Quality Engineer
at Scitex Recruitment
Hamilton, Waikato, New Zealand -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 01 Aug, 2024 | Not Specified | 05 May, 2024 | N/A | Analytical Skills,Iso Standards,Regulatory Requirements | No | No |
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Description:
- Play a critical role in ensuring the safety and efficacy of life-saving products
- Development and growth potential within a cutting-edge industry.
- Based in Te Rapa with flexibility in working hours.
Are you passionate about ensuring the quality and safety of life-changing pharmaceutical and medical device products? Join this dynamic team as a Validation Engineer, where you will play a crucial role in bringing new products into production and shaping the future of healthcare.
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.
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.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Engineering pharmacy or related fields
Proficient
1
Hamilton, Waikato, New Zealand