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Senior Quality Engineer-Remote
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Republic of Ireland
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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.
Diagnostics Supply Chain Project Manager Engineering Medical Device Chemistry Laboratory Scientist IT Microbiology Cork City Product Development Engineer Mayo Limerick PhD Pharmaceutical Dublin Academic Manufacturing Executive Allied Healthcare Pharma Sales Quality Engineering Biotechnology Packaging Engineer Sales and Marketing Sales and Marketing Life Science Scientific Quality Assurance Clinical Research Biopharmaceutical Connected Health Cork Quality Control Supply Chain Validation Engineer Academic Medical Affairs Scientist
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Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
This site uses cookies. More information on cookies can be found in our Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328
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