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<h3>Job Description</h3>
Job Description
Job Title: Bench Chemist
Job Description
We are seeking a skilled Bench Chemist to join our dynamic team. The ideal candidate will perform a variety of chemical analyses and support laboratory operations. The role involves working with raw materials, in-process samples, and finished goods using advanced testing methods.
Responsibilities
<ul>
<li>Run LC and GC testing of raw materials, in-process samples, and finished goods.</li>
<li>Prepare samples across matrices, run calibration curves, and conduct system suitability and integration review.</li>
<li>Perform wet chemistry techniques such as pH measurement, titrations, and loss on drying (LOD).</li>
<li>Conduct first-line instrument care, including column maintenance, addressing leaks, and replacing pump seals, while adhering to IQ/OQ/PQ guidelines.</li>
<li>Provide basic troubleshooting and maintenance for laboratory instruments.</li>
<li>Support method validation work focusing on accuracy, precision, and limits of detection (LOD) and quantification (LOQ).</li>
<li>Flexibly support laboratory needs, including inventory management, lab clean-up, and peer review of notebooks.</li>
<li>Draft and review standard operating procedures (SOPs).</li>
</ul>
Essential Skills
<ul>
<li>Master's degree in Chemistry or Analytical Chemistry with 3-5 years of experience in a quality control laboratory, preferably in the food or supplement industry.</li>
<li>Proven ability to operate HPLC and GC independently.</li>
<li>Experience with natural product or lipid-rich matrices, focusing on small molecule testing such as vitamins, fats, emulsifiers, and actives.</li>
<li>Working knowledge of USP/AOAC methods and cGMP documentation.</li>
<li>Proficiency with chromatography software such as OpenLab and ChemStation.</li>
<li>Strong laboratory safety mindset and approach to work.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Chemistry or Analytical Chemistry with 3-5 years of relevant laboratory experience.</li>
<li>wet chemistry, organic chemistry, formulation, and research &amp; development.</li>
</ul>
Work Environment
The position is based in a laboratory environment with a standard work schedule of Monday to Friday, from 8 AM to 5 PM.
Job Type &amp; Location
This is a Contract to Hire position based out of Hadley, Massachusetts.
Pay and Benefits
The pay range for this position is $40.00 - $40.00/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 Hadley,MA.
Application Deadline
This position is anticipated to close on Oct 31, 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.

Bench Chemist - Food

<h3>Job Description</h3>
Job DescriptionJob Title: Biologist Location: Boston, MA Duration: 18 Months+ (Possibilities of Extension) Shift: Standard shift Pay range: $50 - $55/ hr. on W2 Required Experience: 0-3 years Job Description: 
<ul>
<li>We are seeking a highly skilled, passionate, and motivated scientist to join our diabetes team. </li>
</ul>
 Responsibilities:
<ul>
<li>This position will play a key lab-based role in advancing iPSC stem cell engineering at Client and will contribute to the development of the next generation of islet cell therapies. </li>
<li>Successful candidates will have experience with human iPSC cell culture, differentiation, banking, gene editing, molecular biology techniques, and assay development. </li>
<li>This position will report to Director – Islet Cell Therapy, Stem Cell Biology and Cell Engineering.</li>
<li>Enabling and advancing iPSC gene editing, cell line development and evaluation of differentiated cells.</li>
<li>Routine iPSC cell culture, passaging, and media making.</li>
<li>Optimize workflows for iPSC CRISPR based gene-editing, gRNA screening, and delivery.</li>
<li>Optimize and perform assays for on-/off-target analysis via PCR and NGS workflows.</li>
<li>Generate clonal gene edited iPSC lines and characterize via flow cytometry, ddPCR, dPCR and qPCR.</li>
<li>Culture and execute routine directed differentiation of human iPSCs to pancreatic islets performing drug substance assessments such as cell counts, viability, metabolite assessments.</li>
<li>Assist scientists in the team to evaluate and design mitigation strategies to ensure genomic stability of the iPSC lines and drug substance.</li>
<li>Collaborate cross-functionally to support transfer of R&amp;D assays to GMP.</li>
<li>Maintain accurate and detailed records of all experiments, synthesize results, prepare reports, and present in meetings. Contribute to SOP development.</li>
<li>Work seamlessly in executing workplans and meeting deadlines.</li>
</ul>
 Qualification/ Requirements:
<ul>
<li>BS/MS in Stem Cell Biology, Cell Biology, Bioengineering, or a related field of relevant industry experience in gene editing and cell therapy.</li>
<li>3+ years for MS</li>
<li>5+ years for BS</li>
<li>Extensive hands-on experience with human iPSC culture, gene editing, and molecular biology techniques.</li>
<li>Proficiency in gene editing and cell line development, including optimization of protocols, familiarity with flow-based sorting. Hands-on experience with cell delivery methods of gene editing tools.</li>
<li>Excellent communication and interpersonal skills, with the ability to work effectively in a team-oriented environment.</li>
<li>Strong organizational skills and diligent record keeping.</li>
<li>Experience in pancreatic islet directed differentiation is highly desirable</li>
<li>Hands-on experience in transitioning research-grade processes to GMP-grade is highly desirable.</li>
</ul>
 Additional information:
<ul>
<li>Position located in Seaport, Boston MA. This position has mandatory weekend cell culture responsibilities on rotation basis.</li>
</ul>
 #sczr2

