25 product manager English-speaking jobs in Visp

Represent Drug Product QA topics during regulatory inspections. ... Work closely with QC-Project Leader (QC-PL) and MSAT for New-Product-Introductions (NPI). ... Review and release product specific documentation such as process descriptions and workflows, recipes ... also found on What you will do: Establish Quality Agreements (QAA) in close collaboration with Drug Product ... Act as point of contact for Drug Product QA related questions, topics and complaints from customers related

Drug Product experience is a strong advantage. ... What we’re looking for: 2–4 years of GMP shopfloor experience (ideally sterile Drug Product / Fill & ... What you’ll do: Carry out end‑to‑end Drug Product manufacturing under GMP: batch execution, documentation

Process knowledge in the area of sterile drug product is advantageous. ... What you will do: Author and adapt MES/PCS Recipe based on the Drug Product Processes. ... Responsible for defining the overall concept for MES recipes used in Drug Product Operations Visp to ... If you're passionate about applying your expertise to optimize drug product manufacturing and truly make

Matter Expert (SME) in environmental qualification, manufacturing environment analytical testing, and product

contamination control strategy within a GMP-regulated bioconjugates environment, directly impacting product

The EHS Manager drives the successful implementation and continuous improvement of Environmental, Occupational

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).

Your work will directly contribute to robust processes and successful product delivery.  ... for process monitoring Support Continuous Process Verification (CPV) and generate control charts and product

you will do: Execute manual visual inspection Executes manufacturing activities in the area of Drug Product ... 4 years of experience GMP environment on the shopfloor (preferably in sterile manufacturing of Drug Product

safety, product quality & cGMP compliance are implemented. ... Perform assessments for all product-related changes, assesses relevance to regulatory filings, decide ... representative he/she will be a key member in cross-functional project teams ensuring measures for product ... Ensure all deviations are appropriately investigated and recorded, direct the investigations of customer product

Lead and deliver customer programs from technology transfer to GMP manufacturing, ensuring quality, timelines, and cost-effectiveness. Act as a trusted partner for customers, fostering transparent communication and collaboration.

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.

Lead and deliver customer programs from technology transfer to GMP manufacturing, ensuring quality, timeliness, and cost-effectiveness. Act as a trusted partner and main point of contact for customers, fostering transparent communication and long-term collaboration.

to the Executed Batch Records, clarify with the operations team and evaluate with the responsible QA Manager

Analyze and clarify comments within Batch Records in collaboration with Operations and the responsible QA Manager

manufacturing lifecycle, acting as the key link between process knowledge, manufacturing execution and product ... such as: microbial upstream and/or downstream processes and process parameters and their impact on product

eliminating deviations Participating in audits and visits Executes Visual Inspection in the area of Drug Product

Prepare and approve risk assessments and product statements.

eliminating deviations - Participating in audits and visits - Executes Visual Inspection in the area of Drug Product

eliminating deviations - Participating in audits and visits - Executes Visual Inspection in the area of Drug Product