Documentation Job Vacancies in Baddi

Key Responsibilities:1. Supervise packing operations: Monitor and oversee the packing process to ensure products are packed efficiently and according to company standards.2. Train and mentor packing staff: Provide guidance and support to packing team members, ensuring they understand their tasks and perform them effectively.3. Ensure compliance with safety regulations: Implement safety protocols and procedures to prevent accidents or injuries during the packing process.4. Maintain inventory accuracy: Keep track of inventory levels and update records to ensure accurate stock counts at all times.5. Coordinate with other departments: Collaborate with other teams such as production, quality control, and logistics to ensure smooth operations and timely delivery of products.6. Resolve packing issues: Address any packing-related problems or discrepancies and find solutions to prevent them from recurring.Required Skills and Expectations:- Minimum 1 year of experience in a packing supervisory role.- High school diploma or 12th pass qualification.- Strong leadership and communication skills.- Attention to detail and ability to multitask.- Knowledge of safety regulations and procedures.- Ability to work well under pressure and meet deadlines.- Proficiency in basic computer skills for maintaining inventory records.

Job Opening: Quality Assurance (QA) Officer with IPQA ResponsibilitiesLocation: On-site Nalagarh, Himachal PradeshExperience: 3+ years mandatory experienceQualification: B. Pharm / M. PharmLanguage & Software Skills: Proficiency in English and Microsoft Office (Word, Excel, PowerPoint) MandatoryAbout the Role:We are hiring a knowledgeable and proactive Quality Assurance (QA) Officer to join our pharmaceutical manufacturing unit in Nalagarh. This role combines core QA responsibilities with In-Process Quality Assurance (IPQA) oversight on the production floor. The ideal candidate will ensure regulatory compliance, documentation accuracy, and continuous quality improvement throughout the production lifecycle.Key Responsibilities: Core QA Functions:Review and approve Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).Manage deviations, validations (mandatory), change controls, CAPAs, and maintain documentation as per regulatory norms.Conduct internal quality audits and assist in external audits by clients or regulatory agencies.Maintain and update SOPs, manuals, and master documents in accordance with current regulations.Oversee document control systems and archival processes.Train employees on cGMP practices and quality systems.In-Process QA (IPQA) Responsibilities:Monitor critical stages of manufacturing and packing operations to ensure GMP compliance.Line clearance before batch start-up and between changeovers.Sampling of in-process materials and verification of critical process parameters.Real-time review and recording of BMR/BPR entries during production.Ensure proper gowning, hygiene, and sanitation compliance on the shop floor.Immediate reporting and documentation of any deviation or non-conformance observed.Desired Profile:B. Pharm / M. Pharm with a strong academic and technical background.Minimum 3 years of QA experience in a regulated pharmaceutical manufacturing unit.Hands-on experience with IPQA activities and on-floor quality monitoring.Excellent written and spoken English communication skills MandatoryProficiency in Microsoft Office (Word, Excel, PowerPoint) MandatoryGood understanding of WHO-GMP, Schedule M, and other applicable quality regulations.Strong coordination skills, attention to detail, and documentation accuracy.Join a team committed to delivering excellence through quality-first manufacturing.If you're passionate about compliance, process integrity, and hands-on QA work we invite you to apply!#QualityAssurance #IPQA #PharmaJobs #QAOfficer #BPharmJobs #MPharmJobs #PharmaCareers #GMPCompliance #NalagarhJobs #QualityFirst #IndianPharma #HimachalPharmaJobs #AuditReady

Documentation and accounting job