BioProcess Engineer GMP Manufacturing experience

Position: Bio Process Engineer with GMP Manufacturing experience
Greetings,

Seeking Bio Process Engineer with GMP Manufacturing experience (Onsite, Framingham, MA)

Seeking a BIOPROCESS Engineer for my Pharma client in Framingham, MA. 12+ month ONSITE Contract. This is a more junior role, as 1-2 years of experience (Masters degree) or 2-4 years of experience required (Bachelors degree). This an outstanding opportunity for a junior professional that is looking to build broad biopharma expertise and accelerate their career growth.
C2C rate range $50
-52 per hour
. Manager gives a very technical interview.

Client name will not be disclosed until after a qualified candidate resume is presented. Two recent work references will be required from candidates UPON SUBMISSION.
Resumes will be screened by an AI tool and blatant AI generated resumes will be rejected.

REQUIREMENTS:

• Bachelor's degree in Chemical Engineering, Biochemistry, Biotechnology, Bioengineering, or a related life sciences field with a minimum of 2 - 4 years of relevant industry experience;
  OR a Master's degree with a minimum of 1 - 2 years of experience in biopharmaceutical manufacturing, process engineering, or process development.
• Familiarity with upstream and/or downstream bioprocess unit operations (e.g., cell culture, chromatography, filtration) in a GMP manufacturing environments.
• Strong proficiency in Microsoft Excel; comfort with data review, process trending, and technical documentation systems.
• Strong attention to detail, organizational discipline, and the ability to manage multiple priorities within defined timelines.
• Effective written and verbal communication skills in a cross-functional team setting.
• Prior exposure to technology transfer, process characterization, process validation, or manufacturing support activities in a GMP biologics.
• Experience with data visualization tools, process analytics platforms, or digital workflow development.
• Familiarity with quality systems including deviations, CAPAs, change controls, and investigation documentation.
• Exposure to external manufacturing partnerships or CDMO collaboration models preferred
• Experience across multiple biologic modalities (e.g., mammalian, microbial, etc.) preferred
• ONSITE in Framingham, MA.
• Open to candidates willing to relocate at their own expense.
• Ability to gown and work in classified GMP manufacturing areas as needed.
• Ability to work flexible hours to support manufacturing schedules or cross-site coordination across time zones.