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Production Manager (Bio-pharmaceutical)

  • Salary: Up to £1 per annum
  • Job type: Permanent
  • Location: Munster
  • Sector: Science
  • Date posted: 19/10/2018
  • Job reference: BBBH15327

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Production Manager

My client, a world leader in biotechnology are currently seeking a Production Manager to assist with their Upstream/Midstream and/or Downstream processes and to interfaces with other departments, such as Facilities, Process Development, Process Analytical Sciences, Regulatory, Quality Assurance and Quality Control..
In this role with one of the worlds largest biologics production facility, you will be involved with all aspects of production from managing commercial scale manufacturing of recombinant proteins according to approved protocols, regulation, and schedule to managing a team responsible for the manufacture of bulk drug substance in a cGMP regulatory environment.

Role responsibilities:

  • Ensures that the highest safety and housekeeping standards are maintained.
  • Builds strong teamwork and alliances with the other Shift Supervisors/Managers.
  • Ability to train, develop and mentor direct reports and effectively manage the performance of individuals. Works closely with staff to develop and manage individual goals and objectives.
  • Ensures that policies and procedures are effectively executed and that they comply with regulatory requirements.
  • Tracks and trends relevant technical and business process metrics to ensure operations are performing effectively and efficiently.
  • Ensures the effective use of material, equipment and personnel in producing quality products.
  • Provides technical input to resolve process problems.
  • Leads and implements continuous improvement initiatives.
  • Represents manufacturing during regulatory audit tours. Performs cGMP audits of production area.
  • Participates in safety, process and environmental investigations. Reviews alert and action limits as needed and implements corrective action as appropriate.

Role Requirements:

  • Requires a 3rd Level Qualification in Life Sciences with 7+ years of relevant experience in manufacturing within the Biopharma industry.
  • Requires 5+ years supervisory experience.
  • Knowledge of cGMP and ICH guidelines.

For more information on this and other potential opportunities please contact Kathryn on 016455250 for a confidential conversation.