Company
pharmaceutical
PackagingSupervisor
Neural analysis suggests this role is
optimal for Mid candidates.
“Packaging Supervisor. Skills: packaging operations, people management, problem-solving, project management. Supervise daily operations. Ensure packaging areas are maintained”
What You'll Achieve.
ensuring packaging processes are executed in a compliant, safe, effective, and efficient manner; driving team performance; ensuring commitments are met; keeping colleagues engaged, focused, and aligned with operational goals; Ensure production processes meet standard lead times and output targets; optimizing Overall Equipment Effectiveness (OEE); Ensure delivery of products that meet customer expectations; Maintaining schedule adherence against the production plan; Ensing achievement of committed production volumes and targets
Industry & Context.
Proven problem-solving and decision-making abilities; deviation investigations; OOS/OOL/OOT analysis; Identifying root causes; implementing effective solutions; preventing recurrence
What They're Looking For.
Must Have
Bachelor’s degree in Pharmacy from a reputable university, Minimum 3 years of experience in the pharmaceutical industry, particularly in manufacturing or packaging operations, interpersonal and communication skills, Demonstrated people management experience, Proven problem-solving and decision-making abilities, Proficiency in written and spoken English and local language, Ability to communicate effectively across departments and with external stakeholders, including regulatory agencies, organizational and project management skills, Ability to work collaboratively in a team environment, Proven ability to manage multiple priorities simultaneously
Nice to Have
Trained and/or certified in Six Sigma or Lean methodologies, with demonstrated application in process improvement initiatives, Proficiency in SAP and serialization systems
What You'll Do.
Supervise daily operations
Ensure packaging areas are maintained
Ensure production processes meet targets
Optimize Overall Equipment Effectiveness (OEE)
Verify critical processes in daily production
Review GMP documentation
Ensure personnel are trained
Manage procurement of manufacturing supplies
Develop and maintain GMP documentation
Actively participate in gap assessments
Identify root causes and implement solutions
Ensure delivery of products
Maintain schedule adherence
Achieve committed production volumes
Support internal and external audits
Support validation and qualification activities
Support Integrated Manufacturing (IMEX) initiatives
Support site-level projects
Drive team engagement
Promote effective communication
How You'll Work.
Team & Collaboration
Ability to communicate effectively across departments and with external stakeholders; Ability to work collaboratively in a team environment; Drive team engagement and promote effective communication within the team
Communication Scope
interpersonal and communication skills; Proficiency in written and spoken English and local language; Ability to communicate effectively across departments and with external stakeholders, including regulatory agencies; effective communication
Process & Methodology
organizational and project management skills, project management
Full Job Description
## **Position Purpose** To provide direct support, supervision, and guidance to operators, ensuring packaging processes are executed in a compliant, safe, effective, and efficient manner. As a front-line leader, maintaining a strong leadership presence on the production floor is essential to driving team performance, ensuring commitments are met, and keeping colleagues engaged, focused, and aligned with operational goals. ## **Primary Duties** * Supervise daily operations to ensure compliance with Quality, Safety, and operational efficiency by: \- Ensuring packaging areas, equipment, and facilities are well-maintained, clean, organized, and safe. \- Ensure production processes meet standard lead times and output targets while optimizing Overall Equipment Effectiveness (OEE) through efficient resource utilization and continuous performance monitoring. \- Verifying critical processes in daily production, including line clearance, cleanliness verification, Lot Start-Up verification, In Process Control, and printing verification (Batch No., Manufacturing Date, Expiry Date, HET). \- Reviewing GMP documentation (e.g., batch records, logbooks) to ensure all activities follow approved procedures and are documented in accordance with Data Integrity and Good Documentation Practices (GDP) principles. \- Ensuring all personnel performing packaging activities are properly trained and qualified. \- Managing the procurement of manufacturing supplies in line with approved budgets. * Develop and maintain GMP documentation, including: \- Master Batch Record, \- Standard Operating Procedures (SOPs), covering machine operation, cleaning, handling, and related activities in compliance with cGMP and Pfizer Quality Standard. * Actively participate in: \- Gap assessments, deviation investigations, OOS/OOL/OOT analysis, and product complaints (including rework, complaint handling, and recall). \- Identifying root causes, implementing effective solutions, and preventing recurrence through CA
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