4 Batch Documentation Jobs

As a Capsule Filling Machine Operator SA9 at Lavanya Healthcare Limited in Dera Bassi, Punjab, your main responsibility is to efficiently operate and maintain the SA9 Capsule Filling Machine. You will be tasked with ensuring the accurate filling of hard gelatin capsules in accordance with cGMP, safety, and quality standards. Your key responsibilities will include setting up and running the SA9 Capsule Filling Machine according to the daily production plan, loading empty capsules and powder/blend into appropriate hoppers and magazines, monitoring capsule weight, alignment, and sealing during production runs, conducting in-process checks, ensuring cleanliness and line clearance of machine parts, performing routine lubrication and minor troubleshooting, recording production data, maintaining hygiene and safety at the workstation, and assisting in preventive maintenance activities and equipment calibration. To qualify for this role, you should have a 12th-grade education and at least 13 years of hands-on experience operating SA9 or similar capsule filling machines in a pharmaceutical or nutraceutical setting. Strong knowledge of capsule filling processes, GMP, documentation practices, and regulatory compliance is essential. Basic mechanical skills for minor adjustments and troubleshooting, ability to work in shifts, attention to detail, and quality focus are also required. Preferred qualifications include experience with various capsule sizes and formulations, as well as familiarity with validation and audit procedures. This is a full-time position that requires the use of personal protective equipment. The job involves day shifts and weekend work only. As a part of the benefits package, Provident Fund is offered. If you encounter any deviations, machine malfunctions, or product non-conformities, it is crucial to report them promptly to the production supervisor or quality team. Your dedication to following SOPs, maintaining cleanliness, and upholding quality standards will contribute to the success of the production process.,

To carry out filling and packing activities as per BFR, BPR & SOPs while maintaining current GMP standards in the production area/activities. Follow the day-to-day production schedule diligently and ensure completion of production activities (filling & packing) as per the schedule. Adhere to operating instructions for shift activities received from superiors/Manager. In case of any abnormality in the production area/activities, have the authority to immediately halt the activity and notify the production Manager. Maintain manufacturing records online and ensure compliance with data integrity practices. Responsible for indenting, issuing, and submitting BFR/BPR. Verify Raw material & Packing material during receipt and perform SAP posting as per BFR & BPR. Facilitate sample request/submission to QC after filling activity and transfer finished goods through Finished Goods Transfer Note. Conduct cleaning of filters & storage tanks as per schedule, maintaining cleanliness in the production area as per SOP. Ensure cleaning of AHU filters as per schedule and monitor stock levels of consumables, Log books & status labels. Perform preventive maintenance of equipment as per schedule and maintain temperature & RH within SOP limits in the production area. Coordinate with service departments (QA, QC, stores, E & M and SCM) for various production-related activities. Adhere to safety instructions/procedures and ensure the use of safety outfits while working. Responsible for taking on the work of a senior in their absence or upon authorization from the senior. Qualifications - Bachelor's Degree in Pharmacy or equivalent Required Skills - Manpower handling - Good communication skills - Shift in-charge - Batch documentation Piramal Group, over the three decades of its existence, has pursued both organic and inorganic growth strategies. Driven by core values, Piramal Group is committed to inclusive growth while upholding ethical and values-driven practices. Equal employment opportunity is a fundamental principle guiding employment decisions based on merit, qualifications, skills, performance, and achievements. Ensuring equal opportunity for all applicants and employees in personnel matters is a key focus, including recruitment, selection, training, placement, promotion, compensation, and working conditions, with provisions for reasonable accommodation for qualified individuals with disabilities and religious observance or practice-related needs. About The Team Piramal Critical Care (PCC), a subsidiary of Piramal Pharma Limited (PPL) under Piramal Enterprises Limited, is a global player in hospital generics and the third-largest producer of Inhaled Anaesthetics. PCC's vision is to provide critical care solutions globally and facilitate sustainable and profitable growth for stakeholders. With a wide presence across the USA, Europe, and over 100 countries, PCC's product portfolio includes Inhalation Anaesthetics like Sevoflurane, Isoflurane, Halothane, and Intrathecal Baclofen therapy. PCC operates state-of-the-art manufacturing facilities in the US and India, compliant with inspections by US FDA, UK MHRA, and other regulators. The dedicated global workforce of more than 400 employees across 16 countries drives PCC's expansion in the critical care space. Committed to corporate social responsibility, PCC collaborates with partner organizations to provide hope, resources, and environmental care, aligning with Piramal Group's ethos. Job Info - Job Identification: 8852 - Job Category: Production - Posting Date: 06/11/2025, 01:15 PM - Degree Level: Bachelor's Degree - Job Schedule: Full time - Location: Piramal Enterprises Limited. Factory: Digwal, Medak, Telangana, 502321, IN,

Job Overview We are looking for a qualified and experienced Manufacturing Chemist having worked in cosmetics and OTC production background to oversee the manufacturing processes of cosmetics and OTC products in accordance with industry standards, regulatory requirements, and company protocols. The ideal candidate will ensure accurate batch preparation, maintain compliance with GMP standards, and support production efficiency. Key Responsibilities Take batches of cosmetic & OTC Supervise and manage the manufacturing of cosmetic and OTC topical formulations (creams, ointments, gels, etc.). Oversee end-to-end production management, including planning, scheduling, and resource optimization. Ensure accurate execution and documentation of batch manufacturing records (BMRs) in compliance with SOPs and regulatory standards. Maintain full compliance with GMP, Schedule M, and Drugs & Cosmetics Act requirements. Coordinate with QA/QC, R&D, Procurement, and Warehouse teams to ensure smooth production operations and on-time delivery. Conduct and document in-process quality checks and validations. Operate and maintain key manufacturing equipment (mixers, vessels, filling lines). Monitor inventory levels of raw materials and coordinate with the store and procurement departments. Lead shop floor teams to maintain hygiene, safety, and operational efficiency. Support regulatory inspections, client audits, and continuous improvement initiatives. Qualifications & Requirements Bachelors degree in Pharmacy (B.Pharm) or Chemistry; M.Pharm preferred. Minimum 3-5 years of experience as a Manufacturing Chemist in cosmetics, pharma, or FMCG sector. Valid license as a Manufacturing Chemist under the Drugs & Cosmetics Act is preferred. Strong knowledge of formulation, scale-up, and batch documentation. Familiarity with GMP, SOPs, and regulatory compliance. Excellent attention to detail and strong organizational skills. Experience in working in export oriented units is preferable. What We Offer Competitive salary based on experience Opportunities for growth within a GMP-certified facility Professional and supportive work environment Exposure to domestic and international product development

Conduct preliminary review of: Batch Documentation Certificates of Analysis (CoAs) Change controls, deviations, and investigations Support preparation, review, and maintenance of: Specifications Test methods Master Manufacturing and Packaging Records Product artworks and labeling components Coordinate with contract manufacturing organizations (CMOs) for resolution of documentation queries and ensure timely turnaround. Assist in documentation for supplier qualification and product transfers. Maintain and update product master data in SAP, including: Material codes Specifications and test parameters Change control linkages Artwork version control Track and report progress on key quality actions and compliance metrics. Assist in preparing for regulatory and customer audits. Ensure proper documentation archiving, version control, and compliance with document retention policies.