This role involves working within the Ampoules and Eye Drops department, focusing on manufacturing, dispensing, filling, and sterilization operations. The primary objective is to ensure that production targets are met efficiently while strictly adhering to Good Manufacturing Practices (GMP), Environmental Health and Safety (EHS) guidelines, and all relevant regulatory standards. The position requires close attention to detail, maintaining compliance, and supporting continuous improvement initiatives within the production environment.
Key Responsibilities
- Complete all manufacturing, dispensing, filling, and sterilization tasks for Ampoules and Eye Drops in a timely manner, following local Standard Operating Procedures (SOPs).
- Promote safety within the work area by encouraging Zero Waste initiatives and actively participating in ZAP (Zero Accident Program) and ZIP (Zero Incident Program) reporting.
- Maintain accurate daily records related to production output, downtime, preventive maintenance, and other operational data specific to Ampoules and Eye Drops.
- Ensure full compliance with GMP requirements such as proper labeling and line clearance, as well as EHS standards including zero unauthorized access and Lockout-Tagout (LOTO) procedures.
- Complete Batch Manufacturing Records (BMR) and logbooks accurately, adhering to Good Documentation Practices (GDP).
- Identify, document, and report any deviations from approved SOPs during manufacturing, dispensing, filling, and sterilization processes.
- Uphold data integrity standards and continuously enhance data integrity controls aligned with ALCOA+ principles within all manufacturing operations.
Required Qualifications
- Minimum education of Matriculation, High School Diploma, or equivalent.
- 1 to 3 years of experience in manufacturing or packaging operations.
- Ability to read, understand, and follow written procedures and technical instructions accurately.
- Familiarity with GMP and workplace health and safety regulations.
- Comfortable handling hand tools and basic production equipment.
- Reliable attendance and willingness to work on-site shifts as required.
- Basic proficiency in spoken and written Urdu or English to ensure clear communication and reporting.
Skills
- Strong attention to detail and commitment to data integrity.
- Digital fluency and familiarity with GxP regulations.
- Knowledge of lean management principles and packaging operations.
- Problem-solving capabilities and production management experience.
- Awareness of quality and regulatory compliance requirements and risk management.
About the Company
GSK is a global biopharmaceutical company dedicated to uniting science, technology, and talent to advance the prevention and treatment of diseases. The company aims to positively impact the health of 2.5 billion people by the end of the decade through innovation in specialty medicines and vaccines. GSK focuses on key therapeutic areas including respiratory, immunology and inflammation, oncology, HIV, and infectious diseases. The company fosters a culture of ambition for patients, accountability for impact, and integrity, providing an environment where employees can thrive and contribute meaningfully to global health outcomes.
Important Notice to Employment Agencies
GSK does not accept unsolicited referrals from employment businesses or agencies for vacancies posted. Agencies must obtain prior written authorization from GSK’s commercial and human resources departments before submitting candidates. Any referrals made without such authorization will be considered unauthorized, and GSK will not be liable for any fees related to those referrals.
Applicants interested in this position are encouraged to apply online through the official application process.