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Phosphoramidite Scientist - Process Research & Development
Veranova
Research and development technician job in Devens, MA
Discover Veranova: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.
Role Overview:
The Scientist role within the Chemical Development group will focus on the synthesis, process development, and analytical strategy for protected phosphoramidite precursors used in therapeutic oligonucleotide API manufacturing. This position is key to building Veranova's commercial capability in producing high-quality oligonucleotide building blocks. The ideal candidate will have strong expertise in phosphoramidite chemistry, including impurity profiling and customer-specific requirements. This role will also collaborate closely with the Analytical Team to establish robust characterization and control strategies that ensure exceptional product quality.
Core Responsibilities:
Develop and optimize synthetic routes for protected Phosphoramidite subunits used in therapeutic oligonucleotide API synthesis.
Identify and mitigate side reactions commonly associated with Phosphoramidite chemistry.
Define and implement specifications aligned with customer expectations for commercial-grade oligonucleotide precursors.
Provide expert guidance to the Analytical Team on the selection and application of appropriate analytical methods for product and impurity characterization, based on prior experience and industry standards.
Collaborate with cross-functional teams including Analytical Development, Quality, and Manufacturing to ensure successful scale-up and tech transfer.
Prepare technical documentation including batch records, specifications, and development reports in accordance with SOPs and cGMP guidelines.
Present scientific findings and project updates to internal stakeholders and external customers.
Support the establishment of quality and regulatory standards for commercial production of oligonucleotide precursors.
Contribute to project planning, budgeting, and timeline management for precursor development programs.
Other duties as assigned .
Qualifications:
Required
BS in Organic Chemistry or equivalent with 3-5 years related experience in a pharmaceutical industry, or
MS in Organic Chemistry or equivalent with 0-2 years related experience in the pharmaceutical industry.
Ability to read, analyze, and interpret English-language chemical periodicals, scientific journals, and regulatory documents.
Experience with organic synthesis and process development
Experience with common analytical techniques such as HPLC, GC, NMR, UV, and LC-MS.
Experience in establishing integrated plans with defined resources and tasks.
Ability to write clear and concise technical reports.
Good understanding of Microsoft Office and statistical software.
Demonstrate ability to exercise good judgment and make decisions quickly.
Good written and verbal communication skills.
Ability to work independently and in a team environment.
Salary Range : $110,000 - $120,000 annual base salary
Our Commitment:
Health & Wellness: Comprehensive health & wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies.
Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs.
Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.
Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Even if you don't meet every qualification, we encourage you to apply. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team.
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship.
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting.
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice .
$110k-120k yearly 4d ago
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Downstream Scientist - Top Pharmaceutical Company
Insight Global
Research and development technician job in Andover, MA
We are looking for a Downstream Scientist to join our client's Manufacturing Sciences and Technology (MSAT) organization based in Andover, MA. The MSAT downstream purification team supports purification process development and optimization for commercial processes and next generation process development.
This person will be expected to execute and qualify various downstream purification unit operations, ensure the proper and timely execution of purification processing at both pilot and/or bench scale of various biologics using a variety of unit operations, such, depth filtration, TFF (UF/DF), and chromatography.
Experience with process development and characterization for a polysaccharide based programs and/or second-generation process development of biologics using various purification techniques.
Independently plan, design, and execute downstream experiments to enable technology transfer of polysaccharide programs and/or second-generation purification processes to receiving units.
Direct hands on experience with operation and maintenance of downstream equipment (AKTAs, Repligen TFF, etc.. and associated analytical tools (SoloVPE and Stunner etc..)
Proficient with data analysis, technical writing, reporting, and presenting to internal teams.
Support investigational studies and purification process troubleshooting as needed.
Drive a culture of safety, continuous improvement and operational excellence initiatives within department.
Independently plan, prepare, execute, and conclude critical material production campaigns.
Emphasize strong communication, teamwork, growth mindset and cross functional collaboration with other project teams as needed
EDUCATION AND EXPERIENCE
Bachelor's degree or higher in a relevant discipline with at least 3 years of applicable bioprocess experience.
Experience with process purification of biomolecules (mAbs, vaccines, etc…) from harvest to drug substance
Familiarly working in GxP cross matrix organizations
Lab-scale purification process development and troubleshooting experience with standard downstream equipment (e.g. AKTAs, Repligen TFF, etc…)
Direct hands on experience and knowledge of templated processes such as mAbs, pDNA, mRNA etc…
Proficient experience with data analysis tools such as Minitab, JMP, etc…
Working knowledge of PAT applications development and implementation from bench scale to pilot
Experience with HTS instrumentation for protein purification and process development
Working knowledge of GxP/ICH/Quality compliance systems of the biopharmaceutical industry
$70k-104k yearly est. 2d ago
Research Associate - Injectable Formulation
JMD Technologies Inc.
Research and development technician job in Lexington, MA
Prepare injectable (parenteral) peptide and protein formulations to support in vivo and in vitro animal studies, including buffer, excipient, and surfactant selection
Execute preclinical formulation development activities to support early research and screening programs
Perform biophysical characterization and stability studies to assess formulation performance and robustness
Support animal dosing studies by preparing, documenting, and delivering study-ready formulations
Maintain accurate experimental records using ELN (Electronic Laboratory Notebook) and manage formulation requests/workflows
Operate, maintain, and troubleshoot formulation, biophysical, and analytical laboratory instruments
Analyze experimental data and contribute to scientific documentation and reporting
Collaborate closely with cross-functional research teams to resolve formulation challenges and meet project timelines
$59k-86k yearly est. 3d ago
Research Associate - Upstream Cell Culture
Spectraforce 4.5
Research and development technician job in Framingham, MA
Research Associate I
Assignment Duration: 12 Months
Work Arrangement: Onsite
Work Schedule
M-F 9 AM-5 PM EST (May require weekend work)
HM Notes:
Possibility of extension
• Local candidates ONLY
• References will be requested for finalists
• ***Weekend works is required and is occasionally. This is a rotating, schedule 1-4 hours on 1 weekend day and will include a Saturday or Sunday.
