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Avishek Singh
Life Science

00353872827991
[email protected]
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Details

Bioprocess Associate


Reference:AS0 Location: Louth
Qualification:CertificateExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Production Engineer, Production Supervisor

We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Louth. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

Duties:

  • Support operations team to consistently deliver on specific Key Performance Indicators (KPIs), e.g. Environmental Health and Safety (EHS) metrics, Production Plan, Overall Equipment Effectiveness (OEE), compliance and team training.
  • Execute commercial manufacturing processes according to established work instructions and
  • Standard Operating Procedures (SOPs).
  • Ensures that all assigned task related to manufacturing documentation support is in accordance with good manufacturing practices.
  • Routinely talk about any safety issues you are concerned about.
  • Work as part of a dedicated process team where flexibility and teamwork are a key requirement.
  • Generate SOPs/ Work Instructions (WIs) to ensure compliance with regulatory standards.
  • Maintain/ support a high standard of safety/ Good Manufacturing Practice (GMP) compliance at all times.
  • Determine solutions by referencing relevant past experiences as part of problem solving activities.
  • Get actively involved by participating in inspections, GEMBA’s and Go-See’s.
  • Act as a team member on process deviation reviews and Gemba walkdowns.
  • Mentor new members of staff in specific plant activities.
  • Be prepared to answer auditor questions during site walkdowns.
  • Engage in implementing innovative solutions that drive a high performance organisational culture that accommodates rapid growth and highly dynamic expectations ensuring attainment of site operational and development goals.
Education and Experience :
  • Level 7 qualification in a science or engineering discipline, or level 6 with a minimum of 3+ years’ experience in a GMP Manufacturing environment.
  • Experience of Upstream/ Downstream Processing.
  • Start-up experience in a large-scale commercial drug substance facility, or similar.
  • A proven ability to work with automated systems such as Manufacturing Execution System (MES), Systems Applications and Products (SAP), Delta V etc.
If interested in this posting please feel free to contact Avishek Singh on +353 (0)87 282 7991 or [email protected] for further information.