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<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
<ul>
<li>Support the Drug Substance Process Development (DS PD) team by packing out critical consumables in appropriate tissue culture suites and bioreactor bays</li>
<li>Prepare custom tubing assemblies used in routine bioreactor operations; package assemblies and sterilize by autoclaving, when directed</li>
<li>Assist the&nbsp;DS PD team in preparing and aliquoting pre-made cell culture media</li>
<li>Provide occasional coverage for cell culture media manufacturing efforts</li>
<li>Perform routine bioreactor manipulations (e.g., sampling, cell counting, metabolite analysis, media exchange) during weekdays. Weekend rotating coverage is expected due to the cell culture nature.</li>
<li>Document real-time bioreactor observations and sample measurements according to company procedures, work instructions, job aids, and SOPs</li>
<li>Work with the health and safety of yourself and your teammates in mind; comply with all applicable local, state, federal, and company EHS regulations</li>
</ul>
Qualifications 
Basic Minimum Qualifications:
<ul>
<li>B.S. with 2 years of experience (OR M.S. + 0 years of experience) in a scientific or engineering discipline that incorporates biology and chemistry curricula</li>
<li>Prior experience working in a BSL1+ “wet laboratory” environment</li>
<li>Extensive experience with aseptic technique and working within a biosafety cabinet</li>
<li>Proficiency with mammalian cell culture</li>
<li>Proficiency with bioreactors, peristaltic pumps, and TPE tube welders</li>
<li>Strong organizational, time management, and troubleshooting abilities with excellent verbal and written communication skills.</li>
<li>Ability to design experiments and interpret data, keep accurate records, follow instructions, and comply with company policies.</li>
<li>Ability to work independently and as a part of a team, self-motivation, adaptability, and a positive attitude.</li>
<li>Applicant should be able to safely lift up to 50 lbs</li>
</ul>
Desired Qualifications:
<ul>
<li>Experience working with stem cells in a BSL2+ laboratory</li>
<li>Familiarity with electronic lab notebook (ELN) documentation.</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
 Additional Information 
The position is&nbsp;full-time, Monday through Friday, with rotating work on weekends (2-4 hours per day).&nbsp;Candidates currently living within a commutable distance of&nbsp;Boston, MA&nbsp;are encouraged to apply.
<ul>
<li>Comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Hourly rate is between&nbsp;$38.00-41.00</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Drug Substance Process Development Scientist

