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Commissioning & Qualification Engineer
Eingestellt von Optimus Search
Gesuchte Skills: Engineering, Engineer, Client
Projektbeschreibung
COMMISSIONING & QUALIFICATION ENGINEER
Location: Near Brussels
Salary: €500 per day
Contract: 12 months
My client is a global Pharmaceutical company who thanks to their recent expansion, are looking to bring on a talented Commissioning and Qualification (C&Q) Engineer to join their team near Brussels, Belgium.
RESPONSIBILITIES
- Be responsible for managing the different phases of commissioning, (start-up, qualification) making sure they remain compliant with client requirements and contract conditions.
- You will establish procedures for qualification in accordance with international standards (FDA, EMA, ICH, ASTM E2500, GAMP).
- You will write qualification documents,
- You will perform FAT/SAT and Equipment Commissioning,
- You will coordinate and execute qualification (IQ, OQ) tests,
- You will work in close collaboration with production, EHS, engineering, maintenance, QC, QA
- You will ensure handover with final users.
RESPONSIBILITIES
- Master's degree in engineering (pharmaceutical, chemical or biochemical )
- Fluent written and oral French & English languages.
- At least 2 years of relevant experience in commissioning & Qualification
- Previous experience working in a GMP environment.
- Must have a strong knowledge of the Pharmaceutical industry.
- Good interpersonal communication skills, negotiation skills, with the ability to work well equally as part of a team and independently.
If this sounds like a role that suits your skill set and you would like to find out more, please get in touch with (see below) to kickstart the next stage of your career!
Location: Near Brussels
Salary: €500 per day
Contract: 12 months
My client is a global Pharmaceutical company who thanks to their recent expansion, are looking to bring on a talented Commissioning and Qualification (C&Q) Engineer to join their team near Brussels, Belgium.
RESPONSIBILITIES
- Be responsible for managing the different phases of commissioning, (start-up, qualification) making sure they remain compliant with client requirements and contract conditions.
- You will establish procedures for qualification in accordance with international standards (FDA, EMA, ICH, ASTM E2500, GAMP).
- You will write qualification documents,
- You will perform FAT/SAT and Equipment Commissioning,
- You will coordinate and execute qualification (IQ, OQ) tests,
- You will work in close collaboration with production, EHS, engineering, maintenance, QC, QA
- You will ensure handover with final users.
RESPONSIBILITIES
- Master's degree in engineering (pharmaceutical, chemical or biochemical )
- Fluent written and oral French & English languages.
- At least 2 years of relevant experience in commissioning & Qualification
- Previous experience working in a GMP environment.
- Must have a strong knowledge of the Pharmaceutical industry.
- Good interpersonal communication skills, negotiation skills, with the ability to work well equally as part of a team and independently.
If this sounds like a role that suits your skill set and you would like to find out more, please get in touch with (see below) to kickstart the next stage of your career!
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Ingenieurwesen/Technik