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Manager Bioreactor Jobs (NOW HIRING)

Sanofi EU

Production Operator

Jersey City, NJ

$24 - $32/hr

... Bioreactor and Media Preparation areas with minimum supervision and effective communication to management. Secondary responsibilities will be to aid in the troubleshooting of problems as they arise ...

Sanofi EU

Biomanufacturing Technician

Newark, NJ

$24 - $32/hr

... Bioreactor and Media Preparation areas with minimum supervision and effective communication to management. Secondary responsibilities will be to aid in the troubleshooting of problems as they arise ...

Sanofi EU

Biomanufacturing Technician

Yonkers, NY

$24 - $32/hr

... Bioreactor and Media Preparation areas with minimum supervision and effective communication to management. Secondary responsibilities will be to aid in the troubleshooting of problems as they arise ...

Sanofi EU

Production Operator

Paterson, NJ

$24 - $32/hr

... Bioreactor and Media Preparation areas with minimum supervision and effective communication to management. Secondary responsibilities will be to aid in the troubleshooting of problems as they arise ...

Sanofi EU

Biomanufacturing Technician

Jersey City, NJ

$24 - $32/hr

... Bioreactor and Media Preparation areas with minimum supervision and effective communication to management. Secondary responsibilities will be to aid in the troubleshooting of problems as they arise ...

Sanofi EU

Production Operator

Manhattan, NY

$24 - $32/hr

... Bioreactor and Media Preparation areas with minimum supervision and effective communication to management. Secondary responsibilities will be to aid in the troubleshooting of problems as they arise ...

Sanofi EU

Production Operator

Newark, NJ

$24 - $32/hr

... Bioreactor and Media Preparation areas with minimum supervision and effective communication to management. Secondary responsibilities will be to aid in the troubleshooting of problems as they arise ...

Sanofi EU

Production Operator

Pearl River, NY

$24 - $32/hr

... Bioreactor and Media Preparation areas with minimum supervision and effective communication to management. Secondary responsibilities will be to aid in the troubleshooting of problems as they arise ...

Sanofi EU

Biomanufacturing Technician

Paterson, NJ

$24 - $32/hr

... Bioreactor and Media Preparation areas with minimum supervision and effective communication to management. Secondary responsibilities will be to aid in the troubleshooting of problems as they arise ...

Sanofi EU

Biomanufacturing Technician

Manhattan, NY

$24 - $32/hr

... Bioreactor and Media Preparation areas with minimum supervision and effective communication to management. Secondary responsibilities will be to aid in the troubleshooting of problems as they arise ...

Sanofi EU

Biomanufacturing Technician

Pearl River, NY

$24 - $32/hr

... Bioreactor and Media Preparation areas with minimum supervision and effective communication to management. Secondary responsibilities will be to aid in the troubleshooting of problems as they arise ...

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Manager Bioreactor information

What is the difference between Manager Bioreactor vs Bioprocess Engineer?

AspectManager BioreactorBioprocess Engineer
CredentialsBachelor's or Master's in Biotechnology, Chemical Engineering, or related field; leadership experienceBachelor's or Master's in Biotechnology, Chemical Engineering, or related field; technical expertise
Work EnvironmentOversees bioreactor operations, manages teams, ensures complianceDesigns and optimizes bioprocesses, conducts experiments, analyzes data
Industry UsageCommonly employed in biotech manufacturing facilitiesFound in R&D labs and production settings within biotech and pharma

The Manager Bioreactor primarily oversees bioreactor operations and team management, focusing on production efficiency and compliance. In contrast, the Bioprocess Engineer concentrates on designing and optimizing bioprocesses, often working in research and development. Both roles require similar educational backgrounds but differ in responsibilities and focus areas within the biotech industry.

What are the key skills and qualifications needed to thrive as a manager bioreactor?

To thrive as a Manager Bioreactor, you need a strong background in biotechnology, bioprocess engineering, or a related field, often with a relevant degree and experience in bioreactor operations. Familiarity with process control systems, SCADA software, and GMP compliance, along with certifications like Six Sigma or Lean Manufacturing, is typically required. Leadership, problem-solving, and effective communication are vital soft skills for managing teams and resolving technical challenges. These skills ensure efficient, high-quality bioproduction and regulatory compliance in a complex manufacturing environment.

What is a manager bioreactor?

A Manager Bioreactor oversees the operation and maintenance of bioreactor systems used in the production of biological products, such as pharmaceuticals or vaccines. They manage a team of technicians and scientists to ensure efficient and safe bioprocessing, monitor process parameters, and troubleshoot equipment issues. Additionally, they are responsible for maintaining compliance with regulatory standards, optimizing production processes, and coordinating with other departments to meet production goals.

