Validation Lead

Life Science Consultants; Dublin; On-site; EUR 70,000 - 95,000; Full time

Job summary

Life Science Consultants is sourcing a Validation Lead for a South Dublin based biopharmaceutical company. The role requires 7+ years in Validation, Engineering, Microbiology or Quality and hands-on experience with sterile/biotech equipment.

The successful candidate will coordinate validation activities and approve planning documents, ensuring quality and compliance. This contract opportunity targets individuals eligible to work in Ireland, with visa requirements (Stamp 1G/Stamp 4) noted.

Qualifications

• BS degree with 7+ years of experience in Validation, Engineering, Microbiology or Quality.
• Extensive knowledge and demonstrated experience managing validation activities for Pharmaceutical/Biotechnology projects.
• Experience of sterile/biotech equipment within the pharmaceutical industry is preferred.

Responsibilities

• Coordinates and supervises all validation activities.
• Approves validation planning documents detailing overall strategy for the project.
• Develops and approves the master list of validation test documents and activities.

Skills

Validation

QRAES

URS

TPBN1_IJ

Education

BS degree in Validation/Engineering/Quality

Job description

Job Description

LSC have a great contract opportunity for a Validation Lead to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. If you have 7+ years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you!

ABOUT THE PROJECT - KEY RESPONSIBILITIES

• Coordinates and supervises all validation activities.
• Approves validation planning documents detailing overall strategy for the project.
• Develops and approves the master list of validation test documents and activities.
• Reviews and approves all C&Q summary reports and validation summary reports.
• Ensures all Validation Engineers who perform validation activities have relevant training assigned.
• Assist in the development of User Requirement Specifications (URS's) and Quality Risk Assessment for Equipment and Automated Systems (QRAES).

ABOUT YOU - ARE YOUR SKILLS A MATCH

BS degree with 7+ years of experience in Validation, Engineering, Microbiology or Quality. Extensive knowledge and demonstrated experience managing validation activities for Pharmaceutical/Biotechnology projects. Experience of sterile/biotech equipment within the pharmaceutical industry is preferred.

Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!

Skills: Validation QRAES URS TPBN1_IJ