MSAT Bioprocess Specialist Job at SRG (Falkirk)

MSAT Bioprocess Specialist

We are working with a leading biopharmaceutical manufacturer who are seeking an ...

Location

United Kingdom , Falkirk

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

BSc (Hons) or equivalent in a Science or Engineering discipline
Proven GMP biologics manufacturing or process development experience
Strong organisational and stakeholder influencing skills
Demonstrated project management capability and ability to meet deadlines
Experience in process scale-up/transfer and providing manufacturing support
Effective communication across all levels
Experience evaluating materials for process suitability and writing GMP batch records

Job Responsibility

Lead the technology transfer of new and existing biologics processes into GMP manufacturing
Prepare, review, approve and issue GMP manufacturing documentation, including batch records
Define scale-up criteria and develop process mass balances and flow diagrams
Specify large-scale equipment and assess material suitability for GMP use
Generate quality documentation for raw materials and equipment
Work within the site Quality Management System, raising and managing change controls
Conduct and close investigations, deviations and CAPAs
Project manage the introduction of processes into manufacturing from end to end
Perform risk assessments aligned with ICH Q9 principles
Collaborate cross-functionally with MSAT, Development, Manufacturing, QA, Supply Chain, Engineering and Project Management teams, as well as relevant external partners

Fulltime

MSAT Bioprocess Specialist

We are working with a leading biopharmaceutical manufacturer who are seeking an ...

Location

United Kingdom , Falkirk

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

BSc (Hons) or equivalent in a Science or Engineering discipline
Proven GMP biologics manufacturing or process development experience
Strong organisational and stakeholder influencing skills
Demonstrated project management capability and ability to meet deadlines
Experience in process scale‑up/transfer and providing manufacturing support
Effective communication across all levels
Experience evaluating materials for process suitability and writing GMP batch records

Job Responsibility

Lead the technology transfer of new and existing biologics processes into GMP manufacturing
Prepare, review, approve and issue GMP manufacturing documentation, including batch records
Define scale‑up criteria and develop process mass balances and flow diagrams
Specify large‑scale equipment and assess material suitability for GMP use
Generate quality documentation for raw materials and equipment
Work within the site Quality Management System, raising and managing change controls
Conduct and close investigations, deviations and CAPAs
Project manage the introduction of processes into manufacturing from end to end
Perform risk assessments aligned with ICH Q9 principles
Collaborate cross‑functionally with MSAT, Development, Manufacturing, QA, Supply Chain, Engineering and Project Management teams, as well as relevant external partners

What we offer

Competitive package
Extensive benefits package

MSAT Bioprocess Specialist

We are working with a leading biopharmaceutical manufacturer who are seeking an ...

Location

United Kingdom , Falkirk

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

BSc (Hons) or equivalent in a Science or Engineering discipline
Proven GMP biologics manufacturing or process development experience
Strong organisational and stakeholder influencing skills
Demonstrated project management capability and ability to meet deadlines
Experience in process scale‑up/transfer and providing manufacturing support
Effective communication across all levels
Experience evaluating materials for process suitability and writing GMP batch records

Job Responsibility

Lead the technology transfer of new and existing biologics processes into GMP manufacturing
Prepare, review, approve and issue GMP manufacturing documentation, including batch records
Define scale‑up criteria and develop process mass balances and flow diagrams
Specify large‑scale equipment and assess material suitability for GMP use
Generate quality documentation for raw materials and equipment
Work within the site Quality Management System, raising and managing change controls
Conduct and close investigations, deviations and CAPAs
Project manage the introduction of processes into manufacturing from end to end
Perform risk assessments aligned with ICH Q9 principles
Collaborate cross‑functionally with MSAT, Development, Manufacturing, QA, Supply Chain, Engineering and Project Management teams, as well as relevant external partners

What we offer

Competitive package
Extensive benefits package

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Expiration Date

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Expiration Date

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valid driver's license
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MSAT Bioprocess Specialist

Job Description

Job Responsibility

Requirements

Nice to have

What we offer

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