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<h3>Job Description</h3>
Job Description
Job Title: Associate Scientist
Location: Andover MA 01810
Duration: 12 months 
Discovery BA group – general job description
<ul>
<li>
Responsible for the qualification and execution of ligand-binding assays (e.g. MSD, Gyrolab, ELISA) in support of Client's biotherapeutic programs.
</li>
<li>
Provide sample analysis and data delivery of drug and/or biomarker/biomeasures in a fast paced and dynamic environment.
</li>
<li>
Perform data analysis and interpretation and draw conclusions regarding progress and results of work, utilizing the data for appropriate decision making. Gather input from colleagues, literature, and additional resources to assist in project advancement.
</li>
</ul>
Education:
<ul>
<li>
BSc with at least 2+ years or MSc with at least 1+ years relevant experience with ligand binding assays.
</li>
<li>
Knowledge and hands-on experience executing laboratory experiments utilizing various platforms and demonstrated analytical problem-solving skills.
</li>
<li>
Ability to author technical documents such as data summary reports and analytical procedures.
</li>
<li>
Strong organizational, time management skills, and collaborative skills.
</li>
</ul>
*No PhD
Company DescriptionWe believe in service that helps you solve a problem, move forward with a project, manage a difficult situation, or simply check something off your list. 
<h3>Company Description</h3>
We believe in service that helps you solve a problem, move forward with a project, manage a difficult situation, or simply check something off your list.

Associate Scientist

<h3>Job Description</h3>
Chief Scientific Officer - Confidential Client (Biotechnology, Boston, MA) 
About the Company Our client is a cutting-edge biotechnology company dedicated to developing next-generation gene editing and gene therapy solutions for serious diseases. With a proprietary platform and strong financial backing, they are advancing multiple programs in CNS and neuromuscular disorders with the mission of delivering functional cures.
The Role The Chief Scientific Officer will serve as the scientific and strategic leader, driving discovery, translational, and preclinical efforts across the company's therapeutic portfolio. This executive will play a pivotal role in shaping the company's scientific vision and advancing novel programs toward clinical development.
Key Responsibilities
<ul>
<li>
Provide overall scientific and R&amp;D leadership across CNS and neuromuscular disease programs.
</li>
<li>
Lead teams spanning discovery, translational biology, and preclinical development.
</li>
<li>
Develop and execute strategies to progress gene editing/gene therapy programs from target validation to IND/CTA.
</li>
<li>
Partner with executive leadership, investors, and external collaborators to align R&amp;D with corporate strategy.
</li>
<li>
Stay at the forefront of advances in CNS, neuromuscular, and gene editing/therapy fields to maintain the company's leadership position.
</li>
</ul>
Qualifications
<ul>
<li>
PhD or MD/PhD in neuroscience, genetics, molecular biology, or related discipline.
</li>
<li>
10+ years of leadership experience in biotechnology or pharmaceutical R&amp;D.
</li>
<li>
Deep expertise in CNS or neuromuscular disorders and gene editing/therapy modalities (AAV, LNP, base or prime editing, etc.).
</li>
<li>
Demonstrated track record progressing programs through IND/CTA and into early clinical development.
</li>
<li>
Strong leadership, communication, and collaborative skills with the ability to inspire teams and engage stakeholders.
</li>
</ul>
Why Join? This is a rare opportunity to lead the scientific direction of a company at the forefront of gene editing, backed by a proprietary platform and committed to transforming patient outcomes in areas of urgent need.

