Stein, Aargau, Switzerland · Hybrid
The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Be part of a dynamic, fast-paced project environment where no two da…
Skills: QA Operations, Stakeholder Management, Aseptic Fill & Finish, GMP Compliance, Quality Strategy
Stein, Aargau, Switzerland · On-site
The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Join Lonza as an Associate Director, Technology Transfer (Global MSA…
Skills: Technology Transfer, Drug Product Development, GMP Change Management, Aseptic Manufacturing, Lyophilization
Stein, Aargau, Switzerland · On-site
The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Lead a high-impact MSAT team through a demanding CAPEX growth projec…
Skills: People Leadership, Sterile Fill & Finish, MSAT, Technology Transfer, Process Performance Qualification
Stein, Aargau, Switzerland · Hybrid
Die Bachem-Gruppe investiert in einen neuen geplanten Standort im Sisslerfeld (BSF) in der Nordwestschweiz. Dieser Schritt ist Teil der langfristigen Strategie, die Produktionskapazitäten bis zum Ende des Jahrzehnts ausz…
Skills: Process Technology, GMP Compliance, Downstream Processing, Dispensation, Cleaning Validation
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Lead and develop a team of QA experts to create and execute the overall quality strategy for new commercial production lines. Act as the lead subject matter expert for GMP issues and maintain local and global quality systems in compliance with regulatory standards.
Requires a university degree in Life Sciences and extensive senior QA experience in GMP pharmaceutical manufacturing, specifically as a deputy for Qualified Person in Switzerland or EU. Must be fluent in English with at least basic German skills and have a proven track record in direct-line leadership.
The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
Be part of a dynamic, fast-paced project environment where no two days are the same—this is a unique opportunity to help build multiple new commercial production lines and shape the future of manufacturing from the ground up. We are looking for a confident and collaborative leader with QA Operations experience in pharma manufacturing, strong stakeholder management skills, and an assertive mindset; experience in aseptic fill & finish is a plus. Check out Your Career in Drug Product Services at Lonza!
This role is primarily based on site. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. We offer flexibility to work remotely for no more than 20% of your time. Requests are considered on a case‑by‑case basis, in line with business needs.
An agile career and a dynamic work culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits.
The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits
Lead, develop and grow a team of QA Experts. Create and lead the overall Quality strategy
Partner with Senior Project Directors and Senior Project Leadership Team to ensure alignment of Manufacturing and support functions in executing strategy
Act as Lead SME for significant quality / GMP issues
Develop, direct and maintain the local Quality System. Contribute to the development and maintenance of global quality systems in line with Lonza Corporate requirements & standards as well as current regulatory requirements meeting Swissmedic, US FDA and European requirements
Perform independent review and approval of project documents. Take part in investigations, troubleshooting, audits and inspections
Identify opportunities for optimization of operational procedures in order to improve quality and efficiency within area of responsibility
Implement a learning culture and vertical/horizontal knowledge management
You have current or previous direct-line leadership experience
You have the agility, assertiveness and communication skills needed to excel in this highly dynamic project phase
Eligible to work as as deputy for Qualified Person/FvP in Switzerland or EU as well as extensive work experience in a senior QA role in the GMP controlled pharmaceutical manufacturing environment (e.g. QA Operations), preferably experience in aseptic fill&finish processes
Excellent working knowledge of current ICH, PIC/S, EU and US regulatory requirements and their implementation
Experience in managing customer audits and inspections such as Swissmedic, USFDA, EMA, MHRA Audits
University degree in Life Science (Pharmacy, Biology or similar field)
Fluent English and at least basic knowledge of German (plus the willingness to improve your German skills fast in case it is not fluent yet)
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Making the Medicines of Tomorrow
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow. Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs. For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
Offices: Muenchensteinerstr. 38, Basel, 4002, CH · 8830 Biggs Ford Road, Walkersville, MD 21793, US · 35 Tuas South Ave 6, SG, 637377, SG · 228 Bath Road, Slough, Berkshire SL1 4DX, GB · Rottenstrasse 6, Visp, VS 3930 , CH
There are currently 24 open management & leadership positions in Stein, Switzerland listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Bachem, Lonza, Syngenta Group, among others. Browse the listings above to see every active employer.
Yes — 13 of the 24 open management & leadership positions offer remote or hybrid work (0 remote, 13 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
