Bioprocess Engineer

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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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

• Bachelors degree in Chemical Engineering Bioengineering Biotechnology Biochemistry Life Sciences or a related field with 2 4 years of relevant industry experience; OR
• Masters 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.