Deputy Manager, Production

Pristine Pharmaceuticals

Pristine Pharmaceuticals

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Summary

• Vacancy: 01
• Location: Patuakhali
• Minimum Salary: Negotiable
• Experience: 8 to 12 years
• Published: 9 Nov 2024

Requirements

Education

• Master of Pharmacy (M.Pharm), Bachelor of Pharmacy (B.Pharm)

Experience

• 8 to 12 years
• The applicants should have experience in the following business area(s):
  Pharmaceutical/Medicine Companies, Healthcare/Lifestyle product

Responsibilities & Context

The role of a Deputy Manager in Production at Pristine Pharmaceuticals typically involves overseeing manufacturing operations, ensuring quality and regulatory compliance, and optimizing production processes to meet organizational goals. Here are key responsibilities for this role:

1. **Production Planning and Execution**:

– Develop and implement production schedules to meet daily, weekly, and monthly targets.

– Allocate resources effectively and manage the team to ensure timely completion of production batches.

2. **Quality and Compliance**:

– Ensure that production processes adhere to Good Manufacturing Practices (GMP) and other regulatory requirements.

– Coordinate with the quality assurance (QA) team to address any deviations, non-conformities, or quality issues.

3. **Process Optimization**:

– Identify areas for efficiency improvement and implement process enhancements to reduce waste, lower costs, and increase output.

– Monitor and control production parameters to ensure product consistency and quality.

4. **Team Supervision and Development**:

– Supervise production staff, provide guidance and training, and manage team performance.

– Ensure adherence to safety standards and motivate the team to follow protocols.

5. **Inventory and Resource Management**:

– Monitor inventory levels of raw materials and ensure timely procurement to avoid production delays.

– Collaborate with procurement and supply chain teams to optimize resource use.

6. **Documentation and Reporting**:

– Maintain accurate production records and logs in compliance with industry standards.

– Prepare production reports, analyze performance data, and report issues or achievements to higher management.

7. **Cross-functional Collaboration**:

– Work closely with R&D, QA, and maintenance teams to coordinate activities and resolve any production-related issues.

– Participate in audits and inspections and assist in implementing corrective actions if necessary.

8. **Continuous Improvement**:

– Participate in initiatives to improve production processes, including Lean Manufacturing, Six Sigma, or other methodologies.

This role is central to maintaining efficient production workflows and ensuring high-quality output in a regulated pharmaceutical environment.

Workplace

Work at office

Employment Status

Full Time

Job Location

Patuakhali

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