Biologist

<h3>Job Description</h3>
Job DescriptionPay: $17.50 per hourJob description:
Now Hiring: Chemical Mixer – Manufacturing Location: Holyoke Ma Schedule: Monday to Friday 8am-4:40pm Pay: $17.50
Are you detail-oriented, safety-conscious, and ready to work in a hands-on manufacturing environment? We’re looking for a Chemical Mixer to join our team and help produce high-quality products in a fast-paced facility!
What You’ll Be Doing:
<ul>
<li>Measure, mix, and blend chemicals according to precise formulas and safety protocols</li>
<li>Operate and maintain mixing equipment and machinery</li>
<li>Follow batch records and production schedules</li>
<li>Perform quality checks and report any inconsistencies</li>
<li>Maintain a clean, safe, and organized work area</li>
</ul>
What We’re Looking For:
<ul>
<li>Experience in chemical mixing or manufacturing preferred</li>
<li>Strong attention to detail and commitment to safety</li>
<li>Ability to read and follow instructions and production documentation</li>
<li>Physically able to lift up to 50lbs and stand for extended periods</li>
<li>Team player with a positive attitude and good communication skills</li>
</ul>

Chemical Mixer

<h3>Job Description</h3>
Job DescriptionJob Title: Bench Chemist
Location: Hadley, MA
Job Type: Contract-to-Hire
Schedule: Monday–Friday, 8:00 AM – 5:00 PM
Overview:
We’re seeking a detail-oriented and experienced Bench Chemist to join our team. This role is ideal for someone with a strong background in analytical chemistry who thrives in a fast-paced lab environment. You’ll be responsible for performing chemical analyses on raw materials, in-process samples, and finished products using advanced instrumentation and wet chemistry techniques.
Key Responsibilities:
<ul>
<li>Perform LC and GC testing on various sample types, including raw materials and finished goods.</li>
<li>Prepare samples, run calibration curves, and conduct system suitability and integration reviews.</li>
<li>Execute wet chemistry procedures such as pH measurement, titrations, and loss on drying (LOD).</li>
<li>Conduct first-line instrument maintenance (e.g., column care, leak checks, pump seal replacement) in compliance with IQ/OQ/PQ standards.</li>
<li>Troubleshoot and maintain lab instruments to ensure optimal performance.</li>
<li>Support method validation efforts, focusing on accuracy, precision, LOD, and LOQ.</li>
<li>Assist with lab operations including inventory, cleanliness, and peer review of lab notebooks.</li>
<li>Draft and review SOPs to support quality and compliance.</li>
</ul>
Qualifications:
<ul>
<li>Master’s degree in Chemistry or Analytical Chemistry with 3–5 years of QC lab experience (food or supplement industry preferred).</li>
<li>Proficient in operating HPLC and GC systems independently.</li>
<li>Experience with small molecule testing in complex matrices (e.g., vitamins, fats, emulsifiers).</li>
<li>Familiarity with USP/AOAC methods and cGMP documentation.</li>
<li>Skilled in chromatography software (OpenLab, ChemStation).</li>
<li>Strong commitment to lab safety and quality standards.</li>
</ul>
Preferred:
<ul>
<li>Bachelor’s degree in Chemistry with equivalent experience.</li>
<li>Background in wet chemistry, organic chemistry, formulation, or R&amp;D.</li>
</ul>
Pay and Benefits
The pay range for this position is $40.00 - $40.00/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 Hadley,MA.
Application Deadline
This position is anticipated to close on Oct 30, 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.

