Hi,
My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.
I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.
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https://www.linkedin.com/company/99455976/
Role: Bioprocess Engineer
Location: Framingham, MA (100% Onsite)
Duration: 12+ Month Contract
Position Overview:
We are seeking motivated Bioprocess Engineers to support biopharmaceutical manufacturing operations, process engineering initiatives, and technology transfer activities within a GMP-regulated environment. This is an excellent opportunity for early-career professionals looking to gain hands-on experience supporting biologics manufacturing, process optimization, validation, and cross-functional manufacturing support.
The ideal candidate will have experience in upstream and/or downstream bioprocessing and a strong interest in process improvement, manufacturing support, and biologics production.
Key Responsibilities
- Support upstream and downstream bioprocess manufacturing operations in a GMP environment.
- Assist with process monitoring, data analysis, process trending, and performance evaluations.
- Participate in technology transfer, process characterization, and process validation activities.
- Support manufacturing investigations, deviations, CAPAs, and change control initiatives.
- Collaborate with Manufacturing, Quality, Process Development, Validation, and Engineering teams.
- Generate and maintain technical documentation, reports, and process records.
- Analyze process data and identify opportunities for process improvements and operational efficiencies.
- Support manufacturing readiness, troubleshooting, and continuous improvement initiatives.
- Work closely with internal teams and external manufacturing partners when required.
Required Qualifications
- Bachelor's degree in Chemical Engineering, Bioengineering, Biotechnology, Biochemistry, Life Sciences, or a related field with 2–4 years of relevant industry experience; OR
- Master's degree with 1–2 years of experience in biopharmaceutical manufacturing, process engineering, or process development.
- Experience supporting biopharmaceutical or biologics manufacturing operations.
- Familiarity with upstream and/or downstream unit operations, including:
- Cell Culture
- Chromatography
- Filtration
- Strong proficiency in Microsoft Excel and data analysis.
- Excellent organizational, documentation, and communication skills.
- Ability to manage multiple priorities in a fast-paced GMP environment.