Data Integrity Expert - Basel

We are seeking an experienced Data Integrity Expert to support pharmaceutical and biotechnology clients in the Basel region. · Degree in Life Sciences, Pharmacy, Biotechnology, Chemistry, Engineering, or related field. · 5+ years of experience in Data Integrity, Quality Assurance ...

Join our growing Drug Product Services team and help shape the future of pharmaceutical manufacturing In this role, you'll take the lead and oversight on qualification and validation activities for state-of-the-art equipment and infrastructure supporting aseptic fill & finish lin ...

Join our growing Drug Product Services team and help shape the future of pharmaceutical manufacturing In this role youll take lead on qualification and validation activities for state-of-the-art equipment supporting aseptic fill & finish lines. · An agile career dynamic work cult ...

We are looking for a QA Expert to join our growing Drug Product Services team in Stein, Switzerland. In this role, you'll take the lead on qualification and validation activities for state-of-the-art equipment and infrastructure supporting aseptic fill & finish lines. · Act as re ...

The actual location of this job is in Stein, AG, Switzerland. Join our growing Drug Product Services team and help shape the future of pharmaceutical manufacturing In this role, you'll take the lead and oversight on qualification and validation activities for state-of-the-art equ ...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections. · ...

We are seeking a highly experienced · GCP QA Subject Matter Expert to support a leading Biopharma client during a period of rapid clinical portfolio expansion and integration activities.This is a high-impact, hands-on role requiring a technical expert to ensure the highest stand ...

We are currently looking for a CSV Specialist · to support computerized systems validation activities on a · GMP pharmaceutical site · in the · Basel area. · ...

Location: Basel · Workload: 90 % · Duration: 5 months · Position Summary · The Biomarker Lead (BML) within the Biomarker Development group is responsible for defining and delivering integrated biomarker strategies across an Immunology portfolio spanning early and late clinical de ...

Senior Application Manager & Domain Expert · Location: Basel, Switzerland · Experience: 10–12 years · This is a senior technical leadership role responsible for end-to-end ownership of building management, time tracking, and people-operations applications in a GxP/GMP-regulated e ...

About Us · For more than 30 years, ATP-CGPharm has been supporting clients in the Life Science Industry with a broad range of services in facility and process-engineering, commissioning, qualification & validation, consulting in quality assurance and quality control, environmenta ...

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The department is responsible for process analytics during the manufacturing of chemically synthesized Active Pharmaceutical Ingredients (APIs). We are seeking motivated individuals to actively contribute to a variety of engaging tasks within our Manufacturing Analytics Team. · ...

The lead auditor will assume target- and timely planning, independent implementation, · timely communication of the results of end-to-end audits. He/She will write meaningful reports, · act as a sparring partner for management and monitor the implementation of measures. · The lea ...

You will be responsible for maintaining and leveraging our unique data integration platform, supporting ongoing AI model development, and ensuring the seamless continuation of our R&D data workflows. This is a hands-on role for a data scientist who can quickly get up to speed on ...

Assuming the role of lead auditor including target- and timely planning independent implementation and timely communication of the results of end-to-end audits. · ...

Role Summary · We are looking for a highly experienced Senior Application Manager & Domain Expert to oversee and enhance our portfolio of Building Management (REFS), Time Tracking, and P&O applications within a GxP/GMP‑regulated global enterprise. · In this senior role, you will ...

Quality Specialist · Location: · Basel area · Length: · 6-Month · Workload · : 100% · Start Date: · ASAPWe are supporting a leading laboratory services environment in the Basel area and are looking for an experienced Quality Specialist to strengthen ongoing QC operations. This ro ...

+ Scientist IMP In-Process Controls with hands-on analytical expert and at least three years of experience mastering physical-chemical techniques like chromatography within a cGMP environment. · Provide essential guidance to laboratory colleagues on the planning, execution and co ...

The department of Analytical Research & Development is responsible for process analytics during the manufacturing of Active Pharmaceutical Ingredients APIs This includes reaction controls and the analysis of isolated intermediates strictly adhering to cGMP safety and regulatory r ...