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<h3>Job Description</h3>
Job Description
Our 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 seeking a Scientist I/II, Viral Vector Process Development to join our team in Boston, MA and help push the boundaries of gene therapy process development. This role is for a technical expert who will conduct lentiviral (LV Edge) and adeno-associated viral (AAV Edge) vector-based process engineering for gene therapies, design complex experimental approaches to improve our workflows and systems, and coordinate project efforts. While primarily focused on viral vector process engineering, there is a high degree of cross-functionality within the Process Development group that will also include working on biologics processes (CHO Edge).
The successful candidate will work closely with Asimov’s Synthetic Biology and Cell Line Development teams, as well as interfacing with external partners. This role reports to the Head of Process Development and is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the future of biological engineering.
About the Role:
<ul>
<li>
Be involved in projects that include media/feed optimization, bioreactor process development, process scale-up and characterization at Ambr15, Ambr250, and benchtop scale, along with analytical assay development focused primarily on LV/AAV, with overlap into biologics.
</li>
<li>
Work together with the Commercial team to technology transfer developed upstream processes to external partners.
</li>
<li>
Create and optimize throughput and robustness of workflows for cell line characterization (transient/stable), small scale screening assays, and product quality assessment.
</li>
<li>
Collaborate with our internal process modeling team to test hypotheses for developing robust predictive models using DOE approaches, machine learning algorithms, and multi-omics analysis.
</li>
<li>
Author, review, and approve process development reports and technology transfer protocols.
</li>
<li>
Support clarifications, downstream processing/purification, and product quality assessment with analytical tools.
</li>
<li>
Represent the process development team on cross-functional projects, making decisions for process development activities and effectively communicating results, progress and plans.
</li>
</ul>
About You:
<ul>
<li>
You have a Bachelors in Biological Engineering, Chemical Engineering, Cell Biology, Molecular Biology, or a related field with 6-8 years of hands-on industry experience performing viral vector process development in support of gene therapies; alternatively, a MS with 3-4 years or PhD with 0-2 years of this type of experience.
</li>
<li>
You’re a creative problem solver and get excited about the opportunity to drive the creation of industry-disruptive technology.
</li>
<li>
HEK293-based viral vector process development is squarely in your wheelhouse. Additional CHO-based experience is not required but preferable.
</li>
<li>
You have experience with Ambr15, Ambr250, and/or benchtop scale viral vector bioreactor processes. Analytical development and downstream purification experience is also highly preferable.
</li>
<li>
Being detail-oriented isn’t just a sound bite for you, it’s part of your DNA. Keeping track of a bunch of moving parts is easy for you because you’re highly organized. It’s not your first time following a standardized workflow or pipeline.
</li>
<li>
Experience in the technology transfer of manufacturing processes and CMC filing in the pharmaceutical industry is desirable.
</li>
<li>
You are an expert in spreadsheets such as Google Sheets or Excel and ideally Spotfire, Google Apps Script (JavaScript) and/or BigQuery to facilitate data management and analysis.
</li>
<li>
Experienced with using DOE software to develop robust experiments. Familiarity with implementing algorithm-based design approaches is a plus.
</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.
Compensation Range: $120K - $130K

Scientist, Viral Vector Process Development

<h3>Job Description</h3>
Job Description
Our 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.
Compensation Range: $150K - $175K

Senior Computational Biologist

<h3>Job Description</h3>
Job Description
Our 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 seeking a Scientist, Biologics Cell Line Development to join our team in Boston, MA and help push the boundaries of biotherapeutic cell line development. This role is for a technical expert who will conduct CHO-based cell line engineering for biologic therapeutics, design complex experimental approaches to improve our workflows and systems, coordinate project efforts, and mentor junior scientists.&nbsp;
 
