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Bioprocess Manufacturing Manager Jobs (NOW HIRING)

ProcessHQ, Inc.

QA/QC Director

Glendale, CA · On-site

$100K - $200K/yr

... our bioprocess manufacturing offerings. Key Responsibilities: * Develop, implement, and maintain Quality Management Systems (QMS) in compliance with ISO 9001-2015. * Manage and maintain ISO 9001 ...

ProcessHQ, Inc.

QA/QC Director

Glendale, CA · On-site

$100K - $200K/yr

... our bioprocess manufacturing offerings. Key Responsibilities: * Develop, implement, and maintain Quality Management Systems (QMS) in compliance with ISO 9001-2015. * Manage and maintain ISO 9001 ...

ProcessHQ, Inc.

QA/QC Director

Glendale, CA · On-site

$100K - $200K/yr

... our bioprocess manufacturing offerings. Key Responsibilities: * Develop, implement, and maintain Quality Management Systems (QMS) in compliance with ISO 9001-2015. * Manage and maintain ISO 9001 ...

Lonza

Manufacturing Bioprocess Technician

Vacaville, CA · On-site

$43K - $69K/yr

Join Lonza in Vacaville, CA, as a Manufacturing Technician - Bioprocess and be part of a hard ... Manage inventory and process systems, maintaining accurate records and ensuring safety and ...

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Bioprocess Manufacturing Manager information

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$39.5K

$99.2K

$148.5K

How much do bioprocess manufacturing manager jobs pay per year?

As of Sep 8, 2026, the average yearly pay for bioprocess manufacturing manager in the United States is $99,198.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,500.00 and $118,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Bioprocess Manufacturing Manager jobs?

For Bioprocess Manufacturing Manager jobs, the most frequently searched job titles are:

Infographic showing various Bioprocess Manufacturing Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $99,198 per year, or $47.7 per hour.

Bioprocess Engineer

Framingham, MA • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Re-posted 29 days ago

Job description

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.

You can also follow Stark Pharma Solutions on LinkedIn for the latest job updates:

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.