Compliance Expert Vials Volume (m/w/d)

Randstad (Switzerland) Ltd.

Date de publication :
08 novembre 2024
Taux d'activité :
100%
Lieu de travail :Kaiseraugst

job details

For one of our clients, an international pharma company in Kaiseraugst, we are looking for an end-to-end Compliance Expert Vials Volume to join the Compliance Unit.

General information:

Start date: 02.01.2025

Latest possible start date: 01.03.2025 (earlier start date preferred)

Planned duration of employment: 1 year

Extension: possible

Workplace: Kaiseraugst

Workload: 80-100%

Home office: Possible in exceptional cases

Travel: No

Team: approx. 26 team members

Working hours: Standard

Tasks & responsibilities:

Ensuring GMP-compliant documentation of operational and production processes and their completion

Preparation, implementation and follow-up of internal or external inspections, as well as close cooperation with internal and external interfaces

Initiation and processing of risk analyses

Processing of QRM assessments

Initiation and processing of deviations, changes, processing of complaints and carrying out checks for completeness

Creation and updating of work procedures (SOPs) to ensure GMP-compliant operational and production processes

Coordination of higher-level GMP projects across departments

Must Haves:

Completed Bachelor's / Master's degree in the field of pharmaceutical manufacturing or a related field

Min. 1-3 years of professional experience in pharmaceutical production, development, quality assurance and control or a related industry

A team-oriented mindset with a view to continuous improvement of processes and the ability to deliver consistent performance at a high level in a constantly changing environment