The successful candidate will also work closely with Asimov’s synthetic biology and process development teams.&nbsp; This is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the future of biological engineering.
About the Role: 
<ul>
<li>
You’ll perform CHO cell line development processes including transfection, cloning, characterization, and cell banking using state-of-the-art equipment.
</li>
<li>
You’ll drive innovation through the development of novel cell line development workflows and applications.
</li>
<li>
You’ll identify emerging practices for biologics cell line development and manufacturing to shape scientific strategies and develop improved workflows.
</li>
<li>
You’ll represent the cell line development team on cross-functional projects, making decisions for cell line activities and effectively communicating results, progress and plans.
</li>
</ul>
About You: 
<ul>
<li>
You have a Ph.D. in Biological Engineering, Cell Biology, Molecular Biology, or a related field with &lt;3yrs experience after graduation.
</li>
<li>
Your training has provided you with a depth of knowledge in areas of biology relevant to how mammalian cells regulate transcription, translation, protein folding &amp; assembly, intracellular trafficking and/or secretion.
</li>
<li>
You have an interest in genetically engineering cells to support clinical development of human therapeutics.
</li>
<li>
You have established yourself as an emerging innovator and are interested in applying your knowledge and curiosity to work collaboratively and cross functionally to develop enhanced platforms for production of therapeutic proteins.
</li>
<li>
You’re a creative problem solver and get excited about the opportunity to drive the creation of industry-disruptive technology.
</li>
<li>
You are an expert in spreadsheets such as Google Sheets or Excel and ideally Spotfire, Google Apps Script (JavaScript) and/or BigQuery to facilitate data management and analysis.
</li>
<li>
You are experienced with electronic lab notebooks (Benchling) and document your experiment meticulously.
</li>
<li>
Prior experience genetically engineering CHO cells to express mAbs &amp; bsAbs is desirable but not required.
</li>
<li>
Don’t let this stop you from applying, but it’s also a plus if you are familiar with cell culture liquid handling automation, ambr bioreactors, and/or ddPCR.
</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.
Compensation Range: $120K - $130K

Scientist, Biologics Cell Line Development

<h3>Job Description</h3>
We are seeking a highly skilled, passionate, and motivated scientist to join our diabetes research team. This position will play a key lab-based role in advancing iPSC stem cell engineering and contribute to the development of the next generation of islet cell therapies.
Responsibilities:
<ul>
<li>Enable and advance iPSC gene editing, cell line development, and evaluation of differentiated cells.</li>
<li>Perform routine iPSC cell culture, passaging, and media preparation.</li>
<li>Optimize workflows for iPSC CRISPR-based gene editing, gRNA screening, and delivery.</li>
<li>Develop and perform assays for on-/off-target analysis using PCR and NGS workflows.</li>
<li>Generate clonal gene-edited iPSC lines and characterize them via flow cytometry, ddPCR, dPCR, and qPCR.</li>
<li>Culture and execute routine directed differentiation of human iPSCs to pancreatic islets, performing assessments such as cell counts, viability, and metabolite analysis.</li>
<li>Assist scientists in evaluating and designing mitigation strategies to ensure genomic stability of iPSC lines and drug substances.</li>
<li>Collaborate cross-functionally to support the transfer of R&amp;D assays to GMP environments.</li>
<li>Maintain accurate and detailed experimental records, synthesize results, prepare reports, and present findings in meetings.</li>
<li>Contribute to the development and refinement of SOPs.</li>
<li>Execute work plans efficiently and meet established deadlines.</li>
</ul>
Qualifications:
<ul>
<li>BS or MS in Stem Cell Biology, Cell Biology, Bioengineering, or a related field.</li>
<li>3+ years of relevant industry experience for MS candidates, or 5+ years for BS candidates.</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 protocol optimization and flow-based sorting.</li>
<li>Hands-on experience with delivery methods for gene editing tools.</li>
<li>Strong communication and interpersonal skills, with the ability to work effectively in a collaborative team environment.</li>
<li>Excellent organizational skills and attention to detail in record keeping.</li>
<li>Experience in pancreatic islet directed differentiation is highly desirable.</li>
<li>Experience in transitioning research-grade processes to GMP-grade is highly desirable.</li>
</ul>

Biologist

<h3>Job Description</h3>
Job Description
Description
• Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP • Conduct routine testing or other analysis in a specific group or department setting. • Conduct advanced testing and/or critical testing, as required. • Operate specialized equipment or conduct specialized skill testing • Working knowledge of raw materials testing and release • Lead investigation activities. • Ensure compliance to all data integrity and cGMP practices, procedures, and expect • Ensure compliance with all good documentation practices. • Other duties and responsibilities as assigned by the Head of the Department or Section Head
 
Skills
Hplc, Gmp, Karl Fisher, Particle size, icp, gc-ms, quality control, raw material, data entry, Wet chemistry, Analytical chemistry
 
