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<h3>Job Description</h3>
I am partnered with an exciting client of ours who is looking to grow their QC team! They are currently looking for Three QC Chemists to join their team, located in Boston. 
 
Duties and Responsibilities: 
<ul>
<li>Support QC, Manufacturing, R&amp;D, and QA with raw materials, in-process materials, finished product, stability studies and special project. </li>
<li>Perform all physical, chemical and microbiological testing activities. </li>
<li>Assist in writing Standard operating Procedures (SOP's).</li>
</ul>
 
Experience Needed:
<ul>
<li>Bachelors Degree in Chemistry or related field.</li>
<li>2-3 years of experience within the Pharmaceutical Space. NOT ACADEMIC </li>
<li>Performed routine Analytical Chemistry, Method Development, and Validation alongside Stability Studies and Chemical testing.</li>
</ul>

Quality Control Chemist

<h3>Job Description</h3>
Job DescriptionSalary: 
Description: 
We are seeking an experienced Quality Control Microbiologist to join Marianas Technical Operations organization, advancing personalized medicine and radiopharmaceuticals. This person will be responsible for routine microbiological testing including environmental monitoring, environmental monitoring performance qualifications, growth promotion, bioburden, endotoxin, and sterility testing to support product release. In addition to supporting routine testing, this role will ensure that work is completed with SOPs and adheres to strict quality standards.
 
Illustrative Breadth of Responsibilities:
<ul>
<li>Perform environmental monitoring and environmental monitoring performance qualifications (viable, non-viable, and surface monitoring) of classified areas and maintain database of recovered data and isolates to actively trend EM data.</li>
<li>Perform bioburden, endotoxin, and sterility testing to support product release.</li>
<li>Conduct growth promotion testing and release of media.</li>
<li>Ensures aseptic operator qualification and process simulations are performed aseptically according to GMP compliance.</li>
<li>Microbial enumeration and data analysis from microbiological testing.</li>
<li>Experienced with raw material testing is considered a plus.</li>
<li>Identifying, investigating, and resolving microbial action limits, Out of Specification (OOS) results, and deviations.</li>
<li>Maintain laboratory equipment in accordance with internal procedures.</li>
<li>Adhere to SOPs to ensure high quality standards.</li>
<li>Track progress against project timelines, generate regular status updates, and communicate progress and risks to management.</li>
<li>Adhere to safe laboratory practices.</li>
<li>Multi-task across several projects and manage time effectively to achieve results.</li>
<li>Perform other duties as assigned.</li>
</ul>
Requirements/Skills:
<ul>
<li>Bachelors degree in microbiology or related field with a minimum of two years of experience working in a GMP environment in the pharmaceutical or biotechnology industry. Experience working with radiopharmaceuticals will be considered as a plus.</li>
<li>Experience with cGMP and GMP regulations.</li>
<li>Commitment to maintain data integrity through strict adherence to standardized procedures and relevant compliance requirements.</li>
<li>Good understanding of the radiation safety regulations and guidelines is preferred.</li>
<li>Comfortable handling radioactivity and follow proper ALARA (As Low As Reasonably Achievable) technique Strong communication skills, with motivation to work effectively and cooperatively with others, and to establish and maintain good working relationships.</li>
</ul>
Mariana Oncologys Principles
<ul>
<li>Building a Legacy</li>
<li>Execution Excellence</li>
<li>Courage of our Convictions</li>
</ul>

