
Manufacturing Professional
1 week ago
We are seeking a skilled and detail-oriented professional to join our manufacturing team.
Key Responsibilities:- Develop and review functional standard operating procedures
- Prepare Master Formula Records (MFR) and Product Information Sheets (PORM)
- Design pre-validation protocols and reports
- Coordinate with cross-functional teams for review, corrections, and approvals
- Bachelor's degree in Pharma or related field
- 3-5 years of experience in documentation management and training coordination within pharmaceutical manufacturing
- Strong understanding of Good Manufacturing Practices (GMP), SOPs, and regulatory requirements
- Excellent communication and interpersonal skills
- Detail-oriented with strong organizational and time management abilities
- Ability to work effectively in a fast-paced environment and prioritize tasks accordingly
About the role:
This is an exciting opportunity to contribute to the success of our global manufacturing organisation.
As a valued member of our team, you will play a vital role in ensuring the quality and efficiency of our manufacturing processes.
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