Bench Chemist

<h3>Job Description</h3>
Job Description
Nanobiosym is an innovative company in Cambridge, MA that is developing novel technologies to address a broad range of diseases. Nanobiosym was founded by an MIT/Harvard alum to work at the interface of physics, nanotechnology, and biomedicine. This hypergrowth company allows for unique career opportunities with strong long-term incentives. Nanobiosym is currently seeking top notch candidates to help the company scale up its operations.
 
Nanobiosym is looking for a General Supervisor for its High-Complexity Testing CLIA LAB. The role and requirements are below. The purpose of the Laboratory General Supervisor is to serve as a general supervisor under CLIA 42 CFR 493.1449 regulations for a molecular diagnostics lab. You will assist the Clinical Laboratory Director in day-to-day personnel, workflow, quality control, and equipment management. You are responsible for ensuring that the tests meet all regulatory requirements and coordinating with the laboratory staff to review data for accuracy and issue tests reports in a timely manner. 
 
Job Responsibilities:
<ol>
<li>Provide leadership and directs a team of technologists through positive communication and support </li>
<li>Train new personnel with regard to technical and operational procedures </li>
<li>Ensure all laboratory members are proficient in assay processing including biannual (first year and subsequent annual competency training) </li>
<li>Organize specimens required to be run </li>
<li>Review data for concordant analysis, write-up results, and file data with the assay tested under competency runs </li>
<li>Annually evaluate and document the performance of all testing personnel </li>
<li>Create daily/weekly technologist schedule for molecular diagnostic assays </li>
<li>Setting-up equipment and resources for the laboratory </li>
<li>Monitor examinations to ensure that acceptable levels of analytic performance are maintained and meet TATs </li>
<li>Ensure that all remedial actions are taken whenever test systems deviate from the laboratory's established performance specification </li>
<li>Report quality issues directly to the Clinical Laboratory Director </li>
<li>Track proficiency testing for the validated assay in the laboratory that includes calendar tracking, and following through concordance analysis and finalizing all documents in the database for any future inspections </li>
<li>Maintain all Quality Management System on instrument maintenance programs, i.e. preventative maintenance, cleanliness and maintains records of service in compliance CAP </li>
<li>Maintain and manage daily performance and workload distributed throughout the laboratory </li>
<li>Review issues regarding problem cases with Clinical Laboratory Director to get direction for troubleshooting and next step directions </li>
<li>Work with the lab team to monitor and maintain inventory of supplies, place orders of materials </li>
<li>Participate with Clinical Laboratory Director in managing all governmental and regulatory audits </li>
<li>Mange and monitor Quality Control (QC), Quality Assurance (QA), Safety and Inspection practices to assure compliance with CLIA and MA regulations </li>
<li>Develop, implement and maintain SOPs as per CLIA and MA regulation </li>
<li>Maintain a flexible schedule to meet laboratory goals</li>
</ol>
 
