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Production OSD- Executive
4 weeks ago
Ensure compliance with cGMP (current Good Manufacturing Practices), regulatory requirements, and company policies and procedures.
Collaborate closely with cross-functional teams including Quality Assurance, Regulatory Affairs, Engineering, and Supply Chain to optimize production processes and resolve any issues or challenges.
Drive continuous improvement initiatives to enhance operational efficiency, productivity, and quality within the Production Oral Solid Dosage department.
Develop and implement training programs to ensure that staff are adequately trained and competent to perform their roles effectively.
Monitor and analyze key performance indicators (KPIs) to assess departmental performance and identify areas for improvement.
Requirements Strong understanding of cGMP requirements and regulatory guidelines applicable to pharmaceutical manufacturing.
Proven leadership experience with the ability to effectively manage and develop a diverse team.
Excellent communication, interpersonal, and problem-solving skills.
Ability to thrive in a fast-paced environment and adapt to changing priorities.
Experience with continuous improvement methodologies (e.g., Lean, Six Sigma) is desirable.
Prior experience in a supervisory or managerial role within a pharmaceutical manufacturing environment is highly preferred.
Benefits .
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