Technical Project Lead | Process Equipment Engineering (6-month mission)

  • Valais, Switzerland
  • GXP CONSULTING
  • Temps plein
  • Prรฉsentiel

Description de l'emploi:

Recrutis is supporting one of its clients, a leading pharmaceutical site engaged in a major equipment and process engineering programme, in the search for a Technical Project Lead.

๐—ช๐—ต๐˜† ๐˜๐—ต๐—ถ๐˜€ ๐—ฟ๐—ผ๐—น๐—ฒ

You are the technical anchor of a live engineering programme: you translate user requirements into engineered solutions, own the P&ID lifecycle, and steer external vendors on their technical deliverables. You also sit at the interface between technical and non-technical stakeholders, turning complex engineering into clear business implications.

๐—ž๐—ฒ๐˜† ๐—ถ๐—ป๐—ณ๐—ผ๐—ฟ๐—บ๐—ฎ๐˜๐—ถ๐—ผ๐—ป

On-site presence ยท Consulting mission, 6 months ยท Pharmaceutical / GMP ยท English required (knockout), German a strong asset ยท 3โ€“5 years in project engineering or project management in (bio)chemical or pharmaceutical industries, with international exposure.

๐—ฆ๐—ฐ๐—ผ๐—ฝ๐—ฒ

Review and approval of engineering documentation: URS, TS, document lists, design specs, FAT/SAT protocols and validation reports; support FS and qualification documents.

Development, check and approval of P&IDs (Status AC); support adjustment from Status CE.

Support P&ID walkdowns and Mechanical Completion; follow up and close out punch lists.

Ensure company standards and applicable GMP regulations are met across the engineering process.

Support commissioning and qualification of equipment and technical systems.

Drive execution with external vendors, contractors and equipment suppliers on technical deliverables.

๐—ฃ๐—ฟ๐—ผ๐—ณ๐—ถ๐—น๐—ฒ โ€” ๐—ฅ๐—ฒ๐—พ๐˜‚๐—ถ๐—ฟ๐—ฒ๐—ฑ ๐—ฐ๐—ฟ๐—ถ๐˜๐—ฒ๐—ฟ๐—ถ๐—ฎ (๐—ธ๐—ป๐—ผ๐—ฐ๐—ธ๐—ผ๐˜‚๐˜)

3โ€“5 years in project engineering or project management for (bio)chemical or pharmaceutical industries, with international experience.

Proven experience in a similar role on process equipment in a pharmaceutical environment.

Technical knowledge of the engineering disciplines in a pharmaceutical / cGMP environment.

Hands-on command of the engineering documentation lifecycle (URS, TS, FAT/SAT, P&IDs).

Strong written and spoken English.

๐—ฆ๐˜๐—ฟ๐—ผ๐—ป๐—ด ๐—ฎ๐˜€๐˜€๐—ฒ๐˜๐˜€

German language skills ยท solid project management track record ยท excellent command of MS Office and Visio ยท strong influencing and communication skills across all levels.

๐—ฃ๐—ฟ๐—ผ๐—ฐ๐—ฒ๐˜€๐˜€ โ€” Confidential recruitment process. Response within 48 hours for applications meeting required criteria. Active mandate, priority review.

๐˜๐˜ข๐˜ฃ๐˜ณ๐˜ช๐˜ค๐˜ฆ ๐˜Š๐˜ข๐˜ต๐˜ต๐˜ข๐˜ฏ๐˜ต โ€” ๐˜๐˜ฐ๐˜ถ๐˜ฏ๐˜ฅ๐˜ฆ๐˜ณ, ๐˜™๐˜ฆ๐˜ค๐˜ณ๐˜ถ๐˜ต๐˜ช๐˜ด | ๐˜Œ๐˜น๐˜ฑ๐˜ฆ๐˜ณ๐˜ต & ๐˜Œ๐˜น๐˜ฆ๐˜ค๐˜ถ๐˜ต๐˜ช๐˜ท๐˜ฆ ๐˜š๐˜ฆ๐˜ข๐˜ณ๐˜ค๐˜ฉ ๐˜ช๐˜ฏ ๐˜“๐˜ช๐˜ง๐˜ฆ ๐˜š๐˜ค๐˜ช๐˜ฆ๐˜ฏ๐˜ค๐˜ฆ๐˜ด