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<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
This position is in the Biologics Purification Development team of the Product Development Science and Technology department at Bioresearch Center.
</li>
<li>
The candidate will be involved with all aspects of protein purification and protein chemistry to support biopharmaceutical process development.
</li>
<li>
Execute high through put scale down robotic purification as part of early and late stage process development, viral clearance, process characterization, and continuous process improvement studies.
</li>
<li>
Perform basic data acquisition and analysis, and documentation in electric lab notebooks.
</li>
<li>
Will develop economical, robust steps for recovering the target protein from bioreactor harvests using chromatography, filtration, and other separation techniques; developing downstream purification processes to be transferred to manufacturing; and perform laboratory scale process characterization studies.
</li>
<li>
Perform various bioanalytical assays, including HPLC, ELISAs and SDS-PAGE, to aid in rapid process development.
</li>
<li>
As appropriate, the candidate may supply technical support for pilot and/or GMP manufacturing of clinical materials.
</li>
</ul>
Qualifications:
<ul>
<li>
BS in Chemical Engineering, Biochemistry, or Chemistry with 3-5 years experience; OR
</li>
<li>
Master's Degree with 2 years' experience 
</li>
<li>
Strong biological scientific understanding.
</li>
<li>
Experience with chromatography and filtration for biologics purification
</li>
<li>
Experience with bioanalytical assays and methods preferred
</li>
<li>
Strong written, oral, and collaborative skills in order to effectively communicate experimental procedures and results.
</li>
<li>
Experience with Lab work particularly with process development
</li>
<li>
Small scale Chromatography, high throughput, AKTA is a huge plus 
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Biologist

<h3>Job Description</h3>
Job Description
Production Technician – Biotechnology
We’re seeking a detail-oriented and safety-conscious Production Technician to join our biotechnology team. In this role, you’ll be responsible for executing defined production procedures in a GMP-regulated environment, supporting manufacturing operations, and maintaining a clean, organized, and safe workspace.
Responsibilities:
<ul>
<li>Perform production tasks according to established schedules and procedures.</li>
<li>Ensure compliance with company policies and cGMP regulations.</li>
<li>Maintain a safe work environment and actively participate in site safety initiatives.</li>
<li>Execute lab start-up and shutdown procedures.</li>
<li>Keep work areas clean and well-stocked with necessary supplies.</li>
<li>Operate and monitor equipment including spectrophotometers, pH meters, and automated systems.</li>
<li>Perform routine tasks such as buffer preparation, pH testing, UV measurements, and fraction collection.</li>
<li>Support synthesis and purification processes, including equipment cleaning, solution prep, and column packing.</li>
</ul>
Qualifications:
<ul>
<li>Biotechnology certificate or college degree preferred.</li>
<li>2–5 years of experience in a GMP-regulated environment.</li>
<li>Hands-on experience with pH testing, aseptic technique, buffer preparation, and chromatography.</li>
<li>Strong attention to detail and ability to follow SOPs and safety protocols.</li>
</ul>
Top Skills:
<ul>
<li>pH testing</li>
<li>Aseptic technique</li>
<li>Buffer preparation</li>
</ul>
If interested, please reach out to directly to Lindsee Allienello at lallienello @ actalentservices.com. 
Pay and Benefits
The pay range for this position is $30.00 - $31.25/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 &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;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 Milford,MA.
Application Deadline
This position is anticipated to close on Sep 26, 2025.
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 <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Manufacturing Chemist

