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Manager Bioreactor Jobs in Washington (NOW HIRING)

Azaaki Solutions

Be Seen First

Biomanufacturing Associate

Rockville, MD · On-site

$31.50/hr

... train, bioreactor set up, fermentation monitoring and/or harvest). * Follow instructions when ... Informal coaching or project management experience is desirable. * Qualified as a LEAN trainer or ...

BTS Bioenergy

Wastewater Operator

Jessup, MD · On-site

$22.25 - $30.75/hr

This position reports to the supervisor on duty, Asst. Plant Manager and Plant Manager and reports ... Knowledge and experience operating a Membrane Bioreactor desirable. * Familiarity with ...

Guidehouse

Scientist

Gaithersburg, MD · On-site

$74K - $124K/yr

... bioreactor systems. * Extensive hands-on experience with aseptic technique and mammalian cell ... Be able to independently design experiments and work plans and manage project timelines for ...

Guidehouse

Scientist

Gaithersburg, MD · On-site

$74K - $124K/yr

... bioreactor systems. * Extensive hands-on experience with aseptic technique and mammalian cell ... Be able to independently design experiments and work plans and manage project timelines for ...

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Manager Bioreactor information

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 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 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.

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 most commonly searched types of Bioreactor jobs in Washington?

The most popular types of Bioreactor jobs in Washington are:

What are popular job titles related to Manager Bioreactor jobs in Washington?

For Manager Bioreactor jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Manager Bioreactor jobs in Washington look for?

The top searched job categories for Manager Bioreactor jobs in Washington are:

What cities in Washington are hiring for Manager Bioreactor jobs?

Cities in Washington with the most Manager Bioreactor job openings:

Manager Bioreactor jobs near you
Infographic showing various Manager Bioreactor job openings in Washington as of August 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Biomanufacturing Associate

Azaaki Solutions

Rockville, MD • On-site

$31.50/hr

Contractor

This job post has expired 2 days ago. Applications are no longer accepted.

Job description

Title: BMA Upstream

BMA I Pay Rate $25.50

BMA II Pay Rate $28.50
Location: Rockville MD 20850

Duration: 4+Months

Description:

Initial shift schedule (core hours) is 8:00 am - 4:30 pm w/ 30 min unpaid lunch Monday through Friday
OT and weekend work may become required
there is a possibility of extension or conversion at end of 6 months

Position Summary:

The Biomanufacturing Associate II plays an integral role within CRL’s gene therapy manufacturing function by applying biological, bioprocess, manufacturing, mechanical, application, system, and technology principles, processes, procedures, inputs, and outputs, for designated production processes and handovers within a regulated environment to ensure the timely production and release of quality products, based on client specifications.

Key Responsibilities and Duties:

  • Apply and adhere to SOPs, cGMP, GLP, Quality, and Safety requirements.
  • Effectively execute a range of tasks, in line with SOPs, in the following area:
    • Upstream Activities (e.g., solutions, media aliquot, and buffer preparation and autoclave materials for cell culture, staging of raw materials, seed train, bioreactor set up, fermentation monitoring and/or harvest).
  • Follow instructions when performing planned manufacturing activities, in alignment with the batch record.
  • Prepare, edit, and complete quality documents. Well-versed in applying GDP.
  • Ensure data integrity - accurately document and review work prior to submission.
  • Document, record, investigate, and report observed process variances/deviations, in real time.
  • Follow instructions when operating equipment. Prepare, clean, and maintain equipment/tools.

Title: BMA Downstream

Location: Rockville MD 20850

Duration: 4+Months

Pay Rate $31.50/hr.

Qualifications:

  • HS Diploma/equivalent and 6 years of related experience, A.S. with 5 years, or a B.S. in biology/life sciences, bioengineering, or related discipline with 3 years of related experience.
  • Prior cell/gene therapy experience in a highly technical role, covering a wide range of tasks, within a cGMP/biotech manufacturing environment or related industry/role.
  • Informal coaching or project management experience is desirable.
  • Qualified as a LEAN trainer or willing to become qualified.

 Pay Rate $23.5/hr.

Initial shift schedule (core hours) is 8:00 am - 4:30 pm w/ 30 min unpaid lunch Monday through Friday
OT and weekend work may become required
there is a possibility of extension or conversion at end of 6 months

Preferred Qualifications for the role

? High School Diploma or Associate Degree with 0-2 years of experience in Downstream biologic production processes in a GMP environment in a Life Sciences Company; or

? Bachelor of Science in science or Engineering and 0-1 years of experience in Downstream biologic production processes in a GMP environment in a Life Sciences Company

? Basic knowledge and understanding of purification processes

? Ability to obtain sufficient hands-on experience with chromatography systems (AKTA systems at different scales) and approaches (Affinity, IEX, MMC), TFF modalities, and single use mixing systems

? Ability to learn to operate manual and semi-automated equipment in support of routine production with supervision? Experience in the preparation of buffers