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Biotech Production Supervisor

  • Salary: Negotiable
  • Job type: Permanent
  • Location: Limerick
  • Sector: Other
  • Date posted: 21/02/2018
  • Job reference: J382078A

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Biotech Production Supervisor

Biotech Production Supervisor required to join a leading biopharmaceutical company in the South West.

Responsible to provide direction/leadership and establishes objectives/methodologies to the cleanroom clean-tech team to ensure a state of compliance. Also reviews/analyzes environmental data and prepares/presents reports for both clinical and commercial manufacturing areas.


  • Oversees all aspects of respective areas of operations.
  • Plan, schedule, and provide work direction to team to ensure environmental policies and compliance.
  • Monitor industry trends to ensure the latest in clean room cleaning technologies are implemented regularly.
  • Formulate the basis for studies to better characterize and/or improve the process area cleanliness and related compliance
  • Monitor liquid & solid waste disposal programs to ensure proper handling and disposal to protect health and the environment.
  • Ensures that safety standards are maintained at all times.
  • Conduct safety monitoring, identify and mitigate risks.
  • Analyze, interpret and report assessment results and recommendations to team members.
  • Manage inventory levels for all cleaning and gowning supplies.
  • Monitor cleaning schedules, progress, data, and work quality.
  • Conduct trouble-shooting and environmental excursion investigations.
  • Draft and implement long-term planning for the process, staff, and budget.
  • Perform personnel management functions (i.e. annual employee evaluations, coaching, disciplining, etc.).
  • Prepare reports by collecting, analyzing, and summarizing information and trends.
  • Represent MFG during regulatory inspections to respond to and address environmental issues and solutions.
  • Develop and implement department policies.
  • Ensure that policies and procedures are effectively administered and comply with regulatory requirements.
  • Interfaces with other departments, such as Facilities, Process Development, Process Analytical Sciences, Regulatory, Quality Assurance and Quality Control.
  • Represents Manufacturing at all meetings as required.

Education and Experience:

  • BS/BA in Microbiology or closely related field with 5+ years of relevant cGMP manufacturing experience and some previous supervisory/leadership experience.
  • Will substitute relevant experience in lieu of educational requirement.

For more information contact Paul on 01 6455 250 or email