Single Use Bioreactors jobs

MSAT Upstream Scientist III

Thermo Fisher Scientific · Posted Nov 11, 2026

Open

Plainville, Massachusetts, United States
On-site
Full-time · Senior
$83K–$125K per year

MSAT Upstream Scientist III

Thermo Fisher Scientific · Posted Nov 11, 2026

Open

Plainville, Massachusetts, United States
On-site
Full-time · Senior
$83K–$125K per year

Manufacturing Associate I/ II (Nights)

KBI Biopharma · Posted Nov 11, 2026

Open

Durham, North Carolina, United States
On-site
Full-time · Associate
0–6 years

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Responsible for the execution of Upstream or Downstream production activities for early and late-phase Cell Culture programs within a GMP environment.

Responsibilities

Manufacture cell culture products per manufacturing batch records in compliance with quality standards, company policies and current regulations.
Perform operations in a cleanroom environment, applying controls to ensure aseptic processing including gowning and cleaning procedures.
Document each task involving manufacturing procedures (i.e. SR’s, EPR’s and BR’s) following GDP at the time of execution.
Ensure all items are issued and accounted for during the execution of a record (i.e. SR, EPR and BR)
Demonstrate and apply understanding of current Good Manufacturing Practices (cGMP) and how they apply to specific tasks and responsibilities.

Requirements

Bachelor’s degree in a related scientific or engineering discipline
High school diploma
Nice to have: Fermentation
Nice to have: Purification unit operations
Nice to have: Single-use platform technology

Skills

Cell culture GMP GDP

Manufacturing Associate I/II

KBI Biopharma · Posted Nov 11, 2026

Open

Durham, North Carolina, United States
On-site
Full-time · Associate
0–6 years

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The Manufacturing Associate I/II is responsible for the execution of Upstream or Downstream production activities for early and late-phase Cell Culture programs within a GMP environment.

Responsibilities

Manufacture cell culture products per manufacturing batch records in compliance with quality standards, company policies and current regulations.
Perform operations in a cleanroom environment, applying controls to ensure aseptic processing including gowning and cleaning procedures.
Document each task involving manufacturing procedures (i.e. SR’s, EPR’s and BR’s) following GDP at the time of execution.
Ensure all items are issued and accounted for during the execution of a record (i.e. SR, EPR and BR)
Demonstrate and apply understanding of current Good Manufacturing Practices (cGMP) and how they apply to specific tasks and responsibilities.

Requirements

Bachelor’s degree in a related scientific or engineering discipline
High school diploma
Nice to have: Single-use platform technology

Skills

GMP GDP GLP Aseptic technique

Manufacturing Associate I/ II

KBI Biopharma · Posted Nov 11, 2026

Open

Durham, North Carolina, United States
0–6 years

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Manufacturing Associate I/II (Nights) responsible for execution of upstream or downstream production activities for early and late-phase cell culture programs within a GMP environment.

Responsibilities

Manufacture cell culture products per manufacturing batch records in compliance with quality standards, company policies and current regulations.
Perform operations in a cleanroom environment, applying controls to ensure aseptic processing including gowning and cleaning procedures.
Document each task involving manufacturing procedures (i.e. SR’s, EPR’s and BR’s) following GDP at the time of execution.
Ensure all items are issued and accounted for during the execution of a record (i.e. SR, EPR and BR).
Demonstrate and apply understanding of current Good Manufacturing Practices (cGMP) and how they apply to specific tasks and responsibilities.

Requirements

Bachelor’s degree in a related scientific or engineering discipline
High school diploma
Nice to have: Single-use platform technology

Skills

Good Manufacturing Practices (cGMP)Good Documentation Practices (GDP)Good Laboratory Practices (GLP)

Manufacturing Associate I

KBI Biopharma · Posted Nov 11, 2026

Open

Durham, North Carolina, United States
On-site
Full-time · Entry
0–5 years

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The Manufacturing Associate I is responsible for the execution of Upstream or Downstream production activities for early and late-phase Cell Culture programs within a GMP environment.

