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Search Results for Validation Manager
Job Title. Location Salary Actions

Technical Writer/ Validation Specialist

Technical Writer/Validation Specialist Our Client is recruiting a Validation Specialist based in the Dublin office and reporting directly to the Operations Manager. The successful candidate will be responsible for the day-to-day administration of Validation Protocols which involves liaising with our Quality, Sales and Service Teams, Technical Support Engineers/ Subject Matter Experts, Suppliers and Customers. Role: • Administration of the Validation System including the development and maintenance of IQ/OQ and PQ/ RQ/ PV protocols. • Li...

Location: Dublin,
Technical Writer/ Validation Specialist
Dublin Not Disclosed

Validation Engineer contactor

Our biotech client require a Validation Engineering contractor for an initial 12 month period. Superb remuneration available. Easy to convert to becoming a cont

Location: Dublin,
Validation Engineer contactor
Dublin Not Disclosed
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Validation Manager Career Profile

Validation Manager

The Validation Manager is responsible for the Validation and coordination of operation of machinery and process within the plant. This may be IT systems, various pieces of machinery or Cleaning processes. Salaries start at ca.€32,000 for an entry level position, with an experience Validation Manager being able to command €80,000+. Again, it's an area where many consult on short term contracts, when there is lots of project and construction work in the market.

Key Responsibilities of the Validation Manager

  • To manage all operational validation activities within the client's organisation.
  • To continue to develop and implement a compliant validation strategy for our client.
  • To continue to develop and implement an efficient compliant and cost effective calibration and maintenance programme.
  • To work closely with all departments and the Quality Department to ensure the operation of a validated environment according to GMP and other regulatory requirements
  • Be capable of delivering high level reporting to the client's directors.
  • Manage the process for the creation of documentation and requirements to include but not limited to the following:
  • Computer Systems Validation Plans
  • Equipment Validation Plans
  • Cleaning Validation Plans
  • Utility/Facility Validation Plans
  • Components Area Validation Plans
  • Tissue Business Master Validation Plan
  • Despatch Validation Plans
  • Environmental Monitoring Validation Plans
  • Quality Control Validation Plans
  • Scheduling, Planning and review of validation activities.
  • Manage all facets of assigned validation projects while maintaining strong communication with client representative on project status and assistance needed.

Skills & Qualifications:
  • Third level degree in a science/engineering/computer subject as a minimum.
  • At least 5 years experience Validation Management experience ideally within the clinical, medical, laboratory or pharmaceutical industry.
  • Good understanding and application of GMP and regulatory requirements.
  • Experience of wide range of validations including Computer Systems Validation, equipment, cleaning and utility and facilities validation plans.
  • Excellent communication / interpersonal skills
  • Previously have managed or supervised a team of experienced engineers in a similar industry.
  • Be a motivator and leader for such a team.
  • Attention to detail.
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