Quality Control Analyst II, Microbiology

<h3>Job Description</h3>
Job Description
This is an unpaid internship of 15-29 hours per week in the Corporate Lexington location based on the candidate's availability 
Come join an exciting and innovative company that puts the “care” back in healthcare! 
At KabaFusion, our patients come from all walks of life and so do we. We hire GREAT people, period! Our culture celebrates and supports the differences that make us unique. Here, it doesn’t matter what your role is, your hard work and dedication is not only recognized but celebrated. Join us and find out why this is the place to excel and do your best work. 
About Us: 
What started as a single pharmacy in 2010 has grown into KabaFusion becoming the largest privately held home infusion company in the country. We have a national network of pharmacies and nursing offices strategically placed to service 40+ states. Couple that with over 30 years of combined experience and it’s no wonder why KabaFusion is the industry leader in home infusion. 
This is an exciting time to intern at an industry-leading fast-growing national specialty home infusion company to work with patient datasets and gain exposure to senior leadership. The overarching goal of this internship is to gain an understanding of the ways cutting-edge therapeutics impact patient outcomes with detailed information culled through data analytics techniques. 
Essential Duties
<ol>
<li>Assist with ongoing research projects.</li>
<li>Assist in literature reviews, data collection and presentation preparation.</li>
<li>Accurately and efficiently perform data entry and analysis.</li>
<li>Answer questions about the effectiveness of therapies and patient outcomes.</li>
</ol>
Education and Skills
<ol>
<li>College student or recent graduate preferred, with coursework in data analytics and an interest in health sciences.</li>
<li>Advanced skills in workplace tools, including Microsoft Office, required. </li>
<li>Strong interpersonal, verbal, and written communication skills. </li>
<li>Advanced level of multi-tasking and problem-solving skills, with attention to detail. </li>
<li>Ability to maintain confidentiality. </li>
<li>Ability to work with and analyze large datasets, preferred. 
 To learn more about KabaFusion, please visit our careers page: <a href="https://www.kabafusion.com/careers/" target="_blank">https://www.kabafusion.com/careers/</a>
Join us and find out why this is the place to excel and do your best work.
</li>
</ol>

Internship, Department of Clinical Affairs

<h3>Job Description</h3>
Job Description
Our client is seeking an organic chemist to join their Process Chemistry group. This contract position resides within the Pharmaceutical Sciences organization. The candidate will work full-time onsite and execute laboratory activities related to the development of robust drug substance manufacturing processes across various phases of drug substance development. The ideal candidate will conduct multi-step organic synthesis, route scouting and optimization, purification and characterization of intermediates and final compounds to support drug substance scale-up activities.
An ideal candidate will have a strong foundation in modern synthetic organic chemistry and analytical techniques such as NMR, LCMS, UPLC/HPLC (Empower proficiency) and an understanding of early drug development processes and experiments. Experience in small-molecule process development and scale up is highly desired, however not required.
Responsibilities&nbsp;
<ul>
<li>Participate in the design, planning and execution of multi-step synthesis, process research and development as a cross-functional team member.</li>
<li>&nbsp;Collaborate with cross-functional teams to ensure successful project outcomes.</li>
<li>Implement process enhancements, scientific approaches and technical improvements to deliver robust chemical processes.</li>
<li>Document and report experimental results and findings.</li>
<li>Draft and review technical documents (development reports, patent applications, tech transfer documents etc.) Maintain an accurate, timely and compliant laboratory notebook.</li>
<li>Maintain laboratory equipment and ensure compliance with safety regulations.</li>
</ul>
Requirements&nbsp;
<ul>
<li>An ideal candidate would have a B.S. or M.S. in Chemistry, or a related field with 3+ years of experience in pharmaceutical research or laboratory setting or, Ph.D. with 0-3+ years of experience.</li>
<li>Strong knowledge of organic chemistry.</li>
<li>Experience with early phase route development and process optimization Proficiency in using analytical instruments (HPLC/UPLC, NMR, LCMS) and software.</li>
<li>Strong analytical and problem-solving skills.</li>
<li>Strong written and verbal communication skills.</li>
<li>Ability to work independently and as part of a team.</li>
<li>Strong organizational and time management skills.</li>
<li>Ability to effectively prioritize and manage multiple tasks and compounds Ability to adapt to change and to work optimally within a variety of situations Ability to build productive working relationships across functions and highly diverse groups of individuals Self-motivated and willing to “learn on the job” and ask for assistance when needed Ability to make a significant impact in a results-driven environment where accountability is key.</li>
<li>A team player, who listens effectively and invites response and discussion A collaborator who communicates in an open, transparent, complete, timely and consistent manner</li>
</ul>
Company DescriptionBeacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations. Beacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S. Whether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities. 
<h3>Company Description</h3>
Beacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations.\r\n\r\nBeacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S.\r\n\r\nWhether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities.