Top Skills Details
Hplc,Gmp,Karl Fisher,Particle size,icp,gc-ms,quality control
 
Additional Skills &amp; Qualifications
Frist Shift- General Shift: 8:30AM – 5:00PM Monday -Friday Level II Pay Rate- $5,000K-$82,500K Level III-$83,000-$90,000 They’re hiring across levels (QC Chemist II &amp; III). QC Chemist II should be between 2-3 years’ experience in industry. Co-op experience in a cGMP pharmaceutical manufacturing setting is also acceptable especially for a level I. QC Chemist III should be at least 3-5 industry experience not academic experience. I’d prefer to focus on the Level II based on our previous experience with the hiring team and the level of expertise they desire. • Bachelor's degree (BS or BA), physical sciences required • Master's degree preferred • Minimum of 3-5+ years' experience. • Proficiently speak English as a first or second language • Proficiently communicate and understand (read and write) scientific work in English • Have excellent organization, learning and teaching skills required to work in teams • Ability to understand and analyze complex data sets.
 
Experience Level
Intermediate Level
Job Type &amp; Location
This is a Permanent position based out of Fall River, MA.
Pay and Benefits
The pay range for this position is $65000.00 - $90000.00/yr.
Health Vision Dental 401K
Workplace Type
This is a fully onsite position in Fall River,MA.
Application Deadline
This position is anticipated to close on Nov 24, 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.

Quality Control Chemist II, III

<h3>Job Description</h3>
Job Description
Description
• Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP • Conduct routine testing or other analysis in a specific group or department setting. • Conduct advanced testing and/or critical testing, as required. • Operate specialized equipment or conduct specialized skill testing • Working knowledge of raw materials testing and release • Lead investigation activities. • Ensure compliance to all data integrity and cGMP practices, procedures, and expect • Ensure compliance with all good documentation practices. • Other duties and responsibilities as assigned by the Head of the Department or Section Head
 
Skills
Hplc, Gmp, Karl Fisher, Particle size, icp, gc-ms, quality control, raw material, data entry, Wet chemistry, Analytical chemistry
 
Top Skills Details
Hplc,Gmp,Karl Fisher,Particle size,icp,gc-ms,quality control
 
Additional Skills &amp; Qualifications
Frist Shift- General Shift: 8:30AM – 5:00PM Monday -Friday Level II Pay Rate- $5,000K-$82,500K Level III-$83,000-$90,000 They’re hiring across levels (QC Chemist II &amp; III). QC Chemist II should be between 2-3 years’ experience in industry. Co-op experience in a cGMP pharmaceutical manufacturing setting is also acceptable especially for a level I. QC Chemist III should be at least 3-5 industry experience not academic experience. I’d prefer to focus on the Level II based on our previous experience with the hiring team and the level of expertise they desire. • Bachelor's degree (BS or BA), physical sciences required • Master's degree preferred • Minimum of 3-5+ years' experience. • Proficiently speak English as a first or second language • Proficiently communicate and understand (read and write) scientific work in English • Have excellent organization, learning and teaching skills required to work in teams • Ability to understand and analyze complex data sets.
 
Experience Level
Intermediate Level
Job Type &amp; Location
This is a Permanent position based out of Fall River, MA.
Pay and Benefits
The pay range for this position is $65000.00 - $90000.00/yr.
Health Vision Dental 401K
Workplace Type
This is a fully onsite position in Fall River,MA.
Application Deadline
This position is anticipated to close on Nov 27, 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
Fully onsite 8-5. Cambridge site. Must be able to commute to site. Open to relocation candidates but must be willing to start ASAP. Must have: HPLC expertise and hands on lab experience. M.S. and 1 YOE would be ideal. B.S. and 3 YOE would be acceptable but a M.S is preferred. Managers ideal candidate: Someone who has a couple of years experience in biopharma working on bioanalytical assays such as SEC HPLC, Ion Exchange HPLC, and some basic assays like pH, osmolality, protein concentration etc. Good communication skills are also a must as they will work with a big group of people. Job Details: 1+ Years w/ Relevant MS OR equivalent 3+ Years w/ Relevant BS To perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. Responsibilities include: 1 Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision, 2 Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of data, 3 Effectively transfers experimental methods from literature to the lab and makes modifications as necessary, 4 Develops and implements new protocols with moderate review, 5 Works efficiently in a matrix team environment and collaborates with coworkers, 6 Communicates data and interpretation to work group, 7 Skilled at developing systems to ensure quality data, 8 Skilled and/or knowledgeable in the use of standard laboratory equipment and with one or more major laboratory instruments/techniques (HPLC, CE, physical property testing...), 9 Effectively trouble-shoots equipment and experimental difficulties, 10 Contributes to internal/external reports, papers, presentations, regulatory documents, invention disclosure submissions and/or patents, 11 Participates in department-wide support efforts such as safety, recruiting and committees, 12 May train staff and/or supervise others, 13 Coordinates and organizes resources needed to complete the task, 14 Understands when to seek input and when to make independent judgments. Requirements: Minimum BS degree (MS is preferred) in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences, Biology or related discipline and at least 2 year experience in a Biopharmaceutical working environment.
Top 3 Must Have Skill Sets:
BioPharma lab experience is a plus HPLC expertise - able to operate, process data, and report findings into electronic lab notebook. Good organizational skills - must be able to handle multiple tasks and communicate to different teams effectively and efficiently. Experience working in a biopharmaceutical lab showing analytical skills (compendial assays such as pH, osmolality, protein concentration, particle sizing etc).