This will be included in 40 work week and no to exceed 40 hours.
Weekend work is pre-planned through end of year; new hire can swap with colleagues if available.
• Team of 13 members
• No chemicals
• No extreme heat or cold
• Cell culture media preparation
• Ability to lift 10 kg
• Free parking onsite
• Over 3 years of experience and PHD's considered overqualified
• No full gowning requirement
• PPE will be provided
Must Have Skills:
• Bachelor's or master's degree in chemical engineering Biochemical Engineering, Cell Biology, Biochemistry or a related discipline
• Experience can include co-op or internships, 6+ months of experience.
• Understanding of aseptic technique and principles of mammalian cell culture
• Lab operations experience
• Understanding of aseptic technique and principles of mammalian cell culture
• Some lab mammalian cell culture experience, however, microbial experience is not a match
• MS Office, Word, Excel
• Quick learner for new techniques and technology
• Strong attention to details
Preferred Qualifications
• Up to 3 years of professional experience, or including internships
• Experience in the operation of fed-batch and/or perfusion-based cell culture bioreactors
• Knowledge of CMC
• Cell culture platform process at different scales (shake flasks, AMBR, 3L/10L bioreactors, etc.)
• Strong GPA is a plus
Description:
We are seeking a contract upstream Research Associate to join our Cell Culture Platform group in Cell Culture Development department (CCD-CCP). CCD-CCP is a global business unit responsible for the development of cell culture platforms including media and bioprocess technologies for both fed-batch and perfusion from early and late-stage biologics projects, as well as all upstream CMC development activities for early phase projects (up to Phase II).
The candidate will be self-motivated and strongly driven to succeed while demonstrating the ability to function well within a fast-paced and collaborative team-oriented environment. The candidate will also be inquisitive and innovative, exhibiting scientific curiosity and the ability to acquire new skills for fed-batch and perfusion based upstream cell culture processes.
This is an exciting opportunity to learn cutting-edge cell culture techniques and develop cell culture subject matter expertise. This role will have significant impacts on early pipeline projects, next generation cell culture process development and manufacturing strategies within the global network.
Main Duties & Responsibilities
• Require to be on site daily; Weekend work required occasionally.
• Plan and execute experiments to optimize upstream cell culture platform process at different scales (shake flasks, AMBR, 3L/10L bioreactors, etc.)
• Perform upstream experiments and collaborate with other functional groups to speed Phase I pipeline projects
• Contribute to technical reports, experimental protocols, and technical summaries for presentation internally and externally
• Participate in the technology transfer of processes into manufacturing facilities
• Ensure safety and environmental compliance are maintained in the workplace
• Some weekend working may be required for this role
Basic Qualifications
• Bachelor or Master's degree in Chemical Engineering, Biochemical Engineering, Cell Biology, Biochemistry or a related discipline
• Post-education experience ?=3 years
• Understanding of aseptic technique and principles of mammalian cell culture
• Detailed in lab operations and quick learner for new technologies
Preferred Qualifications
• Experience in the operation of fed-batch and/or perfusion-based cell culture bioreactors
• Knowledge of CMC
$68k-96k yearly est. 19h ago
R&D Reliability Engineer
Formlabs 4.3
Research and development technician job in Boston, MA
## R&D Reliability Engineer---To all recruitment agencies: Formlabs does not accept agency resumes. Please do not forward resumes to our jobs alias, Formlabs employees or any other company location. Formlabs is not responsible for any fees related to unsolicited resumes. Unsolicited resumes received will be considered our property and will be processed accordingly.**Department:** Hardware Engineering **Location:** Boston, MA**What Formlabs Does:**At Formlabs, we're building the tools that make it possible for anyone to bring their ideas to life, from cutting-edge products to life-saving medical devices. Our 3D printing technology powers innovation at more than 50,000 industry leaders worldwide, including Apple, Google, Tesla, New Balance, and NASA. Together, we're helping creators design, prototype, and manufacture faster than ever before.We're a team of hands-on builders, engineers, and innovators reinventing how the world makes physical things. If you're ready to shape the future of fabrication, come build it with us.**Your Impact:**The Reliability Engineering Team is the company's independent voice on product robustness, ensuring our hardware products are reliable so that Customers spend more time printing and less time troubleshooting. We architect effective testing strategies, engineer advanced electro-mechanical test rigs, and extract valuable, actionable insights from the data.**R&D Reliability Engineering Team.****What You'll Do:*** Develop, execute, and manage system, subsystem, and component level validation test plans to ensure products meet design and reliability requirements.* Perform hands-on and data-driven root cause analysis (RCA) of electromechanical subsystems and field failures, utilizing common problem-solving methodologies and a "physics of failure" approach.* Design, build, and implement automated testing equipment for subsystem characterization and reliability/environmental testing.* Collaborate with R&D design teams throughout product development to perform risk assessments, manage continuous testing, and contribute to design reviews, influencing product design for reliability from day one.* Analyze field failure data to identify trends, prioritize investigations based on business value, and develop clear, actionable corrective action plans (CAPAs).**Our team did the testing to ensure Form 4 would be the most reliable printer Formlabs has ever built:*** **LCD & Light Engine:** Developed custom rigs to simulate UV light and heat, continuously monitoring performance over thousands of hours.* **Mixer Scraper:** Tested our proprietary debris detection hardware to protect the LPU from damage.* **Z-Axis:** Conducted millions of cycles of accelerated lifetime testing to ensure consistent motion.Tank Film: Developed custom pneumatic fixtures to ensure that tank tension remained high after tens of thousands of layers.* **Cartridge & Dispense System:** Optimized cartridge geometry to ensure reliable dispensing of all kinds of Formlabs materials.