CQV Specialist (m/w/d) 100%

Join Our Dynamic Team in Switzerland

We are seeking talented individuals to contribute to our mission in the pharmaceutical and biotechnology sector. As part of our innovative team, you will play a vital role in ensuring the highest standards in equipment and facilities validation.

Key Responsibilities

• Engage in comprehensive validation activities, including Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, and Risk Assessment.
• Prepare and deliver critical validation documentation deliverables, such as URS, DQ, FMEA, Risk Assessments, FAT, SAT, and protocols (IQ, IOQ, OQ, PQ).
• Execute IQ/OQ and PQ for equipment, systems, and utilities, while documenting the outcomes and recommending efficiencies in the validation approach.
• Stay informed of industry regulatory changes relevant to equipment and facility validation and apply lessons learned to improve processes.
• Carry out assigned Quality Systems activities, including Document Management, Change Control, Non-Conformities, and CAPA’s.
• Write and revise procedures applicable to Engineering activities.
• Support the Engineering group in developing the validation, requalification, and maintenance program.

Your Profile

• Education: Bachelor’s Degree in a Science or Technical field.
• Language Skills: Proficiency in English is essential; knowledge of German is an added advantage.
• Work Experience: 3-6 years in the pharmaceutical industry.
• Skills:
  • Exceptional technical writing abilities with a focus on thorough and accurate documentation.
  • Strong verbal and written communication skills, with an aptitude for effective interdepartmental collaboration.
  • Excellent organizational and time management abilities.

We eagerly anticipate the opportunity to connect with you and discuss how you can become a valued member of our team!