Quality Control Engineer

agap2 Switzerland; Basel; Vor Ort; CHF 80’000 - 100’000; Vollzeit

Zusammenfassung

A leading consulting group in Switzerland is seeking a Quality Control Engineer for the Pharmaceutical/Biotech sectors. The role involves rigorous Quality Control analyses, method validation, and authoring SOPs. Candidates should have an engineering diploma and a minimum of 2 years of experience in Quality Control, with fluency in English preferred. This full-time position offers an opportunity to work on significant projects in a dynamic work environment.

Qualifikationen

• Minimum 2 years of experience in Quality Control within the pharma industry.
• Fluent in English; proficiency in French and German is advantageous.
• Experience in Quality assurance for the QC lab is a plus.

Aufgaben

• Conduct Quality Control analyses on raw materials and finished products.
• Carry out validation and transfer of analytical methods.
• Contribute to the authoring and review of Standard Operating Procedures.

Kenntnisse

Analytical Chemistry

Organic Chemistry

Quality Control

Good Manufacturing Practices

Ausbildung

Engineer diploma in pharmaceutical, quality control, or related fields

Jobbeschreibung

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Specialist in hiring engineers, pharmacists and business managers for Life Science in Switzerland!

Agap2 is a European engineering and operational consulting group founded in 2005, specialized in the industry. We work in the Pharma, Biotechnology, Medical Devices, Energy, Infrastructure, Transportation, Chemicals, and Information Technology sectors.

As a consultant, you will support our clients in project realization on site by bringing your expertise and skills.

You are agile and eager to adapt to different work environments, fueling your curiosity about the biggest projects in our clients' portfolios.

Main responsibilities:

We are looking for a Quality Control engineer to join our team in the Pharmaceutical/Biotech sectors. The key responsibilities are to:

• Conduct rigorous Quality Control analyses on raw materials and finished products using analytical and organic chemistry techniques, ensuring adherence to established quality standards and contributing to product excellence.
• Carry out validation and transfer of analytical methods.
• Contribute to the authoring and review of Standard Operating Procedures (SOPs), Protocols, and Reports related to Good Manufacturing Practices (GMP) within the QC laboratory.
• Formulate and improve strategies and methodologies for designated processes and projects.
• Provide ad-hoc support on CQV activities of QC equipment as needed.

Requirements:

• Engineer diploma or equivalent in pharmaceutical, quality control, analytical chemistry, biotechnology, or related fields.
• Minimum 2 years of experience in Quality Control within the pharma industry.
• Experience in Quality assurance for the QC lab is a plus.
• Fluent in English; French and German are advantageous.
• Swiss (or valid Swiss permit) or EU nationality.

Seniority level

• Entry level

Employment type

• Full-time

Job function

• Engineering, Science, and Manufacturing

Industries

• Engineering Services, Biotechnology Research, and Pharmaceutical Manufacturing

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