CQV Specialist (m/w/d) 100%

Join Our Dynamic Team in Switzerland

We are seeking motivated individuals to contribute their expertise within the pharmaceutical and biotechnology sectors. Become a vital part of a team that values professionalism and innovation.

Key Responsibilities

• Engage in various validation activities, covering Facilities, Utilities, Validation Life Cycle, Technical Documentation, and Risk Assessment.
• Prepare and deliver essential validation documentation, including URS, DQ, FMEA, and protocols for IQ, IOQ, OQ, and PQ.
• Conduct the execution of IQ/OQ and PQ for equipment, systems, and utilities, ensuring comprehensive reporting of validation activities.
• Identify efficiencies within the validation program, apply lessons learned, and stay updated on industry regulatory changes.
• Contribute to assigned Quality Systems activities, including Document Management, Change Control, and CAPA management.
• Draft and revise procedures relevant to Engineering activities, supporting the broader Engineering group in validation and maintenance programs.

Qualifications and Skills

• Education: Bachelor’s Degree in a Science or Technical field.
• Languages: Proficiency in English is essential; knowledge of German is advantageous.
• Experience: 3-6 years in the pharmaceutical industry.
• Skills:
  • Strong technical writing abilities with a commitment to thorough and timely documentation.
  • Exceptional written and verbal communication skills, facilitating effective interdepartmental collaboration.
  • Excellent organizational and time management capabilities.

We eagerly anticipate the opportunity to review your qualifications and engage in an introductory conversation.

The Techfirm Team