**to see a breakdown of these systems in action!****About You:*** Well-versed with complex electromechanical systems and passionate about understanding what it takes to make them work reliably.* Have experience with testing a wide range of sensors, actuators, and mechanical components.* Have experience developing system test plans and know how to execute them efficiently within fast-paced product development timelines.* Can prototype and run your own tests, from experimental setup to hardware and software implementation in Python.* Possess strong data analysis skills, capable of distilling complex test results and field data into clear, concise, and compelling insights that drive action.**Bonus Skills:*** Familiarity with Linux systems and scripting in various languages.* Experience with SQL for data analysis.* Prior experience with field failure analysis or quality engineering roles is a plus.**Our Benefits & Perks:*** Robust equity program to build future wealth through RSUs* Comprehensive healthcare coverage (Medical, Dental, Vision)* Low cost fund options in our 401K and access to advisors* Generous paid Parental Leave (up to 16 weeks)* Tenure-based paid Sabbatical Leave (up to 6 weeks)* Flexible Out of Office Plan - Take time when you need it* Ample on-site parking & pre-tax commuter benefits* Healthy on-site lunches, snacks, beverages, & treats* Regular sponsored professional development opportunities* Many opt-in culture events across our diverse community* And of course… unlimited 3D prints*We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.***Even if you don't check every box, but see yourself contributing, please apply.** Help us build an inclusive community that will change the face of 3D printing.**Compensation**We are all owners of Formlabs and direct beneficiaries of our success. We believe that equity is a critical component of compensation at Formlabs, and we want our newest team members to understand the potential value of their equity compensation. Full time employees receive equity, in the form of RSUs. Your financial investment will grow with us in accordance to your impact.At Formlabs, base pay is one part of our total compensation package and is determined within a range. Your base pay will depend on your skills, qualifications, experience, location and expected impact on the organization.The annual base pay range for this role is:$80,000-$125,000 USD
#J-18808-Ljbffr
$80k-125k yearly 2d ago
Associate Synthetic Chemist
Quadratic 3D, Inc.
Research and development technician job in Boston, MA
We are seeking an enthusiastic Associate Synthetic Chemist to support the discovery of small molecules for next-generation 3D printing resins. You will work hands-on in the lab, executing syntheses of novel molecules, characterizing products, and exploring photochemical and photophysical structure-property relationships. This role is ideal for highly motivated early-career chemists who love synthesis and are excited to accelerate innovation through fast, iterative chemistry. You will be closely mentored by experienced synthetic chemists and will collaborate with analytical scientists and engineers developing our printing systems.
Responsibilities
Design, execute, and troubleshoot small molecule synthetic routes, with a focus on divergent or modular approaches to rapidly generate lead candidates.
Purify products using chromatography and crystallization techniques.
Characterize compounds via UPLC, NMR, UV/Vis and IR spectroscopy, and mass spectrometry.
Work with cross-functional teammates to explore photochemical and photophysical structure-property relationships that drive 3D printing performance.
Maintain excellent electronic lab notebook documentation.
Contribute to management of chemical databases (e.g., commercial, proprietary, and virtual compound libraries).
Minimum Qualifications
Bachelor's degree in Chemistry or a closely related field with equivalent advanced chemistry coursework.
≥2 years of intensive organic synthesis laboratory experience (academic research and/or industrial roles).
Experience with synthetic planning with chemical databases (e.g., SciFinder, Reaxys).
Excellent command of synthetic and physical organic chemistry fundamentals.
Experience with air-sensitive techniques (e.g., Schlenk line), purification (chromatography/crystallization), and data interpretation (NMR / LC-MS).
Evidence of strong documentation and organizational skills, attention to detail, and the ability to manage multiple workflows efficiently.
Evidence of strong collaboration and teamwork talents/skills.
Ability to thrive in a fast-paced, collaborative R&D environment.
Preferred Qualifications
Command of the basics of photochemistry.
Experience with heterocyclic and/or extended aromatic systems, especially those relevant to organic (opto)electronics.
Benefits
We offer competitive compensation packages in our VC-backed startup.
Benefits include a full suite of offerings covering medical, dental, vision and 401k plan.
Beautiful setting looking out over a river and seaport; outdoor seating and picnic areas.
Highly collaborative work environment.
Additional Information
Travel: Occasional travel may be required from time to time
Location: Boston, Massachusetts
We value diversity in our company and are an Equal Opportunity Employer.
$62k-92k yearly est. 19h ago
Biomedical Informatics Associate - Research & Knowledge Graphs
Harvard University 4.2
Research and development technician job in Boston, MA
A prestigious research institution in Boston is seeking an Associate in Biomedical Informatics to support biomedical research training and projects. The role involves developing knowledge graphs, conducting data analyses, and writing research reports under the guidance of experienced mentors. Applicants should have a Bachelor's degree in computer science and a keen interest in healthcare technologies.
#J-18808-Ljbffr
$61k-87k yearly est. 1d ago
Senior Assay Development Scientist/Engineer
Siphox Health
Research and development technician job in Burlington, MA
+++
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 DevelopmentDevelop 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.
$64k-94k yearly est. 19h ago
Quality Control Analyst II - Mansfield, MA area - Contract (Weekend Shift)
Yoh, A Day & Zimmermann Company 4.7
Research and development technician job in Norton, MA
Please send your updated resume to ****************** Quality Control Analyst II - Mansfield, MA area- Contract (Weekend Shift) Mansfield, MA area Contract - (Weekend Shift)
Experienced in performing routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.
Support weekend lab operations and maintain training records.
