Team Leader - Packaging Material

At Julphar, we are on a journey of culture transformation & our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism.

Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents , create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.

Job Summary / Main Purpose

The Packaging Material Team Leader is responsible for overseeing the inspection and quality control of packaging materials at Julphar HQ. This role leads a team within the Quality Control (QC) department, ensuring strict adherence to regulatory guidelines, Good Manufacturing Practices (GMP), and internal quality standards. The role includes managing inspections, audits, data analysis, system updates, and team development. The ideal candidate will hold a bachelor’s degree in Chemistry or Pharmacy and bring more than 10 years of relevant experience in QC/QA within a regulated pharmaceutical environment.

Key Responsibilities

• Oversee the inspection and release of packaging materials in compliance with quality specifications.
• Operate and supervise the use of various QC instruments and equipment based on the section’s requirements.
• Ensure strict adherence to GLP, GMP, safety protocols, and maintain a hygienic laboratory environment.
• Review and verify test data in SAP and ensure accuracy in system entries.
• Prepare, review, and maintain Standard Operating Procedures (SOPs) for packaging material analysis.
• Supervise and guide analysts in the packaging material section, ensuring timely and compliant execution of tasks.
• Authorize release or rejection decisions for packaging materials in SAP based on evaluation outcomes.
• Lead, train, and mentor QC staff to develop technical competencies and maintain motivation levels.
• Analyze quality control data to detect trends and initiate corrective actions as needed.
• Ensure full compliance with current regulatory, cGMP, and company quality standards.
• Conduct investigations for lab incidents, deviations, OOS (Out of Specification), and OOL (Out of Limit) results, and implement CAPAs accordingly.
• Manage and ensure timely closure of quality system records (CAPA, OOS, Deviations, Change Controls) via Amplelogic EQMS.
• Support internal and external audits, respond to observations, and oversee timely closures.
• Promote data integrity, documentation accuracy, and implementation of good documentation practices in the lab.
• Handle any additional responsibilities as assigned by the Head of Department or designee.
  
  

• Strong sense of accountability, ownership, and ethical responsibility.
• Excellent communication, interpersonal, and presentation skills.
• In-depth knowledge of industry standards, regulations (21 CFR Part 11, cGMP, GLP), and audit readiness.
• Strong leadership, team management, and manpower handling skills.
• Analytical mindset with the ability to identify root causes and propose practical solutions.
• High attention to detail and ability to manage multiple priorities and stakeholders.
• Conflict management and cross-functional collaboration capabilities.
• Proactive in identifying opportunities for process improvement and driving compliance.
  
  

• Bachelor’s degree in Chemistry or Pharmacy (mandatory).
• Minimum 10 years of experience in Quality Control and/or Quality Assurance, preferably in a pharmaceutical environment.
• Proven track record in a supervisory or leadership role within QC/QA functions.
• Demonstrated expertise in regulatory audits and compliance with global quality standards.
• Strong problem-solving, analytical, and decision-making skills.
• Experience with SAP and electronic quality systems (e.g., Amplelogic) is preferred.
• Ability to manage complex operational challenges in a fast-paced, regulated setting.