External Manufacturing Assoc Manager

  • Type: Permanent
  • Location: Limerick
  • Salary: Negotiable
  • Job Ref: EMA040119
  • Date Posted January 4, 2019

Our client, a leading pharmaceutical company based in Limerick currently has an opportunity for an External Manufacturing Assoc Manager to join their team. This is a full time, permanent position offering an excellent salary and benefits package.

Main Responsibilities:

  • Serve as the primary operations contact for select Drug Product manufacturing sites.
  • Oversee production on site, co-ordinate the activities at Drug Product manufacturing sites to meet Supply requirements.
  • Liaison between internal IOPS functions and functional groups at DP manufacturing sites or business partners.
  • Coordinated all DP Manufacturing operations at contract and/or business partner manufacturing sites, including but not limited to: scheduling of all batches, supply of materials, direct shipment of bulk and finished product at manufacturing site, track and monitor cycle times, technology transfer execution and providing any required associated reports and technical expertise.
  • Ensure the timely routing and review of all master manufacturing records (MRs), standard operations procedures (SOPs), tech transfer reports, validation master plans, and other documentation related to clinical and commercial drug product manufacturing at drug product manufacturing sites and/or business partners.
  • Provide regulatory filing supports (IND, BLA, MAA, etc.).
  • Maintain required training status on specific work instructions and SOP’s.
  • Lead sub-team in continuous process improvements, system/equipment implementation and/or strategy development.
  • Support all investigations which concern DP Manufacturing or associated shipping operations, when required.
  • Ensure product integrity and company reputation by assisting in the monitoring of cGMP compliance at drug product contract manufacturers.
  • Travel to contract manufacturers or business partners, as required. Ability to travel up to 50%.

Education and Experience:

  • BS/BA in Life Sciences or a related field and 6 years of industry relevant work experience. Relevant experience may be substituted in lieu of educational requirement.
  • Aseptic Parenteral Filling operations or development experience.
  • Previous experience providing technical support and interacting with Contract Manufacturing organisations.
  • Good interpersonal, cross-cultural, communication, negotiation and problem solving skills
  • Good knowledge of industry practices and regulations (e.g. GxP, ISO, ICH, etc.) across multiple health authorities (e.g. FDA, IMB, etc.)
  • Project management (PMP or equivalent) qualification preferable.

For more information on this position please call Rachael O Rourke on 061336136 or apply online and a member of the Harmonics team will be in touch

More Details

For more information on this position please call Rachael O Rourke on 061336136 or apply online and a member of the Harmonics team will be in touch

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