Chief Scientific Officer - Gene Editing

<h3>Job Description</h3>
Job Description
Description
Support development and research of new methods and analytical techniques to be used to release new and existing products 
Validation and verification of analytical methods
perform investigations of out of specification, out of trends, equipment failure, etc. 
Present trending data to support development and validation following GMP guidelines
Perform analytical testing for organic and inorganic chemicals by using FTIR, HPLC, NMR LCMS, GCMS, ICP- MS, GC and wet chemistry
Create test procedures and provide analytical support for certain research products
Top Skills Details
NMR,GCMS,Hplc,FTIR,wet chemistry,analytical chemistry,LCMS
Additional Skills &amp; Qualifications
MS in chemistry or biochemistry with 3-5 years experience or a BS with 5-7 years experience
Experience working with FTIR, HPLC, LCMS, GCMS, ICPMS, NMR
Vast knowledge of following GMP guidelines and procedures
Willingness to train and develop team members
Experience Level
Intermediate Level
Pay and Benefits
The pay range for this position is $75000.00 - $85000.00/yr.
Company provides holiday, vacation, and 401k benefits. They will be able to gain bonuses past on company and personal performance.
Workplace Type
This is a fully onsite position in Tewksbury,MA.
Application Deadline
This position is anticipated to close on Sep 12, 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.

