Responsibilities:

Execute analytical testing for GMP and non-GMP release and stability samples.Adhere to Good Manufacturing Practices by completing and maintaining accurate cGMP documentation (electronic and hard copy) for all work performed.Support daily laboratory operations, including reagent preparation and routine instrument calibration.Maintain laboratory reagent and materials inventory; initiate ordering as needed to ensure uninterrupted operations.Support GMP data review and compliance checks, including data scanning and trend analysis.Assist with method qualification activities for analytical methods used by internal and external contract testing laboratories.Review, write, revise, and execute protocols, reports, test methods, and SOPs as required.Assist in coordinating sample management activities, including shipment, receipt, log-in, and inventory control.Establish and maintain a safe laboratory working environment; proactively identify, address, and correct potential safety hazards.

 

Qualifications:

MS with 3+ year or BS with 5+ years’ experience in analytical development and quality control in pharma/biotechHands on experience with protein analytical techniques—including SEC‑HPLC, CE‑SDS, icIEF, and ELISA—is required; proficiency with peptide mapping and N‑glycan analysis is a strong plusProficiency with laboratory software including Empower, Compass, and SoftMax for routine testing and data analysis.Hands‑on experience working in a GMP regulated environment, including maintaining accurate cGMP documentation, is essential.Strong teamwork and communication skills with demonstrated experience working across cross-functional teams.Experience using LIMS systems to support sample tracking and data management.Ability to work a flexible schedule to accommodate program priorities.Ability to thrive in a fast-paced, innovative environment while remaining flexible, proactive, resourceful, and efficient

Job Type & Location

This is a Contract position based out of Lexington, MA.

Pay and Benefits

The pay range for this position is $40.00 - $45.00/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 & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&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 Lexington,MA.

Application Deadline

This position is anticipated to close on Feb 11, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.