About this role
The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
We're looking for an Investigation Specialist to own critical deviations, drive impactful process changes, and ensure GMP compliance within our sterile manufacturing environment. If you have a scientific degree or equivalent experience, experience in sterile manufacturing, and a knack for thorough investigations, we encourage you to apply!
What you will get:
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. Our full list of tailored local benefits can be found below.
Benefits in Visp: https://bit.ly/3wjkoFi
What you will do:
Proactively driving optimization projects for manufacturing processes.
Owns investigations and critical deviations and assists in decision making on production issues.
Drives process changes, CAPAs, and CAPA efficiency checks related to process within required timelines and through GMP systems (e.g. Trackwise, SAP, MES, training, etc.)
Performs retraining/awareness sessions as CAPA identified during the investigation/deviation.
What we are looking for:
Bachelor's or Master's Degree in Pharmaceutical Technology, Chemistry, Pharmacy or equivalent work experience.
At least one year of experience in Sterile Manufacturing in operations and/or QC/QA.
Previous experience with investigation/deviation management in TW and CAPA definition.
Proficient in English, German is an advantage.
Familiarity with GMP requirements, quality procedures and SOP execution.
Good interpersonal skills with a variety of interfaces within the organization and within the shopfloor.
Structured, focused, proactive and well-organized working demeanor.
High motivation and collaboration focused; oriented towards finding solutions and driven by science.
About Lonza
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.
Ready to shape the future of life sciences? Apply now.
Other facts
About Lonza
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.
What you'll do
- The Investigation Specialist will own critical deviations and drive impactful process changes to ensure GMP compliance. They will also assist in decision-making on production issues and perform retraining sessions as needed.
Ready to join Lonza?
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