Scientist - GMP Quality & Technical Writing (Hybrid, Devens MA)

We are seeking a Scientist to join our client’s Manufacturing Sciences & Technology team in Devens, MA. This role supports the Materials and Cryogenics Science group in the life cycle management of raw materials, consumables, and single-use systems used in biopharmaceutical commercial manufacturing.

You will collaborate closely with Manufacturing, Quality Assurance, Quality Control, Supply Chain, and Procurement on cross-functional teams to ensure GMP compliance and continuity of supply.

Key responsibilities include :

• Qualify alternative raw material suppliers and partner with Procurement to identify new options.
• Recommend and lead necessary testing to qualify materials for GMP manufacturing.
• Author technical equivalency assessments, specification comparisons, material characterization reports, and change controls.
• Support material and consumable manufacturing investigations.
• Manage supplier change notifications and evaluate risks to maintain GMP compliance.
• Contribute to risk assessments and material specification development.
• Partner with cross-functional teams to deliver results in a fast-paced, matrixed environment.

Requirements

Bachelor’s or Master’s degree in Material Science Engineering, Chemistry, or related field with 2+ years of industry experience , or a PhD.

Strong technical writing skills and ability to author GMP documentation.

Experience in cross-matrix team environments and stakeholder collaboration.

Proven ability to manage multiple projects in a fast-paced setting.

Independent contributor with strong communication and interpersonal skills.

Experience with GMP change controls and investigations preferred.

Familiarity with analytical techniques (FTIR, SEM-EDS, etc.) and data trending / analysis a plus.

Awareness of cGMP regulations and compliance requirements.

Benefits

Competitive hourly rate : $67.20 – $75.20 / hr (W-2 only, no C2C)

Hybrid schedule (50% onsite Tue–Thu; full onsite during the first month)

12-month contract with possible extension

Health benefits, holiday pay, and 401(k) program

Paid time off (UTO) and professional development support

Employee referral bonus program

Opportunity to contribute to high-impact projects with a leading biopharma company