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<h3>Job Description</h3>
Job DescriptionJob Title: Clean Room Operator
1st &amp; 2nd Shift
Job Description
We are seeking a dedicated Clean Room Operator with a passion for quality and a strong sense of responsibility. This role requires flexibility in working overtime and the ability to stand for the entire shift with minimal downtime. You will work in a clean room environment, utilizing small hand tools and components, and have the opportunity to multitask across multiple workstations. This is an exciting chance to grow with a company in its early stages, where wearing many hats is encouraged.
Responsibilities
<ul>
<li>Manufacture, inspect, and package products following written processes.</li>
<li>Work at a pace that meets established time standards while ensuring product quality.</li>
<li>Identify quality issues or workmanship deficiencies related to equipment, assembly and inspection processes, materials, and manufacturing environment.</li>
<li>Comply with cGMP requirements by maintaining individual training records and adhering to documented manufacturing practices and procedures.</li>
<li>Maintain a clean, safe, and organized work environment.</li>
<li>Comply with all company policies and procedures.</li>
<li>Perform other duties as assigned.</li>
</ul>
Essential Skills
<ul>
<li>High School Diploma or equivalent.</li>
<li>One year of clean room experience.</li>
<li>Prior experience in a medical device manufacturing setting.</li>
<li>Ability to read and understand policies, procedures, and processes written in English.</li>
<li>Good hand-eye coordination and attention to detail.</li>
<li>Effective communication skills.</li>
<li>Demonstrated ability to achieve quality and labor time targets.</li>
</ul>
 Pay and Benefits
The pay range for this position is $22.00 - $24.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Billerica,MA.
Application Deadline
This position is anticipated to close on May 30, 2025.
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 Operator

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
Responsible for conducting an independent research project under the co-mentorship and supervision of research scientists.
</li>
<li>
Attend on-boarding and training sessions
</li>
<li>
Plan, design, and execute a research project as agreed upon your scientist co-mentors (aka "Supervisors")
</li>
<li>
Actively participate in weekly Summer Internship Program professional development sessions/workshops
</li>
<li>
Present research project at an end of program poster session
</li>
<li>
Adhere to all policies
</li>
</ul>
QUALIFICATIONS:
<ul>
<li>
Enrolled in a US academic institution and have completed at least 3 semesters
</li>
<li>
Have a GPA of at least 3.0 on a 4.0 scale
</li>
<li>
Have a strong desire to pursue a graduate-level STEM degree for biomedical research
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Scientific Associate

<h3>Job Description</h3>
Job Description
The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. 
WORKING AT GENEZEN
Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.
JOB SUMMARY
The QC Microbiology Supervisor will lead, plan, organize, guide, and be responsible for the coordination/performance of the QC Microbiology Laboratory Operations,
This position is located in Lexington, MA and will supervise the 2nd shift which will operate M-F from 1:00-9:30pm. The Supervisor will report to the Manager of Microbiology.
ESSENTIAL JOB FUNCTIONS
<ul>
<li>Oversee the execution of monitoring for controlled environments and utility systems within the Manufacturing Facility. Ensure execution is compliant with appropriate regulatory requirements and guidelines using approved Standard Operating procedures (SOPs). </li>
<li>Serve as an SME and provide guidance and support for critical QC Microbiology assays and methods.</li>
<li>Provide leadership, coaching, mentoring and training of QC Microbiology staff, aiding in employee development and performance. </li>
<li>Ensure QC Microbiology testing is completed, reviewed, and reported in a compliant manner and results are timely delivered to clients.</li>
<li>Maintain all aspects of QC Microbiology day-to-day operations and scheduling to align with all aspects of GXP requirements.</li>
<li>Manage data and trending in support of environmental monitoring and utility monitoring reports.</li>
<li>Represent QC Microbiology at cross-functional meetings and interact with internal customers, clients and external vendors.</li>
<li>Perform QC Microbiology testing as required, including bioburden, endotoxin of in-process, product and utility samples. </li>
<li>Perform EM and utility related monitoring, as necessary. </li>
<li>Identify continuous improvement opportunities. Design, implement and maintain resulting systems.</li>
<li>Ensure a safe working environment and compliance with OSHA, EHS, Quality, and cGMP procedures and policies is maintained.</li>
<li>Author and revise SOPs, protocols and technical reports to meet industry standards, as necessary.</li>
<li>Oversee QC sample submission and processing activities, and ensure testing is performed accordingly. </li>
<li>Initiate and collaborate on change controls, deviations, and Out of Specification (OOS), Out of Tolerance (OOT) investigations related to QCM and assist with non-conformance investigations. </li>
<li>Serve a system owner of QC Microbiology controlled temperature units, respond per on-call schedule to CMS alarms, including off-hours and weekends </li>
</ul>
SPECIAL WORK REQUIREMENTS
<ul>
<li>Ability to troubleshoot equipment and microbiological testing methods.</li>
<li>Ability to adapt to schedules and priorities changes based on business needs</li>
<li>Experience creating comprehensive department schedules</li>
<li>Leadership experience within a high functioning team</li>
<li>Other duties, as assigned. </li>
</ul>
KNOWLEDGE, SKILLS AND EXPERIENCE
EDUCATION / CERTIFICATIONS / LICENSES
Essential/Desired
Bachelor's degree in microbiology; other related science will be considered. 
Essential
ON-THE-JOB EXPERIENCE