What are some common challenges faced by a manager bioreactor, and how can they be addressed?

A Manager Bioreactor often faces challenges such as maintaining optimal bioprocess conditions, troubleshooting equipment malfunctions, and ensuring strict adherence to regulatory and safety standards. Managing production schedules while balancing the needs of cross-functional teams, such as quality assurance and process development, can also be demanding. These challenges can be addressed through strong communication skills, proactive maintenance protocols, ongoing staff training, and staying updated with the latest bioprocessing technologies. Building collaborative relationships across departments is essential for resolving issues quickly and ensuring the smooth operation of bioreactor systems.
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Manager Bioreactor jobs near you
Infographic showing various Manager Bioreactor 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.

Continuation Engineer

Cell Culture Company, LLC

Minneapolis, MN • On-site

Full-time

Re-posted yesterday

Job description

Job Title:                                Continuation Engineer
Location:                                Minneapolis, MN
Immediate Supervisor:         Senior Director, Manufacturing
Travel Requirements:           0-10%
Education:                             B.S. or B.A. degree, minimum
Experience:                            3+Years Related Experience
Status:                                    Full-Time
Compensation:                      Salaried/Exempt
CELL CULTURE COMPANY OVERVIEW
Cell Culture Company (C3) is a contract development and manufacturing organization (CDMO) focused on custom protein production for therapeutic and diagnostic industries. C3 also manufactures, distributes and services AcuSyst perfusion bioreactor systems.
Our advantage is our ability to deliver the highest levels of quality while reducing financial risk and increasing speed to market for our customers. Our employees are experts in cell culture, purification, and quality control. C3 has serviced 1,700+ organizations globally.
Located in Minneapolis, Minnesota, C3 is headquartered at a 33,000-square foot facility that houses corporate offices, bioreactor manufacturing operations, a GMP-compliant custom mammalian and protein production space, and a distribution center.
GENERAL SUMMARY
C3 is currently recruiting for the position of Continuation Engineer, whose primary responsibility will be to support the manufacture of bioreactor instruments, disposables, and accessories. This role identifies and implements new and replacement parts to maintain current disposable and instrumentation product lines. Additionally, this role drafts and reviews complicated work instructions, drawings, and specifications with feedback from the manufacturing team. This team is tasked with meeting growth demands while maintaining stringent quality standards required through ISO 9001:2015.
Candidates must have experience meeting corporate goals related to production schedules, process optimization, cost control. This position will collaborate with the account services, supply chain, quality, engineering, and accounting departments to maintain sustainability of our products, resolve issues, and ensure on-time delivery of quality products to our customers.
DUTIES AND RESPONSIBILITIES
  • Create and update manufacturing and safety procedures. Evaluate drawings, bill of materials, SOPs, and other documents when required to ensure they are accurate, clear, concise, and user-friendly.
  • Work with quality control to ensure all manufactured products are within specifications.
  • Work with the assemblers/technicians on the flow and function of the disposable and instrumentation manufacturing areas to enable high productivity and provide a safe working environment.
  • Contribute with hands-on work to meet production schedules as needed.
  • Prepare for and participate in customer and supplier audits.
  • Participate in CAPA investigation and resolution process.
  • Participate in new/replacement product design
  • Facilitate the transition of new parts to production.
  • Other duties as assigned
QUALIFICATIONS
  • Strong leadership with excellent written and oral communication skills and the ability to maintain accurate documentation. Must have demonstrated ability to solve problems, think critically, make decisions, remain organized, multi-task, manage time, plan, and accomplish goals using interpersonal and organizational skills. Must be able to maintain a sense of urgency necessary to meet goals, objectives, and deadlines.
  • Familiarity with RoHS, CE, ISO, FDA, and other relevant regulations and classifications.
  • Experience manufacturing a complicated product line, preferably complex instrumentation and single-use disposables that are manufactured in a QSR, ISO, or similar environment.
  • Demonstrated success in Lean Process Improvement.
  • Ability to read and revise drawings/schematics/BOMs and review document change orders.
  • Advanced ability to use computers to plan, execute, communicate, present, and analyze using Microsoft office suite and Solidworks
  • Ability to maintain confidentiality at all times.
WORKING CONDITIONS
  • Clean room and electronics manufacturing environment with routine tools, a variety of equipment, and custom fixtures.
  • Office with accessibility to standard equipment, computer, copier, fax, and phone.
  • Use of computer system requiring frequent mental and visual attention.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the position.

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