Process Chemist

<h3>Job Description</h3>
Job Description
Scientist II/ Senior Scientist – Viral Vector / Discovery &nbsp;
(Hybrid – Greater Boston, on-site lab work required)&nbsp; NOTE: Applicants must be legally authorized to work in the United States on a permanent basis. At this time, the Company does not provide, and will not provide in the future, sponsorship for employment visas.
Why Work With Us?&nbsp;
At Candel, our people drive our mission to transform cancer care. We value curiosity, collaboration, and bold science in a supportive environment where everyone has visibility and impact. You’ll join a team that embraces creativity, trusts its people, and fosters growth through coaching and open discussion. This is the place to bring your ideas forward, dig deep into data, and see your work make a real difference for patients.&nbsp;
Our Science: Advancing Cancer Immunotherapies&nbsp;
Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies designed to stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs, advancing novel treatments through discovery, IND-enabling studies, and into clinical development. With positive Phase 3 results for our lead candidate and multiple pipeline programs on the horizon, it’s an exciting time to join us. Learn more: <a href="http://www.candeltx.com&amp;nbsp" target="_blank">www.candeltx.com&amp;nbsp</a>;
Position Summary&nbsp;
This is a highly visible, hands-on role reporting directly to the VP of Research. As Scientist II /Senior Scientist, (We will determine final title and level based on your experience and background.) you’ll balance bench work and strategic contributions to advance novel viral vectors into IND-enabling studies and first-in-human trials. You’ll gain full-spectrum exposure across discovery, development, regulatory, and clinical programs, while contributing to the future of Candel’s viral immunotherapy platform.&nbsp;
We’re looking for a scientist who thrives in a fast-paced biotech with a “can-do” mindset — someone versatile enough to design experiments at the bench, analyze data, and present insights across functions. If you’re inquisitive, data-driven, and energized by the chance to innovate while still being hands-on, this role offers both the challenge and growth you’re seeking.&nbsp;
What You Will Do&nbsp;
<ul>
<li>
Support scientific strategy and execution for viral immunotherapy programs from discovery through IND-enabling studies.&nbsp;
</li>
</ul>
<ul>
<li>
Design and optimize viral vectors (e.g., HSV) for therapeutic applications, including genome engineering and payload design.&nbsp;
</li>
</ul>
<ul>
<li>
Oversee and perform in vitro and ex vivo assays to evaluate vector potency, transduction efficiency, and immunological activity.&nbsp;
</li>
</ul>
<ul>
<li>
Collaborate closely with cross-functional teams including CMC and Regulatory to ensure seamless program progression.&nbsp;
</li>
</ul>
<ul>
<li>
Guide the development and transfer of analytical and process development methods to the CMC team.&nbsp;
</li>
</ul>
<ul>
<li>
Mentor and manage junior scientists and research associates; foster a culture of scientific rigor, innovation, and collaboration.&nbsp;
</li>
</ul>
<ul>
<li>
Contribute to regulatory documentation, including IND-enabling study design and data interpretation.&nbsp;
</li>
</ul>
<ul>
<li>
Stay current with scientific literature and emerging technologies in viral vector design, immunotherapy, and oncology.&nbsp;
</li>
</ul>
What You Will Bring&nbsp;
<ul>
<li>
Ph.D. in Virology, Molecular Biology, Immunology, or related field with 3–5+ years biotech industry experience&nbsp;
</li>
</ul>
<ul>
<li>
Extensive hands-on experience with viral vector systems, including design, production, purification, and characterization; HSV experience a plus&nbsp;
</li>
</ul>
<ul>
<li>
Strong background in mammalian cell culture, transduction assays, and molecular biology techniques (qPCR, ELISA, flow cytometry)&nbsp;
</li>
</ul>
<ul>
<li>
Demonstrated experience developing and implementing platform-based approaches in cell and gene therapy (e.g., scalable vector design, modular assays, standardized workflows)&nbsp;
</li>
</ul>
<ul>
<li>
Familiarity with IND-enabling studies, GLP/GMP environments, and regulatory expectations for gene therapy products&nbsp;
</li>
</ul>
<ul>
<li>
Comfort running your own bench work while also contributing strategically&nbsp;
</li>
</ul>
<ul>
<li>
Proven ability to thrive in a lean, entrepreneurial environment without big-pharma infrastructure&nbsp;
</li>
</ul>
<ul>
<li>
Curious, data-driven mindset — eager to ask questions, revisit data, and generate new insights&nbsp;
</li>
</ul>
<ul>
<li>
Excellent written and verbal communication skills with confidence to present across levels and functions&nbsp;
</li>
</ul>
<ul>
<li>
Must be legally authorized to work in the United States. Sponsorship is not available; U.S. citizenship or permanent residency is required&nbsp;
</li>
</ul>
Preferred Attributes&nbsp;
<ul>
<li>
Desire to grow into leadership, with experience mentoring or guiding junior staff&nbsp;
</li>
</ul>
Work Environment&nbsp;
This is a hybrid role based in Greater Boston, with significant on-site lab work (bench and data analysis). Expect to be onsite most of the week to fully engage with research, team collaboration, and laboratory execution.&nbsp;
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tfgqQ3Hl92