5-15 years of Microbiology laboratory-based experience in a QC testing capacity within a cGMP setting. 
Required
Prior supervisory experience. 
Desired
SKILLS / ABILITIES

Excellent microbiological skills and technical experience in GXP environment. 
Essential
Thorough understanding of industry and regulatory testing requirements for QC Microbiology.
Essential
Computer literacy (MS Word, Excel, and LIMS)
Essential
Must possess excellent communication and organizational skills.
Essential
Detail-Oriented
Essential
Self-organized
Essential
Work Environment:
<ul>
<li>Regularly sit or stand for long periods of time </li>
<li>Work in a BSL 2 environment</li>
</ul>
Movement:
<ul>
<li>Work in a BSL 2 environment</li>
</ul>
Lifting
<ul>
<li>Frequently lift and/or move up to 25 pounds </li>
</ul>
Vision
<ul>
<li>Frequently utilize close vision and the ability to adjust focus</li>
</ul>
Communication
<ul>
<li>Frequently required to communicate by talking, hearing, using telephone and e-mail</li>
</ul>
GENEZEN'S CURES VALUE-BASED COMPETENCIES
Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
Resilience &amp; Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. 
Execute with Excellence &amp; Integrity We are dedicated to delivering quality results and upholding ethical principals.
olutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner.
GENEZEN'S BENEFITS
<ul>
<li>Paid vacation days, amount based on tenure</li>
<li>Paid sick time</li>
<li>10 observed holidays + 2 floating holiday + 1 volunteer day</li>
<li>401(k) plan with company match up to 6% of salary, vested immediately</li>
<li>Share Appreciation Rights</li>
<li>Choice of several healthcare plans</li>
<li>FSA and HSA programs</li>
<li>Dental &amp; vision care</li>
<li>Employer-paid basic term life/personal accident insurance</li>
<li>Voluntary disability, universal life/personal accident insurance</li>
<li>Accidental Death &amp; Dismemberment (AD&amp;D) Insurance</li>
</ul>
ADDITIONAL DETAILS
<ul>
<li>Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time.</li>
<li>This position requires a criminal background check.</li>
<li>Genezen is an Equal Opportunity Employer.</li>
<li>Genezen participates in EVerify.</li>
<li>Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.</li>
</ul>
Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts. 
Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

QC Supervisor, Microbiology (2nd Shift, 1pm-9:30pm)

