Manufacturing Engineer
- France
- Contract
- CAPEX Projects
Our client, a global biotechnology organisation, is recruiting for a Manufacturing Engineer to join their capital project in the South of France. This new build facility will house a therapeutic protein production plant, and we are looking for a Manufacturing Engineer to help expand our client's biotech operations throughout Europe.
Responsibilities
- Responsible for the Manufacturing Equipment within the Multi-Product Cell Culture (MPCC) building, including but not limited to Bioreactors, Depth Filtration, Centrifugation, Chromatography, Ultrafiltration/Diafiltration and Process Support systems.
- Provide support to Manufacturing with main focus on troubleshooting Equipment and Automation issues, and supporting/leading Process Equipment Investigations.
- Engineering owner for specific Manufacturing areas and systems, focused on acquiring an in depth knowledge of process operations and process equipment to support Manufacturing, Quality, Automation and Validation.
- Ensuring all the systems are in compliance with all Regulatory requirements including Quality (cGDP/GMP’s), and EHS requirements & procedures.
- Supporting internal and external audits as the Manufacturing Engineering Technical resource.
- Responsible for Clean in Place (CIP) and Steam in Place (SIP) changes, support of Validation including periodic assessment.
- Accountable for redlining, reviewing and approving of Automation Functional Specifications and ensuring implementation of software changes to the PAS.
- Co-ordination of Maintenance activities and monitor reliability of equipment, including review and approval of Preventative Maintenance (PM), Drawing updates, and support of out of Specification investigations related to Calibration of critical equipment..
- BS in Engineering (Chemical or Mechanical preferred)
- 2-3 years plus experience (or equivalent) with manufacturing equipment support in the Biotechnology manufacturing industry.
- Knowledgeable and experienced in engineering principles related to typical biopharmaceutical upstream and downstream processing and support equipment including but not limited to bioreactors, filtration and ultra-filtration, CIP, SIP, centrifugation, chromatography, autoclaves, and parts washers.
- Candidates must be effective in both a team environment and an individual contributor role with minimal supervision.
If this role is of interest, please apply now.
#LI-CO1
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
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