Executive / Assistant Manager – Production
Location: Nashik, Maharashtra, India
Industry: Pharmaceutical Manufacturing
Employment Type: Full-Time
Experience Required: 7–10 Years
Education: B.Pharm / M.Pharm
About the Company
GSK is a global biopharmaceutical organization focused on uniting science, technology, and talent to get ahead of disease together. With 37 global manufacturing sites, GSK delivered 1.7 billion packs of medicines and over 409 million vaccine doses in 2024.
The Nashik manufacturing site plays a strategic role in producing high-quality medicines using advanced pharmaceutical manufacturing technologies, robotics, digital systems, and AI-enabled smart operations.
Position Overview
The Executive / Assistant Manager – Production will act as a First Line Leader (FLL) responsible for leading shop-floor production teams to ensure safe, compliant, and reliable pharmaceutical manufacturing operations.
This role requires a minimum of 70% shop-floor presence, ensuring real-time process control, cGMP compliance, and consistent achievement of safety, quality, service, and cost targets.
Key Responsibilities
Production & Process Management
Lead ointment manufacturing and packaging operations within a regulated pharmaceutical facility
Ensure compliance with cGMP, QMS, EHS, and regulatory standards
Perform process confirmations based on 4M methodology (Material, Manpower, Method, Measurement)
Provide line clearance and area readiness during batch manufacturing and changeovers
Ensure adherence to Standard Operating Procedures (SOPs) and Leader Standard Work
Conduct management monitoring audits as per schedule
Maintain audit readiness for internal and external inspections
Performance Management & Operational Excellence
Deploy structured performance management processes using accurate production data
Identify real-time operational issues and lead structured problem-solving initiatives
Manage deviations, conduct root cause analysis, and implement CAPA
Restore operations to standard following safety, quality, or output deviations
Participate in governance, safety, and performance review meetings
Ensure accurate data entry in SAP, VQMS, VQD, Workday, and related systems
Monitor cost budgets and drive efficiency improvements within the production area
People Leadership & Team Development
Lead, coach, and develop production teams to consistently meet safety, quality, and output targets
Implement development plans using structured learning methodologies (70:20:10 framework)
Ensure training compliance and skill development tracking
Conduct performance reviews and capability enhancement initiatives
Manage disciplinary procedures, absence management, and grievance handling as per site policy
Demonstrate leadership behaviors aligned with organizational values
Educational Qualifications
Mandatory: B.Pharm or M.Pharm
Preferred Specialization: Ointment Manufacturing / Pharmaceutical Packaging Operations
Experience Required
Minimum 7–10 years of experience in pharmaceutical manufacturing
Proven experience in ointment production and/or packaging operations
Leadership experience in a cGMP-regulated environment
Exposure to regulatory audits and inspections
FDA certification as Competent Technical Staff (Mandatory)
Technical Skills & Competencies
Strong knowledge of cGMP, regulatory compliance, QMS, and EHS standards
Expertise in deviation management, CAPA, and audit readiness
Advanced proficiency in MS Word, Excel, and PowerPoint
Strong communication and cross-functional coordination skills
Data-driven decision-making and operational problem-solving capability
Why Apply for This Role
This opportunity offers hands-on leadership responsibility in pharmaceutical manufacturing operations, with clear growth pathways in production management, regulatory compliance, and operational excellence within a globally recognized biopharmaceutical organization.
Important Notice
GSK does not charge any fees during the recruitment process. Applicants should ensure that all official communications originate from verified “gsk.com” email domains. Unauthorized agencies are not permitted to submit candidate referrals without prior written authorization.
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