Scientist II / Senior Scientist - - Viral Vector / Discovery

<h3>Job Description</h3>
Job DescriptionJob Title: Associate Scientist – iPSC-Derived Neuron Models Location: Lexington, MA, 02421 Duration: 1 year+ (Possibility of Extension) Onsite, 5 days/wk Pay Rate: $44.72-$51.43/Hour. on W2 TOP SKILLS PER MGR:
<ul>
<li>Human iPSC-derived neuron culture experience</li>
<li>Gene perturbations using siRNA and/or CRISPR</li>
<li>Cell-based molecular and biochemical assays including 1) immunocytochemistry, 2) qPCR, 3) ELISA, 4) micro-electrode array (MEA), and 5) fluorescence microscopy (at least 2-3 of these 5 skillsets).</li>
</ul>
 JOB DESCRIPTION: Position Summary: We are seeking a highly motivated and detail-oriented scientist to join our Humanized In Vitro Model Development team. The successful candidate will contribute to the development of human iPSC-derived neuronal models and assays to support drug discovery and translational research. This is an exciting opportunity to work at the forefront of human-relevant neuroscience in a collaborative and innovative environment. Key Responsibilities: • Culture, differentiate, and maintain human iPSC-derived neurons. • Perform routine cell-based and molecular assays including immunocytochemistry, qPCR, ELISA, MEA, luciferase, western blot, and fluorescence microscopy. • Conduct functional gene perturbations and pharmacological interventions. • Support assay development and optimization for phenotypic screening and mechanistic studies. • Analyze and interpret experimental data, maintain accurate records, and present findings in team meetings. • Collaborate cross-functionally with scientists in different units. • Contribute to protocol development, SOP documentation, and continuous improvement initiatives. Qualifications: • Bachelor’s or Master’s degree in Neuroscience, Cell Biology, Stem Cell Biology, or a related field. • LEVEL II - Minimum of 2 years of hands-on experience with human iPSC-derived neuronal cell models and assays. • LEVEL III - Minimum of 5 years of hands-on experience with human iPSC-derived neuronal cell models and assays. • Proficiency in cell-based assay techniques and fluorescence microscopy. • Strong organizational and communication skills. • Ability to work independently and collaboratively in a fast-paced research environment. • Comfortable working with electronic lab notebooks. Preferred Skills: • Experience with CRISPR editing, RNA-seq, calcium imaging, high-content imaging, or complex co-culture systems is plus. • Knowledge of automated liquid handling systems and high-throughput screening platforms. • Familiarity with cardiometabolic diseases is a plus. #sczr2