Assist in lab equipment and inventory maintenance, including reagent and sample prep
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the . All qualified applicants are welcome to apply
Estimated Min Rate: $30.80
Estimated Max Rate: $44.00
What's In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh's network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh's extensive talent community that will provide you with access to Yoh's vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:
Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
Health Savings Account (HSA) (for employees working 20+ hours per week)
Life & Disability Insurance (for employees working 20+ hours per week)
MetLife Voluntary Benefits
Employee Assistance Program (EAP)
401K Retirement Savings Plan
Direct Deposit & weekly epayroll
Referral Bonus Programs
Certification and training opportunities
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit ************************************************ to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh's hiring clients' preferences. To learn more about Yoh's privacy practices, please see our Candidate Privacy Notice: **********************************
$30.8 hourly 2d ago
Quality Control Analyst II
Talentburst, An Inc. 5000 Company 4.0
Research and development technician job in Norton, MA
Industry: Pharmaceuticals
Title: Quality Control Analyst II
Duration: 11 months contract (+Possibility of extension)
This is an onsite role in Norton, MA, with occasional responsibilities at other Client locations. Weekend coverage is required. First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training.
Description:
The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. This position enhances QC efficiency and effectiveness.
Key Responsibilities'
Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.
Support weekend lab operations and maintain training records.
Assist in lab equipment and inventory maintenance, including reagent and sample prep.
Review data timely and qualify as a data reviewer.
Perform operational assignments (raw material processes, environmental monitoring, in-process testing).
Contribute to updating controlled documents (SOPs, work instructions, test methods).
Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH).
Participate in continuous improvement initiatives and cross-functional collaboration.
Support regulatory submissions, inspection readiness, and audits
Qualifications:
B.S. in chemistry, biology, biochemistry, or related field.
4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent.
Experience in method transfer/implementation; understanding of method lifecycle management preferred.
Strong technical writing, data analysis, problem-solving, and organizational skills.
Excellent communication and teamwork.
Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred
$60k-83k yearly est. 2d ago
QC Analyst
Tandym Group
Research and development technician job in Woburn, MA
A recognized pharma company is actively seeking a new Quality Control (QC) Analyst for a great entry-level position with their QC Bioassay group. In this role, the QC Analyst will be trained to perform cell-based bioassays, ELISAs, and other biological methods in a GMP-regulated setting, while also supporting external laboratory testing.
Responsibilities:
Learn and perform immunoassays (e.g., ELISA) and cell-based assays under supervision in a GMP environment to support product release and stability testing
Assist in drafting and reviewing standard operating procedures (SOPs) and technical documents
Support method transfer, qualification of critical reagents, and other assay-related activities
Participate in the review and basic trending of QC data
Assist with routine laboratory upkeep, including cell culture maintenance, instrument calibration, and inventory tracking
Collaborate with internal teams and external partners as part of cross-functional project support
Contribute to investigations and deviation reports under guidance
Perform other duties, as needed
Qualifications:
Bachelor's Degree in Cell Biology, Molecular Biology, Biochemistry, or a related scientific field
Familiarity with basic Lab techniques and Data Analysis methods
Strong organizational, communication, and interpersonal skills
Detail-oriented and eager to develop problem-solving skills in a regulated lab environment
Enthusiasm for learning and the ability to work both independently and within a team
Desired Skills:
Academic or internship experience with Mammalian Cell Culture and/or ELISAs
$48k-78k yearly est. 2d ago
Quality Control Analyst II
Advantage Technical
Research and development technician job in Norton, MA
Quality Control Analyst II Norton 45 per hour
This is an onsite role in Norton, MA.
First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training.
Perform routine and non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies in accordance with SOPs
Support weekend laboratory operations and maintain required training records
Assist with laboratory equipment and inventory maintenance, including reagent and sample preparation
Review data in a timely manner and serve as a qualified data reviewer
Perform operational assignments such as raw material processing, environmental monitoring, and in-process testing
Contribute to the creation and updating of controlled documents, including SOPs, work instructions, and test methods
Follow internal policies, SOPs, and applicable regulatory standards (GMP, GLP, ICH)
Participate in continuous improvement initiatives and cross-functional collaboration
Support regulatory submissions, inspection readiness, and audits
Qualifications
Bachelor's degree in Chemistry, Biology, Biochemistry, or a related field
4-8 years of pharmaceutical or biotech experience in GMP QC or equivalent environments
Experience with method transfer and implementation; understanding of method lifecycle management preferred
Strong technical writing, data analysis, problem-solving, and organizational skills
Excellent communication and teamwork abilities
Proficiency in LabWare LIMS, Microsoft Excel, Word, and PowerPoint preferred
$49k-79k yearly est. 2d ago
R&D Technologist
Gorton's 4.4
Research and development technician job in Gloucester, MA
Gorton's is seeking a passionate and technically skilled Associate Food Technologist to join our Innovation Team, supporting the development of next-generation frozen seafood products. This role will contribute to product ideation, formulation, and commercialization, with a focus on innovation while upholding our commitment to quality, sustainability, and consumer satisfaction.
What You'll Do:
- Support and potentially lead the creation of new frozen seafood products and improvements to existing products.
- Conduct bench-top formulation, prototype development, and plant trials.
- Develop and optimize cooking instructions and recipes for consumer use.
- Support multiple projects simultaneously and prioritize tasks for robust development plans.
- Maintain detailed records of formulations, testing protocols, and ingredient specifications.
- Ensure all products meet Gorton's quality standards, regulatory requirements (FDA, CFIA), and shelf-life expectations.
- Apply scientific principles and analytical thinking to solve problems and improve products.
- Demonstrate understanding of manufacturing systems, processes, and policies.
- Support production facility tests and process scale-up development.
- Contribute to ingredient optimization, cost savings, and sustainable sourcing initiatives.
