Executive - QA (IPQA)

USV (Pharma) is Hiring Senior Manager - QA (Sterile) for USFDA Formulation Manufacturing Plant based at Daman near Vapi. We are looking for dynamic professionals having more than 15 years of experience in hard core injectables (Liquid Vials, Ophthalmic and Pre-filled syringes).The incumbent must be having the thorough knowledge of IPQA, Qualification and...

Position : Manager - Inprocess Quality Assurance (OSD)1) In-process Quality Assurance (Oral Solids)Partake in controlling, implementing, executing the activities of Quality Assurance.To carry out sample management.Verification of online rejection and destruction if any.Co-ordination and execution of validation and qualification activities.To check the...

Hands-on experience in monitoring manufacturing and packaging processes, line clearance, and in-process checks.Proficiency in DOC-MS systems, SOP preparation, deviation handling, and change control.Involvement in TT activities including protocol review, execution, and coordination between RCD and manufacturing.Familiarity with validated software systems that...

Assist in operation and monitoring of tablet compression machines (e.g., Cadmach, Korsch, Fette). Support batch execution as per defined BMR parameters — weight, thickness, hardness, and appearance. Help in machine setup, cleaning, and changeover activities as per SOPs. Perform and record in-process checks ensuring compliance with BMR and GMP. Maintain...

Supervise and monitor vial, ampoule, and PFS packing lines as per BPR and SOPs. Ensure proper functioning of labeling, sealing, inspection, and serialization machines. Review and maintain Batch Packing Records (BPRs), logbooks, and line clearance documentation. Coordinate with QA, Engineering, and Warehouse teams for smooth batch execution. Ensure...

Operate coating machines (e.g., Auto Coater, Pan Coater) as per SOPs.Assist in setup, loading, and unloading of tablets in the coating machine.Monitor process parameters (spray rate, temperature, pan RPM, etc.) during coating.Follow Batch Manufacturing Record (BMR) instructions during batch execution.Maintain real-time documentation of operations and...

Job Description: - Arrange and follow up on special lab testing request (aging test, compression set etc) - Arrange and involve in routine testing of rubber masterbatch and compound - Maintain good 5S housekeeping for physical testing lab, raw material storage area, lab mixing and curing area - Certify the Delivery Order (OQC) and ensure compliance to...

**Key Responsibilities**: - **Incoming Material QC**:Manage and ensure compliance in incoming raw material testing. Develop and implement QC inspection plans for incoming raw materials within defined timeframes. - **Revalidation Process**:Track the revalidation process of raw materials, intermediates, and finished goods. - **Instrument...

We are hiring for QC- QA Executive. Location - Daman Working hrs - 12 hrs shift Diploma in plastic processing technology / science graduate with CIPET diploma - Thorough knowledge of QC, Lab testing procedures - Knowledge of ISO 9000 documentation - Familiar with injection moulding and extrusion Minimizing customer complaints. Technical Co-ordination...

To ensure the quality and consistency of Tin and Can Products throughout the manufacturing process. 1. Conduct regular inspection of raw materials (tin plate and cans) 2. Monitor the Production process to identify and rectify any quality defects. 3. Inspect Finished Products to ensure they meet specific dimensions and weight. 4. Document detailed record...

**Daman** Should have knowledge of analytical analysis, Quality Control - Experience- 4 - 8 Years- Salary- 1 Lac 75 Thousand To 4 Lac P.A.- Industry- Manufacturing / Production / Quality- Qualification- B.Pharma, M.Pharma- Key SkillsQuality Control Quality Audit Quality Asurance Qa Analyst **About Company** - Company Name**Our Client - Limited Pharma...

Job Title: Lead QA Engineer (Manual + Automation) Location: Remote (India)Client Domain: Product-based company HRMS (Human Resource Management System) applications focused on SaaS-based HRMS solutions for public sector organizationsAbout the Role:We are seeking an experienced and detail-oriented Lead QA Engineer with strong expertise in both manual and...

Job Description Job Purpose To oversee and manage day-to-day production activities in the Oral Solid Dosage (OSD) manufacturing area, ensuring compliance with cGMP, USFDA, and other regulatory requirements while meeting production targets. Key Responsibilities - Supervise and execute production operations for granulation, compression, coating, and capsule...

Title: Sr Executive - Production QMSDate: Dec 18, 2025Location: Dadra - PlantCompany: Sun Pharmaceutical Industries LtdJob Purpose:To ensure compliance with cGMP, USFDA, and other regulatory requirements by implementing and maintaining Quality Management System (QMS) practices within the Production department. Responsible for documentation, deviation...

Job Description Job Purpose To ensure compliance with cGMP, USFDA, and other regulatory requirements by implementing and maintaining Quality Management System (QMS) practices within the Production department. Responsible for documentation, deviation handling, and continuous improvement initiatives to maintain product quality and regulatory compliance. Key...

Job Description Job Accountabilities -: Support shift in charge for shift co-ordination work. Priorities the samples for testing. Provide right containers to collect samples, identifies right carriers to distribute samples and designate right location for pre-testing storage. Ensure the usability of the chemicals / standards to use in the test and performs...