<h3>Job Description</h3>
Job Description
Production Technician – Biotechnology
We’re seeking a detail-oriented and safety-conscious Production Technician to join our biotechnology team. In this role, you’ll be responsible for executing defined production procedures in a GMP-regulated environment, supporting manufacturing operations, and maintaining a clean, organized, and safe workspace.
Responsibilities:
<ul>
<li>Perform production tasks according to established schedules and procedures.</li>
<li>Ensure compliance with company policies and cGMP regulations.</li>
<li>Maintain a safe work environment and actively participate in site safety initiatives.</li>
<li>Execute lab start-up and shutdown procedures.</li>
<li>Keep work areas clean and well-stocked with necessary supplies.</li>
<li>Operate and monitor equipment including spectrophotometers, pH meters, and automated systems.</li>
<li>Perform routine tasks such as buffer preparation, pH testing, UV measurements, and fraction collection.</li>
<li>Support synthesis and purification processes, including equipment cleaning, solution prep, and column packing.</li>
</ul>
Qualifications:
<ul>
<li>Biotechnology certificate or college degree preferred.</li>
<li>2–5 years of experience in a GMP-regulated environment.</li>
<li>Hands-on experience with pH testing, aseptic technique, buffer preparation, and chromatography.</li>
<li>Strong attention to detail and ability to follow SOPs and safety protocols.</li>
</ul>
Top Skills:
<ul>
<li>pH testing</li>
<li>Aseptic technique</li>
<li>Buffer preparation</li>
</ul>
Pay and Benefits
The pay range for this position is $30.00 - $31.25/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 &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;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 Milford,MA.
Application Deadline
This position is anticipated to close on Sep 29, 2025.
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 <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job Description
We are currently seeking a Lead Scientist / Engineer with a PhD in Systems &amp; Control, Biomedical Engineering, Applied Mathematics, or a related quantitative field, and 5–6+ years of experience in applied modeling and estimation. This role will function as a senior member of the company’s algorithm team. It will involve designing and implementing Etiometry’s next-generation physiologic risk and treatment-prediction algorithms. The position will require close collaboration with Etiometry’s data science, product, and clinical teams to translate physiologic and clinical requirements into real-time decision support tools deployed in the ICU.
Responsibilities
<ul>
<li>
Lead the design, implementation, and validation of algorithms that predict patient trajectories and responses to interventions (e.g., fluids, vasoactives, ventilator changes).
</li>
<li>
Extend Etiometry’s existing ODE-based physiologic models with advanced estimation methods (e.g., Kalman filters, Bayesian inference, particle filters).
</li>
<li>
Integrate data-driven approaches (e.g., neural networks, probabilistic ML, hybrid mechanistic/ML frameworks) with classical physiology-based models.
</li>
<li>
Translate physiologic and clinical requirements into quantitative risk indices for FDA-regulated software.
</li>
<li>
Work with real-world ICU data, including physiologic waveforms, vital signs, and laboratory values.
</li>
<li>
Mentor junior scientists and collaborate with engineers, clinical experts, and regulatory affairs to bring models from research → cleared product.
</li>
</ul>
Basic Qualifications
<ul>
<li>
PhD in Systems &amp; Control, Biomedical Engineering, Applied Mathematics, Electrical/Mechanical Engineering, or a related field.
</li>
<li>
5–6+ years of experience (industry or postdoctoral) in applied modeling, estimation, or control systems.
</li>
<li>
Strong background in dynamical systems &amp; ODE/PDE modeling.
</li>
<li>
Strong background in state estimation techniques (Kalman filters, stochastic processes, Bayesian methods).
</li>
<li>
Working knowledge of machine learning (neural networks, probabilistic ML, data-driven system identification).
</li>
<li>
Proficiency in scientific computing in Python (NumPy, SciPy, PyTorch, TensorFlow).
</li>
<li>
Strong communication and organization skills.
</li>
<li>
Proven ability to work in cross-disciplinary teams and translate theory into applied solutions.
</li>
</ul>
Desired Qualifications
<ul>
<li>
Experience working with clinical monitoring data (ICU waveforms, vital signs, laboratory data, EHR integration).
</li>
<li>
Familiarity with computational physiology or biomedical modeling.
</li>
<li>
Knowledge of medical device software lifecycle (IEC 62304, FDA 510(k)).
</li>
<li>
Experience mentoring junior scientists or leading research projects.
</li>
</ul>
About Etiometry
Etiometry is the market leader in predictive analytics for the Intensive Care Unit. Our system leverages real-time patient data to provide clinicians with actionable information that improves care for the most vulnerable patients. In use at some of the best medical institutions across three continents, the Etiometry Platform has a proven track record in improving outcomes while reducing hospital costs. Our next generation of algorithms will go beyond monitoring risk to forecasting how treatments will affect patient physiology — giving clinicians foresight to guide critical interventions. By joining Etiometry, you will be at the forefront of clinical innovation, working with a passionate team of engineers and scientists with the mission of transforming the delivery of critical care. You will become an integral part of a dynamic team whose work will directly impact patients worldwide and shape the future of ICU analytics.