<h3>Job Description</h3>
Job Description
Job Description: Cleanroom Technician (2nd Shift) Location: Mansfield Shift: 1st and 2nd Shift - $18-24/hr. (2 dollar differential on 2nd shift, base pay of $18-20) Employment Type: Full-Time
Overview:
Join our team as a Cleanroom Technician on 2nd shift. In this role, you’ll work in a Class 7 cleanroom, assembling small parts, handling electromechanical assemblies, and ensuring sterile products are cleaned, sealed, and labeled. This position requires attention to detail and technical skills in assembly, measurement, and machine setup.
Key Responsibilities:
<ul>
<li>
Assemble small parts using tools and optical microscopy.
</li>
<li>
Mix two-part solutions for molding and joining processes.
</li>
<li>
Perform machine setups for ultrasonic welders and heat-sealing equipment.
</li>
<li>
Clean, pouch, seal, and label sterile products.
</li>
<li>
Measure using lab equipment and maintain accurate documentation.
</li>
<li>
Read and interpret blueprints and procedures.
</li>
<li>
Work collaboratively and communicate effectively with the team.
</li>
</ul>
Qualifications:
<ul>
<li>
Ability to work in a cleanroom with gowning.
</li>
<li>
Strong manual dexterity for small part assembly.
</li>
<li>
Experience with electromechanical assemblies and troubleshooting.
</li>
<li>
Familiarity with MS Office, especially Access.
</li>
<li>
Attention to detail and ability to work with inspection tools.
</li>
</ul>
#KPB
Company DescriptionMicro Tech Staffing Group is one of the top staffing firms on the Eastern Seaboard. Since 1985 we have taken great pride in providing quality staffing services to businesses in the fields of Information Technology, Engineering, Manufacturing, Life Sciences, and Finance &amp; Administration. With offices in Massachusetts, New Hampshire, Rhode Island, Connecticut, Maine, Virginia, North Carolina and Georgia, Micro Tech places an average of 2,000 highly-skilled employees daily 
<h3>Company Description</h3>
Micro Tech Staffing Group is one of the top staffing firms on the Eastern Seaboard. Since 1985 we have taken great pride in providing quality staffing services to businesses in the fields of Information Technology, Engineering, Manufacturing, Life Sciences, and Finance &amp; Administration. With offices in Massachusetts, New Hampshire, Rhode Island, Connecticut, Maine, Virginia, North Carolina and Georgia, Micro Tech places an average of 2,000 highly-skilled employees daily

Cleanroom Assembler 1st and 2nd shift $18-24/hr.

<h3>Job Description</h3>
Job Description
Responsibilities: Under general supervision, perform all aspects required for the completion of all electric Geographic Information Systems (GIS) work closure and mapping activities. Perform administrative support activities of various degrees of complexity, and to perform as required such duties as:
<ul>
<li>Perform and complete "As Built" design changes for construction and confirming work requests and post updates to Smallworld GIS</li>
<li>Check construction and retirement orders together with their completion reports in the field against the actual installations and retirements of equipment</li>
<li>Perform and complete all types of Data Model changes and map/drawing changes</li>
<li>Assist with the design of Underground systems such as Conventional Manhole, Duct and URD systems utilizing computer systems and perform "As Built" design changes</li>
<li>Provide support to the Regional Control Centers and other clients to ensure accuracy of systems</li>
<li>Assist in recording on appropriate prints or drawings additions and retirements of facilities as shown on construction and retirement orders and associated completion reports</li>
<li>Analyze completion reports and reconcile with information added to or removed from the prints or drawings relating to any asset classes</li>
<li>Work proficiently in MS Office, GIS and EAM Applications</li>
<li>Make contacts with other districts and departments in connection with job duties</li>
<li>Assemble, maintain and/or transcribe information from various sources, prepare and maintain reports, correspondence and records, forms and orders.</li>
<li>Make arithmetical computations; maintain statistical information.</li>
<li>Check data for accuracy and otherwise assist in completing various types of orders, reports, invoices.</li>
<li>Communicate with customers or their representatives, outside agencies, and other departments.</li>
<li>Update company records including but not limited to maps and various reports.</li>
<li>Perform administrative support activities associated with the tasks and responsibilities of the department.</li>
</ul>
Requirements
AAS Degree in applicable Engineering Technology as posted, i.e. GIS, Computer Science, Electrical, Mechanical, or Civil/Structural. For GIS postings, candidates must have an AAS degree in GIS/Computer Science or two (2) years of design work experience in GIS
<ul>
<li>Must pass validated aptitude test</li>
<li>Ability to read maps and construction drawings and knowledge of equipment and materials used in electric plant</li>
<li>Thorough familiarity with applicable accounting procedures.</li>
<li>Thorough familiarity with applicable computer and software systems and procedures.</li>
<li>Ability to direct the work of others engaged in all administrative support activities as required.</li>
<li>Ability to handle contacts with customers, contractors and other departments.</li>
<li>Ability to handle duties which require independent judgment.</li>
<li>Satisfactory completion of validated skills testing (keyboarding), as determined by the Company</li>
<li>Ability to satisfactorily interact with customers, outside agencies and other departments.</li>
<li>Ability to handle duties that require independent judgment.</li>
<li>Ability to make arithmetical computations.</li>
<li>Familiarity with computer applications normally required in a business environment.</li>
<li>Satisfactory completion of validated skills testing (keyboarding), as determined by the Company.</li>
</ul>
Benefits
MWResource offers medical, dental and vision coverage through Capital Blue Cross, short- and long-term disability coverage, employer paid life insurance, and participation in the MWResource 401K plan for US based consultants.
MWResource does not discriminate based on race, gender, color, religion, national origin, age, disability, veteran status, or anything else that makes you part of any group.
Candidates must be authorized to work in the United States.
Candidates will be required to pass a background check and drug screening.
Please note we are not open to outsourcing our recruitment needs.

