Production Incharge

8 years

12 - 15 Lacs

Posted:21 hours ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

This role is for one of the Weekday's clients

Salary range: Rs 1200000 - Rs 1500000 (ie INR 12-15 LPA)

Min Experience: 8 yearsLocation: Baddi, Himachal PradeshJobType: full-timeWe are seeking an experienced

Production In-charge

to supervise the complete manufacturing lifecycle of soft gelatin capsules while ensuring compliance with

GMP, revised Schedule M, and industry quality standards

. This role requires strong leadership, process ownership, and the ability to drive operational efficiency while maintaining strict documentation and regulatory compliance.

Requirements

Key Responsibilities

  • Plan, organize, and execute production schedules to achieve output goals and optimal resource utilization.
  • Oversee all stages of softgel manufacturing including gelatin and fill preparation, encapsulation, drying, polishing, sorting, and packing.
  • Ensure continuous compliance with quality standards and manage in-process controls in collaboration with Quality Control teams.
  • Supervise equipment operation, cleaning, and maintenance; coordinate with engineering for servicing, repairs, and calibration.
  • Monitor availability of raw materials and packaging components in partnership with warehouse and supply chain teams.
  • Lead, train, and oversee production staff; reinforce safety, hygiene, and performance standards on the shop floor.
  • Ensure accurate and timely completion of production documentation (BMR/BPR) aligned with ALCOA+ and cGMP requirements.
  • Develop, review, and implement SOPs; support equipment and process validation activities.
  • Investigate deviations, drive CAPA implementation, and maintain compliance records for audits and regulatory inspections.
  • Collaborate with QA, QC, Engineering, and Warehouse teams to support internal and external audits.

Required Skills & Experience

  • Bachelor's degree in Pharmacy (B.Pharm) or related scientific qualification.
  • 8-10 years of supervisory or managerial experience in pharmaceutical manufacturing, preferably in soft gelatin capsule production.
  • Strong knowledge of cGMP, revised Schedule M guidelines, and regulatory compliance.
  • Experience in production planning, process optimization, and equipment oversight.
  • Proven leadership, team management, and problem-solving skills.
  • Excellent documentation, communication, and decision-making ability.
  • Hands-on understanding of validation, SOP development, deviation handling, and CAPA execution.

Nice-to-Have

  • Experience supporting regulatory audits including WHO, USFDA, etc.
  • Exposure to Lean Manufacturing and continuous improvement practices.
  • Familiarity with advanced or automated softgel encapsulation technologies.

Skills

Production Planning
  • Manufacturing Operations
  • Soft Gelatin Capsule Production
  • SOP
  • GMP
  • Team Leadership
  • CAPA
  • Process Compliance
  • Pharmaceutical Production

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