Production Incharge

24 hours ago


Baddi Himachal Pradesh, India Weekday AI Full time

This role is for one of the Weekday s clients Salary range Rs 1200000 - Rs 1500000 ie INR 12-15 LPA Min Experience 8 years Location Baddi Himachal Pradesh JobType full-time We 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 o Manufacturing Operations o Soft Gelatin Capsule Production o SOP o GMP o Team Leadership o CAPA o Process Compliance o Pharmaceutical Production



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