QA Validation Specialist

允; Wallis; Vor Ort; CHF 70’000 - 85’000; Vollzeit

Zusammenfassung

A leading company in the pharmaceutical sector is seeking an Entry Level Validation Specialist in Valais, Switzerland. This role focuses on ensuring compliance in biopharmaceutical manufacturing through validation activities, documentation, and collaboration with various departments. Candidates should have a Master's degree in a relevant field and project management experience in a GMP environment. The position offers a 7-month contract and a commuting allowance.

Leistungen

7-month contract with Oxford Global Resources

Commuting allowance

Qualifikationen

• Experience in project management within a GMP environment.
• Background in MSAT, Quality Assurance, or Operations.

Aufgaben

• Design and implement process validation plans compliant with industry standards.
• Draft, review, and finalize validation protocols, reports, and assessments.
• Collaborate with R&D on process characterization.

Kenntnisse

Project Management

Organizational Skills

Ausbildung

Master's degree in Chemistry

Master's degree in Biology

Master's degree in Biotechnology

Master's degree in Chemical Engineering

Jobbeschreibung

Entry Level Validation Specialist - Valais, Switzerland

Are you seeking your next opportunity in the pharmaceutical industry? Read on!

About the Client

Our client is a global leader in biotech and pharmaceutical manufacturing, with a prominent presence in Switzerland. Their facility in the Valais region is at the forefront of bioprocessing innovation, offering a unique alpine setting and a collaborative environment for professionals to grow their careers.

Job Description

This role involves leading validation activities to ensure compliant and consistent biopharmaceutical manufacturing. You will be responsible for process documentation, regulatory interactions, and cross-department collaboration, from design to ongoing verification, maintaining high quality standards. The position provides exposure to both technical and strategic quality operations.

Responsibilities

1. Design and implement process validation plans compliant with industry standards.
2. Draft, review, and finalize validation protocols, reports, and assessments.
3. Collaborate with R&D on process characterization.
4. Evaluate and approve changes, deviations, and non-conformance reports.
5. Develop and maintain the continued process verification strategy.
6. Participate in Product Quality Reviews for lifecycle monitoring.
7. Coordinate with internal stakeholders to align validation and quality efforts.
8. Engage with regulatory authorities as needed.

Minimum Requirements

• Master's degree in Chemistry, Biology, Biotechnology, Chemical Engineering, or related field.
• Experience in project management within a GMP environment.
• Background in MSAT, Quality Assurance, or Operations.
• Exposure to biologics, especially mammalian systems, is advantageous.
• Strong organizational skills and ability to manage multiple priorities.
• Fluent in English; German skills are a plus.

Benefits

• 7-month contract with Oxford Global Resources.
• Work at a leading pharmaceutical facility.
• Commuting allowance.

Preferred Skills

• Project Management
• Valais, Switzerland

Work Experience

• Project Management
• Finance & Accounting
• Healthcare

Languages

• English