System Validation Professional
6 days ago
We are seeking a skilled Computer System Validation Engineer to join our team. The ideal candidate will have experience in pharmaceutical engineering and a strong background in commissioning, qualification, and validation of various systems within the industry.
Key Responsibilities- Provide technical guidance on the commissioning, qualification, and start-up of various equipment and facilities.
- Lead the development of key qualification deliverables during the project lifecycle to ensure project success.
- Prepare protocols, execute protocols, summarize data, resolve deviations, and prepare final reports.
- C coordinate meetings with cross-functional departments to drive project progress, facilitate decisions, and provide updates.
- Excellent written and spoken English is required, including the preparation of technical documents.
- Years of experience: 5+ years in commissioning, qualification, or validation of various systems within the pharmaceutical/biotech industry.
- Knowledge of cGMP operations, including SOPs, Change Controls, and Validation.
- Experience with developing and executing validation projects.
- Knowledge of GAMP and Data Integrity requirements.
- Previous Pharmaceutical/Biotech experience is mandatory for this role.
We offer competitive wages, opportunities for travel, and a team mentality that sets us apart from our competitors. Our consultants come from different areas of the Pharmaceutical/Biotech/Medical Device industries and have extensive experiences obtained from world-class organizations.
About UsWe value everyone's unique talents and work together to support our clients. We strive to cultivate the best working environment where empowerment, passion, and perseverance are nurtured.
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