GIS Analyst

<h3>Job Description</h3>
Job Description
Job Title: Quality Control (QC) Chemist (Method Validation) Work Location: Fall River, MA&amp; Work Hours: 8:30AM – 5:00PM (may vary based on business needs)&amp; 
Reports To: Quality Control manager
The Quality Control Chemist is an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory.
Duties and Responsibilities • Preparation of protocols and execution of analytical method validation / verification / method transfer. • Working knowledge on cleaning validation (residue analysis). • Conduct routine testing or other analysis in a specific group or department setting. • Conduct advanced testing and/or critical testing, as required. • Operate specialized equipment or conduct specialized skill testing • Working knowledge of raw materials testing and release • Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP • Lead investigation activities. • Ensure compliance to all data integrity and cGMP practices, procedures, and expect • Ensure compliance with all good documentation practices. • Other duties and responsibilities as assigned by the Head of the Department or Section Head
Education and Experience: • Bachelor's degree (BS or BA), physical sciences, Chemistry preferred • Proficiently speak English as a first or second language Proficiently communicate and understand (read and write) scientific work in English • Must be authorized to work permanently in the United States without company sponsorship • Have excellent organization, learning and teaching skills required to work in teams • Ability to understand and analyze complex data sets. • Working knowledge of Microsoft Office programs and other scientific based software. • Experience in Inhalation products (MDI) is a plus

QC Chemist

<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 
We are seeking a scientist with strong organizational skills, excellent oral and written communication, and keen attention to detail. The ideal candidate will support the development, optimization, and qualification of analytical methods in a compliance-based environment. This role involves method development, process support, documentation, and potential technology transfer, along with some analytical testing. The ability to work independently and collaboratively, along with self-motivation, adaptability, and a positive attitude, is essential.
Responsibilities Include:&nbsp;
<ul>
<li>Contributing as part of a small team of scientists towards the development/optimization, and qualification of analytical methods to be used in support of biological therapeutic product release and characterization testing in a compliance-based environment</li>
<li>90% Method development,&nbsp;qualification, and process supporting related work, as well as associated protocol/report documentation and presentations;
<ul>
<li>May include technology transfer activities, regulatory support, and possible project team participation</li>
</ul>
</li>
<li>10% Analytical testing
<ul>
<li>Liquid Chromatography&nbsp;and Plate-Based&nbsp;</li>
</ul>
</li>
<li>Independently executes method development for: elucidation and monitoring of functional properties of protein therapeutics and the quantitation of process- and product-related impurities</li>
</ul>
Qualifications 
The Ideal Candidate will Have:&nbsp;
<ul>
<li>Experience in high throughput technologies and automated liquid handling systems – TECAN, Hamilton, etc.&nbsp;</li>
<li>Experience working in a GMP/GLP environment&nbsp;</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis, and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives</li>
<li>Understands and applies advanced scientific principles, theories, concepts, practices, and standards to process and product development</li>
</ul>
Minimum Qualifications:&nbsp;
<ul>
<li>BS in&nbsp;Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration
<ul>
<li>2 years of demonstrated work experience with cell-based assays</li>
</ul>
</li>
<li>Or MS in&nbsp;Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration
<ul>
<li>6 months of Demonstrated experience with cell-based assays&nbsp;</li>
</ul>
</li>
<li>Experience with&nbsp;experience working with sterile cell culture and execution of cell-based and plate-based immunological methods such as Bioassay, ELISA, Octet protein binding assays, Host Cell Protein assays, Activity and Binding assays</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with the Region Recruiter</li>
<li>45-60 Minute Virtual Interview with the Manager and/or Group Leader</li>
<li>30 Minute Virtual Meeting with the Site Director&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, Monday-Friday from 8 am-5 pm. Candidates living within a commutable distance of Lexington, Massachusettes, and the surrounding areas are encouraged to apply.&nbsp;&nbsp;
<ul>
<li>Excellent full-time benefits including 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 holiday</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Bioassay Scientist