Lead Algorithm Scientist Engineer

<h3>Job Description</h3>
Job DescriptionProduct Development Engineer/Scientist About actnanoWe are a dynamic materials technology company in Malden, MA. With a strong global technical team, we develop and manufacture coatings that protect printed circuit boards in electronics, allowing them to function in water-laden environments. We work with the biggest brands in the consumer electronics and automotive industries to increase product reliability and improve product performance in wet and humid conditions. Not only do we provide a portfolio of coatings, but we also work closely with our customers to help solve some of their most difficult problems through rapid innovation and ingenuity. About this RoleWe are seeking a roduct Development Engineer/Scientist to join our talented and diverse technical team in Malden, MA. This position will focus on developing novel coatings platforms from lab-to-scale to address customer needs. A bachelor’s degree or higher in Mechanical, Chemical or Electrical Engineering, Chemistry, Materials Science,or associated technical field is required. Fluency in Mandarin, Spanish, or German preferred but not required. Candidate must be legally allowed to work in the US. Key Responsibilities
<ul>
<li>Develop novel coating platforms, test metrics, and design experiments by working in a lab-based environment with minimal day-to-day guidance.</li>
<li>Develop hypotheses and conduct experiments to improve understanding and performance of actnano’s coating technology by coordinating with various team members.</li>
<li>Communicate technical advances internally with other members of the company and interact with external vendors, independent testing laboratories, and customers to explain and troubleshoot application of the technology.</li>
<li>Support scaling of coating from lab or pilot scale to a manufacturing environment.</li>
<li>Collaborate with sales or technical service to address customer requests.</li>
<li>Expand actnano’s coating portfolio by innovating on current coating technology and developing new coating platforms.</li>
<li>Some international and domestic travel required. </li>
</ul>
This position is based in Malden, MA, accessible via the Orange Line. The salary range for this position is $75,000 – $90,000 per year, which reflects the base pay the Company reasonably and in good faith expects to pay at the time of this posting. &nbsp;
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I3Y9Z3UrYH

Product Development Engineer / Scientist

<h3>Job Description</h3>
Job Description
At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking treatments including MACI (knee cartilage repair), Epicel and Nexobrid (burn care). 
Position Summary: 
This role is primarily responsible for calibrating and coordinating the calibration of a diverse range of electrical and mechanical equipment while adhering to good manufacturing practices. The role may also perform and/or assist with the installation, maintenance, testing and repair and of the equipment.
Schedule: This position is in-office Monday-Friday.
Position Scope:
<ul>
<li>Manage vendors and calibrates instruments such as, RO systems, clean steam generators, autoclaves, parts washer systems, lab equipment, and manufacturing equipment. </li>
<li>Develop and maintain the Blue Mountain Regulatory Asset Manager (BMRAM) system.</li>
<li>Maintain all calibration records and instrument tagging. </li>
<li>Write/develop Standard Operating Procedures (SOPs), and/or protocols.</li>
<li>Write initial deviations using the QMS system.</li>
<li>Assist in change control documentation and deviation notifications.</li>
<li>Serve as information resource for validation technicians, contractors and vendors.</li>
<li>Perform scheduled, new and emergency calibrations activities with vendors on all critical process equipment and lab instrumentation ensuring compliance with SOPs and cGMPs.</li>
<li>Troubleshoot instrument control loops like temperatures, pressure, flow controllers, etc.</li>
<li>Follow all environmental, health, and safety requirements and protocols.</li>
<li>Understand schematics, logic ladder diagrams, and P&amp;IDs.</li>
<li>Identify/coordinate inventory for spare parts used on critical instruments.</li>
<li>Support operations during 1st shift and be available after hours as needed to support the business.</li>
<li>Assist in equipment selection, specification and commissioning.</li>
<li>Other duties as assigned.</li>
</ul>
Qualifications: 
<ul>
<li>Bachelors degree in STEM or High School degree with equivalent years of experience.</li>
<li>Minimum 6+ years related experience in the areas such as temperature, pressure, flow (liquid &amp; gas), pH, conductivity, humidity, lab instrumentation controllers, depyrogenation oven, steam generators, steam boilers, air compressor, vacuum pumps, and lab instrumentation.</li>
<li>Knowledge of pharmaceutical manufacturing process equipment and lab instrumentation.</li>
<li>Basic knowledge on cleanroom classifications.</li>
<li>Familiarity with FDA, cGMP, SOPs, ASNI/NCSL, EU and ISO standards.</li>
<li>Good organizational skills.</li>
<li>Experience utilizing quality manage systems like Trackwise and BMRAM preferred.</li>
<li>Excellent verbal, writing and interpersonal communication skills.</li>
<li>Ability to gown and gain entry to manufacturing areas wearing personal protection equipment - safety glasses, gloves, gowns, etc. </li>
<li> Ability to be available after hours as needed to support the business.</li>
<li>Ability to lift up to 25 lbs.</li>
</ul>
Why Vericel?
<ul>
<li>Cutting-Edge Science: Work with a leading regenerative medicine product that is transforming patient care.</li>
<li>Career Growth: Be a part of a growing organization with opportunities to expand your impact.</li>
<li>Collaborative Culture: Work alongside a team of dedicated professionals who are passionate about improving lives.</li>
</ul>
EEO Statement
All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, sexual orientation, gender identity, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of disability. Vericel Corporation is an Equal Opportunity/Affirmative Action Employer.
Vericel Corporation is VEVRAA federal contractor and desires priority referrals of protected veterans for job openings at all locations within the state.