Associate Scientist iPSC-Derived Neuron Models

<h3>Job Description</h3>
Job Description
JOB SUMMARY
The Cultivation Technician will perform manual labor to assist in the upkeep, stocking, and fulfillment of growing cannabis, including, but not limited to; watering, feeding, pruning, cloning, cleaning, and transplanting. This position will report to the Cultivation Manager. 
PRIMARY RESPONSIBILITES 
<ul>
<li>Daily care of cannabis plants, including watering, pruning and trimming, inspecting the plants. </li>
<li>Fertilizing and providing nutrients to the plants according to cultivation protocols</li>
<li>Careful monitoring of the plants for any signs of growing issues or problems; treatment for disease or infestation.</li>
<li>Ensure the appropriate information is accurate and listed clearly in accordance with the state regulations and company standard operating procedures.</li>
<li>Carefully follow directions as provided by the Cultivation Department</li>
<li>Willingness to continue to learn best practices of cannabis cultivation with a strong interest in horticulture, agriculture and greenhouse operating systems.</li>
<li>Sweeping, mopping and all other required cleaning</li>
<li>Cleaning of the plant housing devices</li>
<li>Maintenance and cleaning of the plant tables</li>
<li>Maintenance of the plant pots</li>
<li>Reporting any issues to management to ensure a timely fix</li>
</ul>
JOB REQUIREMENTS 
<ul>
<li>Must be 21 years or older</li>
<li>Well organized and ability to keep deadlines</li>
<li>Ability to work in a team environment to achieve company goals</li>
<li>Effective time-management skills and ability to multi-task</li>
<li>Ability to work in a fast-paced, changing, and challenging environment</li>
<li>The willingness to continue to learn and grow with the company, improve cultivation skills and gain greater knowledge of cultivation processes.</li>
<li>Basic Excel, Word, and general computer knowledge</li>
<li>Full knowledge of all applicable law, regulations, and requirements; maintaining facility at 100% compliance at all times; this includes being up to date on any changes to current applicable laws/regulations </li>
<li>Must be and remain compliant with all regulatory requirements for working in the cannabis industry</li>
<li>Must be able to obtain and retain a Registered Agent Card issued by the state of operation</li>
<li>Must be focused, pay close attention to detail</li>
<li>Must be able to internalize training and follow instructions </li>
<li>Must be able to communicate clearly and effectively</li>
<li>Other duties and responsibilities</li>
</ul>
COMPANY OVERVIEW
Ascend Wellness Holdings (AWH) is a vertically integrated cannabis cultivator, processor and provisioning center operator with assets in Illinois, Maryland, Massachusetts, Michigan, New Jersey, Ohio and Pennsylvania. We seek to foster a robust and inclusive cannabis industry through a premium, unmatched customer-focused retail experience. We are looking to build a world-class team that will help carry out our mission of helping to shape the future of cannabis as a leading healthcare solution. We are committed to improving the quality of our patient's lives by offering unrivaled quality, consistency and meticulously curated products that satisfy our customers unique, individual needs. When it comes to customer service experience, our dispensaries will set a new standard of excellence, emphasizing health and wellness by a highly knowledgeable team. A team that is committed to our values, our people, and our communities; we are looking for people who are inspired by our vision and stay dedicated to our mission as we continuously expand.
EEO STATEMENT 
Ascend Wellness Holdings, Inc. ("AWH") and its subsidiaries is an equal opportunity employer and celebrate the population of differences and does not discriminate in its hiring / hiring practices, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected by law. #LetsAscend