Qualifications:
<ol>
<li>Qualified as a Director for high-complexity testing; </li>
<li>OR Qualified as a Technical Supervisor for high complexity testing; </li>
<li>OR Doctoral degree in clinical laboratory science or chemical, physical or biological science with 1 year training and experience in high-complexity testing; </li>
<li>OR Master's degree in clinical laboratory science, medical technology or chemical, physical or biological science and 1 year training and experience in high-complexity testing; </li>
<li>OR Bachelor's degree in clinical laboratory science, medical technology or chemical, physical or biological science and 1 year training and experience in high-complexity testing;</li>
<li>OR Associate degree in medical laboratory technology (or pulmonary function) and 2 years laboratory (or blood gas analysis) training or experience, or both, in high complexity testing Refer to the CLIA regulation 42CFR493.1461 for additional qualifications </li>
</ol>
 Job Posted by ApplicantPro

General Supervisor for High Complexity CLIA LAB

<h3>Job Description</h3>
Job Description
At Curaleaf, we're redefining the cannabis industry with a strong commitment to quality, expertise, and innovation. As a leading global cannabis provider, our brands—including Curaleaf, Select, and Grassroots—offer premium products and services in both medical and adult-use markets.
Join us at Curaleaf to be part of a high-growth, purpose-driven company that champions corporate social responsibility through our Rooted in Good initiative, supporting community outreach and positive change. Here, you'll have the opportunity to make a meaningful impact, drive innovation, and help shape the future of cannabis.
Lab Processing Supervisor- 2nd Shift
Job Type: Full Time, Exempt Shifts: 3:30pm-11:30pm M-F Salary Range: 57k - 69k + bonus Location: Webster, MA
POSITION SUMMARY:
The Processing Lab Supervisor will supervise and optimize all the tasks in the Post Processing Lab and will assist the Lab Manager and Manufacturing team by maintaining quality control measures in the extraction and purification processes and thereby ensuring the delivery of high-quality product. This Supervisor carries out day-to-day tasks including prepping for distillation runs, formulations, and Ethanol extractions, and maintaining paperwork using good documentation practices. The Laboratory Supervisor will be a hands-on working supervisor responsible for extraction team training and schedule coordination between early and late overlapping shifts.  
ESSENTIAL DUTIES AND RESPONSIBILITIES:
<ul>
<li>Directly supervises the Post Processing staff and accomplishes department results by communicating job expectations; weekly and monthly planning; monitoring, and appraising job results; coaching, counseling, and disciplining employees; initiating, coordinating, and enforcing systems, policies, and procedures. </li>
</ul>
<ul>
<li>This position and all output metrics report directly to the Lab Manager. These reports will include all daily production metrics, establishing actual vs. expected production results with explanations of variances, staff absences and all associated production paperwork. </li>
</ul>
<ul>
<li>Shows the capability to effectively communicate with management and co-workers on a professional basis. This will include all team members, leads, supervisors, and upper management. </li>
</ul>
<ul>
<li>Preparing for efficient production by reviewing the manufacturing schedule; studying and clarifying specifications; calculating batch requirements; assembling and weighing plant materials and supplies for extractions, distillations and formulations. </li>
</ul>
<ul>
<li>Ensure proper scheduling of Post Processing team, accounting for PTO and call offs when applicable. </li>
</ul>
<ul>
<li>Performing all training required for Post Processing team, including maintaining all required documentation. </li>
</ul>
<ul>
<li>Operating highly sophisticated extraction and processing equipment; Processing concentrate, extracts and formulated products. </li>
</ul>
<ul>
<li>Cleaning and maintaining lab equipment and laboratory facility following current good manufacturing practices (cGMP), and standard operating procedures; complying with legal regulations. </li>
</ul>
<ul>
<li>Operating, maintaining, adjusting, trouble shooting, and repairing laboratory equipment such as extractors, heaters, chillers, vacuum pumps, balances, centrifuges, distillation units and other laboratory equipment. </li>
</ul>
<ul>
<li>Operating extraction equipment to extract crude oil utilizing Ethanol as a solvent in a C1D2 environment. </li>
</ul>
<ul>
<li>Operating highly sophisticated purification equipment to convert crude oil into decarboxylated oil. </li>
</ul>
<ul>
<li>Following procedures for extract purification, including ethanol addition, winterization, filtration, rotary evaporation, decarboxylation and distillation. </li>
</ul>
<ul>
