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Microbiology Quality Lab Supervisor

Location: Limerick
Experience:5-7 Years
Job Type:Permanent
Salary:Not Disclosed
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Microbiology Quality Lab Supervisor
Our Limerick based client are currently recruiting for a Microbiology Quality Lab Supervisor to join their team on a permanent basis. As Micro Quality Lab Supervisor you will manage all aspects of the Quality Assurance Microbiology whilst ensuring all testing & quality requirements related to all products meet company requirements. You will provide technical leadership and establish appropriate systems to ensure departmental compliance with regulatory requirements.

• Supervises the performance, review and scheduling of laboratory personnel & provide training development
• Oversee microbiology and coordinates sampling activity in support of routine testing etc
• Coordinate and prioritise laboratory activity in support of routine testing, product release, product shelf-life, process non-conformances, complaint investigations, regulatory submissions, etc
• Act as a technical expert and approval authority on relevant technical issues, protocols, SOPs, methods, etc
• Implement cost improvement projects within department and in support of internal customers
• Oversee safety & environmental requirements for Raw Material/Chemistry lab and ensures lab meets all safety requirements
• Track, report, & improve key quality indicators for laboratory compliance and efficiency
• Performs other related duties as assigned by management
• Plan and manage annual spending and headcount budget
• Act as the contact for regulatory groups on scientific issues and audit

• Minimum of a level 8 bachelors degree in a related science/management related field
• 5+ years industry experience working in a Quality Assurance and/or Research and Development
• Minimum of 2 years managerial experience or advanced management training
• Understanding of basic Chemistry / Microbiology / sterilization / Stability / Quality System principles and practices
• Technical depth to make solid business decisions
• Ability to interpret GMP’s, regulations, corporate and company policy
• Thorough knowledge of FDA and International Regulatory requirements
• Excellent organizational, interpersonal, written and oral communication skills required
• Proven leadership and problem-solving skills
• Ability to work on own initiative and flexible work ethic
• Innovative development techniques and strategic thinking abilities
• Ability to prioritize and handle multiple tasks, and to facilitate and resolve cross-functional activities and issues

If you would like further Information you can contact the recruiter directly:

Sinead Cullen | Tel: +353 (0) 1 507 9252


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