QC Micro Manager

LSC, Life Science Consultants; Dublin; On-site; EUR 70,000 - 90,000; Full time

Job summary

LSC, Life Science Consultants, is seeking a QC Micro Manager for a contract role at a South Dublin biopharmaceutical site that focuses on Formulation, Fill Finish and Packaging.

You will lead QC Microbiology readiness, support GMP documentation, and mentor QC personnel in a GMP environment. Eligibility to work in Ireland (Stamp 1G/Stamp 4) is required due to visa conditions.

Qualifications

• 6+ years of biopharmaceutical QC experience, or related Quality Control/GMP laboratory experience within the pharmaceutical or medical device industry, is preferred.
• Bachelor's degree in a Science-related field is required.
• Strong leadership and people-management capability.

Responsibilities

• Support the planning and implementation of QC Microbiology activities associated with the expansion of manufacturing operations at the site.
• Lead and coordinate QC Microbiology readiness activities, ensuring appropriate planning and execution in advance of operational requirements.
• Support the development, review and implementation of GMP documentation, including procedures, protocols, reports and other controlled documentation required to establish and maintain QC Microbiology operations.
• Support resource, training and qualification planning to ensure QC Microbiology personnel are appropriately prepared for future operational requirements
• Support the establishment, implementation and maintenance of Environmental Monitoring and other microbiological testing programmes, as applicable.
• Supervise and/or manage QC Microbiology personnel as required and provide effective coaching, development and technical leadership.

Skills

QC Leadership

Biopharma QC

GMP Experience

Education

Bachelor's degree in Science

Job description

LSC have a great contract opportunity for a QC Micro Manager to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
If you have 6 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:

• Support the planning and implementation of QC Microbiology activities associated with the expansion of manufacturing operations at the site.
• Lead and coordinate QC Microbiology readiness activities, ensuring appropriate planning and execution in advance of operational requirements.
• Support the development, review and implementation of GMP documentation, including procedures, protocols, reports and other controlled documentation required to establish and maintain QC Microbiology operations.
• Support resource, training and qualification planning to ensure QC Microbiology personnel are appropriately prepared for future operational requirements
• Support the establishment, implementation and maintenance of Environmental Monitoring and other microbiological testing programmes, as applicable.
• Supervise and/or manage QC Microbiology personnel as required and provide effective coaching, development and technical leadership.

ABOUT YOU - ARE YOUR SKILLS A MATCH?

• 6+ years of biopharmaceutical QC experience, or related Quality Control/GMP laboratory experience within the pharmaceutical or medical device industry, is preferred.
• Bachelor's degree in a Science-related field is required.
• Strong leadership and people-management capability.

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!