Join Our Team as a CQV Specialist (m/w/d)
We are seeking new team members to contribute to our efforts in the pharmaceutical and biotechnology sectors here in Switzerland.
What We Are Looking For
The Commissioning Qualification Validation Engineer will execute a variety of tasks related to the validation of equipment and facilities. Key responsibilities include:
- Coordinating the installation of equipment and drafting the IQ/OQ/PQ protocols.
- Executing IQ/OQ/PQ protocols and documenting results according to cGMP requirements.
- Getting involved in all validation activities, including but not limited to:
- Facilities
- Utilities
- Validation Life Cycle
- Execution
- Technical Documentation
- Process
- GAP Analysis
- Risk Assessment
- Preparing validation documentation such as URS, DQ, FMEA, and Protocols (IQ, IOQ, OQ, PQ).
- Writing reports on completed validation activities and identifying efficiencies in the validation program approach.
- Staying informed about industry regulatory changes relevant to equipment and facility validation.
- Performing assigned Quality Systems activities, including Document Management System, Change Control, Non-Conformities, and CAPAs.
- Writing and revising procedures applicable to Engineering activities.
- Supporting the Engineering group in preparing the validation, requalification, and maintenance program.
Your Background and Experience Should Include
- Education: Bachelor’s Degree in Science or a Technical field.
- Language: English is required; German is a significant plus.
- Work Experience: 3-6 years in the Pharma Industry.
- Skills:
- Excellent technical writing skills with the ability to document all work thoroughly, accurately, and in a timely manner.
- Strong written and oral communication skills to work effectively across departments.
- Exceptional organizational and time management capabilities.
We look forward to your application. Apply online using the form below. Please note that only applications matching the job profile will be considered.
Your Techfirm Team