<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 
Seeking a scientist to perform analytical testing for biologic product release and characterization in a cGMP/GLP environment. Responsibilities include routine testing, documentation, troubleshooting HPLC/UPLC/CE methods, and ensuring compliance.
Responsibilities Include:&nbsp;
<ul>
<li>Contributes as part of a team of AD scientists towards execution&nbsp;of various analytical methods to support biological therapeutic product release and characterization testing in a compliance-based environment.</li>
<li>Independently performs routine testing such as but not limited to SEC, CEX, RP, P20, P80, CE, iCE, cIEF, CE-SDS, Titer, Peptide, and Glycan mapping - using established Test Methods, including associated protocol/report documentation and presentations.</li>
<li>Conducts work in compliance with cGMP/GLP, safety, and regulatory requirements.</li>
<li>Responsible for working on other non-lab-based tasks from time to time if assigned.</li>
<li>Demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis,&nbsp;and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives.</li>
<li>Demonstrate HPLC, UPLC, and/or CE troubleshooting capabilities.</li>
</ul>
Qualifications 
The Ideal Candidate will Have:&nbsp;
<ul>
<li>Experience with ELISA techniques</li>
<li>Ability to quickly learn new techniques</li>
<li>Strong multitasking and organizational skills</li>
<li>Attention to detail with accurate record-keeping</li>
<li>Ability to follow instructions and adhere to company policies</li>
</ul>
Minimum Qualifications:&nbsp;
<ul>
<li>Bachelor’s or Master’s in Cell and Molecular Biology, Biochemistry, Pharmaceutical, or other science-related degree concentration</li>
<li>Equivalent directly related work/internship experience with HPLC/UPLC required.</li>
<li>Knowledge of principles of HPLC/UPLC/CE and theories of relevant techniques and a&nbsp;basic understanding of industry practices and standards required</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with the Region Recruiter</li>
<li>45-60 Minute Virtual Interview with the Manager and/or Group Leader</li>
<li>30 Minute Virtual Meeting with the Site Director&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, Monday-Friday from 8 am-5 pm. Candidates living within a commutable distance of Lexington, Massachusettes, and the surrounding areas are encouraged to apply.&nbsp;&nbsp;
<ul>
<li>Excellent full-time benefits including 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 holiday</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

HPLC Scientist

<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 
Technical expert that will drive late-stage process development activities of novel antibody-drug conjugates (ADCs).&nbsp; Independently identify, develop, and execute laboratory experiments to address critical project needs.&nbsp; Continuously seek to improve existing laboratory methods and processes.&nbsp; Read and adapt literature to accomplish assignments.&nbsp; Demonstrate mastery of a broad range of experimental techniques and methods of data analysis.&nbsp; Collaborate effectively with cross-functional groups ensure robust process scale-up and tech transfer to manufacturing sites.
Responsibilities:
<ul>
<li>
List up to 10 main responsibilities for the job. Include information about the accountability and scope.
•Independently design and conduct critical experiments that further project goals.
•Implement and may innovate new experimental protocols/techniques.
•Understand the goal and maintain a high proficiency in his/her projects as well as the overall
program.
•Interpret results and draw conclusions from own multistage experiments, note significant
deviations, then suggest, design, and pursue relevant experiments.
•Understand relevant scientific literature and apply theoretical framework to solving problems within
scientific discipline in a timely manner.
•Perform routine and complex tasks competently and independently and generate reliable and
consistent results.
•Impact projects mostly through lab and/or pilot plant based activities.
•Responsible for compliance with all applicable Corporate and Divisional policies and procedures.
•Understand and adhere to corporate standards regarding code of conduct, safety, appropriate
handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care
where applicable.
</li>
</ul>
Qualifications 
<ul>
<li>
•Bachelor’s Degree or equivalent education with typically 5 years of experience, or Master’s Degree
or equivalent education with typically two years of experience.
•Theoretical and practical knowledge to carry out the job functions.
</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​
​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive 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 determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with 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>

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