Aurobindo Pharma, a global pharmaceutical leader, is seeking a highly motivated and experienced Validation Engineer to join our dynamic team in Malta. This is an exciting opportunity to contribute to the production of high-quality pharmaceutical products in a rapidly growing and innovative environment. If you are a detail-oriented individual with a passion for quality assurance and a proven track record in validation within a manufacturing setting, we encourage you to apply.
About Aurobindo Pharma
Aurobindo Pharma is a leading multinational pharmaceutical company with a strong presence across the globe. We are committed to developing and manufacturing high-quality, affordable medicines that improve the lives of patients worldwide. Our Malta facility plays a crucial role in our global operations, and we are constantly investing in our infrastructure and personnel to maintain our position at the forefront of the pharmaceutical industry. We offer a supportive and collaborative work environment where innovation is encouraged and professional development is prioritized. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Key Responsibilities of the Validation Engineer
As a Validation Engineer at Aurobindo Pharma Malta, you will play a critical role in ensuring the consistent quality and compliance of our manufacturing processes. Your responsibilities will include, but are not limited to:
- Developing and executing validation protocols: This involves creating detailed plans for validating equipment, processes, and systems in accordance with Good Manufacturing Practices (GMP) and regulatory requirements.
- Performing equipment qualification (EQ) and process qualification (PQ): You will be responsible for conducting IQ, OQ, and PQ activities to ensure that equipment and processes meet predefined specifications and perform consistently.
- Documenting and reporting validation activities: Maintaining meticulous records of all validation activities, including protocols, reports, and deviations, is essential to ensure regulatory compliance.
- Supporting the investigation of deviations and CAPAs: You will be involved in investigating any deviations from established procedures and implementing corrective and preventive actions (CAPAs).
- Staying abreast of regulatory changes: Keeping up-to-date with the latest GMP guidelines and regulatory requirements is crucial for maintaining compliance.
- Collaborating with cross-functional teams: Working effectively with engineers, operations personnel, and quality assurance teams is essential for successful validation activities.
- Participating in continuous improvement initiatives: Identifying opportunities for improvement in validation processes and implementing them to enhance efficiency and effectiveness.
Required Skills and Qualifications
To succeed in this role, you must possess the following:
- Education: A higher diploma in engineering (MQF Level 5 or higher) is required. A Bachelor’s degree in Engineering or a related scientific field is highly preferred.
- Experience: At least two years of experience in a pharmaceutical or other regulated manufacturing environment, with a strong focus on validation activities, is essential.
- Communication Skills: Excellent written and spoken English communication skills are crucial for effective collaboration and documentation.
- Technical Skills: Proficiency in Microsoft Office Suite (Word, Excel, Outlook) is necessary. Experience with validation software and data management systems is highly advantageous.
- Organizational Skills: Meticulous attention to detail, strong organizational skills, effective planning, and excellent time management abilities are critical for success in this role. The ability to manage multiple projects simultaneously and meet deadlines is essential.
Why Choose Aurobindo Pharma Malta?
Aurobindo Pharma Malta offers a competitive salary and benefits package, including:
- Competitive Compensation: We offer a salary commensurate with experience and qualifications.
- Comprehensive Benefits: We provide a comprehensive benefits package that includes health insurance, pension plan, and paid time off.
- Professional Development: We are committed to supporting the professional development of our employees through training opportunities and career advancement prospects.
- Collaborative Environment: We foster a collaborative and supportive work environment where teamwork and innovation are highly valued.
- Global Opportunities: As part of a global organization, you will have opportunities for career growth and development within Aurobindo Pharma worldwide.
How to Apply
If you are interested in this exciting opportunity to join our team, please submit your CV and cover letter to: HRMALTA@AUROBINDO.COM
