Production Shift Supervisor

Job Description:
Educational and Experience Requirements:
Education:

- Bachelor’s degree in pharmacy (B Pharm) or Chemical Engineering.
- Graduated from a reputed university or college, such as NITs, RECs, or Tier-1 state colleges.

Experience:

- 3 to 7 years of experience in manufacturing or production.

Job Description

Mixing and Filling Operations- Expert in liquid-liquid and solid-liquid mixing and filling processes.- Proficient in packaging operations with a focus on accuracy, hygiene, and efficiency.

Regulatory Compliance- Implement and oversee manufacturing practices in strict adherence to FDA, WHO, and cGMP guidelines.- Ensure processes meet global quality and safety standards.

Project Management- Successfully managed projects aimed at cycle time reduction, productivity improvements, and line balancing.- Demonstrated ability to drive cross-functional teams towards project milestones and KPIs.

Safety & Risk Analysis- Conduct Pre-Startup Safety Reviews (PSI), HAZOP, and Process Hazard Analysis (PHA) for new product introductions.- Lead all Process Hazard Management activities for existing products to ensure safe and reliable operations.

Process Analysis & Optimization- Perform process capability studies, What-if analyses, and variability studies to optimize performance.- Define and refine key process parameters such as cycle time, lead time, takt time, and line balancing.

Process & Equipment Qualification- Lead and support process qualifications, change control, and IQ/OQ (Installation & Operational Qualification).- Accountable for equipment calibration and maintaining validation records.

Operational Excellence- Foster shop floor discipline, team engagement, and a culture of 5S, system adherence, and compliance.- Drive continuous improvement through SPC (Statistical Process Control) and process mapping.

Documentation & Training- Manage production reporting and ensure all process documentation is up to date.- Conduct training programs for team members on SOPs and best practices.

Customer-Centric Quality Management- Conduct root cause analyses for customer complaints and deviations.- Implement Corrective and Preventive Actions (CAPA) to drive continuous quality improvements.

Operational Management- Monitor and maintain line flow, output, and process control for optimal production efficiency.

Capacity Planning & Resource Management- Develop and execute capacity plans, shift planning, material issuance, and manpower loading. Improvement Initiatives- Spearhead yield improvement, OEE (Overall Equipment Effectiveness), and automation projects. Process Redesign & Layout Optimization- Identify opportunities and implement process redesigns, layout modifications, and workflow enhancements to boost efficiency and reduce waste.

1. Certifications- Six Sigma Green Belt certification is preferred (not mandatory).

2. Regulatory & Industry Compliance- Proven experience working with FDA, WHO, and cGMP standards.- Sound understanding of ICH and WHO guidelines related to pharmaceutical manufacturing and quality systems.

3. Technical Proficiency- Hands-on experience in commissioning and qualification processes (IQ, OQ, PQ).- Familiarity with validation protocols and regulatory documentation.

4. Industry Exposure- Demonstrated exposure to the pharmaceutical and healthcare industries, preferably in manufacturing or process engineering roles.

5. Corporate Experience- Experience working in multinational corporations (MNCs) is preferred.- Ability to work within structured environments and adhere to global corporate policies.

6. Career Stability- Shows a stable career progression with limited job-hopping. 3M Global Terms of Use and Privacy Statement