Analytical Chemist

<h3>Job Description</h3>
Job DescriptionThe Company We are Alloy Therapeutics—a biotechnology ecosystem company empowering the global scientific community to make better medicines together. Through a community of partners, we democratize access to pre-competitive tools, technologies, services, and company creation capabilities that are foundational for discovering and developing therapeutic biologics. The company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to the largest biopharma. At Alloy, we believe our industry should compete on getting the best drugs to patients as quickly as possible, not exclusive access to the best platforms. As a reflection of our relentless commitment to the scientific community, we reinvest 100% of our revenue in innovation and access to innovation. MAY THE BEST DRUG WIN. Alloy is headquartered in Waltham, MA with additional labs in Cambridge, UK; Basel, Switzerland, and Athens, GA. Successful members thrive in our shared culture of accountability, deliberate trust, and open communication. As a team we aspire to work together to exceed expectations and collectively contribute across the global organization to always maintain our nimble, startup culture. This is an on-site and full-time position in Waltham, MA. At Alloy, we have an ethos of “Mentorship-By-Apprenticeship” in all of our positions.&nbsp;&nbsp;We strive to have workers in the office when needed to interact organically and face-to-face.&nbsp;&nbsp;Of course, as a lab-based operation, our cells and animals grow 7 days a week, 365 days per year.&nbsp;&nbsp;We respect and value our colleagues for their hard work that requires them to be in the lab every day.&nbsp;&nbsp;We ask our people who have more flexible accommodations, like this position, to appreciate their colleagues who have less flexibility.&nbsp;&nbsp;We are all one team! The Team Alloy’s In Vitro Pharmacology team collaborates with drug discovery partners to conduct in vitro studies on therapeutic candidates across diverse modalities. Our team delivers comprehensive functional screening and characterization of biologics to support discovery and selection of lead candidates. Primary modalities are monoclonal, multispecific, and TCR-mimic antibodies, but also include cell therapies and genetic medicines. As Alloy Tx enters its next phase of growth, we are expanding our capabilities to include mechanistic studies that enhance preclinical development and further advance our translational research efforts. The Role&nbsp; We are seeking a highly motivated Scientist for in vitro screening and pre-clinical development to join our dynamic and fast-paced team. In this role, you will support the execution of in vitro functional cell-based assays to evaluate the potency, mechanism of action, and pharmacological properties of biologic therapeutics. This role requires exceptional organizational skills, a commitment to scientific excellence, and the ability to adapt to a dynamic environment. You will report to the Head of In Vitro Pharmacology and will work collaboratively in a matrixed environment to drive biologics discovery while supporting rapid decision-making in a fast-moving biotech setting. How You’ll Drive Impact&nbsp;
<ul>
<li>Execute: Support in vitro functional characterization of drug candidate molecules.</li>
<li>Develop: Bring a proactive mindset to optimize workflows for more efficient and effective data generation.</li>
<li>Deliver: Support screening campaigns to meet experimental timelines for monoclonal and multispecific antibodies, as well as TCR-mimic antibodies.</li>
<li>Collaborate: Work closely across multi-disciplinary teams in biologics discovery programs spanning all Alloy sites. Engage with an inclusive and collaborative work environment.</li>
<li>Communicate: Clearly convey scientific concepts, experimental results, and interpretations to internal and external stakeholders.&nbsp;</li>
</ul>
 Principal Responsibilities&nbsp;
<ul>
<li>Expand, bio-bank and characterize primary and immortalized cell lines to validate target expression and enable downstream assays.</li>
<li>Generate engineered cell lines using lentiviral, CRISPR or other techniques.&nbsp;</li>
<li>Support day-to-day lab and experimental workflows, including cell line inventory maintenance.</li>
<li>Execute cell-based functional assays using high-throughput approaches in primary cells, immortalized reporter cell lines, and other disease-relevant cellular systems.</li>
<li>Process human leukopaks, isolate and characterize human PBMCs.</li>
<li>Present experimental data and findings during team meetings.</li>
<li>Ensure timely and successful execution of project activities according to plan.</li>
<li>Maintain detailed and accurate laboratory records in compliance with industry standards.</li>
<li>Maintain laboratory organization and ensure compliance with safety protocols.</li>
</ul>
 Qualifications
<ul>
<li>PhD in Cell or Molecular Biology, or a related field, with 0-2 years (Scientist I) or 3-5 years (Scientist II) of relevant industry experience.&nbsp;</li>
<li>Direct experience with cell line engineering (CRISPR, lentiviral, etc) required.</li>
<li>Flow cytometry and fundamental cell and molecular biology techniques required.</li>
<li>Significant cell culture experience with primary and immortalized cell lines.</li>
<li>Experience handling human blood, leukopak processing, and PBMC isolations.</li>
<li>Hands on experience isolating and/or expanding primary immune cell subsets preferred.</li>
<li>Direct experience with high-throughput cell-based assays a plus.</li>
<li>Experience with live cell imaging (i.e. Incucyte) a plus.</li>
<li>Excellent organization, clear communication and teamwork abilities in a multidisciplinary setting.&nbsp;</li>
<li>Thrives working on a team and collaborating with others to achieve project goals.</li>
<li>Enjoys a dynamic and exciting work environment.&nbsp;</li>
<li>Detail oriented, with rigorous scientific thinking and a passion for drug discovery to improve patients’ lives.</li>
</ul>
Taking Care of Our People We support the individuality of what people need to do outside of work to empower them to do their best at work. While you focus on making better medicine together, we focus on programs and benefits that support a diverse and growing team. Whether you’re single, in a growing family, or nearing retirement, Alloy offers a variety of comprehensive and competitive benefits starting from day one. Compensation
<ul>
<li>Competitive base and equity compensation commensurate with level of experience and independence</li>
<li>401(k) company match</li>
</ul>
Health &amp; Family
<ul>
<li>Generous personal and family medical, dental and vision benefits with 100% of premiums and deductibles covered</li>
<li>Company-paid disability (STD, LTD) and life insurance</li>
<li>Paid parental leave</li>
<li>Family planning support up to $45,000 (e.g., IVF/PGT, adoption, surrogacy, egg retrieval)</li>
</ul>
Unique Perks
<ul>
<li>Unlimited PTO (paid time off) and flexible schedules</li>
<li>Annual stipend for continuing education with commitment to your career through individualized professional development plan</li>
<li>Wellness and Extensive Employee Assistance Program (EAP) including resources for mental wellness</li>
</ul>
Pay Transparency At Alloy Therapeutics, we believe in fostering trust and open communication. For this role, the estimated annual base salary range is $130,000 - $145,000, with the final offer based on factors like your experience, skills, and alignment with our needs.
Additionally, this role is eligible for equity compensation, reflecting our commitment to shared success as we work together to make better medicines.
We are proud to offer competitive compensation and benefits, aiming to support our team’s professional and personal well-being. If you have any questions about pay or benefits, we’re here to help.
Alloy Therapeutics is an equal opportunity employer.&nbsp; All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, veteran status, disability, or other legally protected status.&nbsp; If you are unable to submit an application because of incompatible assistive technology or a disability, please contact us at <a href="mailto:recruiting@alloytx.com" target="_blank">recruiting@alloytx.com</a>.&nbsp; We will make every effort to respond to your request for disability assistance as soon as possible. &nbsp;
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Scientist I/II, In Vitro Pharmacology

