Biologics MSAT Validation Engineer for Process Excellence

SIRE LIFE SCIENCES

Leiden

On-site

EUR 52,000 - 76,000

Full time

14 days+

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

The Company in Leiden is seeking an Engineer MSAT Validation to support process validation activities within biologics drug substance manufacturing. You will collaborate with technical, quality, and manufacturing teams to ensure validated, compliant, and optimized processes.

Ideal candidates hold a Master’s degree (or Bachelor + 2+ years) and possess knowledge of GMP, ALCOA+ data integrity, and validation activities, with fluent English communication.

Qualifications

  • Master’s degree with up to 2 years of relevant experience, or Bachelor’s with 2+ years in industry.
  • Experience in a biopharmaceutical, pharmaceutical, or regulated manufacturing environment.
  • Knowledge of GMP regulations and ALCOA+ data integrity principles.
  • Understanding of validation and qualification activities.
  • Fluent English communication and strong documentation skills.

Responsibilities

  • Plan, coordinate, and execute process validation activities.
  • Conduct mixing validation, buffer hold time validation, microbial hold time validation, and moist heat sterilization validation.
  • Prepare, review, and maintain validation protocols, reports, and support documentation.
  • Support validation and qualification activities for both new and existing manufacturing processes.
  • Execute performance qualification activities related to change controls and improvement projects.
  • Collaborate with cross functional teams to deliver validation activities according to project timelines.
  • Ensure GMP compliance and ALCOA plus data integrity principles.
  • Identify opportunities for process optimization, standardization, and continuous improvement.
  • Support adherence to quality, safety, and regulatory requirements.

Skills

GMP knowledge
ALCOA+ data integrity
Validation methods
Documentation
Project planning
English communication

Education

Master’s degree in Biotechnology
Master’s degree in Biochemical Engineering
Bachelor’s degree in related field

Job description

The Company in Leiden is seeking an Engineer MSAT Validation to support process validation activities within biologics drug substance manufacturing. You will collaborate with technical, quality, and manufacturing teams to ensure validated, compliant, and optimized processes.

Ideal candidates hold a Master’s degree (or Bachelor + 2+ years) and possess knowledge of GMP, ALCOA+ data integrity, and validation activities, with fluent English communication.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

MSAT Validation Engineer — Biopharma Process Innovator
MSAT Validation Engineer — Biopharma Process Innovator

SIRE LIFE SCIENCES • Leiden

On-site
EUR 60,000 - 80,000
Engineer MSAT Validation
Engineer MSAT Validation

SIRE LIFE SCIENCES • Leiden

On-site
EUR 52,000 - 76,000
Validation Engineer
Validation Engineer

Progressive • Leiden

On-site
EUR 48,000 - 68,000
Manager MSAT Cleaning Validation
Manager MSAT Cleaning Validation

Leiden Bio Science Park • Leiden

Hybrid
EUR 120,000 - 180,000
MSAT Validation & Lifecycle Lead, Leiden
MSAT Validation & Lifecycle Lead, Leiden

Bristol-Myers Squibb • Leiden

Hybrid
EUR 95,000 - 135,000
Senior MSAT Validation & Lifecycle Manager
Senior MSAT Validation & Lifecycle Manager

Bristol-Myers Squibb • Leiden

On-site
EUR 110,000 - 160,000
MSAT Process Engineer
MSAT Process Engineer

Walker Cole International • Hoofddorp

Hybrid
USD 69,000 - 117,000
Bioprocess Validation Engineer
Bioprocess Validation Engineer

SIRE LIFE SCIENCES • Leiden

On-site
EUR 55,000 - 90,000
Bioprocess Validation Specialist
Bioprocess Validation Specialist

SIRE LIFE SCIENCES • Leiden

On-site
EUR 55,000 - 90,000
MSAT Validation Engineer
MSAT Validation Engineer

SIRE LIFE SCIENCES • Leiden

On-site
EUR 60,000 - 80,000