132 Job openings found

Position: QA Asst Manager ( OSD , ORAL LIQUID & OINTMENT FACILITY) Position: QA Asst. Manager Vacancy: 01 Location: VAPI- GUJARAT Experience: 10 to 15 Years Qualification: B. Pharma / M. Pharma Core Technical Expertise:  IPQA (In-Process Quality Assurance): Hands-on experience in monitoring manufacturing and packaging processes, line clearance, ...

Position:          Sr. Officer - IPQA Location:          Bhimpore - Daman Experience:       6 - 8 Years Industries:        Medical Device Responsibilities: IPQA (In-Process Quality Assurance) Monitoring Supervise and monitor all IPQA activities in manufacturing areas. Ensure compliance with cGMP guidelines during production processes. Line clearance verification before batch ...

Qualification & Experience M.Pharm / M.S / B.S in Chemistry, Pharmaceutics or related discipline 3–5 years of experience in R&D (DQA) Strong knowledge of GMP, GCP, GLP and 21 CFR 210/211 Experience with dermatology products or medical devices is an advantage Key Responsibilities Review development documents, analytical methods, R&D trials, lab notes, PDR, MFR, and batch ...

The job description is as below: Purpose of the RoleTo ensure timely, accurate, compliant, and scientifically justified responses to regulatory and customer queries related to pharmaceutical and medical device testing, in alignment with global regulatory and accreditation requirements. Key Responsibilities 1. Regulatory Query ManagementReceive, log, track, and respond to regulatory queries, including US ...

Position:           Executive - Utility & Maintenance Location:          Vapi Experience:       4 - 6 Years Industries:        Pharma API   Responsibilities: Planning and execution of routine maintenance activities. Check utility daily Log sheet. Co- ordination with all departments pertaining to maintenance activity. Carry out all the maintenance activities as ...

Job Description   Preferred experience 10-12 years (L3 Support) The Middleware Administrator supports and documents the installation, configuration, capacity planning, upgrading, problem resolution and debugging of all middleware product environments Coordinates environment configuration activities to ensure integration and alignment with other IT technology, processes, systems, applications, and environments Document middleware platforms and related infrastructure as ...

Position:          QC Executive Location:         Bhimpore - Daman Experience:      5 - 8 Years Industries:       Medical - Device   Responsibilities: Preparation and review of QC documents (SOPs, protocols, reports) Equipment qualification, validation, and method verification Handling QMS activities (OOS/OOT, deviations, CAPA, change control) Review and approval of analytical data, including CTL samples Required Skills: Good documentation ...

Position:         Officer/Executive - Design & Development Location:        Dabhel - Daman Experience:     2 - 3 Years Industries:      Pharma    Responsibilities: Design & Drafting Create and revise 2D and 3D mechanical designs using AutoCAD, Solid Edge, and SolidWorks. Develop detailed engineering drawings for pharmaceutical equipment, piping layouts, utility systems, and plant infrastructure. Design ...

Key Responsibilities: Handle QMS activities including CAPA, Change Control, Deviation, and OOS/OOT. Prepare, review, and maintain QMS documentation as per cGMP and regulatory guidelines. Support internal audits, external audits, and regulatory inspections. Ensure timely closure of quality incidents and continuous improvement initiatives. Coordinate with cross-functional teams for compliance and quality culture. Requirements: B.Pharm / M.Sc (Chemistry) with ...

Responsibilities Perform and supervise In-Process Quality Assurance (IPQA) OR QA checks during API manufacturing operations. Conduct on-line review of Batch Production Records (BPR) and ensure adherence to approved procedures. Ensure sampling, line clearance, and process compliance as per GMP/cGMP norms. Identify, record, and support resolution of deviations, non-conformances, and quality incidents during manufacturing. Support quality investigations and prepare required ...