Associate Scientist-HPLC (SEC/ Ion Exchange)

<h3>Job Description</h3>
Job Description
At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases. 
Why Choose Editas?
At Editas Medicine, we’re a team of passionate problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what’s possible in medicine, come join us and become an Editor!
Decoding The Role:
Editas is seeking a highly motivated Associate Scientist to join our Genomics &amp; Bioinformatics Group. In this role, you will use various CRISPR delivery systems to execute high-throughput screens to identify lead guides across our internal programs. You will be responsible for experimental design, analysis, and summarizing screens. In addition to screening efforts, you will be responsible for inventory and distribution of reagents within Sample Management. 
An ideal candidate has extensive experience handling and troubleshooting primary cells (HSC, T cells, Hepatocytes) and has experience screening in these cell types using various CRISPR delivery systems, including RNP and LNPs. The candidate should have a strong track record of creative thinking, strong drive, and the ability to be nimble while supporting multiple programs at a given time. Familiarity with liquid handling robots, such as the Biomek I7, and acoustic liquid transfers, like the Echo, is a plus. 
The position requires working effectively in a multi-disciplinary team, excellent written and verbal communication skills, and a capacity for creativity and innovation to efficiently execute screens that support the company achieve corporate objectives.
Requirements
Characterizing Your Impact:
As the Associate Scientist, Genomics and Bioinformatics you will:
<ul>
<li>Contribute to experimental design, execute screens, with editing and/or functional assays as readouts for internal programs. </li>
</ul>
<ul>
<li>Analyze and summarize screening results into proper documentation (ELN, Study Reports) and presentation slides.</li>
<li>Assist with Sample Management Support. </li>
</ul>
The Ideal Transcript:
To thrive in this role, you’ll need:
Minimum Qualifications 
<ul>
<li>B.S. in cell biology, or related field with 5+ years of relevant experience in industry; or M.S. in cell or molecular biology with 3+ years of relevant experience in industry</li>
<li>Independently design and run screening experiments, extract gDNA, submit for sequencing, analyze, and present data</li>
<li>Extensive experience handling primary cell lines. Proficient in performing cell-based assay development. Demonstrated ability to handle multiple cell lines simultaneously. </li>
<li>Proficient in multi-color flow cytometry, including design and data analysis using FlowJo.</li>
<li>Experience working with different screening modalities such as guide RNAs and LNPs.</li>
<li>Demonstrated ability to formulate both RNP and LNPs</li>
<li>Capable of independently using data analysis software such as PRISM, Tableau</li>
<li>Desire to learn new techniques and share expertise with colleagues</li>
<li>Self-motivated, detail-oriented problem solver with strong troubleshooting skills</li>
<li>Outstanding organizational skills and ability to multi-task in a fast-paced environment</li>
<li>Excellent communication and interpersonal skills fostering effective teamwork</li>
</ul>
Fundamentals That Set You Apart
Preferred Qualifications
<ul>
<li>Proficient in executing and analyzing functional assays including ELISAs and western blots</li>
<li>Familiar in molecular biology analyses such as qPCR and ddPCR</li>
<li>Prior experience operating lab automation including both liquid handling robots (Biomek I7s, Mantis, Echo) and plate readers (Envision). Bonus if prior experience writing methods on liquid handling robots. </li>
</ul>
Benefits
Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Stock Purchase Plan, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy.
Salary Range: 
$105,000 - $118,000
Pay Transparency
Editas Medicine is committed to transparency and accuracy in our hiring practices. The anticipated salary range for each position is posted within the role. The final salary offer will be determined based on a comprehensive assessment of the candidate's qualifications, including education, training, and relevant experience. Additional factors such as external market conditions, the role's criticality, and internal equity will also be considered. Editas Medicine's compensation philosophy ensures fair and equitable pay practices.
Aspire to be an Editor? We invite you to apply and join us at the forefront of innovation and be a key contributor to realizing Editas Medicine's mission of developing transformative medicines for people living with serious diseases.