<li>Assisting with the development of further purification processes and in-process materials, including processes for new products. </li>
</ul>
<ul>
<li>Maintaining inventory records of supplies, materials, equipment PMs as required, and preparing requisitions as needed. </li>
</ul>
<ul>
<li>Maintaining strict inventory within state-issued cannabis inventory software, MJ Freeway, via regular cycle counts of WIP inventory. </li>
</ul>
<ul>
<li>Storing supplies and equipment, disposing of waste according to state guidelines, and keeping laboratory, storerooms and working areas organized. </li>
</ul>
<ul>
<li>Performing clerical work related to laboratory activities such as word processing, record keeping, data logging and filing. </li>
</ul>
<ul>
<li>Maintaining material safety data sheets for all department chemicals and products. </li>
</ul>
<ul>
<li>Performing related duties as assigned </li>
</ul>
<ul>
<li>Perform other duties as assigned. </li>
</ul>
Supervisory Responsibilities: 
This position directly supervises the work activities of others and makes recommendations concerning selection, termination, performance appraisal, and professional development 
QUALIFICATIONS:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. 
Minimum Qualifications: 
<ul>
<li>BS/BA Degree or greater in Chemistry, Bio-Chemistry or similar. </li>
</ul>
<ul>
<li>Minimum of 2 years' experience in a lab or manufacturing setting. </li>
</ul>
<ul>
<li>Minimum of 2 years' experience leading and managing a team. </li>
</ul>
<ul>
<li>Experience with scientific writing for processes, training, and procedures that require documentation </li>
</ul>
<ul>
<li>Knowledge of and hands-on experience with Ethanol Extraction, Winterization &amp; Filtration, Rotary Evaporation, Distillations and Product Formulations. </li>
</ul>
<ul>
<li>Ability to draft weekly and monthly schedule for department processes, as well as establish daily metrics for each process on a week by week basis. </li>
</ul>
<ul>
<li>Ability to Follow health and safety practices and precautions applicable to an extraction laboratory </li>
</ul>
<ul>
<li>Experience with proper and safe handling and disposal of harmful chemicals, substances, and hazardous wastes </li>
</ul>
<ul>
<li>Experience with computer systems, software, and hardware common to laboratories </li>
</ul>
<ul>
<li>Experience with record keeping procedures, as well as regular audits of team's production sheets to ensure accuracy and completeness. </li>
</ul>
Preferred Qualifications: 
<ul>
<li>1-year experience in the cannabis industry preferred </li>
</ul>
<ul>
<li>QA/QC experience with HPLC and GC analysis preferred but not required. </li>
</ul>
Physical Requirements: 
<ul>
<li>Must be able to stand for prolonged periods of time, along with frequent bending </li>
<li>Close vision (unobstructed vision at 20 inches or less) </li>
<li>Manual dexterity sufficient to reach/handle items, work with fingers </li>
<li>Ability to lift to 50 pounds and push up to 100 pounds with assistance </li>
</ul>
Massachusetts Hiring Range$57,000—$69,000 USD
What We Offer:
<ul>
<li>Career Growth Opportunities</li>
<li>Competitive Pay and Benefits</li>
<li>Generous PTO and Parental Leave</li>
<li>401(K) Retirement Plan</li>
<li>Life/ Disability Insurance</li>
<li>Community Involvement</li>
<li>Referral Bonuses and Product Discounts</li>
</ul>
Benefits vary by state, role type, and eligibility. 
Follow us on Social Media: Instagram: @curaleaf.usa Twitter: @Curaleaf_Inc LinkedIn: Curaleaf LinkedIn
Curaleaf Holdings, Inc. (TSX: CURA) (OTCQX: CURLF) ("Curaleaf") is a leading international provider of consumer products in cannabis with a mission to enhance lives by cultivating, sharing, and celebrating the power of the plant. As a high-growth cannabis company known for quality, expertise and reliability, the Company, and its brands, including Curaleaf, Select, Grassroots, JAMS, Find and Zero Proof provide industry-leading service, product selection and accessibility across the medical and adult-use markets. Curaleaf International is the largest vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence
Our Vision: To be the world's leading cannabis company by consistently delivering superior products and services and driving the global acceptance of cannabis. 
Our Values:
<ul>
<li>Lead and Inspire. </li>
<li>Commit to Win. </li>
<li>ONE Curaleaf. </li>
<li>Driven to Deliver Excellence. </li>
</ul>
Curaleaf is an equal opportunity employer. Curaleaf recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, gender identity, sexual orientation, physical ability, age, veteran status, and other protected status as required by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Individuals adversely impacted by the war on drugs are encouraged to apply.
Current Curaleaf employees should apply for open positions through our Internal Job Board, which can be accessed via the link on The Leaf.

