About
Are you passionate about ensuring the quality and safety of life-changing pharmaceutical and medical device products? Join this dynamic team as a Quality Systems / Validation Engineer, where you will play a crucial role in bringing new products into production and shaping the future of healthcare.
Key Responsibilities:
- Conduct validation activities for pharmaceutical / medical device production processes.
- Develop and execute validation protocols, including URS/IQ/OQ/PQ, to ensure compliance with regulatory standards.
- Analyze and interpret validation data, identifying areas for improvement and implementing corrective actions.
- Collaborate with cross-functional teams to integrate validation requirements throughout the product development lifecycle.
- Stay up to date with industry regulations and best practices, applying them to enhance validation processes.
Key Qualifications and Experience:
- Bachelor's degree in Engineering, Pharmacy, or related fields.
- Proven experience in validation activities within the pharmaceutical or medical device industry.
- Familiarity with regulatory requirements such as FDA, cGMP, and ISO standards.
- Strong analytical skills and attention to detail.
- Excellent communication and team collaboration abilities.
Benefits:
- Competitive salary in line with your experience.
- Comprehensive health and wellness benefits package.
- Opportunities for professional development and growth.
- Work in a state-of-the-art facility with cutting-edge technology.
- Collaborative and inclusive work environment fostering innovation.
- Make a meaningful impact on patients' lives by contributing to life-saving products.
Join this high functioning team and be part of a mission to improve lives and create a healthier future.
LANZ has 70+ vacancies
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