Cultivation Technician- Athol

<h3>Job Description</h3>
Job Description
Our Culture: Why work with us?
At Foghorn Therapeutics, we believe in “People First, Mission Always.”
We put “People First” because we know our people are the key to everything we will accomplish. We value the diversity of background, ideas, perspectives and experiences that our team members bring to Foghorn Therapeutics – demonstrated by our community speaking more than 22 languages and representing over 24 nationalities. We value our teammates as people, not just as employees – validated by our actions that let our people know that we care about them, their families, and their lives.
We say “Mission Always” because we know a relentless commitment to our mission will make a difference in the lives of others. We believe our success will come from evaluating the data to follow the science. We work hard to develop a new class of therapies that could improve the lives of over 2.5 million people with cancer.
Our culture is focused on succeeding through the evaluation of data, not people. And in that, relationships can flourish and develop.
Our Science:
The groundbreaking science behind our therapies continues to yield vital insights into diseases that have confounded physicians and researchers. Our core scientific approach is centered on the chromatin regulatory system, which opens and closes the right sections of DNA at the right time. Breakdowns in the chromatin regulatory system lead to a wide range of diseases, including cancer, impacting millions of people.
Our proprietary Gene Traffic Control® platform is a powerful tool for understanding and modulating the chromatin regulatory system. We are pursuing multiple treatments for breakdowns in this system. We are the only company with the ability to study and target the chromatin regulatory system at scale, in context, and in an integrated way. 
Job Summary
Foghorn Therapeutics is seeking a motivated Principal Scientist to join the drug product development group within Chemistry Manufacturing and Controls (CMC) to pursue an exciting role in cutting-edge formulation development and drug delivery technologies to support our portfolio. The individual will be responsible to take a leadership role in development of specialty drug delivery technologies and will be responsible to lead and execute the assessments of various innovative drug delivery technologies for development of complex injectables and solid oral dosage forms to support Foghorn’s portfolio at both preclinical and clinical stages. Based on experience level, the candidate will lead the CMC laboratory activities in-house and/ or also represent their function in program/ project teams allowing opportunities for cross-functional involvement/ collaboration. The candidate will also eventually support clinical formulation development and manufacture at CDMOs and regulatory filings.
Requirements
Requirements
Minimum Qualifications
<ul>
<li>PhD in chemical engineering, pharmaceutics, chemistry, material science or related field</li>
<li>5+ years of industry experience in drug delivery areas or formulation/drug delivery experience in the pharmaceutical industry for Sr. Scientist. </li>
<li>Experience in LAI (long-acting injectables)</li>
</ul>
Preferred Qualifications and Role Expectations
<ul>
<li>Prior experience and a good understanding of one or more long acting or targeted drug delivery technologies such as nanosuspensions, liposomes, PLGA microspheres technology are preferred.</li>
<li>Excellent scientific knowledge in formulation technologies, material science, chemistry, preformulation and formulation sciences – experience / exposure in drug delivery, complex / long acting parenterals, modified release formulation platforms are a significant plus and will be preferred</li>
<li>Laboratory based skills including various drug delivery platforms, analytical characterization is a must.</li>
<li>Ability to learn rapidly, have a flexible mindset and to be able to adapt to fast paced highly matrixed environments</li>
<li>Effective verbal and written communication skills</li>
<li>A desire to be part of a highly innovative company aimed at helping patients with serious diseases</li>
</ul>
Benefits
Foghorn Therapeutics is pleased to provide you and your family with a comprehensive suite of benefits, including:
<ul>
<li>Highly competitive and inclusive medical, dental and vision coverage options</li>
<ul>
<li>BCBS PPO and PPO HSA plans</li>
<li>BCBS Dental Plan</li>
<li>EyeMed Vision Plan </li>
</ul>
<li>FSA and HSA for medical expenses and dependent care expenses</li>
<li>401(k) Program via Fidelity with the company match</li>
<li>Corporate Wellness Program</li>
<li>Unlimited Paid Time Off policy</li>
<li>Winter shut down</li>
<li>12 weeks of 100% paid parental leave for birthing/primary parent and primary guardian in case of adoption and 3 weeks of 100% paid parental leave for non-birthing/non-primary parent/guardian.</li>
<li>Paid Life, LTD and STD insurance coverages, as well as voluntary benefit options</li>
<li>Free parking, subsidized commuter passes, or a $100 monthly stipend for walking/biking to work</li>
<li>Company lunches on Wednesdays </li>
</ul>
Foghorn Therapeutics is a smoke-free, alcohol-free and drug-free work environment. Foghorn is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Foghorn Therapeutics will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Principal Scientist, Drug Product Development