Lab Processing Supervisor

<h3>Job Description</h3>
Job DescriptionOur mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We're developing a mammalian synthetic biology platform––from cells to software––to enable the design and manufacture of next-generation therapeutics. We are searching for a Senior Computational Biologist with multi-disciplinary skills in computational biology, machine learning, and applied mathematics to join our team. This role bridges the gap between sequence-level design and systems-level dynamics, focusing on the development and application of sophisticated models that integrate diverse biological data. The ideal candidate will be adept at building data-driven, mechanistic, and hybrid models to decipher complex biological processes and guide the engineering of therapeutic molecules and systems. You will leverage everything from high-dimensional omics datasets to time-course bioprocess data to create predictive models that drive genetic design and optimize bioprocess development. Join our team to contribute at the cutting-edge of innovation in biology and computational science, shaping the future of therapeutic innovation. About the Role:
<ul>
<li>Design and implement sophisticated models—including data-driven (ML/AI), mechanistic (e.g., ODE-based), and hybrid approaches—to predict and optimize the performance of biologics and vector manufacturing processes.</li>
<li>Develop models that predict functional outcomes such as transgene expressibility, protein stability, and product quality attributes from nucleic acid and amino acid sequence features</li>
<li>Develop new models to predict developability attributes such as expressibility, secretability, aggregation, and stability of biologics, from sequence.</li>
<li>Create multi-scale models of cellular behavior, integrating omics data (RNA-seq, proteomics, etc.) to simulate gene expression, protein secretion dynamics, metabolism, and cell phenotype.</li>
<li>Work in close collaboration with bench scientists to guide rational experimental design, using techniques like Bayesian Optimization to ensure that data generation is maximally informative for modeling and yields actionable insights.</li>
<li>Contribute to our long-term computational strategy by exploring novel algorithms, modeling frameworks, and data integration techniques to solve critical challenges in synthetic biology and therapeutic development.</li>
</ul>
About You:
<ul>
<li>You have a Ph.D. in Bioengineering, Computational Biology, Computer Science, Applied Mathematics, or a related quantitative field.</li>
<li>You are proficient in sequence-based analysis and have hands-on experience integrating large-scale omics datasets (e.g., NGS, RNA-seq, proteomics) to inform model development and validation.</li>
<li>You are an expert in applying machine learning and advanced mathematical techniques (e.g., dynamical systems, differential equations, stochastic modeling) to biological systems, with at least 3 years of experience in a pharmaceutical or biotechnology industry setting.</li>
<li>You have a strong background in modeling dynamic biological systems, such as gene regulatory networks, metabolic pathways, or cell population dynamics.</li>
<li>You are a skilled programmer, fluent in Python and associated scientific computing/ML libraries.</li>
<li>You excel at communicating complex scientific and mathematical concepts effectively to colleagues with diverse backgrounds and expertise.</li>
<li>You are a collaborative, impact-driven scientist, passionate about working in a fast-paced, research-focused environment to engineer biology.</li>
</ul>
We're fueled by a vision to transform biological engineering into a fully-fledged engineering discipline. Should you join our team, you will grow with a constantly evolving organization and push the frontiers of synthetic biology. Company culture is key to Asimov, and ours is a culture of recombination; we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives.