<h3>Job Description</h3>
Job Description
&nbsp;
&nbsp;
<ul>
<li>We are hiring immediately for a full time METROLOGY TECHNICIAN position.</li>
<li>Location: AstraZeneca - 35 Gatehouse Drive, Waltham, Massachusetts 02451. Note: online applications accepted only.</li>
<li>Schedule: Full time; Monday through Friday, 7:00 am to 3:30 pm. More details upon interview.</li>
<li>Requirements: Prior metrology technician experience is preferred.
<ul>
<li>Equipment Certification:&nbsp;Manage and support vendor certification for&nbsp;Biosafety Cabinets (BSCs),&nbsp;Ventilated Balance Enclosures (VBEs),&nbsp;Down Draft Tables, Calibrate&nbsp;5 Gas Meters, DP sensors&nbsp;and&nbsp;Animal Transfer Stations.</li>
<li>Vendor Coordination:&nbsp;Serve as the primary point of contact for external service providers, managing schedules and overseeing&nbsp;on-site vendor maintenance&nbsp;and repairs..</li>
<li>Water Systems:&nbsp;Manage and perform routine maintenance and&nbsp;preventive maintenance (PMs) on Millipore&nbsp;(Reverse Osmosis) units to ensure high-purity water standards.</li>
</ul>
</li>
<li>Pay Range: $40.00 per hour to $50.00 per hour.</li>
</ul>
&nbsp;
ESFM is the corporate Integrated Facilities Management (IFM) division of Compass Group USA and a Keystone member of the International WELL Building Institute (IWBI).&nbsp;
&nbsp;
We Make Applying Easy!&nbsp;Want to apply to this job via text messaging? Text JOB&nbsp;to 75000&nbsp;and search requisition ID number&nbsp;1498467.
The advertised program is a conversational recruiting assistant that helps you apply to jobs with Compass Group. Message frequency varies. Message and data rates may apply. Text STOP to opt out or HELP for help. Terms and conditions: <a href="http://olivia.paradox.ai/moSkg" target="_blank">http://olivia.paradox.ai/moSkg</a>
Rooted in hospitality, ESFM elevates the workplace experience as the single source of innovative FM solutions that ensure a safe, healthy, and sustainable environment. ESFM’s clients include many household names from Life Science, Technology, Oil &amp; Gas and Manufacturing markets.
&nbsp;
ESFM self-performs 80% of all IFM solutions provided to clients. Their portfolio of service categories includes Environment, Health &amp; Safety, Facilities Maintenance &amp; Engineering, Sustainability, Janitorial &amp; Industrial Cleaning, Laboratory Support and Workplace solutions.&nbsp;&nbsp;This self-performance model creates a consistent hospitality experience for clients, resulting in higher engagement and productivity from their employees.
&nbsp;
In 2020, ESFM (formerly Eurest Services) won the George Graves Award for Facility Management Achievement from the International Facilities Management Association (IFMA).
&nbsp;
Job Summary
 Summary: Delivers lab services at client locations. Essential Duties and Responsibilities: 
<ul>
<li>Isolates and cryopreserves primary PBMCs from both whole blood and leukopaks.</li>
<li>Handles and processes primary blood and tissue from mouse and primate sources.</li>
<li>Maintains sterile technique while culturing isolated primary cells.</li>
<li>Performs established flow cytometry protocols on a routine basis.</li>
<li>Completes daily maintenance and QC protocols on flow cytometers.</li>
<li>Conducts analysis of flow cytometry data (FlowJo).</li>
<li>Records results and uploads to relevant databases.</li>
<li>Processes customer requests from receipt until completion.</li>
<li>Maintains clear and accurate laboratory records.</li>
<li>Identifies and reports unusual results/outcomes.</li>
<li>Maintains clean and orderly lab space.</li>
<li>Maintains inventory of laboratory reagents and supplies.</li>
<li>Performs other duties as assigned.</li>
</ul>
 Qualifications: 
<ul>
<li>Minimum two years of professional experience using sterile technique.</li>
<li>Minimum two years of professional experience with primary cell isolations.</li>
<li>Minimum one year professional experience performing in vitro cell based assays.</li>
<li>Previous flow cytometry experience required.</li>
<li>Experience conducting multiplex ELISAs &amp; protein labeling strongly preferred.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Bachelors degree in lab-based biomedical, pharmaceutical or biological sciences strongly preferred.</li>
</ul>
Associates at ESFM are offered many fantastic benefits.
Full-time and part-time positions offer&nbsp;the following benefits to associates:&nbsp;Retirement Plan,&nbsp;Associate Shopping Program,&nbsp;Health and Wellness Programs,&nbsp;Discount Marketplace,&nbsp;Identity Theft Protection,&nbsp;Pet Insurance,&nbsp;Voluntary Benefits, including Critical Illness Insurance, Accident Insurance, Hospital Indemnity Insurance, Legal Services, and Choice Auto and Home Program
Full-time positions also offer&nbsp;the following benefits to associates:&nbsp;Medical,&nbsp;Dental,&nbsp;Vision,&nbsp;Life Insurance/AD,&nbsp;Disability Insurance,&nbsp;Commuter Benefits,&nbsp;Employee Assistance Program,&nbsp;Flexible Spending Accounts (FSAs)
Associates may also be eligible for paid and/or unpaid time off benefits in accordance with applicable federal, state, and local laws.&nbsp;For positions in Washington State, Maryland, or to be performed Remotely, click here or copy/paste the link below for paid time off benefits information.
<a href="https://www.compass-usa.com/wp-content/uploads/2023/08/2023_WageTransparency_ESFM.pdf" target="_blank">https://www.compass-usa.com/wp-content/uploads/2023/08/2023_WageTranspa…</a>
About Compass Group: Achieving leadership in the foodservice and facility management industry
&nbsp;
Compass Group is an equal opportunity employer.&nbsp; At Compass, we are committed to treating all Applicants and Associates fairly based on their abilities, achievements, and experience without regard to race, national origin, sex, age, disability, veteran status, sexual orientation, gender identity, or any other classification protected by law.
Qualified candidates must be able to perform the essential functions of this position satisfactorily with or without reasonable accommodation. Disclaimer: this job post is not necessarily an exhaustive list of all essential responsibilities, skills, tasks, or requirements associated with this position. While it is intended to be an accurate reflection of the position posted, the Company reserves the right to modify or change the essential functions of the job based on business necessity. We will consider for employment all qualified applicants. Candidates’ employment is subject to a background check.
Applications are accepted on an ongoing basis.
ESFM maintains a drug-free workplace.
ESFM&nbsp;

