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Tier-1 employer and common mid-level manufacturing role create moderate competition.
Role requires regulated pharma manufacturing skills and cGMP experience, limiting cross-industry transferability.
Explicit degree, cGMP experience, and 6+ years requirement make shortlisting highly strict.
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Manage projects and lead a team handling people, technology, and financial resources in sterile pharmaceutical manufacturing.
Drive process and product improvements and risk-managed problem solving in compliance with regulatory and cGMP standards.
Develop and manage process operators, implement Lean Tools, set SMART objectives, and optimize manufacturing operations performance.
B-Pharm or M.Sc degree.
6+ years of experience in sterile Pharma/Biopharma manufacturing operations.
Working knowledge of Upstream/Downstream cGMP manufacturing operations and regulatory compliance.
Not explicitly mentioned: Notice period.
Proven leadership experience in regulated pharmaceutical manufacturing operations, preferably managing diverse teams.
Experienced with Lean Tools implementation and continuous process improvement methods.
Comfortable leveraging AI tools like ChatGPT or Microsoft Copilot for problem-solving and operational enhancements.