Senior Computational Biologist

<h3>Job Description</h3>
Job Descriptionjob summary: 
This role as a Quality Control Associate I, Microbiology in Norwood, MA, is a fantastic opportunity for a detail-oriented individual with a STEM degree and 6 months to 2 years of GMP QC microbiology experience.
You will be the key player in Environmental Monitoring (EM) and Critical Utilities sampling (WFI, Compressed Gas), ensuring the cleanroom environment is compliant. The position requires strong hands-on skills with equipment like particle counters and viable air samplers, combined with the ability to manage data using LIMS and other electronic databases. If you are proficient in GMP, microbiology, and aseptic techniques, and are ready to apply your troubleshooting skills to support critical quality systems, this contract role offers vital experience in a regulated setting.
Shifts: 
1 st Shift: Wednesday through Saturday, 7am-5pm
2 nd Shift: Wednesday through Saturday, 10am-8pm
2 nd Shift: Sunday through Wednesday, 10am-8pm
 location: Norwood, Massachusetts job type: Contract salary: $30 - 37 per hour work hours: 11 to 7 education: Bachelors responsibilities: 
<ul>
<li>Conduct Environmental Monitoring (Routine, In-Process, and EMPQ's), WFI Sampling, and Compressed Gas Sampling.</li>
<li>Maintain lab equipment and perform housekeeping tasks.</li>
<li>Write, revise, and follow SOPs, protocols, and reports.</li>
<li>Ensure data entry, review, and trending are performed using LIMS.</li>
<li>Collaborate with internal and external labs for sample coordination and testing.</li>
<li>Troubleshoot equipment and test methods.</li>
<li>Support quality systems records such as deviations, change controls, and CAPAs.</li>
<li>Participate in audits and continuous improvement initiatives.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>STEM degree with 6 months - 2 years of experience in a GMP QC laboratory setting, focusing on microbiology.</li>
<li>Hands-on experience with particle counters, viable air samplers, and gas equipment. </li>
<li>Proficiency with Microsoft Office Programs and electronic databases (LIMS, SAP, eQMS).</li>
<li>Excellent troubleshooting skills and the ability to communicate scientific issues clearly.</li>
<li>Knowledge of GMP, microbiology, aseptic techniques, and general laboratory instrumentation.</li>
<li>Familiarity with relevant FDA, EU, ICH guidelines, and regulations.</li>
</ul>
#LI-KH1
 skills: Quality control, SOP, FDA, MS-WORD, MS-EXCEL, Microbiology, ICH Regulations, GMP (Good Manufacturing Practice), Environmental Sampling, LIMS (Laboratory Information Management System 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. 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.