- Continuously seek process and product improvements, challenging the status quo appropriately.
- Collaborate with cross-functional teams (marketing, operations, procurement, supply chain, finance, sales) to execute initiatives.
- Organize, facilitate, and lead product evaluation sessions, including cuttings and sensory panels, to assess internal prototypes and benchmark competitive products.
- Communicate project status, findings, and recommendations clearly to managers and cross-functional teams.
- Partner with Quality Assurance and Regulatory teams to ensure compliance with food safety standards.
- Conduct product presentations at sales and management meetings.
- Keep up with new technologies, ingredients, regulations, and industry trends.
- Leverage internal and external data to meet consumer needs and guide decisions.
- Support proper ingredients inventory of the lab for tests and experiments.
- Perform lab management tasks such as cleaning, sorting, and storing lab equipment.
What You'll Need:
- Bachelor's degree in Food Science, Chemistry, Microbiology, Biology, or related field with >2 years of relevant lab experience in food product development or manufacturing.
- Excellent oral and written communication abilities; able to translate technical concepts for diverse audiences.
- Ability to work independently and collaboratively with minimal supervision.
- Strong quantitative, analytical, and project management skills.
- Demonstrated ability to tackle new and unfamiliar tasks with minimal assistance.
- Basic culinary skills for creative recipe development and comfort in a product development kitchen.
- Good interpersonal skills and ability to work well on teams.
- Experience with experimental design and statistical analysis are a plus.
- Flexibility for early plant tests and willingness to travel (up to 30%).
- Proficiency in Microsoft Office, formulation software, and data analysis tools.
- Willingness to taste fish and shellfish prototypes and discriminate subtle flavor differences.
- Ability to lift up to 50 lbs.
Pay Range:
$60,632 - $71,240/Annual
$60.6k-71.2k yearly 60d+ ago
R&D Analytical Chemist
Dupont de Nemours Inc. 4.4
Research and development technician job in Marlborough, MA
Are you looking to power the next leap in the exciting world of advanced electronics? Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics.
At Qnity, we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us.
We are seeking a hands-on, self-motivated Analytical Chemist to support New Product Development (NPD) and commercial product support across the ACP portfolio; ranging from metallization/plating chemistries to advanced packaging polymers and formulated materials. This role will lead development, implementation, and continuous improvement of analytical and characterization methods for specially synthesized raw materials (small molecules through complex polymers) and finished products, partnering closely with cross-functional stakeholders (DE, NPD, Manufacturing, Quality, and Technical Service) to enable scale-up, specifications, and customer support.
Key responsibilities
* Analytical method development & execution: Develop, optimize, and run analytical/characterization methods for raw materials, intermediates, and formulated products supporting NPD milestones and commercial needs.
* Core techniques: Apply techniques such as CVS, HPLC/UPLC, GPC, % solids, titrations, potentiostatic measurements, surface tension, cloud point, densitometry, and rheology (and related wet/physical methods).
* Other techniques relevant: ICP-OES/ICP-MS for metals/impurities, UV-Vis, FTIR, NMR, IC, TOC, DSC/TGA, particle size/zeta potential, SEM/EDS
* Method validation, transfer, and sustainment: Author/maintain methods, validation protocols/reports, and ensure robust method transfer to R&D and Manufacturing as needed.
* Data integrity & documentation: Maintain high-quality written documentation (methods, validation, batch/lot data packages, change control / MOC) and ensure traceable, audit-ready records.
* Troubleshooting & investigations: Support root-cause investigations, out-of-spec troubleshooting, and customer complaint response in collaboration with Quality/Manufacturing.
* Statistical/data analysis: Use statistical tools to analyze method performance, capability, trends, and investigation data (DOE, GR&R, SPC as applicable).
* Safety & teamwork: Work safely with hazardous chemicals in a collaborative, fast-paced lab environment; communicate clearly in both informal updates and formal presentations.
Required qualifications
* Education: B.S. in Chemistry, Biology, Chemical Engineering, Materials Science, or related field.
* Experience: 3-5 years of hands-on experience in analytical chemistry supporting R&D/NPD, development engineering, manufacturing, or quality environments. (Experience characterizing small molecules, polymers, and/or inorganic/metal-containing chemistries is strongly valued.)
* Demonstrated ability to follow procedures with high repeatability, strong attention to detail, and commitment to safe lab practices.
* Strong written and verbal communication skills; able to translate data into clear technical conclusions and recommendations.
* Strong data analysis capability; JMP/Minitab (or similar) preferred.
Preferred qualifications
* Demonstrated success developing/validating new analytical methods and supporting method transfer.
* Experience supporting semiconductor materials (e.g., plating baths, photoresists, dielectrics, silicones, packaging polymers) and working across interdisciplinary teams.
* Six Sigma (Green/Black Belt) or demonstrated experience applying structured problem-solving tools.
Join our Talent Community to stay connected with us!
Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information.
Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page.
We use Artificial Intelligence (AI) to enhance our recruitment process.
$100k-115k yearly est. Auto-Apply 3d ago
Quant Researcher & Developer
Jpmorgan Chase & Co 4.8
Research and development technician job in Boston, MA
JobID: 210670287 JobSchedule: Full time JobShift: Base Pay/Salary: Boston,MA $150,000.00-$224,000.00 Join Us at 55ip & Help the Wealth Management Industry Move Forward Working at 55ip means standing at the intersection of finance and technology-and at the cutting-edge of wealth management. We've been making rapid progress on our mission: to break down barriers to financial progress for financial advisors and their clients. Our Boston- and Mumbai-based team has built and brought to market a tax-smart investment strategy engine delivering an intuitive experience and intelligent automation. Driven by strategic partnerships with world-class asset management firms, such as BlackRock and J.P. Morgan, we've experienced breakthrough growth over the last year. Today, over 110 financial advisor firms with $90 billion in assets (and counting) are using 55ip.
