Senior Consultant – Hygiene Projects – 6939 – ADA
Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is recruiting for a Senior Consultant – Hygiene Projects for a contract until 31st March 2027. TThis is a hybrid role based with 2-3 days onsite presence required in Visp, Switzerland.
Main Responsibilities
* Ensure the effective implementation and continuous improvement of hygiene standards at the site
* Act as an interface and key link between all departments involved in contamination control, including Production, QA, Monitoring, Engineering and EHS
* Plan, lead and execute hygiene projects in the areas of material transfer, gowning, cleaning, disinfection and cleanroom behavior
* Take responsibility for planning, coordinating, and performing Cleanroom Performance Qualifications (PQs) in compliance with GMP and site requirements
* Prepare, maintain and update hygiene-related documentation in accordance with GMP standards
* Investigate deviations within hygiene and environmental monitoring processes, perform root cause analyses, define and track CAPAs
* Initiate and own related change requests (CRs)
* Manage and execute deviation investigations and ensure timely closure in compliance with quality system requirements
* Identify and implement improvement measures to harmonize and standardize hygiene processes across different production areas
* Prepare and represent hygiene topics during internal and external audits as well as inspections by authorities and customers
* Develop and deliver targeted training programs to strengthen hygiene awareness, and consistent hygiene standards across the site
Qualifications and Experience
* Relevant working/residency permit or Swiss/EU-Citizenship required
* Degree or vocational education in a scientific discipline such as Chemistry, Pharmaceutical Technology, Pharmacy, Bioprocess Engineering, or equivalent
* Professional experience in a GMP-regulated environment, ideally in contamination control, cleanroom hygiene, or quality management
* Strong knowledge of GMP regulations and experience in preparing and maintaining GMP documentation (SOPs, CAPAs, deviations, change controls)
* Excellent command of English, both written and spoken; good German skills are an advantage
* Analytical mindset with a structured and solution-oriented approach
* Strong communication and collaboration skills across multidisciplinary team
* Independent, committed and responsible personality with a high level of quality awareness
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