Metrology Lead

<h3>Job Description</h3>
Job DescriptionSenior Product Development Engineer/Scientist About actnanoWe are a dynamic materials technology company in Malden, MA. With a strong global technical team, we develop and manufacture coatings that protect printed circuit boards in electronics, allowing them to function in water-laden environments. We work with the biggest brands in the consumer electronics and automotive industries to increase product reliability and improve product performance in wet and humid conditions. Not only do we provide a portfolio of coatings, but we also work closely with our customers to help solve some of their most difficult problems through rapid innovation and ingenuity. About this RoleWe are seeking a Senior Product Development Engineer/Scientist to join our talented and diverse technical team in Malden, MA. This position will focus on developing new platform technologies for environmental protection and implementing at our customers around the world. A master’s or doctorate in Mechanical, Chemical or Electrical Engineering, Chemistry, Materials Science, or associated technical field is required. Fluency in Mandarin, Spanish, or German preferred but not required. Candidate must be legally allowed to work in the US. Key Responsibilities
<ul>
<li>Develop functional materials, test methods, and implementation solutions for the environmental protection of automotive and consumer electronics.</li>
<li>Maintain project plans, timelines, and deliverables related to product launch strategy.</li>
<li>Communicate technical advances and project strategy to a global team of technical and sales personnel.</li>
<li>Work autonomously on open-ended projects, from new coating development to novel application techniques.</li>
<li>Expand actnano’s IP portfolio by innovating on coatings and application technology.</li>
<li>Serve as the subject matter expert on coatings and participate in developing customer implementation strategies.</li>
<li>Collaborate with cross-functional teams and maintain project plans, timelines, and deliverables for product launches.</li>
<li>Mentor technicians and co-ops on conducting experiments for coating development.</li>
<li>International and domestic travel is required.</li>
</ul>
This position is based in Malden, MA, accessible via the Orange Line. The salary range for this position is $115,000 – $125,000 per year, which reflects the base pay the Company reasonably and in good faith expects to pay at the time of this posting. &nbsp;
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Senior Product Development Engineer / Scientist