If we look a little different, it's because we are. We're entrepreneurs, product pros, investment scientists, and customer advocates who aim to deliver an exceptional experience-and have fun doing it. Like lots of companies, we've got a deep bench of smart, talented, creative people, but our superpower is something else: hustle. That extra push when others would quit, that new approach nobody else has tried, that ability to thrive at 30,000 feet or dig into the details-and to do it all with humility, empathy, and respect. As we enter an exciting new chapter as a separately-branded subsidiary of J.P. Morgan, we're looking for top talent-with hustle-to join us on our path to becoming an industry standard.
Overview
The 55ip Quant team is looking for a quantitative professional to research, implement, test, and maintain the core algorithms of its technology-enabled investment platform for large investment advisory (RIA) & wealth management firms. The ideal candidate has a background in optimization and statistical modules using software design constructs and tools. The candidate will be motivated, a problem solver, and an effective team player looking to make a significant impact in supporting research projects and who can grow as an independent researcher.
Responsibilities
* The end-to-end research, development, and maintenance of investment algorithms
* Contribute to development and maintenance of optimization models
* Take part in building out the research and development framework
* Thoroughly vet investment algorithmic results
* Contribute to the research data platform design
* Investigate datasets for use in new or existing algorithms
* Participate in agile practices
* Liaise with stakeholders to gather & understand the functional requirements
* Take part in research & code reviews
* Develop code using high quality standards and best practices, conduct thorough end-to-end unit testing, and provide support during testing and post go-live
* Support research innovation through the creative and aggressive experimentation of cutting-edge hardware, advanced analytics, machine learning techniques, and other methods
* Collaborate with technology teams to ensure appropriate requirements, standards, and integration
Requirements
* Experience in a quantitative role
* Proficient in Python, Git and Jira
* Professional experience with commercial optimizers (Gurobi, CPLEX) is a big plus
* Master's degree in computer science, computational mathematics, or financial engineering
* Excellent mathematical foundation and hands-on experience working in the finance industry
* Proficient in quantitative, statistical, and ML/AI techniques and their implementation using Python modules such as Pandas, NumPy, SciPy, SciKit-Learn, etc.
* An understanding of or exposure to financial capital markets, various financial instruments (such as stocks, ETFs, Mutual Funds, etc.), and financial tools (such as Bloomberg, Reuters, etc.)
* Experience in direct-indexing products is a big plus
* Strong communication (written and oral) and analytical problem-solving skills
* Strong sense of attention to detail, pride in delivering high quality work and willingness to learn
* Knowledgeable in SQL
* Agility: Able to shift gears and react quickly to timely requests
* Hustle: Self-motivated, proactive, responsive-ability to think strategically but also willing to dig into the details and tactics
About 55ip
55ip is a financial technology company whose purpose is to break down barriers to financial progress. Wealth management enterprises and financial advisors use 55ip's tax-smart investment strategy engine to dramatically improve their efficiency and effectiveness. 55ip's intuitive experience and intelligent automation elevate portfolio design and delivery, helping advisors save time and drive better outcomes for their clients. At the heart of the experience is 55ip's ActiveTax Technology, which includes tax-smart transitions, management, and withdrawals. 55ip is becoming the industry standard by connecting to platforms where advisors manage their client accounts, enhancing workflow and reducing the need to move the assets. More information is available at ******************
$150k-224k yearly Auto-Apply 60d+ ago
R&D Analytical Chemist
Qnity
Research and development technician job in Marlborough, MA
**Are you looking to power the next leap in the exciting world of advanced electronics?** Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics.
At **Qnity** , we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us.
We are seeking a hands-on, self-motivated Analytical Chemist to support New Product Development (NPD) and commercial product support across the ACP portfolio; ranging from metallization/plating chemistries to advanced packaging polymers and formulated materials. This role will lead development, implementation, and continuous improvement of analytical and characterization methods for specially synthesized raw materials (small molecules through complex polymers) and finished products, partnering closely with cross-functional stakeholders (DE, NPD, Manufacturing, Quality, and Technical Service) to enable scale-up, specifications, and customer support.
**Key responsibilities**
+ Analytical method development & execution: Develop, optimize, and run analytical/characterization methods for raw materials, intermediates, and formulated products supporting NPD milestones and commercial needs.
+ Core techniques: Apply techniques such as CVS, HPLC/UPLC, GPC, % solids, titrations, potentiostatic measurements, surface tension, cloud point, densitometry, and rheology (and related wet/physical methods).
+ Other techniques relevant: ICP-OES/ICP-MS for metals/impurities, UV-Vis, FTIR, NMR, IC, TOC, DSC/TGA, particle size/zeta potential, SEM/EDS
+ Method validation, transfer, and sustainment: Author/maintain methods, validation protocols/reports, and ensure robust method transfer to R&D and Manufacturing as needed.
+ Data integrity & documentation: Maintain high-quality written documentation (methods, validation, batch/lot data packages, change control / MOC) and ensure traceable, audit-ready records.
+ Troubleshooting & investigations: Support root-cause investigations, out-of-spec troubleshooting, and customer complaint response in collaboration with Quality/Manufacturing.
+ Statistical/data analysis: Use statistical tools to analyze method performance, capability, trends, and investigation data (DOE, GR&R, SPC as applicable).
+ Safety & teamwork: Work safely with hazardous chemicals in a collaborative, fast-paced lab environment; communicate clearly in both informal updates and formal presentations.
**Required qualifications**
+ Education: B.S. in Chemistry, Biology, Chemical Engineering, Materials Science, or related field.