METROLOGY TECHNICIAN (FULL TIME)

<h3>Job Description</h3>
Job DescriptionSalary: $50,000 - $70,000 
JOB SUMMARY
The Environmental Monitoring Microbiologist conducts cleanroom monitoring activities to ensure the air, surfaces, and critical utilities utilized for pharmaceutical product manufacturing meet cGMP requirements. These samples are collected according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures.
 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Collects Environmental Monitoring Samples at client manufacturing sites on a daily basis in the greater Boston area.</li>
<li>Sample collection types include: air viable, surface viable, water and compressed gas samples. Samples are then subsequently submitted to the lab for analysis.</li>
<li>Understands the importance of aseptic technique and the critical role it plays in EM sample collection.</li>
<li>Documents work in a clear and organized manner.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
<li>Under close supervision will be trained to become proficient at assigned tasks in order to become subject matter experts.</li>
<li>Performs routine data generation and problem solving with a minimal rework.</li>
<li>Works under close supervision to ensure all work performed is executed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>
<li>Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.</li>
<li>Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.</li>
</ul>
 
SHIFT
Wednesday - Saturday 1st Shift
 
REQUIREMENTS &amp; QUALIFICATIONS
Qualifications include a BA or BS degree in Microbiology or related science discipline with 0-2 years of related experience is required. Knowledge of cGMP and related compliance regulations and guidances is preferred.

Microbiologist I, EM

<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development.
 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Prepares and analyzes products to determine chemical and physical properties.</li>
<li>Will perform work under partial supervision and will provide over site to projects and assist other Chemists as needed.</li>
<li>Works under partial supervision with chemists and other client personnel regarding research, procedures performed, related results and prepares reports.</li>
<li>Is a subject matter expert in some techniques and will mentor others. Work to learn and improve on others techniques and tasks.</li>
<li>Performs data generation, analysis and more complicated problem solving with a minimal rework.</li>
<li>Reviews and assesses deviations; includes performing risk assessments, participating in root cause analysis investigations, tracking, follow-up and reporting.</li>
<li>Works under partial supervision to ensure all work performed is performed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>
<li>Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.</li>
<li>Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.</li>
<li>Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.</li>
<li>Documents work in a clear and organized manner.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
</ul>

REQUIREMENTS &amp; QUALIFICATIONS
Qualifications include a Bachelors degree in Chemistry or a related discipline is required with 1+ years of related experience. Knowledge of cGMPs and related compliance regulations and guidances required.
 
MINIMUM SKILLS REQUIREMENTS
<ul>
<li>Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.</li>
<li>A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.</li>
<li>Must have excellent organizational, verbal communication and technical documentation skills.</li>
<li>Solid computer skills.</li>
<li>Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