<h3>Job Description</h3>
Job Descriptionjob summary: 
<ul>
<li>As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. </li>
<li>Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatments streamlined, easily accessible, and globally produced. If you share their goal of approaching healthcare in a novel way, look no further - apply for your dream job now!</li>
<li>A position is available for a bioanalytical bench scientist to join a bioanalytical mass spectrometry laboratory in the Pharmacokinetics Dynamics and Metabolism department. This lab-based role will focus on supporting Antibody Drug Conjugate (ADC) related bioanalytical activities. This includes LC-MS based assay development for ADCs, study sample analysis, data reporting, LC-MS instrument operation and maintenance. The successful candidate is detail-oriented and, following training, can operate independently. This position requires demonstrated experience in successfully executing complex bioanalytical procedures. Previous experience in small molecule LCMS assay is desired. Previous experience in handling ADC molecules, immunoanalytical workflows and quantitative LC-MS assay techniques is a plus. We are looking for a scientist passionate about learning and quickly applying new skills to project needs.</li>
</ul>
 location: Andover, Massachusetts job type: Contract salary: $40.05 - 42.78 per hour work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Preparation of samples for mass spectrometry analysis</li>
<li>Design of experiments in collaboration with colleagues</li>
<li>Conduct analytical experiments and method development as needed</li>
<li>Identify and exploit new scientific concepts</li>
<li>Interpretation and documentation of experimental results</li>
<li>Communication of experimental results to team members</li>
<li>Maintain high quality record in electronic lab notebook</li>
</ul>
 qualifications: 
Required:
<ul>
<li>BS/MS degree in chemistry, biological sciences, biochemistry or related fields (NON-PhD)</li>
<li>Bachelors Degree with a minimum of 3+ years of experience OR</li>
<li>Master's Degree with a minimum of 1+ years of experience</li>
<li>Experience with LC-MS biological sample preparation involving a multi-step process to isolate, purify, and concentrate the analytes of interest for the LCMS analysis</li>
<li>Experience with the operation of LC-MS instrument and familiar with related operation software (Analyst, Xcalibur or Skyline)</li>
</ul>
Nice to have:
<ul>
<li>ADC</li>
</ul>
#LI-PV1
 skills: Cell Biology, Biology, Chemistry, Biologics, Mass Spectrometry (MS) 
 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.

Bench Scientist, ADC LCMS

<h3>Job Description</h3>
Job Description
Position Summary
Responsibilities will vary from performing one procedure or work instruction to a number of analytical, microbiological or quality system procedures for a cGMP sterile facility. Precision and accuracy in performance of the work instructions and data collection is essential. Must be able to maintain laboratory records for process control and comply with quality system and safety requirements. Initial proficiency testing must be passing and competency will be verified periodically thereafter. 
Duties and Responsibilities
<ul>
<li>Perform sample log-in and ensure samples are appropriately labeled</li>
<li>Accurately document results</li>
<li>Environmental monitoring of graded spaces</li>
<li>Collection and testing of WFI, RODI water and tap water</li>
<li>Coordination of packing and shipment of samples to contract testing laboratories</li>
<li>Maintenance and daily verification of laboratory instrumentation</li>
<li>Maintenance of laboratory supplies</li>
<li>Maintain storage of samples in accordance with established SOPs</li>
<li>Maintain regular communication with internal management regarding samples, schedules, customer requirements, problems, delays and/or complaints</li>
<li>Conduct multiple test steps at once</li>
<li>Input test result entry into the database and generate reports</li>
<li>Ability to work unscheduled and overtime hours as needed</li>
<li>Other duties as assigned</li>
</ul>
Regulatory Responsibilities 
<ul>
<li>Conduct all work in compliance with FDA, 21 CFR 820, 21 CFR 210 and 211, and other regulatory agency requirements sufficient to apply to quality operations and compliance</li>
</ul>
Supervisory Responsibilities
<ul>
<li>N/A</li>
</ul>
Experience
<ul>
<li>Up to two (2) years of experience working in a cGMP laboratory environment</li>
</ul>
Education
<ul>
<li>Bachelor’s degree in Biology, Microbiology, Chemistry and/or Physical Sciences</li>
</ul>
Knowledge, Skills &amp; Abilities
<ul>
<li>Possess working knowledge of aseptic testing techniques, principles, tools and instruments involved in the sample preparation and performance of microbiological assays</li>
<li>cGLP</li>
<li>Perform complex work instructions and/or operate sophisticated equipment under general supervision</li>
<li>Resolve routine problems</li>
<li>Experience with Microsoft Office, and general computer proficiency</li>
<li>Effective communication and availability</li>
</ul>
Physical Requirements

<ul>
<li>Ability to meet gowning requirements</li>
<li>Ability to remain stationary for prolonged periods of time</li>
<li>Ability to lift up to 25 lbs. as required</li>
<li>Satisfactory audio-visual acuity</li>
<li>Ability to walk between locations </li>
<li>Fine and gross motor skills to manipulate equipment and tools</li>
</ul>

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