Manufacturing Engineer

Quanta part of QCS Staffing; Toulouse; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A global biotechnology organization in Toulouse is seeking a Manufacturing Engineer to support the expansion of their therapeutic protein production plant. Responsibilities include managing manufacturing equipment, troubleshooting automation issues, and ensuring compliance with regulatory requirements. The ideal candidate will have a BS in Engineering, 2-3 years of experience in the biotech sector, and strong knowledge of manufacturing equipment. This is a contract position in the life sciences field.

Qualifications

• 2-3 years experience in biotechnology manufacturing equipment support.
• Knowledge of biopharmaceutical upstream and downstream processing equipment.
• Ability to work both in teams and independently with minimal supervision.

Responsabilités

• Manage Manufacturing Equipment in the Multi-Product Cell Culture building.
• Support Manufacturing by troubleshooting Equipment and Automation issues.
• Ensure compliance with Regulatory requirements.
• Coordinate Maintenance activities and monitor equipment reliability.

Connaissances

Manufacturing Equipment support

Troubleshooting Equipment and Automation

Process Equipment Investigations

Regulatory compliance

Clean in Place (CIP)

Steam in Place (SIP)

Formation

BS in Engineering (Chemical or Mechanical preferred)

Description du poste

Manufacturing Engineer – Upstream & Downstream – Contract – Toulouse – Life Sciences

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.

Qualifications & Experience

• 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.