Chemist II

<h3>Job Description</h3>
Job DescriptionDescription Applies advanced scientific principles and expertise in the design and development of analytical methods to support the development of new products and technologies for Ascensus and our customers. Leverages experimental design, scientific principles, laboratory techniques, analytical methods, and guidance from personal and shared sources of subject matter relevant in the delivery on assigned projects. Works collaboratively with internal R&amp;D colleagues, operations, and quality with a high degree of independence. Experienced in finding relevant detailed scientific literature for informed research and proactively maintains awareness of advances in relevant chemistry and scientific principles.&nbsp; Essential Functions and Responsibilities· &nbsp; Highly proficient in lab and analytical equipment set up and related activities. Experience with method development and validation&nbsp; for NMR, HPLC, UPLC, GC, FTIR, MS, CHN, TGA, and DSC.&nbsp; · &nbsp; Proficient in wet chemistry and able to work with other instruments for physical/chemical&nbsp; characteristics of the products like particle size, melting point, polarimeter, Refractive index and other instrumental and non-instrumental techniques.&nbsp; · &nbsp; Leads development and mentors others on how to develop new analytical techniques and solve new analytical challenges in support the development of new products and technologies from R&amp;D to production to meet customer requirements. · &nbsp; Maintains high quality lab records and follows all standard operating procedures. Writes clear and concise methods and analytical reports.&nbsp; ·&nbsp; &nbsp; Presents highly detailed results to peers, managers, and non-technical audiences. Proactively seeks opportunities to update stakeholders on projects and new technologies.&nbsp; ·&nbsp; &nbsp; Maintains a clean, uncluttered, work area at all times.&nbsp; ·&nbsp; &nbsp; Conducts all work in a safe and professional manner. Follows all safety principles and uses all required PPE in conducting work. Actively participates in the development of safety programs for the lab (Job Hazard Analysis, Audits, Waste Management.) · &nbsp; Ensures all developed methods meet level of detection, level of quantification, and statistical requirements. ·&nbsp; &nbsp; Leverages all available sources of scientific information (e.g. literature, internal reports, subject matter experts, patents, articles, A.I., etc.) in the feasibility and directed design stages of product development.&nbsp; · &nbsp; Makes strong observations, suggestions, or improvements for analytical experiments. · &nbsp; Attends approved meetings, seminars, and educational opportunities. · &nbsp; Able to run instrument qualification/calibration as needed. ·&nbsp; &nbsp;Other duties as assigned. Qualifications Minimum Qualifications&nbsp; ·&nbsp; &nbsp; &nbsp; &nbsp; Demonstrates an advanced proficiency in analytical chemistry and statistics.&nbsp;·&nbsp; &nbsp; &nbsp; &nbsp; Highly proficient in lab and analytical equipment set up and related activities.&nbsp;·&nbsp; &nbsp; &nbsp; &nbsp; Advanced understanding of the use and maintenance analytical instrumentation.&nbsp;·&nbsp; &nbsp; &nbsp; &nbsp; Recognizes problems and troubleshoots using root cause analysis.·&nbsp; &nbsp; &nbsp; &nbsp; Skilled at making strong and frequent observations, documenting them in reports daily.·&nbsp; &nbsp; &nbsp; &nbsp; Routinely makes strong data driven suggestions for improvements to analytical experiments.&nbsp; ·&nbsp; &nbsp; &nbsp; &nbsp; Highly experienced in working with and developing analytical methods for products which may have special hazards (air sensitive, moisture sensitive, pyrophoric, high energy, toxic, high potency, etc.). Advocates for innovation and improvement at multiple levels. Leads others to do the same.&nbsp;
<ul>
<li>Proven skilled innovative problem solver.&nbsp;</li>
</ul>
·&nbsp; &nbsp; &nbsp; &nbsp; Adept in presenting findings and making strong data-driven recommendations in a group setting.
<ul>
<li>Demonstrated working knowledge of collaboration tools (e.g. Teams, Salesforce, SharePoint, electronic notebooks, etc.) to drive engagement and deliver results.&nbsp;</li>
</ul>
·&nbsp; &nbsp; &nbsp; &nbsp; Consistently represents the analytical group in PHA and safety related activities.·&nbsp; &nbsp; &nbsp; &nbsp; Awareness of state of the art development techniques, tools, and processes (e.g. stage gate, design for six sigma, design thinking, lean, etc.). Educational Requirements:&nbsp; ·&nbsp; &nbsp; &nbsp; &nbsp; BS Degree with 10 + years relevant experience desired, or·&nbsp; &nbsp; &nbsp; &nbsp; MS Degree with 5 + years relevant experience desired, orPhD Degree with 2 + years relevant experience desired Benefits
<ul>
<li>Medical, Dental, Vision - effective day one of employment.</li>
<li>401(k) with company match with immediate vesting - effective first of the month, following date of hire.
<ul>
<li>First 3% is matched dollar-for-dollar.&nbsp;</li>
<li>Second 3% is matched at 70 cents on the dollar.&nbsp;</li>
</ul>
</li>
<li>3 Weeks' Vacation.</li>
<li>12 Paid Holidays.</li>
<li>Basic Life, AD&amp;D, STD, and LTD provided at no cost to employee.</li>
</ul>

