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Details
Manufacturing Biotech Associate 24/7 Shift
Reference: | AS20487 | Location: |
Meath |
Qualification: | Degree | Experience: | See description |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
Manufacturing Biotech Associate 24/7 Shift
AS20487
11 Months
Meath
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Meath. 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.
- Level 7 qualification in a science or engineering discipline, or level 6 with a minimum of 4+ 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.
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