50 Job openings found

Position:        R&D Officer Location:       Silvassa Experience:   2 - 5 Years Industries:    Pharma  Responsibilities: Preparation, review, and control of R&D documents such as SOPs, specifications, logbooks, and formats. Maintain document control systems as per cGMP and regulatory requirements. Ensure timely issuance and retrieval of controlled documents. Coordinate with various departments for document approval and ...

Position:       QA Officer. Location:       Daman Experience:    1 - 3 Years Industries:     Pharma Responsibilities: Ensure compliance with cGMP, GLP, and regulatory requirements. Review and approve Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and analytical reports. Handle deviations, change controls, CAPA, OOS, OOT, and risk assessments. Conduct line clearance, in-process checks, and shop ...

Position:      Asst. Manager/Manager - QA Location:      Kadi - Ahmedabad  Experience:   5 - 7 Years Industries:    Pharma Responsibilities: Quality Assurance & Compliance Ensure compliance with cGMP, GLP, and regulatory requirements (WHO, USFDA, MHRA, etc.) Handle audits (internal, external, regulatory) and ensure audit readiness at all times Review and approve SOPs, BMRs, BPRs, protocols, and reports Documentation Management Oversee ...

📋 Documentation & Compliance Preparation, review, and control of SOPs, BMRs, BPRs, and other GMP documents Ensure proper documentation practices (GDP compliance) Handling change control, deviation, and CAPA 🏭 Shop Floor QA Activities Line clearance before batch initiation In-process checks and verification Monitoring of manufacturing and packing activities 🧪 Validation & Qualification Support in process validation, cleaning validation Equipment qualification ...

Role Overview We are seeking a skilled and detail-oriented VMC Programmer with strong expertise in NX-CAM programming and hands-on experience on Cosmos VMC machines with Mitsubishi controllers. The ideal candidate should also have exposure to Fanuc and Sinumerikcontrollers, bringing versatility and adaptability to complex mold-making operations.Key Responsibilities• Programming & Process Development• Develop, ...

We are looking for a meticulous and detail-oriented Billing Executive to manage the entire billing process, including preparing verifying purchase orders, ensuring GST compliance, and maintaining accurate records. The candidate will work closely with the sales, dispatch, and accounts teams to ensure smooth and timely billing operations. Qualification: Bcom, Graduate in ...

Key Responsibilities New Product Development (NPD) Handle complete product development lifecycle including RFQ study, design, development, validation, industrialization, and production launch Develop and review process documents such as PFD, Control Plan, PFMEA, Quality Plan, and work instructions Prepare technical feasibility studies for manufacturing and outsourcing opportunities Ensure products meet customer requirements related to quality, performance, ...

Job Description Summary Responsible for programming a component, feature and or feature set.Works independently and contributes to the immediate team and to other teams across business. Will also contribute to design discussions.Responsible for software lifecycle including activities such as requirement analysis, documentation/procedures and implementation. Job Description Roles & Responsibility In this role, you ...

Position:       Microbiologist Location:      Silvassa Experience:   2 - 3 Years Industries:    Cosmetic Responsibilities:  Swab testing & environmental monitoring  Media preparation & sterilization  GMP & GDP documentation practices  ATP testing for hygiene verification  Sample collection of microbiologically sensitive RM / tankers  Maintain lab records, SOP compliance, and timely reporting  Required Skill Logical thinking. Organizing. Excellent verbal and written communication skills. Required Qualification: - ...

Position:       QA Officer  Location:       Acchad nearby Bhilad Experience:   1 - 2 Years Industries:   Medical Devices Responsibilities: Review QC raw data, BMRs, STPs, and specifications. Monitor compliance with cGMP, GLP, and documentation practices. Conduct GMP training sessions and maintain related records. Handle deviations, change control, CAPA, and non-conformance. Perform self-inspections, audits, and ensure ISO compliance. Familiarity with ...