CQV Specialist (m/w/d) 100%

Join Our Dynamic Team in Switzerland

We are expanding and eager to welcome new professionals to our collaborative environment in the pharmaceutical and biotechnology sector. As part of our team, you will play a crucial role in ensuring the quality and compliance of our operations.

Responsibilities

• Coordinate the installation of equipment and conduct thorough validation activities, including Facilities, Utilities, and Validation Life Cycle.
• Draft and manage documentation such as IQ/OQ/PQ protocols, URS, DQ, FMEA, and Risk Assessments.
• Execute validation protocols and write comprehensive reports on validation activities.
• Identify efficiencies in the validation program approach while applying insights from past experiences and staying updated on industry regulations.
• Engage in Quality Systems activities, including Document Management, Change Control, Non-Conformities, and CAPA.
• Write and revise procedures pertinent to Engineering activities in collaboration with the Engineering team.
• Support the preparation of validation, requalification, and maintenance programs.

Qualifications

• Education: Bachelor’s Degree in a Science or Technical field.
• Language: Proficiency in English; knowledge of German is an advantage.
• Work Experience: 3-6 years in the Pharma Industry.
• Skills:
  • Exceptional technical writing abilities to ensure thorough and timely documentation.
  • Strong written and verbal communication skills for effective interdepartmental collaboration.
  • Excellent organizational and time management skills to handle daily responsibilities efficiently.

We are eager to explore the potential of having you on our team and discuss how your expertise aligns with our mission.

Your Techfirm Team