Quality Specialist - Switzerland (Valais Region)
We are working with a leading pharmaceutical organization that partners with global pharma and biotech companies to develop and manufacture pharmaceutical products. They are expanding their team and looking for a Quality Assurance Specialist to support the product lifecycle at their site in Switzerland.
The Role
As a Quality Specialist, you'll play a key role in ensuring product quality and compliance throughout the full project lifecycle. This is an opportunity to work on innovative medicines in a highly regulated environment, supporting projects from development through to commercial release.
Key Responsibilities
Act as the technical QA representative for client projects, providing expert input on quality-related matters.
Deliver QA oversight across all phases of projects, ensuring compliance with GMP and regulatory standards.
Review and assess product-related quality records for accuracy and completeness.
Support method transfer, qualification, and validation activities in collaboration with QA teams.
Issue batch records and provide technical support for batch documentation review.
Act as a subject matter expert during audits and inspections.
Provide input for regulatory submissions and coordinate timely batch manufacturing and QC release.
Prepare and approve technical documentation such as SOPs, Master Batch Records, specifications, and sampling plans.
What We're Looking For
Relevant degree such as a Science or Manufacturing
Minimum 3 years' experience in a technical QA role within a GMP environment; sterile manufacturing experience is a bonus.
Strong understanding of GMP principles and regulatory compliance.
Excellent communication and teamwork skills, with fluency in English. German is a bonus
Experience in microbiology or QC is advantageous.Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy