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Continuous Process Improvement Jobs In Luzern - 8 Job Positions Available

1 – 8 of 8 jobs

# Associate Director, Planning & Scheduling (m/f/d)Applyremote type: Not Applicablelocations: CHE - Lucerne - Schachen (Werthenstein)time type: Full timeposted on: Posted Todaytime left to apply: End Date: June 13, 2026 (14 days left to apply)job requisition

MSD Malaysia  1 day ago

About the Role To strengthen our Supply Chain team in Lucerne, we are looking for a motivated and detail-oriented Supply Chain Coordinator (f/m/d) - full time or part-time 40-60%. The Supply Chain Coordinator (f/m/d) plays a

GC International AG  1 day ago

Are you passionate about quality, precision, and working in a GMP‑regulated environment? We are currently seeking a detail‑oriented GMP Documentation Specialist (m/w/d) to join our client’s Manufacturing Operations team in a dynamic, fast‑paced biopharmaceutical environment. The

LHH  1 day ago

Location: Vienna, Austria Working hours: Full-time With our unified SaaS platform deltaconX, we simplify regulatory compliance, to streamline transaction reporting processes. Since the market launch in 2013, we have been committed to helping businesses meet evolving

DeltaconX - Unifying Regulatory Compliance  19 hours ago

Job Description Our Manufacturing & Supply Division is dedicated to being the most trusted supplier of biopharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create a reliable global manufacturing network that’s devoted

MSD Malaysia  2 days ago
Aristo Group jobs

The GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation supports ALCOA+ standards and GMP expectations. The role is part of the Operational Excellence team within Manufacturing

Aristo Group  1 day ago
Fortive jobs

Job Summary Responsible for leading and governing Phase In / Phase Out (PIPO) initiatives across the product lifecycle to ensure controlled product changes and PIPO transitions, from a Supply chain perspective with a strong focus on

Fortive  1 day ago
Aristo Group jobs

The Batch Record Reviewer supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation meets ALCOA+ , GDP , and GMP expectations. As part of the Manufacturing Operational Excellence team, this

Aristo Group  1 day ago

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