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Purification/Process Engineer (French Speaking)
Eingestellt von Optimus Search
Gesuchte Skills: Engineering, Engineer, Design
Projektbeschreibung
Purification/Process Engineer (French Speaking)
Belgium (South of Gent)
€450 per day
12-month contract
Optimus Life Sciences are working with a world-leading pharmaceutical company, via a consulting business, to hire a Purification Engineer on a long-term freelance basis. The working on a project to expand the manufacturing capabilities on an existing site and has the potential to last longer than the initial length offered.
The job role will work on the design, construction/modification, commissioning and qualification of Purification/Clean Utilities systems according to EHS, GMP and Best Engineering Practices requirements.
The role oversees responsibilities relating to day to day manufacturing operations for problem-solving/improvement deployment as a Subject Matter Expert regarding purification and clean utilities systems.
If applicable, the freelance Purification Engineer will also assist in the training and mentoring of more junior staff. FLUENCY IN THE FRENCH LANGUAGE IS MANDATORY.
ROLE
- General aspect of project management.
- Detailed Design of new or modified systems.
- Tenders writing, orders handling, following of construction, and start-up of equipment.
- Writing and execution of validation packages (URS/FSDS/Commissioning/engineering part of IQOQ).
- Training of employees impacted by changes and new equipment.
- Ensure compliance with EHS, cGMP, regulatory and Best Engineering Practices requirements.
- Develop technical expertise on purification processes/Clean utilities systems to be a Subject Matter.
REQUIREMENTS
- Master's Degree in an Engineering discipline.
- 7+ years' experience working in a process engineering function within the Pharmaceutical/Biotech industry.
- Knowledge of purification equipment & related clean utilities.
- Must have experience in project: design/construction/commissioning.
- Experience with GEP, GMP and validation approach in the pharmaceutical industry.
- Good written and verbal skills in French and English.
- Working knowledge of current Good Manufacturing Practices (cGMP) and current Good Documentation Practices (cGDP).
If you're interested in knowing more, please send over a CV - Thanks!
Belgium (South of Gent)
€450 per day
12-month contract
Optimus Life Sciences are working with a world-leading pharmaceutical company, via a consulting business, to hire a Purification Engineer on a long-term freelance basis. The working on a project to expand the manufacturing capabilities on an existing site and has the potential to last longer than the initial length offered.
The job role will work on the design, construction/modification, commissioning and qualification of Purification/Clean Utilities systems according to EHS, GMP and Best Engineering Practices requirements.
The role oversees responsibilities relating to day to day manufacturing operations for problem-solving/improvement deployment as a Subject Matter Expert regarding purification and clean utilities systems.
If applicable, the freelance Purification Engineer will also assist in the training and mentoring of more junior staff. FLUENCY IN THE FRENCH LANGUAGE IS MANDATORY.
ROLE
- General aspect of project management.
- Detailed Design of new or modified systems.
- Tenders writing, orders handling, following of construction, and start-up of equipment.
- Writing and execution of validation packages (URS/FSDS/Commissioning/engineering part of IQOQ).
- Training of employees impacted by changes and new equipment.
- Ensure compliance with EHS, cGMP, regulatory and Best Engineering Practices requirements.
- Develop technical expertise on purification processes/Clean utilities systems to be a Subject Matter.
REQUIREMENTS
- Master's Degree in an Engineering discipline.
- 7+ years' experience working in a process engineering function within the Pharmaceutical/Biotech industry.
- Knowledge of purification equipment & related clean utilities.
- Must have experience in project: design/construction/commissioning.
- Experience with GEP, GMP and validation approach in the pharmaceutical industry.
- Good written and verbal skills in French and English.
- Working knowledge of current Good Manufacturing Practices (cGMP) and current Good Documentation Practices (cGDP).
If you're interested in knowing more, please send over a CV - Thanks!
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik