Quality Assurance Specialist

Randstad Group; Schachen; Hybride; CHF 90 000 - 120 000; Plein temps

Résumé du poste

Randstad Group in Switzerland is seeking a Quality Assurance Operations Specialist to support cGMP QA activities at the Schachen site. The role includes batch release support and documentation reviews within the Global Development Quality OPS team.

We require a university degree (bachelor or higher) and German C1 along with English business proficiency. The position allows 2 days per week home office in a hybrid setup and runs until 31.10.2028.

Qualifications

• University degree (bachelor or higher) preferred.
• Experience in a regulated environment is an advantage.
• Previous experience in a similar role.
• German C1 is must have; English business proficient is highly expected.

Responsabilités

• Participate in the release or rejection of GMP materials and components through direct batch release support or involvement with critical program issues.
• Perform documentation, system or other GMP record reviews related to QOS activities.
• Conduct all work to high standards of quantity, integrity, quality and GMP compliance.

Connaissances

Regulated environment experience

GMP documentation

Quality assurance

Formation

Bachelor’s degree or higher

Description du poste

For one of our clients, an international pharmaceutical company, we are seeking aQuality Assurance Operations Specialist.

General Information:

• End Date:31.10.2028
• Home office:Possible, 2 days per week
• Working hours:Standard

About the work:

The Global Development Quality OPS team is responsible to drive or support compliance-based programs and results which include support cross functional projects, solving simple problems, current Good Manufacturing Practices (cGMP) quality initiatives, quality system improvements, quality directives, compliance metrics and monitoring, SOP management, and site procedures at Schachen Site.

Task & Responsibilities:

• Participate in the release or rejection of GMP materials and components either through direct batch release support or involvement with critical program issues.
• Perform documentation, system or any other GMP record review in relationship with the QOS activities
• Conduct all work meeting high standards for quantity, integrity, quality, and GMP compliance

“Day in the job”:

• 3 times per week the day starts at 8:30 with a team meeting to discuss ongoing activities. During the day, the person will work on records review

Requirements:

• University degree (bachelor or higher) is preferred
• Experience in a regulated environment is an advantage
• Previous experience in a similar role
• German C1 is must have, English business proficient is highly expected