+ Experience: 3-5 years of hands-on experience in analytical chemistry supporting R&D/NPD, development engineering, manufacturing, or quality environments. (Experience characterizing small molecules, polymers, and/or inorganic/metal-containing chemistries is strongly valued.)
+ Demonstrated ability to follow procedures with high repeatability, strong attention to detail, and commitment to safe lab practices.
+ Strong written and verbal communication skills; able to translate data into clear technical conclusions and recommendations.
+ Strong data analysis capability; JMP/Minitab (or similar) preferred.
**Preferred qualifications**
+ Demonstrated success developing/validating new analytical methods and supporting method transfer.
+ Experience supporting semiconductor materials (e.g., plating baths, photoresists, dielectrics, silicones, packaging polymers) and working across interdisciplinary teams.
+ Six Sigma (Green/Black Belt) or demonstrated experience applying structured problem-solving tools.
Join our Talent Community (*************************************************************** to stay connected with us!
Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information (**************************************************** .
Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page (*************************************************************************** .
**We use Artificial Intelligence (AI) to enhance our recruitment process.**
The Pay range for this role is $67,200.00 - $105,600.00 Annual
**How Base Pay is Determined:** Qnity has job leveling frameworks that help organize roles based on progressive levels of responsibility, proficiency and qualifications. Each role has an associated pay range (or an established pay rate for some roles) based on the competitive market in each country where we operate. Each individual's pay is based on a variety of factors, including their role and the associated pay range for that role, their geographic location (i.e., country, state, metropolitan area), as well as their skills, experience, education and certifications, and performance.
$67.2k-105.6k yearly 3d ago
Research Associate/Associate Scientist, Assay Development
Spear Bio
Research and development technician job in Woburn, MA
Spear Bio, founded in 2021, is a well-funded and rapidly growing biotech start-up headquartered in Woburn, Massachusetts. Our proprietary technology, Successive Proximity Extension Amplification Reaction (SPEAR), is a novel wash-free immunoassay platform, offering unprecedented sensitivity. We are dedicated to revolutionizing early disease diagnosis and monitoring by providing scalable, ultrasensitive solutions that deliver unparalleled accuracy in measuring low-abundant biomarkers, enabling clinicians and researchers to improve patient outcomes and advance global health.
Research Associate/Associate Scientist:
We are seeking a highly motivated and experienced Research Associate/Associate Scientist to join our growing Assay Development team, with hands-on experience running ultrasensitive immunoassays and the desire to be at the forefront of innovative research. This individual will play a pivotal role in advancing Spear Bio's new range of ultrasensitive immunoassays and assay biomarker programs.
This role is based onsite in our lab in Woburn, MA 5 days/wk.
Responsibilities:
Test and execute immunoassay workflows on high-throughput, semi-automated platforms
Assist in optimizing methods for processing different types of biofluid samples (ie. serum, plasma) for assay development
Set up, calibrate, and maintain laboratory equipment, as specified by the requirements of various projects
Assist in data analysis
Acquire necessary equipment and supplies for various projects
Qualifications:
Master's degree in Biology, Biochemistry, Biophysics, Biomedical Engineering or a related discipline plus 1-3 years of assay development experience in an industry or academic lab
Direct experience running biofluid-based immunoassays and qPCR experimentation is required
Experience with neurodegenerative disease protein biomarkers a plus (ie. pTau217, pTau181, NFL, GFAP, alpha-synuclein, etc.)
Experience characterizing and troubleshooting immunoassays
Strong proficiency in molecular biology lab techniques
General Qualifications:
Self-motivated and ability to perform complex tasks in an effective manner
Ability to follow instructions and grow in a mentorship setting
Excellent organizational and documentation skills
Desire to learn and implement new technologies
Strong presentation and interpersonal skills, ability to build collaborative working relationships, and become a key contributor within the assay development team
Work 5 days/week on site in Woburn, MA. LOCAL CANDIDATES will be given priority consideration for this position.
We offer competitive compensation, meaningful stock ownership, comprehensive benefits, and a great work environment. This is an opportunity to enter an innovative, high-growth startup at an early stage and play an integral role in the company's growth and success. We are focused on identifying candidates who have demonstrated leadership and excellence throughout their careers and are excited by the prospect of building an industry-leading company.
Spear Bio Inc. provides equal opportunity in employment to all persons. No person shall be denied equal access because of race, creed, color, religion, national origin, sex, sexual orientation, gender identity, age, or physical/mental disability.
Spear Bio does not accept resume submissions from external recruiting agencies. Any unsolicited resumes or candidate information submitted without prior written agreement will be deemed the property of Spear Bio, and no placement fees will be paid.
$69k-97k yearly est. Auto-Apply 41d ago
iPSC Production Scientist - Biology
ZP Group 4.0
Research and development technician job in Medford, MA
Piper Health & Sciences is seeking a full-time iPSC Production Scientist to join a growing organization's Bio/Engineering Production team onsite at their Massachusetts location. The ideal candidate will have a strong biology background and hands-on experience in iPSC stem cell culture, differentiation, and QC within a pharmaceutical or biotech environment.
Responsibilities of the iPSC Production Scientist Include:
* Full-time onsite schedule: Monday-Friday, 9:00 AM - 5:00 PM
* Lead and support iPSC production and related lab activities
* Perform hands-on stem cell culture and differentiation
* Execute QC-related tasks in accordance with SOPs
* Maintain accurate lab documentation and records
* Support Bio/Engineering Production workflows
* Follow all safety, GMP, and GLP standards
Qualifications of the iPSC Production Scientist Include:
* Biology degree is strongly preferred (Biomedical Engineering degrees are NOT a fit)
* Proven hands-on experience with:
* iPSC cell culture
* Stem cell differentiation
* Quality Control (QC) processes
* Pharmaceutical or biotech industry experience preferred
Compensation of the iPSC Production Scientist Includes:
* Salary Range: $83,200.00 - $114,000.00 per year (equivalent to $40.00 - $55.00 per hour), based on experience and certifications.
