What are the responsibilities and job description for the Manufacturing Associate position at TSR Consulting?
Bio Process Associate
Location: Devens, MA (100% Onsite)
Duration: 6 Month Contract (Possible Extension)
Pay Range: $20.00 - $30.00/hour (W2)
About the Role
TSR Consulting Services, Inc., a BCforward company, is seeking a highly motivated Bio Process Associate to support one of our leading biopharmaceutical clients in Devens, MA.
This position is ideal for candidates with hands-on GMP manufacturing experience in biotechnology or biopharmaceutical production. The successful candidate will support upstream and/or downstream manufacturing operations while ensuring compliance with GMP regulations, SOPs, and quality standards.
Work Schedule:
- Rotating shift:
- 3 days on (Saturday, Sunday, Monday)
- 2 days off (Tuesday, Wednesday)
- 2 days on (Thursday, Friday)
- 3 days off (Saturday through Monday)
- Must be available to work weekends and holidays as scheduled.
Key Responsibilities
- Execute manufacturing operations in accordance with GMP regulations and written procedures.
- Perform upstream and/or downstream bioprocess manufacturing activities.
- Weigh, verify, and document raw materials.
- Assemble, clean, sterilize, and prepare manufacturing equipment.
- Complete electronic batch records and manufacturing documentation accurately.
- Operate production equipment including bioreactors, chromatography systems, filtration equipment, buffer preparation systems, and harvest equipment.
- Utilize manufacturing automation systems and business applications.
- Support process investigations, validation activities, and continuous improvement initiatives.
- Maintain cleanroom standards and follow all safety requirements.
- Collaborate effectively with Manufacturing, Quality, and cross-functional teams.
Required Qualifications
- High School Diploma required; Associate's or Bachelor's degree in Science, Engineering, Biotechnology, Biochemistry, or a related field is preferred.
- Minimum 1 year of GMP biotechnology or biopharmaceutical manufacturing experience.
- Hands-on experience with upstream and/or downstream manufacturing operations.
- Strong knowledge of GMP regulations and Standard Operating Procedures (SOPs).
- Experience working in a highly automated manufacturing environment.
- Strong teamwork, communication, and problem-solving skills.
- Excellent attention to detail and personal accountability.
- Proficiency with Microsoft Office and web-based applications.
Preferred Qualifications
Experience with any of the following is highly preferred:
- DeltaV
- Syncade
- OSI PI Historian
- SAP
- TrackWise
- Maximo
Must-Have Skills
- GMP/biopharmaceutical manufacturing experience
- Upstream and/or downstream manufacturing operations
- Strong understanding of GMP and SOP compliance
- Experience in automated environments
- Excellent attention to detail
- Strong communication and teamwork skills
- Comfortable working rotating shifts, weekends, and holidays
If you are interested in this opportunity, please apply with your updated resume for immediate consideration.
TSR Consulting Services, Inc. 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 veteran status.
Salary : $20 - $30