to increase crop yields and support environmental stewardship. Our cost-effective biofertilizer leverages and enhances a natural process to deliver significant, sustained nitrogen to the soil. As a Research Associate you will work with the Discovery and Product Development team to plan and execute plant trials to validate product efficacy and test product prototypes. This role will focus on development, implementation, and data collection from plant assays that will lead to understanding the performance of the product. On a regular day, you will support validation of product efficacy through experimental design and set-up. You will implement crop growth protocols, handle microbial cultures, collect assay data, and present results. You will cultivate plants in controlled environmental conditions, monitor plant health and collect key data on plant growth, use and maintain laboratory equipment, and work closely with the broader team in a collaborative effort to meet project goals and timelines. Requirements Qualifications: BS in Plant Biology, Plant Science, Agronomy, Crop Science, Horticulture, or related sciences with at least 1 year of relevant hands-on research experience. Experience working in greenhouses, controlled environmental chambers, and research fields. Experience with plant care and maintenance including seed germination, propagation, seedling care, transplantation, nutrient and fertilizer delivery, plant phenotyping, and stress monitoring. Ability to perform hands-on work in greenhouse, outdoor, and laboratory environments, including standing for extended periods and lifting moderate weights up to 50 lbs. (e.g., trays, soil, supplies). Skilled at implementing standard experimental protocols and workflows including appropriate application of nutrients and/or amendments according to experimental design. Experience working in wet lab settings and practicing safe handling of chemicals and biologicals. Experience with good aseptic technique including handling microorganisms or microbial products under sterile conditions. Proficiency in data collection, management, and presentation including experience in use of Excel and PowerPoint - experience with Prism or other statistical analysis software is ideal. Proficiency in lab record keeping including good note taking practices - experience with electronic lab notebooks like SciNote is ideal. Strong critical thinking skills, demonstrating an ability to identify failure points, troubleshoot experiments, and propose practical solutions. Strong communication skills and the ability to clearly communicate progress, challenges, and results. Willing to work in a collaborative, timeline-driven environment. Salary range $60,000 - $65,000 per year Salary Description $60k - $65k

2 Positions Top skills needed: Broad knowledge of acceptable excipients and equipment/instruments widely used in pre-clinical formulation preparation Form 1 - Research Associate II Function: Discovery Formulations Department: Global Chemistry OBJECTIVES: We are seeking to fill a contractor position reporting to the Global Chemistry organization in Cambridge, MA to prepare formulated API for in vivo PK, pharmacology, and safety studies. This role entails collaboration with a wide range of cross-functional research project teams, external CRO collaborators, and Client Pharm Sci colleagues to develop project specific formulation strategies for in vivo studies (PK, efficacy, tox), enabling the rapid advancement of compounds from PE through CN and CS. ACCOUNTABILITIES: Prepares and optimizes pre-clinical drug formulations using appropriate technology and scientific principles for in vivo PK, Pharmacology, and safety studies Conducts limited screening of known excipients, pH adjustment, etc, and chemical/physical stability check for program compounds. Prepares cassette dosing solutions for PK screening. Conducts experiments and analyzes/shares data to support project progression using analytical instrumentation (HPLC, Mass Spec) to assess formulation stability and chemical stability Accurately records formulation experiments/protocols in an e-notebook Prepares/shares formulation protocols, technical reports, presentations, and regulatory documents as necessary Adherence to lab safety and quality protocols o Ensures formulations meet IUCUC guidelines and industry standards in coordination with in vivo study director o Understanding and ability to implement good laboratory practices, particularly in handling preclinical pharmaceutical small molecule API for neuroscience, immunology, and oncology indications Collaborates with a Global Chemistry manager, cross-functional research project teams, CROs, the Comparative Medicine group, and Pharmaceutical Science colleagues to provide project specific formulations and formulations strategies for in vivo studies (PK, efficacy, tox) Continuous review and learning of formulation science through reading the literature and active engagement with client Pharm Sci group and CROs to guide project formulation strategy Exceptional organizational skills will be required, as the role requires receiving, managing, and delivering on requests from a wide range of groups and teams across the Research organization, often under tight timelines Job Description Form 2 - Research Associate II Direct/In Direct: Managers/Supervisors Global Chemistry Comparative Medicine and Pharm Sci EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS: Bachelor s degree in a chemistry or pharmaceutical science, or equivalent with 5+ years of experience, or Master's degree with 3+ years of experience in formulating small molecule APIs Broad knowledge of acceptable excipients and equipment/instruments widely used in pre-clinical formulation preparation Demonstrates technical knowledge of formulations and pharmaceutics of small molecule APIs including: Solubilizing/solution formulations Solid/suspension formulations Well-versed in analytical instrumentation (HPLC, Mass Spec) to assess: Formulation stability (physical) Chemical stability A good understanding of pre-clinical formulation science Exceptional organizational skills Strong attention to detail, communication, and teamwork PHYSICAL DEMANDS: Manual dexterity required to operate office and lab equipment Carrying, handling and reaching objects up to 25 lbs Prolonged standing and/or sitting Exposure to hazardous/toxic/dangerous chemicals