* Comprehensive Benefits: CIGNA Medical, Dental, Vision; 401k through ADP and sick leave as required by law.
* Ability to work with a well renowned and growing organization that has a robust pipeline and quality culture.
This job opens for applications on 1/12/2026. Applications for this job will be accepted for at least 30 days from the posting date.
#LI-AW1
#LI-ONSITE
keywords: Scientist, iPSC Production, stem cell culture, induced pluripotent stem cells, cell differentiation, quality control, QC, laboratory scientist, cell biology, biotechnology, pharmaceutical production, bioengineering, GMP, GLP, SOP compliance, tissue engineering, regenerative medicine, bioprocessing, cell therapy, stem cell research, lab operations, onsite scientist, Medford MA jobs, contract scientist, PhD biology, master's biology, postdoctoral research, biotech scientist, pharma scientist, cell culture specialist, stem cell specialist, iPSC scientist, QC scientist, bio production scientist, laboratory techniques, cell-based assays, biotech careers, pharma careers, stem cell manufacturing, cell culture workflows, life sciences jobs, biopharma jobs, laboratory compliance, scientific documentation, biotech industry experience, pharmaceutical industry experience, cell line development, research scientist, production scientist, laboratory QC, stem cell differentiation protocols, cell culture maintenance, full-time onsite scientist, bioengineering production team, regenerative biology, tissue culture, cell therapy manufacturing, biotechnology research, pharmaceutical QC, biomanufacturing, cell biology techniques, stem cell QC testing, scientific method, laboratory safety standards, GMP compliance, GLP compliance, biotech contract role, scientist contract position, iPSC culturing, stem cell production, biotech Medford MA, pharma Medford MA, scientific careers, laboratory scientist jobs, cell therapy scientist, bioprocess scientist, QC laboratory scientist, stem cell lab work, biotech production workflows, pharmaceutical production workflows, life sciences contract jobs, biotech contract scientist, pharma contract scientist.
$83.2k-114k yearly 7d ago
Research Technologist - Ordovas-Montanes Lab
Children's Hospital Boston 4.6
Research and development technician job in Boston, MA
This is an opportunity to join Ordovas-Montanes Lab, which specializes in understanding how inflammation drives memory formation in barrier tissues with the goal of developing new therapeutic avenues for human disease. This candidate will contribute to a collaborative project focused on mucosal immunity to respiratory infection and vaccination.
The candidate will work under the direct supervision of Dr. Jose Ordovas-Montanes and be closely integrated within a community of senior scientists, graduate students, and postdoctoral fellows. This position requires substantial technical expertise, the ability to troubleshoot specialized assays, and the capacity to support and train junior lab members as needed.
This role offers the opportunity to develop a wide range of experimental and computational skills while working in an interdisciplinary environment with access to resources across Boston Children's Hospital and Harvard Medical School. The ideal candidate is motivated to understand the biological principles underlying infection-induced inflammatory diseases and may be interested in pursuing future postgraduate education.
Key Responsibilities:
* Independently perform complex experimental workflows, help optimize protocols, and generate high-quality data for single-cell genomics and airway epithelial biology studies.
* Troubleshoot specialized assays.
* Support and train junior lab members as needed.
* Performs routine and highly specialized lab experiments using sophisticated and intricate research equipment and techniques. Performs and devises specialized experiments and research procedures, troubleshooting problems with own and other researchers' results.
* Assists other lab personnel with the use of specialized equipment and techniques within the lab.
Minimum Qualifications
Education:
* Bachelor's degree in biology, immunology, genomics, chemistry, or a related field is required. Master's degree preferred but not required.
Experience:
* Bachelor's and 4 years of relevant experience OR a Master's of Science and 2 years of relevant experience.
* Demonstrated experience performing mammalian cell culture, ideally primary airway epithelial culture or similar complex systems.
* Proficiency in molecular biology techniques.
* Proven ability to independently execute and troubleshoot complex laboratory workflows.
* Experience with single-cell RNA-sequencing methods and data analysis in R and/or python is preferred but not required.
The posted pay range is Boston Children's reasonable and good-faith expectation for this pay at the time of posting.
Any base pay offer provided depends on skills, experience, education, certifications, and a variety of other job-related factors. Base pay is one part of a comprehensive benefits package that includes flexible schedules, affordable health, vision and dental insurance, child care and student loan subsidies, generous levels of time off, 403(b) Retirement Savings plan, Pension, Tuition and certain License and Certification Reimbursement, cell phone plan discounts and discounted rates on T-passes. Experience the benefits of passion and teamwork.
$44k-55k yearly est. 38d ago
R&D Reliability Engineer - Electromechanical Systems & Testing
Formlabs 4.3
Research and development technician job in Boston, MA
A 3D printing technology company in Boston is seeking an R&D Reliability Engineer to ensure product robustness through comprehensive testing strategies. You will build and execute validation plans, analyze failure data, and collaborate with design teams to enhance reliability. The ideal candidate should be proficient with electromechanical systems and data analysis, and can implement tests in Python. This role offers a competitive salary and generous benefits, including equity opportunities.
#J-18808-Ljbffr
$84k-111k yearly est. 2d ago
Learn more about research and development technician jobs
How much does a research and development technician earn in Lowell, MA?
The average research and development technician in Lowell, MA earns between $65,000 and $138,000 annually. This compares to the national average research and development technician range of $55,000 to $125,000.
Average research and development technician salary in Lowell, MA
$95,000
What are the biggest employers of Research And Development Technicians in Lowell, MA?
The biggest employers of Research And Development Technicians in Lowell, MA are:
Velocity Search Group
Joseph's Bakery
Zink Holdings Group
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