16 立讯精密2026年3月21日股价 English-speaking jobs in Sittard

work part-time or full-time (24–40 hours per week) and must be flexibly available between 06:40 and 21 ... Functie-eisenAvailable part-time or full-time (24–40 hours per week) Flexible availability between 06:40 and 21

, you work Parttime or Fulltime (at least 24 hours per week) and you are flexible between 06:40 and 21 ... area  Are available 24 to 40 hours per week, Fulltime / parttime  Can work flexibly between 06:40 and 21

(QP) – Cell & Gene Technologies Location: Geleen, Netherlands Contract: 6-month contract (March 16, 2026 ... – September 15, 2026) Platform: Cell & Gene Technologies About the Role We are seeking an experienced

technical field Strong understanding of GMP, lab data integrity, and regulatory compliance (including 21

Your working hours Part time or full time (from 24-40 hours per week) Flexible between 06:40 and 21 ... job is perfect for you if you: Are available 24-40 hours per week Can work flexibly between 06:40-21

Important: Fully onsite position Fluent in English required Minimum of 3 years experience in a GMP environment

Working together with an international team Working Hours: 24–40 hours per week Shifts between 06:40 – 21

Normally from 08:00 to 17:00, with occasional shifted shifts: 06:40 – 15:40 12:00 – 21:00 A stable schedule

Minimum of 3 years' experience in a GMP environment, ideally as a trainee.

Controller Your Profile Must-haves Bachelor's or Master's degree in Finance or a related field 3–

environment with tight deadlines.Will require travel depending on project needs for a duration of 2-3

Advisor DeWalt NL ApplyLocation: Born, Sittard-Geleen, NetherlandsTime Type: Full timePosted on: Posted 3

What we are looking for Minimum of 3 years of experience in QC or a related role within pharmaceutical

Operational Excellence Trainer needed for a cell and gene therapies company in Geleen. Plan and deliver training sessions, monitor progress, and identify improvement actions. Ensure employees are trained on GMP guidelines and quality standards. Requires a Life Sciences or related degree, 3+ years GMP experience, and strong English communication skills.

organized, and detail-oriented Flexible availability (including evenings and weekends) MBO level 3

What we are looking for 3–5 years of experience in a QC or related GMP-regulated laboratory environment