Switzerland, Visp The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
In this senior MSAT role based in
Visp, Switzerland
, you will play a
key part in safeguarding product quality and patient safety
by driving
risk‑based impurity compliance for Small Molecules
. You will lead impurity risk assessments and shape
robust, pragmatic control strategies across the entire product lifecycle
, in line with
ICH Q3D, ICH Q3C and ICH Q9
.
This position offers a
high level of visibility and impact
at a strategically important manufacturing site. You will work at the interface of MSAT, Compliance and Operations, collaborate closely with cross‑functional teams, influence critical decisions, and actively contribute to establishing sustainable compliance standards within a dynamic GMP environment.
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
Lead and execute impurity risk assessments across the product lifecycle, identifying, assessing and documenting risks and mitigation measures
Define and document scientifically sound, compliant impurity control strategies, including risk‑based testing concepts, acceptance criteria, sampling approaches and periodic reviews
Evaluate manufacturing processes, utilities, equipment contact materials, raw materials, process aids and changes for potential impurity and carryover risks in a GMP environment
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