40 project manager English-speaking jobs in Visp

  • Lonza
  • Visp
  • May 26
Work closely with QC-Project Leader (QC-PL) and MSAT for New-Product-Introductions (NPI). ... Act as QA representative in Project teams and represent QA in customer meetings during Technical Transfer ... - and Site Engineering project / technology transfer to effectively execute tasks related to Drug Product ... Support and approve project / product specific risk assessments or regulatory specific risk or gap assessments ... cross-functional teams, establish and maintain interfaces with the Manufacturing teams, QC, Support Functions, Project
  • Lonza
  • Visp
  • May 20
Central Hygiene Project Manager will ensure the implementation and continuous improvement of hygiene standards at the Visp site. The role involves acting as a key link between departments, leading hygiene projects, and managing Cleanroom Performance Qualifications (PQs).
  • Hays
  • Visp
  • May 24
LogoProject Engineer - CAPEX (m/f/d) Freelance/temporary employment for a project Visp Start date: asap ... success criteria aligned with GMP standards and operational objectives Develop and manage the full project ... coordinate cross-functional teams across operations, engineering, maintenance, and quality Monitor project ... activities Solid understanding of commissioning, qualification, and validation methodologies Strong project ... experience in biopharmaceutical manufacturing or GMP-regulated environments Proven track record in technical project
  • Proclinical
  • Visp
  • May 8
LogoAbility to work effectively in project environments with multiple stakeholders. ... Proclinical is seeking a Project Buyer to support the execution of capital expenditure (Capex) procurement ... Coordinate with Engineering, Project Management, Quality, and Finance teams to ensure schedule adherence ... proactive individual who can work collaboratively with multiple stakeholders and is comfortable in a project-driven
  • ITJOBS
  • Visp
  • May 13
LogoJoin an exciting project environment where you will work across the full validation lifecycle - from
  • ITJOBS
  • Visp
  • June 1
LogoAlessia Biassoli Business Manager Life Sciences +41 41 632 43 59 [email protected]
  • Fusion Consulting
  • Visp
  • May 23
Logoare currently seeking an experienced SAP EWM Functional Consultant to join a leading pharmaceutical project
  • Lonza
  • Visp
  • May 23
Join our Engineering team in Visp as an EI&C IT/OT Senior Project Lead 80-100% (m/f/d) and drive the ... Coordinate and manage external partners and vendors involved in MES or OT‑related project and support
  • Lonza
  • Visp
  • March 20
Four our Site in Visp, we’re currently looking for an EHS Manager Process Safety (m/w/d). ... The EHS Manager Process Safety is, as expert function, responsible for the successful implementation,
  • Hays
  • Visp
  • May 28
LogoBiotechnologist (m/f/d) Freelance/temporary employment for a project Visp Start date: asap Reference
  • Coopers Group AG
  • Visp
  • May 13
LogoJoin an exciting project environment where you will work across the full validation lifecycle - from
  • Lonza
  • Visp
  • April 30
Experience in project or program management, ideally in pharma or CDMO. ... ll be the main link between Lonza and our customers, leading cross-functional teams through the full project ... deliver customer programs across their full lifecycle—from technology transfer to GMP manufacturing and project
  • Lonza
  • Visp
  • March 23
The EHS Manager drives the successful implementation and continuous improvement of Environmental, Occupational
  • Lonza
  • Visp
  • May 7
Calculating and monitoring QC costs in the project. ... Represent QC in project teams. Make decisions independently. ... working with many people in many different business areas and you bring the necessary organizational and project
  • Lonza
  • Visp
  • April 24
What you’ll do: during the project phase Support the project team in defining and setting up innovative ... seeking motivated and resilient individuals to play a key role in vaccine production—both during the project
  • Lonza
  • Visp
  • May 19
MSAT Data Manager (f/m/d) will extract, structure, and curate manufacturing data to support data-driven decisions. Responsibilities include preparing process data for investigations, developing dashboards, and performing statistical analysis to evaluate process performance. The ideal candidate will have experience in biopharma manufacturing, data analytics, or a regulated environment and strong data handling and analysis skills.
  • Lonza
  • Visp
  • June 2
Ability to oversee project execution to identify non-compliance from quality standards. ... Represent QA in project/tech transfer organizations for new biotech manufacturing processes. ... As a Quality and Compliance representative he/she will be a key member in cross-functional project teams ... Ability to prioritize and manage work to critical project timelines in a fast-paced environment.
  • Lonza
  • Visp
  • June 2
You will lead the Spend Optimization Project, addressing approximately 800MCHF in spend across global ... Contract (S2C), prioritizing and following up on Continuous Improvement (CPI) activities as part of Project ... will do: Establish the governance model and setup to successfully lead the 800MCHF Spend Optimization project ... systematic ideation, identify risks early, and ensure timely escalation to senior leadership to maintain project
  • Lonza
  • Visp
  • March 23
What you will do: Coordinate QA interests during different project phases. ... Responsible for project specific QA Operation tasks during Commissioning / Qualification.
  • Lonza
  • Visp
  • May 9
Own defined areas within the site Contamination Control Strategy, ensuring a sustained microbial state of control across facilities, equipment, processes, and supporting systems. Act as the technical lead for contamination control, hygiene, and microbiological QC topics. Provide visible shopfloor presence, hands-on technical support, and leadership on contamination control topics. Develop and improve hygiene concepts, gowning expectations, aseptic behavior, microbial hold times, and bioburden control strategies. Represent CCS and microbiological quality topics in projects, audits, regulatory inspections, and cross-functional governance forums. Drive continuous improvement, KPI delivery, training, and technical guidance.
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