<h3>Job Description</h3>
Job Description
About Discovery Life Sciences:
Discovery Life Sciences (Discovery) is a leading provider of highly characterized human biospecimens and cellular starting materials to advance cell and gene therapy and precision medicine programs for cancer, infectious disease, and other complex conditions. We routinely manage hundreds of studies and expertly test thousands of biospecimens simultaneously. Leading biopharma, diagnostic and academic institutions trust us to quickly deliver high-quality biospecimens and reliable, reproducible biomarker data, so they can outpace their competition and push the leading edge of innovation using our Science at your Service TM business model.
Position Summary:
Discovery is looking for a talented and passionate Senior Scientist to join our dynamic R&amp;D team. As a Senior Scientist, you will participate in the scientific direction and execution of product research and development projects for the preclinical business. We offer an exciting and collaborative work environment where you can unleash your creativity and make a real impact.
A Day in the Life of a Senior Scientist at Discovery Life Sciences:
<ul>
<li>Design, develop, and execute R&amp;D projects in collaboration with cross-functional teams</li>
<li>Lead the execution of projects, including scheduling, and resource planning</li>
<li>Review and interpret data; ensure scientific accuracy and integrity in final reports and conclusions</li>
<li>Maintain accurate documentation and protocols throughout the project lifecycle</li>
</ul>
Must-Have Qualifications (Education, Skills, Experience):
<ul>
<li>PHD biology, toxicology, or a related field</li>
<li>2+ years of postdoctoral experience in pharmacology, toxicology or related science or significant study in the areas of absorption, distribution, metabolism, and excretion (ADME), toxicity and disease modeling as they relate to hepatocyte biology.</li>
</ul>
Key Responsibilities:
<ul>
<li>Bring new innovative ideas and develop them into feasible concepts</li>
<li>Design, develop, and execute R&amp;D projects in collaboration with cross-functional teams</li>
<li>Lead the execution of projects, including scheduling, and resource planning</li>
<li>Review and interpret data; ensure scientific accuracy and integrity in final reports and conclusions</li>
<li>Represent product development during customer engagements on calls or conferences.</li>
<li>Functionally mentoring junior scientific staff, providing guidance on technical execution, experimental design, and professional development</li>
<li>Maintain laboratory operations supporting assigned projects, including procurement of supplies, equipment maintenance, and overall lab functionality</li>
<li>Identify and resolve operational or scientific challenges independently; develop and implement effective solutions</li>
<li>Manage multiple concurrent projects while meeting established timelines and deliverables</li>
<li>Drive innovation to reduce workload and costs, improve operational efficiency, and develop new products and services or scientific capabilities</li>
<li>Coordinate with internal departments such as operations, bioanalytical, and services to ensure alignment on product development and workflow integration</li>
<li>Maintain accurate documentation and protocols throughout the project lifecycle</li>
<li>Use word processing, spreadsheet, statistical, presentation, and database software to support project execution and reporting</li>
<li>Prioritize responsibilities to support project goals</li>
<li>Exercise sound judgment in handling and protecting confidential and proprietary company information</li>
<li>Communicate effectively, both in writing and verbally, including in customer-facing activities and cross-functional collaboration</li>
<li>Establish and maintain professional, cooperative relationships with internal colleagues and external partners</li>
<li>Maintain consistent and reliable attendance, which is an essential function of the role</li>
<li>Perform other related duties as assigned, which may occasionally fall outside the core scope of the position</li>
</ul>
Compensation and Benefits:
Discovery Life Sciences is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $90,000- $135,000. Candidates hired to work in other locations will be subject to the pay range associated with that location, and the actual annualized salary amount offered to any candidate at the time of hire will be reflected solely in the candidate’s offer letter. The exact base pay offered for this role will depend on various factors, including the candidate's qualifications, skills, and experience. Your annual salary is only one part of your total compensation package. Other benefits include:
<ul>
<li>Competitive salary and benefits package options, including a free medical, dental, vision package, life insurance, and disability coverage which start on your first day of employment.</li>
<li>This role is also eligible to earn performance-based incentive compensation, which may include cash bonus(es).  These incentives are discretionary.</li>
<li>401(k) match program which starts on your first day of employment.</li>
<li>Time away from work (Generous vacation and paid time off, your BIRTHDAY, paid parental leave, paid family leave, etc.).</li>
<li>Professional development opportunities and reimbursement for relevant certifications.</li>
<li>Collaborative and inclusive work environment that values diversity.</li>
<li>Team-building activities and social events.</li>
<li>Employee Referral Program and Colleague Recognition Program.</li>
</ul>
Location, work hours, and application details:
<ul>
<li>Malden/Woburn. MA Flexible work schedule, start time between 7am and 9am local time</li>
</ul>
We are actively seeking motivated, dedicated individuals like you to join our thriving organization. As a leader in our industry, we offer unparalleled opportunities for professional growth and success. Apply Now to join our team! Visit dls.com/careers for more details.
*The Discovery Life Sciences Talent Acquisition team proudly manages and represents all Discovery recruitment activities. We respectfully request that third party staffing agencies refrain from submitting candidates or soliciting meetings to discuss recruiting services.

