About the job
We are currently seeking a skilled and motivated Commissioning & Qualification Consultant to join our consultancy department in Terrassa. This role is pivotal in managing and executing projects related to commissioning and validation of pharmaceutical engineering and equipment, tailored to meet the specific requirements of our diverse clientele.
The ideal candidate will possess between 1 to 3 years of relevant experience in validation, qualification, and/or Quality Assurance within the pharmaceutical consulting arena.
Key Responsibilities:
- Develop comprehensive commissioning and qualification documentation for projects, including C&Q Plans, Commissioning Protocols, VMP, URS, RA, DQ, IQ, OQ, PQ, and Traceability Matrices.
- Execute qualifications and commissioning activities as per project scope.
- Communicate and report to the Team Leader/Level 1 Consultants on deliverables prior to submission to clients, raising any concerns or deviations identified.
- Document any incidents related to project development, including deviations from acceptance criteria, extended hours, project changes, or documentation integrity issues, to the Team Leader or Level 1 Consultants.
- Ensure documentation aligns with ALCOA principles for data integrity.
- Generate qualification and commissioning reports.
- Maintain updated records of project activities through defined channels.
- Adhere to company policies and procedures while executing assigned tasks.
- Contribute initiatives for continuous improvement within the department, reporting to the line leader.
- Promote environmental sustainability by supporting company-defined actions and proposing new initiatives relevant to the work area.
- Comply with the Syntegon-Telstar Group's compliance culture and understand applicable regulations for the position.
If you believe that this opportunity aligns with your personal and professional aspirations and meet the qualifications outlined, we encourage you to apply. We look forward to your application!