Responsibilities

Manufacture cell culture products per manufacturing batch records in compliance with quality standards, company policies and current regulations.
Perform operations in a cleanroom environment, applying controls to ensure aseptic processing including gowning and cleaning procedures.
Document each task involving manufacturing procedures (i.e. SR’s, EPR’s and BR’s) following GDP at the time of execution.
Ensure all items are issued and accounted for during the execution of a record (i.e. SR, EPR and BR)
Demonstrate and apply understanding of current Good Manufacturing Practices (cGMP) and how they apply to specific tasks and responsibilities.

Requirements

Bachelor’s degree in a related scientific or engineering discipline
High school diploma
Nice to have: Single-use platform technology

Skills

GMP GDP GLP Aseptic technique

Manager, Manufacturing

Bristol Myers Squibb · Posted Nov 9, 2026

Open

Bothell, Washington, United States
Full-time · Manager
$114K–$138K per year
5+ years

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The Manufacturing Manager I leads and drives the execution of manufacturing processes according to established electronic work instructions and production records for the manufacture of cell therapies with Current Good Manufacturing Practices (cGMP’s).

Compensation

Bothell - WA - US: $113,930 - $138,051

Responsibilities

Manages the creation, implementation and compliance of all Source Governing Documents (including but not limited to: Standard Operating Procedures, Work Instructions, Batch Records, Forms) related to cell therapy operations for self and others
Oversee operations within the requirements of a validated manufacturing system(s)
Plan, assign resources and oversee daily operational activities associated with assigned areas of responsibility while controlling costs
Maintain operating and storage areas to ensure that they are compliant, efficient, effective, safe and always inspection ready
Drives right-first-time initiatives and holds team accountable for compliance performance. Generates solutions for compliance issues.

Requirements

Bachelors in relevant science or engineering discipline

Skills

cGMP cell therapy manufacturing bioprocessing manufacturing

Manager, Manufacturing

Bristol Myers Squibb · Posted Nov 9, 2026

Open

Bothell, Washington, United States
Full-time · Manager
$114K–$138K per year
5+ years

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Compensation

Bothell - WA - US: $113,930 - $138,051

Responsibilities

Manages the creation, implementation and compliance of all Source Governing Documents (including but not limited to: Standard Operating Procedures, Work Instructions, Batch Records, Forms) related to cell therapy operations for self and others
Oversee operations within the requirements of a validated manufacturing system(s)
Plan, assign resources and oversee daily operational activities associated with assigned areas of responsibility while controlling costs
Maintain operating and storage areas to ensure that they are compliant, efficient, effective, safe and always inspection ready
Drives right-first-time initiatives and holds team accountable for compliance performance. Generates solutions for compliance issues.

Requirements

Bachelor's degree in a relevant science or engineering discipline
Nice to have: leadership experience
Nice to have: performance management

Skills

cGMP cell therapy manufacturing

Executive, Manufacturing

Amneal · Posted Nov 5, 2026

Open

Ahmedabad, Gujarat, India
4–10 years

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Upstream & Downstream Process Specialist for Biosimilar manufacturing

Responsibilities

Responsible for upstream process for mammalian/cell culture
Responsible for downstream process for mammalian/cell culture
Prepare SOPs, QMS, qualification and validation of equipment
Batch manufacturing
Prepare QRM, change control, vendor and CFT follow up

Requirements

Life science Graduate / Postgraduate (M.Sc./B.E./B.Tech/M.Tech (Biotechnology/Microbiology))

Skills

Cell culture techniques Single use bioreactors Shake flasks Perfusion technology Chromatography TFF Virus filtration Column packing/unpacking

MSAT Upstream Scientist III

MSAT Upstream Scientist III

Compensation

Responsibilities

Requirements

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Manufacturing Associate I/ II (Nights)

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Requirements

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Manufacturing Associate I/II

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Manufacturing Associate I/ II

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Manufacturing Associate I

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Requirements

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Manager, Manufacturing

Compensation

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Manager, Manufacturing

Compensation

Responsibilities

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Executive, Manufacturing

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Skills

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