Senior Analytical Chemist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Discovery Biotherapeutics at AbbVie is seeking a highly skilled and self-motivated scientist to join a dynamic team supporting design, engineering, and manufacturing of multispecifics. This position will impact projects through engineering, production, and characterization of multispecific biopharmaceutical products. The ideal candidate should have extensive experience with biologics and multispecifics production platforms, analytical characterization, and a proven track record implementing multispecific engineering and production strategies to advance early- and late-stage discovery programs. The applicant should be an enthusiastic, creative scientist who will make tangible contributions to the continuous improvement and innovation within the organization.
Key Responsibilities:
<ul>
<li>Responsible for design, engineering and production of multispecific biologics to support oncology</li>
<li>Evaluate and integrate state-of-the-art technology to improve therapeutic production platforms, and demonstrate creative “out-of-the-box” thinking to solve difficult problems</li>
<li>Serve as a Multispecifics Engineering representative for cross-functional teams, and contribute scientific insights into multiple projects across various therapeutic areas; recognized expert in multispecifics design and production</li>
<li>Serve as the Biologics lead on projects to coordinate activities and transitions from hit generation through candidate nomination</li>
<li>Identify and solve technical problems independently, conceive and implement innovative process research ideas</li>
<li>Ensure consistency and quality of technical reports</li>
<li>Provide project update, analysis and advice to cross-functional teams and senior management</li>
<li>Present original work internally across departments and at internal and external scientific conferences; may author or co-author peer-reviewed scientific papers or patents</li>
</ul>
Qualifications 
<ul>
<li>PhD, MS, or BS degree in Biochemistry, Biochemical engineering or related disciplines with typically 0-5 (PhD), 8-11 (MS), or 10-13 (BS) years of experience,&nbsp;ideally in multispecifics biologics engineering</li>
<li>Extensive experience with protein, biologics, fragments, and multi-specifics design, expression and purification</li>
<li>Design experience of multispefics for ADC is preferred</li>
<li>Experience with purification and automation instruments e.g. Akta, Kingfisher, Hamilton</li>
<li>Sound scientific understanding of current state of protein expression/separation/analytical technologies and ability to explore and develop new approaches for innovative purification</li>
<li>Experience with CRO coordination</li>
<li>Experience with in vitro analytical techniques for protein characterization (e.g. SEC, MS, DSF); experience with developability screening for multispecifics preferred</li>
<li>Strong molecular biology skills (e.g. molecular cloning) and experience with sequence analysis tools (Vector NTI, Geneious, Genedata)</li>
<li>Knowledge of biologic pipeline progression from exploratory through candidate nomination with program management experience preferred</li>
<li>Excellent organizational skills and the ability to manage multiple projects simultaneously and adapt to rapid change in priorities</li>
<li>Candidate must be a goal-oriented team player with excellent verbal and written communication skills, ability to operate in a fast-paced multi-disciplinary environment, and strong can-do attitude</li>
<li>Recognized in the scientific community through a sustained record of peer-reviewed publications and patents preferred</li>
</ul>
Key AbbVie Competencies:
<ul>
<li>Builds strong relationships with peers and cross functionally with partners outside of the team to enable high performance</li>
<li>Learns fast, grasps the “essence” and can change the course quickly where indicated</li>
<li>Raises the bar and is never satisfied with the status quo</li>
<li>Creates a learning environment, open to suggestions and experimentation for improvement</li>
<li>Embraces the ideas of others, nurtures innovation and manages innovation to reality</li>
</ul>
 Position will be filled at level commensurate with extent of education, experience, and accomplishment - Senior Scientist I or Senior Scientist II
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may&nbsp;ultimately&nbsp;pay&nbsp;more or less than the posted range. This range may be&nbsp;modified&nbsp;in the&nbsp;future.&nbsp;​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to&nbsp;participate&nbsp;in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to&nbsp;participate&nbsp;in our long-term incentive&nbsp;programs.&nbsp;​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee&nbsp;remains&nbsp;in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be&nbsp;modified&nbsp;at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist, Multispecific Antibody Engineering (Oncology)