Senior Scientist

<h3>Job Description</h3>
Job Description
About General Fluidics General Fluidics is a clinical diagnostics startup based in Watertown, MA developing the Axess™ platform, a breakthrough point-of-care system that delivers laboratory-grade performance across clinical chemistry, hematology, and immunoassays from a single blood sample. By integrating three “gold standard” analytical technologies into one compact instrument, we are transforming how clinicians access and act on diagnostic data. Learn more at generalfluidics.com.
The Role We are seeking a highly motivated&nbsp;Senior Scientist&nbsp;to join our R&amp;D team and drive expansion of our diagnostic assay menu for veterinary and human health applications. This is a hands-on, experimental role, ideal for a scientist who thrives on creative problem-solving, assay development, and instrumentation work in a startup environment.
Reporting to the VP of Assay Development, you will independently design and execute experiments, interpret data, and optimize assay performance on the Axess™ platform. You’ll collaborate closely with our team of engineers and fellow scientists, contribute to analytical validation efforts, and help accelerate our path to regulatory clearance and product launch. As a company of 10, this is an individual contributor role but carries significant ownership over your workstreams. We value scientists who are resilient, resourceful, and as comfortable running critical assays as they are maintaining lab systems.
Key Responsibilities
<ul>
<li>Lead design, development, and validation of clinical chemistry, hematology, and immunoassays on the Axess™ point-of-care instrument.</li>
</ul>
<ul>
<li>Plan and execute complex experiments independently; analyze, interpret, and present results to guide development decisions.</li>
</ul>
<ul>
<li>Collaborate with engineers on system integration, troubleshooting, and instrument optimization.</li>
</ul>
<ul>
<li>Apply statistical methods and data analysis to support assay performance claims and regulatory submissions.</li>
</ul>
<ul>
<li>Author experimental protocols, technical reports, and supporting documentation in compliance with design control requirements.</li>
</ul>
<ul>
<li>Support quality systems through calibration, control protocols, and proficiency testing.</li>
</ul>
<ul>
<li>Maintain high standards of lab operation including safety, inventory management, and instrument upkeep.</li>
</ul>
<ul>
<li>Mentor junior staff in assay development best practices as needed.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree with 6–8 years, Master’s with 3–5 years, or PhD with 0–2 years of relevant industry R&amp;D experience in biotechnology, molecular biology, or related field.</li>
</ul>
<ul>
<li>Proven experience in assay development, troubleshooting, and data interpretation in an industry setting (not academic or QC/manufacturing).</li>
</ul>
<ul>
<li>Hands-on skills in assay development, reagent preparation, and laboratory techniques (pipetting, biosafety cabinet work, etc.).</li>
</ul>
<ul>
<li>Familiarity with clinical instrumentation (e.g., flow cytometry, hematology analyzers, clinical chemistry, immunoassays) strongly preferred.</li>
</ul>
<ul>
<li>Prior exposure to diagnostic assay validation, design controls, or regulatory submissions strongly preferred.</li>
</ul>
<ul>
<li>Comfortable in a dynamic startup environment: onsite presence, ownership mentality, and willingness to tackle both high-impact experiments and day-to-day lab operations.</li>
</ul>
<ul>
<li>Excellent written and verbal communication skills, with the ability to clearly present scientific concepts and data.</li>
</ul>
Who You Are
<ul>
<li>Curious, creative, and energized by solving open-ended scientific problems.</li>
</ul>
<ul>
<li>Resilient in the face of experimental failure, with the maturity to adapt and keep moving forward.</li>
</ul>
<ul>
<li>Independent and confident in your scientific judgment, while eager to collaborate across disciplines.</li>
</ul>
<ul>
<li>Excited by the opportunity to help build a transformative diagnostic platform from the ground up.</li>
</ul>
Company DescriptionGeneral Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus. 
<h3>Company Description</h3>
General Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus.

Sr. Scientist

<h3>Job Description</h3>
Job Description
Adecco Staffing is assisting a facility in Devens MA in sourcing for an Clean RoomOperator on 1st shift! Ideal candidates have a direct background in a clean-room environment operating machines!

Shift Hours: 5:00AM -4:00PM, Monday-Thursday Pay Rate: $19/hr Job Responsibilities:
• Assisting with 5S and Safety tasks associated with good manufacturing practices • Manufacturing of Extruded tubing • Manufacture of Liquid Silicone Rubber Moulded (LSR) parts • Collecting and recording relevant process data • Assisting engineering with validation and experimental activities • Identifying opportunities for improvement throughout the manufacturing process and working with team members to recommend and implement solutions • Following Clean room policies- gowning up and wearing a mask that covers nose and mouth. • Maintain the tools used to create products. • Keep a clean and well-maintained workspace. • Comply with company regulations and operating procedures • Maintain a helpful and collaborative culture through communication and a strong work ethic • Carry out any other activities to support the business as required Essential Skills and Experience: • Strong Attention to Detail • Troubleshooting &amp; Repairs • Strong Mechanical Background • Direct Background in a Clean Room Environment
 INTERESTED? If so, please apply directly to this posting!
 Pay Details: $19.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to <a href="https://uat.adecco.com/en-us/candidate-privacy" target="_blank">https://uat.adecco.com/en-us/candidate-privacy</a> The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: 
<ul>
<li>The California Fair Chance Act</li>
<li>Los Angeles City Fair Chance Ordinance</li>
<li>Los Angeles County Fair Chance Ordinance for Employers</li>
<li>San Francisco Fair Chance Ordinance</li>
</ul>
 
Massachusetts Candidates Only: 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.

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