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Executive/Assistant Manager - Production

Gsk Plc
GSK plc
7-10 years
Not Disclosed
Nashik, India
10 Feb. 16, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Executive / Assistant Manager – Production (Ointment Manufacturing & Packaging)
Location: Nashik, Maharashtra, India
Department: Manufacturing Operations
Employment Type: Full-Time

About the Company

GSK is a global biopharmaceutical organization committed to uniting science, technology, and talent to get ahead of disease together. With an extensive global manufacturing network of 37 medicines and vaccines sites, GSK delivered over 1.7 billion packs of medicines and 409 million vaccine doses in 2024.

The Nashik manufacturing site plays a critical role in supplying high-quality pharmaceutical products through advanced manufacturing technologies, digital solutions, and robust compliance systems.

Position Summary

The Executive / Assistant Manager – Production will function as a First Line Leader (FLL) responsible for leading shop-floor manufacturing operations in ointment manufacturing and packaging. The role focuses on ensuring safety, quality, compliance, and reliable product supply while driving operational excellence aligned with the Global Manufacturing & Supply (GMS) strategy.

The incumbent will spend at least 70% of working time on the shop floor, ensuring real-time supervision, issue resolution, and adherence to cGMP and regulatory standards.

Key Responsibilities

Production & Process Management

  • Lead daily manufacturing and packaging operations for ointment products

  • Ensure adherence to cGMP, QMS, EHS, and regulatory compliance standards

  • Drive process confirmations aligned with 4M principles (Material, Manpower, Method, Measurement)

  • Manage shift readiness to ensure smooth batch execution and output performance

  • Provide line clearance and ensure process compliance during changeovers

  • Conduct management monitoring audits as per schedule

Operational Excellence & Performance Management

  • Deploy performance management systems and ensure accurate production data tracking

  • Identify real-time issues and implement structured problem-solving methodologies

  • Manage deviations and ensure timely root cause analysis and CAPA implementation

  • Ensure safe and controlled restoration to standard conditions following incidents

  • Support tiered accountability meetings and governance reviews

  • Manage cost awareness within the assigned production area

Systems & Documentation

  • Ensure data entry and compliance within systems such as SAP, VQMS, VQD, and Workday

  • Maintain accurate production documentation and batch records

  • Ensure audit readiness and inspection compliance

People Leadership & Team Development

  • Lead, coach, and develop production operators to achieve safety, quality, and output targets

  • Implement development plans using the 70:20:10 learning methodology

  • Conduct performance reviews, disciplinary procedures, and absence management as required

  • Promote a culture of accountability, teamwork, and continuous improvement

Educational Qualifications

  • B.Pharm or M.Pharm (Mandatory)

  • Specialization in Ointment Manufacturing or Packaging Operations preferred

Experience Required

  • 7–10 years of experience in pharmaceutical manufacturing operations

  • Hands-on experience in ointment production and/or packaging operations

  • Proven experience in shop-floor leadership within a cGMP-regulated environment

  • Exposure to regulatory audits (FDA or equivalent)

  • Certification from FDA as Competent Technical Staff (Mandatory)

Required Skills & Competencies

  • Strong knowledge of cGMP, QMS, and pharmaceutical compliance standards

  • Expertise in deviation management, CAPA, and audit preparedness

  • Practical experience in performance management and production KPI monitoring

  • Advanced proficiency in MS Word, Excel, and PowerPoint

  • Strong leadership, communication, and cross-functional collaboration skills

  • Sound understanding of safety and quality audit requirements

Experience Level

Mid-to-Senior Level (7–10 Years Pharmaceutical Manufacturing Experience)

Why Join GSK?

GSK is committed to delivering innovative medicines and vaccines across key therapeutic areas including respiratory, immunology, oncology, HIV, and infectious diseases. The organization fosters a culture built on accountability, ambition for patients, and ethical leadership, enabling professionals to contribute meaningfully to global healthcare.

Equal Opportunity & Compliance Notice

GSK is an equal opportunity employer committed to inclusion and diversity. The company does not charge any recruitment fees and does not authorize third-party agencies without prior written approval. Applicants are advised to verify communications through official channels ending in “gsk.com”.