<h3>Job Description</h3>
Job DescriptionJob Title: Clean Room AssemblerJob Description
This role involves performing a variety of tasks, ranging from repetitive to non-repetitive production, to assemble component parts into assemblies, sub-assemblies, or completed units using standard operating procedures. The position may require conducting quality inspections on the processing line in accordance with quality specifications.
Responsibilities
<ul>
<li>Assemble component parts into assemblies, sub-assemblies, or completed units.</li>
<li>Follow standard operating procedures to ensure accuracy and quality.</li>
<li>Conduct quality inspections on the processing line as per quality specifications.</li>
<li>Work on basic and routine assignments under close supervision.</li>
<li>Adhere to all quality guidelines and standard operating procedures.</li>
<li>Seek supervisor approval for any deviations from the norm.</li>
</ul>
Essential Skills
<ul>
<li>Basic skills and techniques for completing routine tasks.</li>
<li>Ability to maintain appropriate licenses, training, and certifications.</li>
<li>Experience in cleanroom environments, assembly, and microscope usage.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in assembly or warehouse settings.</li>
</ul>
Why Work Here?
Join a team that values precision and quality. Benefit from a structured work environment with clearly defined procedures and supportive supervision. Enhance your skills with opportunities for training and certification.
Work Environment
Work in a cleanroom environment where you will use microscopes and adhere to standard operating procedures. Enjoy a role that involves routine tasks with close supervision to ensure quality and accuracy.
Job Type &amp; Location
This is a Contract position based out of Chicopee, MA.
Pay and Benefits
The pay range for this position is $17.65 - $19.40/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Chicopee,MA.
Application Deadline
This position is anticipated to close on Jan 30, 2026.

About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Clean Room Assembler

<h3>Job Description</h3>
Job DescriptionProduct Development Scientist – Medical Nutrition 
<ul>
<li>Location: Ayer, MA (On-site) </li>
<li>Industry: Food Production / Medical Nutrition </li>
<li>Experience: Mid-Level (5+ years) </li>
<li>Education: Bachelor’s degree required </li>
<li>Positions: 1 </li>
<li>Relocation: Limited assistance available </li>
<li>Visa Sponsorship: Not available Overview </li>
<li>Seeking a Product Development Scientist to develop and optimize medical nutrition beverage and powder formulations in a manufacturing environment. This role supports product innovation, ingredient initiatives, clinical evidence development, and compliance with GMP and food safety standards. </li>
<li>Responsibilities </li>
<li>Develop and optimize nutritional beverage and powder formulations </li>
<li>Conduct bench-level formulation, testing, and troubleshooting </li>
<li>Execute shelf-life and stability studies </li>
<li>Research and evaluate new ingredients </li>
<li>Support scale-up, manufacturing, and commercialization activities </li>
<li>Collaborate with cross-functional teams (R&amp;D, Quality, Manufacturing, Commercial) </li>
<li>Ensure compliance with GMP and food safety requirements </li>
<li>Support documentation and IP protection efforts Additional Info </li>
<li>On-site role in Ayer, MA </li>
<li>Limited relocation assistance available </li>
<li>No visa sponsorship available </li>
<li>JD Summary:Develop and optimize medical nutrition beverage and powder formulations; apply food science and ingredient expertise; collaborate with Medical Nutrition, Marketing, Sales, Manufacturing; research new ingredients; support clinical evidence development; manage ingredient vendors; support IP protection; ensure GMP, food safety, and workplace safety compliance; participate in conferences and clinician meetings; support manufacturing and new product initiatives. </li>
</ul>
 RequirementsRequirements 
<ul>
<li>Bachelor’s degree in Food Science, Nutrition, or related field (Master’s preferred) </li>
<li>5+ years of product development experience in food, beverage, medical nutrition, supplement, or nutraceuticals </li>
<li>Strong knowledge of ingredient functionality and nutrient stability </li>
<li>Experience with GMPs and FDA food regulations </li>
<li>Hands-on lab and pilot-scale experience required </li>
<li>PLM or formulation software experience preferred </li>
</ul>

Product Development Scientist

<h3>Job Description</h3>
Duration: 1 Year contract
Schedule: Monday to Friday, 8:00 am to 5:00 pm

Job Description:
This position is in the Biologics Purification Development team of the Product Development Science &amp; Technology department at Bioresearch Center. The candidate will be involved with all aspects of protein purification and protein chemistry to support biopharmaceutical process development.