<h3>Job Description</h3>
Job Description
Job Title:&nbsp;Metrologist Chemist
Location:&nbsp;Billerica, MA
Employment Type:&nbsp;Full Time - Permanent 
Experience Level:&nbsp;Intermediate
Overview:
We are seeking a skilled and detail-oriented&nbsp;Metrologist Chemist&nbsp;to support laboratory operations within a pharmaceutical manufacturing environment. This role focuses on ensuring all lab instrumentation is properly validated, calibrated, and compliant with GMP standards. The ideal candidate will have a strong foundation in chemistry and hands-on experience with lab equipment and quality systems.
Key Responsibilities:
<ul>
<li>Validate laboratory instrumentation and ensure alignment with approved analytical methods.</li>
<li>Author and maintain Standard Operating Procedures (SOPs).</li>
<li>Initiate and document deviations within the Quality Management System (QMS).</li>
<li>Coordinate calibration activities and collaborate with vendors to ensure equipment and method validation.</li>
<li>Follow SOPs and adhere to Good Manufacturing Practices (GMP).</li>
<li>Operate and maintain autoclaves and other lab instruments.</li>
</ul>
Required Skills &amp; Knowledge:
<ul>
<li>Chemistry and laboratory instrumentation expertise.</li>
<li>Experience with calibration, change control, and QMS documentation.</li>
<li>Familiarity with autoclaves, pH meters, and other analytical tools.</li>
<li>Proficiency with MasterControl, CMMS, and electronic document management systems (EDMs).</li>
<li>Hands-on experience with pH, conductivity meters, digital multimeters (DMM), and oscilloscopes.</li>
</ul>
Qualifications:
<ul>
<li>Associate degree in a life science discipline.</li>
<li>Minimum of 4 years of experience in a pharmaceutical manufacturing environment.</li>
<li>Strong attention to detail and ability to work independently and collaboratively.</li>
</ul>
Preferred Tools &amp; Platforms:
<ul>
<li>MasterControl</li>
<li>TrackWise</li>
<li>CMMS</li>
<li>EDMs</li>
</ul>
Pay and Benefits
The pay range for this position is $80000.00 - $91000.00/yr.
They get annual bonuses, they get holiday, vacation, as well as 401k and other medical benefits.
Workplace Type
This is a fully onsite position in Billerica,MA.
Application Deadline
This position is anticipated to close on Sep 12, 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.

Metrologist Chemist

<h3>Job Description</h3>
We are looking for a research scientist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.
In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Research and Development Chemist, Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist.
Benefits:
<ul>
<li>This is a full-time or part-time REMOTE position</li>
<li>You’ll be able to choose which projects you want to work on</li>
<li>You can work on your own schedule</li>
<li>Projects are paid hourly starting at $40+ per hour, with bonuses on high-quality and high-volume work</li>
</ul>
Responsibilities:
<ul>
<li>Give AI chatbots diverse and complex chemistry problems and evaluate their outputs</li>
<li>Evaluate the quality produced by AI models for correctness and performance</li>
</ul>
Qualifications:
<ul>
<li>A current, in progress, or completed Masters and/or PhD is preferred but not required</li>
<li>Fluency in English (native or bilingual level)</li>
<li>Detail-oriented</li>
<li>Proficient in chemistry, inductive/deductive reasoning, physical/temporal/ spatial reasoning</li>
</ul>
Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. This job is only available to those in the US, UK, Canada, Australia, or New Zealand. Those located outside of these countries will not see work or assessments available on our site at this time.

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