At a Glance
- Tasks: Ensure compliance and performance of pharmaceutical manufacturing equipment through validation protocols.
- Company: Leading pharmaceutical company focused on operational excellence in Randburg.
- Benefits: Competitive salary, bonuses, medical aid, and professional development opportunities.
- Other info: Stable work environment with generous leave and wellness programs.
- Why this job: Join a dynamic team ensuring high-quality pharmaceutical products and regulatory integrity.
- Qualifications: Bachelor's degree in Engineering and 3 years of validation engineering experience required.
The predicted salary is between 39600 - 48400 £ per year.
About the Role
Our client is seeking a detail-oriented Validation Engineer to ensure the compliance and performance of pharmaceutical manufacturing equipment and systems at their facility in Randburg .
This role is critical for maintaining regulatory adherence and ensuring the reliability of processes that produce high-quality pharmaceutical products.
You will be responsible for developing, executing, and documenting validation protocols for equipment, utilities, and processes.
This is an excellent opportunity for an engineer with a strong understanding of pharmaceutical manufacturing and validation principles to contribute to a leading company in the Gauteng area, ensuring operational excellence and regulatory integrity.
Key Responsibilities
- Develop, execute, and finalize validation protocols (IQ/OQ/PQ) for pharmaceutical manufacturing equipment, utilities, and computerized systems.
- Ensure all validation activities comply with c GMP , FDA, and other relevant regulatory requirements.
- Troubleshoot and resolve deviations identified during validation activities, documenting all findings and resolutions.
- Maintain validation documentation in a state of compliance, including master validation plans, protocols, reports, and change controls.
- Collaborate with engineering, manufacturing, quality assurance, and IT departments to support validation efforts.
- Provide technical expertise and guidance on validation-related issues to project teams and operational staff.
Requirements
- Bachelor's degree in Engineering (Mechanical, Electrical, Chemical, or equivalent).
- Minimum of 3 years of experience in validation engineering within the pharmaceutical, biotech, or medical device industry.
- Strong knowledge of c GMP regulations and validation principles (IQ, OQ, PQ).
- Experience with validation of manufacturing equipment, clean utilities, and computerized systems (e. g., SCADA, DCS, LIMS).
- Excellent documentation, technical writing, and problem-solving skills.
- Ability to work independently and manage multiple validation projects simultaneously.
Benefits
- Competitive annual salary and performance-based bonus opportunities.
- Comprehensive medical aid, life insurance, and retirement fund.
- Opportunities for professional development and training in validation and pharmaceutical compliance.
- A stable work environment with a focus on engineering excellence and regulatory standards.
- Generous annual leave and access to employee wellness programs.
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Validation Engineer - Pharmaceutical Equipment in Southampton employer: Placements24
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We think this is how you could land Validation Engineer - Pharmaceutical Equipment in Southampton
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We think you need these skills to ace Validation Engineer - Pharmaceutical Equipment in Southampton
Some tips for your application 🫡
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✨Understand the Science
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