Responsibilities:
<ul>
<li>Execute high throughput scale down robotic purification as part of early and late stage process development, viral clearance, process characterization, and continuous process improvement studies.</li>
<li>Perform data acquisition and analysis, and documentation in electric lab notebooks.</li>
<li>Will develop economical, robust steps for recovering the target protein from bioreactor harvests using chromatography, filtration, and other separation techniques; developing downstream purification processes to be transferred to manufacturing; and perform laboratory scale process characterization studies.</li>
<li>Perform various bioanalytical assays, including HPLC, ELISAs and SDS-PAGE, to aid in rapid process development.</li>
<li>The candidate must possess strong written, oral, and collaborative skills in order to effectively communicate experimental procedures and results.</li>
<li>As appropriate, the candidate may supply technical support for pilot and/or GMP manufacturing of clinical materials.</li>
<li>Execute new technology/innovation evaluation for purification process.</li>
</ul>
 
Experience:
<ul>
<li>PhD. - Chemical Engineering, Biotechnology, Biochemistry, or Chemistry with 0-2 yrs.</li>
<li>Internship or corporate experience</li>
<li>Laboratory hands on skills</li>
<li>Experience with chromatography and filtration for biologics purification</li>
<li>Experience with bioanalytical assays and methods preferred</li>
</ul>
 
Skills:
a. Strong biological scientific understanding.
 2. Experience with chromatography and filtration for biologics purification
 3. Experience with bioanalytical assays and methods preferred

Education:
<ul>
<li>PhD. - Chemical Engineering, Biotechnology, Biochemistry, or Chemistry with 0-2 yrs. Experience or MS with 4-6 yrs. Experience</li>
</ul>

About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit <a href="http://www.ustechsolutions.com" target="_blank">www.ustechsolutions.com</a>.
 
US Tech Solutions is an Equal Opportunity Employer.All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
 
Recruiter Details:
Name: Muskan
Email: <a href="mailto:Muskan.anjea@ustechsolutionsinc.com" target="_blank">Muskan.anjea@ustechsolutionsinc.com</a>
Internal Id: 26-00642

Purification Scientist III

<h3>Job Description</h3>
Job Description
Title: Research Scientist – Animal Studies Location: Marlborough, MA (Hybrid) Contract Length: 6-12 months with possibility for extension/conversion
General Description
<ul>
<li>Experience with benchtop models using phantoms.</li>
<li>Participation in preclinical investigations with tissue collection and biologic metrics.</li>
<li>Familiar with numerical models with finite element methods.</li>
<li>Skills on data collecting, analyzing, interpreting, and communicating experimental results to the team and organization.</li>
</ul>
Responsibilities and Duties
<ul>
<li>Collaborate with the research team to develop experimental methodologies in benchtop, numerical, and preclinical methodologies.</li>
<li>Execute benchtop and preclinical trial investigations, including collection, analysis, interpretation, and distribution of research findings.</li>
<li>Capacity to integrate research outcomes into meaningful technological advances.</li>
<li>Support regulatory submissions.</li>
<li>Generation of reviews supporting technical documentation and product development phases.</li>
<li>Contribute to the generation of intellectual property for the company.</li>
<li>Interaction with third-party service research providers.</li>
<li>Compilation and analysis of research data for scientific publications and technical writing.</li>
<li>Attendance at relevant scientific conferences and meetings.</li>
</ul>
Requirements
<ul>
<li>Advanced degree in Engineering, Biomedical Engineering, or a related scientific field. A PhD is highly valued.</li>
<li>Previous participation in a multidisciplinary project including benchtop, numerical, and preclinical. Experience pulsed electric fields and electroporation applications is highly valued.</li>
<li>Basic knowledge of electricity, mechanic, human anatomy and physiology.</li>
<li>Self-driven skills for execution and education.</li>
</ul>

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