Associate Scientist, Genomics and Bioinformatics

<h3>Job Description</h3>
Job Description
Position: QC Chemist II / III
Location: Fall River, MA
Type: Direct Placement | First Shift (Monday–Friday, 8:30 AM – 5:00 PM)
A growing pharmaceutical manufacturer in Fall River, MA is seeking experienced Quality Control Chemists to join their team. This is a direct placement opportunity offering competitive compensation and the chance to work in a GMP-regulated environment. The ideal candidate will have hands-on experience with analytical instrumentation and raw material testing, and a strong understanding of cGMP and data integrity practices.
Key Responsibilities
<ul>
<li>Perform routine and advanced analytical testing using instruments such as HPLC, GC, Karl Fischer, ICP, and particle size analyzers.</li>
<li>Conduct raw material testing and release activities in compliance with regulatory standards.</li>
<li>Operate specialized lab equipment and perform wet chemistry techniques.</li>
<li>Lead and support investigation activities related to lab deviations or quality events.</li>
<li>Ensure strict adherence to cGMP, data integrity, and good documentation practices.</li>
<li>Collaborate with team members and department leadership to meet testing timelines and quality standards.</li>
<li>Perform other duties as assigned by department leadership.</li>
</ul>
Required Skills &amp; Qualifications
<ul>
<li>Bachelor’s degree in Physical Sciences (Chemistry, Biology, or related field); Master’s degree preferred.</li>
<li>2–5+ years of industry experience in a GMP pharmaceutical or biotech setting (co-op experience may be considered for entry-level).</li>
<li>Proficiency with analytical instruments including HPLC, GC-MS, Karl Fischer, ICP, and particle size analysis.</li>
<li>Strong understanding of GMP regulations and quality control procedures.</li>
<li>Excellent organizational, communication, and data analysis skills.</li>
<li>Ability to read, write, and communicate scientific information in English.</li>
<li>Comfortable working independently and collaboratively in a fast-paced lab environment.</li>
</ul>
Preferred Qualifications
<ul>
<li>Experience leading investigations or contributing to CAPA activities.</li>
<li>Familiarity with raw material release processes and documentation systems.</li>
<li>Strong attention to detail and ability to manage multiple priorities.</li>
</ul>
If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com 
Job Type &amp; Location
This is a Permanent position based out of Fall River, MA.
Pay and Benefits
The pay range for this position is $65000.00 - $90000.00/yr.
Health Vision Dental 401K
Workplace Type
This is a fully onsite position in Fall River,MA.
Application Deadline
This position is anticipated to close on Nov 21, 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
Title: Logistics Associate II
Pay Rate: $22/hour
Duration: 12-month contract
Location: Portsmouth, NH
Schedule: Monday – Friday, 7:00 AM – 3:30 PM
Job Summary
The Logistics Associate II is responsible for facilitating product shipping and distribution operations. This role involves working closely with management and team members to support logistics systems, implement new strategies, and ensure smooth warehouse operations.
Key Responsibilities
Perform general warehouse duties to support daily operations.
Facilitate product shipping, receiving, and distribution activities.
Collaborate with management on logistics systems and process improvements.
Assist in purchasing, warehousing, distribution, forecasting, and customer service.
Ensure freight is processed efficiently to maximize product service levels.
Process orders, prepare packing lists, and package outgoing materials.
Manage shipping logistics and ensure accuracy and timeliness of all orders.
Track shipment details, locations, and estimated times of arrival (ETAs).
Qualifications
3–5 years of relevant experience in logistics, warehouse operations, or supply chain management.
Strong attention to detail and organizational skills.
Ability to work effectively in a fast-paced environment.

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