QC Microbiology Associate I

<h3>Job Description</h3>
Job Description
LICENSED WILDLIFE SERVICE SPECIALISTS WANTED!
Are you looking to grow your career and earn more than your competition? Dynamic go getters are not only appreciated here, they enjoy amazing work/life balance and award-winning culture. If its time for a change, look no further than Ultra Safe Pest Management, the Boston areas premier pest and wildlife company.Our Industry has evolved quite a bit in recent years. In the past, technicians were primarily focused on pesticide applications. In today’s Pest Industry and especially here at Ultra Safe, pesticide application has become a much smaller part of the pest control process. A more complete and comprehensive integrated approach (IPM) is the preferred method of control.Our service concepts are focused around a “complete” plan of action with the goal of long-term results. This type of work requires the use of specialized equipment, materials and dynamic service methods. The work here is more exciting and rewarding compared to most pest and wildlife control jobs.Job Type: Full-timePay:
$85,000.00 - $100,000.00 per year
Benefits:
<ul>
<li>401(k)</li>
<li>401(k) matching</li>
<li>Dental insurance</li>
<li>Employee discount</li>
<li>Flexible schedule</li>
<li>Health insurance</li>
<li>Life insurance</li>
<li>Paid time off</li>
<li>Professional development assistance</li>
<li>Referral program</li>
<li>Vision insurance</li>
</ul>
Schedule:
<ul>
<li>10 hour shift</li>
<li>Day shift</li>
<li>Monday to Friday</li>
<li>Overtime</li>
<li>Weekend availability</li>
</ul>
Supplemental Pay:
<ul>
<li>Bonus pay</li>
<li>Commission pay</li>
</ul>
License/Certification:
<ul>
<li>MA Driver's License (Required)</li>
<li>MDAR Pest Applicator License (Preffered)</li>
<li>Mass Wildlife PAC Permit/License (Required)</li>
</ul>
Job Type: Full-time
Company DescriptionUltrasafe is a division of Ned’s Home and at Ned's Home, we value your skills, reward your hard work, and invest in your future. We're proud to be recognized as a USA Today Top Workplace for 2025! This award is based on our employee feedback and recognizes outstanding workplace culture. 
<h3>Company Description</h3>
Ultrasafe is a division of Ned’s Home and at Ned's Home, we value your skills, reward your hard work, and invest in your future. We're proud to be recognized as a USA Today Top Workplace for 2025! This award is based on our employee feedback and recognizes outstanding workplace culture.

Wildlife Technician

<h3>Job Description</h3>
Job Description
The Senior Food Scientist role will lead the development and improvement of nutritional beverages and powders from concept to commercialization, driving innovation that ensures exceptional quality, stability, and clinical impact.
Responsibilities
<ul>
<li>Develop and optimize nutritional beverage and powder formulations that meet nutritional, sensory, and stability goals.</li>
<li>Partner with Medical Nutrition, Marketing, and Sales to align product design with business and patient needs.</li>
<li>Research and evaluate new ingredients and explore new medical nutrition opportunities.</li>
<li>Support leadership with technical and scientific expertise for product and clinical development.</li>
<li>Build vendor relationships to source ingredients that meet product requirements.</li>
<li>Present company research at scientific meetings and conferences.</li>
<li>Ensure strong intellectual property protection for new products and processes.</li>
<li>Follow all GMP, food safety, and workplace safety policies.</li>
</ul>
Requirements
MUST HAVES:
<ul>
<li>Bachelor’s degree in Food Science, Nutrition, or related field (Master’s preferred; PhD or PharmD a plus).</li>
<li>5+ years of product development experience from concept to commercialization in nutrition, food, beverage, supplement, nutraceutical, or biotech industries.</li>
<li>Previous experience in basic and applied research and development preferably in small/mid-sized nutrition, food, beverage and/or biotech company.</li>
<li>Strong background in food science, ingredient interactions, and process impact on nutrient stability.</li>
<li>Knowledge of food safety standards and aseptic processing</li>
</ul>
Benefits
<ul>
<li>Competitive salary and performance-based bonus (12.5%) program</li>
<li>Comprehensive health, dental, and vision insurance</li>
<li>Paid time off and holidays</li>
<li>401(k) with company match</li>
<li>Opportunities for professional growth and advancement</li>
<li>Employee discount programs</li>
</ul>

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