Join Our Team as a CQV Specialist (m/w/d)
We are seeking dedicated individuals to become part of our dynamic team in the pharmaceutical and biotechnology sector, based in Switzerland.
What We Are Looking For
The Commissioning Qualification Validation (CQV) Engineer will engage in a variety of tasks associated with the validation of equipment and facilities. Key responsibilities include:
- Coordinating the installation of equipment
- Drafting IQ/OQ/PQ protocols and documenting results in accordance with cGMP requirements
- Executing IQ/OQ/PQ for equipment, systems, and utilities
- Identifying efficiencies in the validation program approach and applying lessons learned
- Staying informed of industry regulatory changes relevant to equipment and facility validation
- Performing Quality Systems activities, including Document Management, Change Control, Non-Conformities, and CAPA’s
- Writing and revising procedures applicable to Engineering activities
- Supporting the Engineering group in preparing the validation, requalification, and maintenance programs
Your Background and Experience Should Include
- Education Required: Bachelor’s Degree in a Science or Technical field
- Language: Proficiency in English; German is a significant advantage
- Work Experience: 3-6 years in the pharmaceutical industry
- Skills:
- Exceptional technical writing skills with a demonstrated ability to document work thoroughly and accurately
- Strong written and oral communication skills, with the ability to collaborate effectively across departments
- Excellent organizational and time management abilities
Apply online using the form below. Please note that only applications matching the job profile will be considered.
We look forward to reviewing your CV and organizing an introductory phone call!
Your Techfirm Team