Average salary: Rs626,730 /yearly
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- ...Key Responsibilities: 1. Develop the global regulatory strategies for biologic products across all development phases (preclinical to post... ...submissions including INDs/IMPDs, BLA/MAA, CTA, DSUR, Annual Reports, as applicable. 4. Post-approval changes (variations,...Regulatory
- ...We are seeking an experienced Regulatory Affairs professional to lead and execute global regulatory strategies for biologic products across... ..., including INDs, IMPDs, BLAs, MAAs, CTAs, DSURs, and Annual Reports , as applicable. Manage post-approval activities ,...Regulatory
- ...vault register and overdue management Review branch operations reports and track exceptional transactions. Handle internal and... ...Knowledge of banking products and services Knowledge of regulatory guidelines and norms Good communication (both verbal and written...RegulatoryWork at officeLocal areaImmediate start
- ...Vapi, Gujarat / Pune, Maharashtra (as per business requirement) Reports To: Manager – Verification & Validation / Head – Quality & R&... ...design requirements, user needs, and applicable medical device regulatory standards. The role plays a critical part in regulatory...Regulatory
- ...trials, ensuring compliance with Good Clinical Practice (GCP), regulatory requirements, and study protocols. Key Responsibilities:... ...maintenance of study documents, including informed consent forms, case report forms, and study logs. 2. Coordinate with study sites to...RegulatoryFull time
- ...utilization of borrowings and compute cost of borrowings 6. MIS Reporting: Preparation of daily MIS of Fund Flow and Cash Flow Statement... ...limits, and handling Forex transactions in compliance with regulatory and internal guidelines. The role requires strong coordination...Regulatory
- ...prepare monthly and annual financial statements along with related reports, perform ledger scrutiny, demonstrate strong analytical skills,... ...management reporting requirements. • Ensure all statutory and regulatory compliances are met on time. MAJOR RESULTS/ACCOUNTABILITY:...Regulatory
- ...Perform and document Analytical Method Validation in accordance with regulatory guidelines. Support Process and Product Quality Assurance (... ...and data reliability. Prepare and review technical reports batch records and regulatory documentation. Collaborate with...RegulatoryFull time
- ...critical for managing multiple warehouse sites and storage containers , ensuring accurate inventory, smooth material movement, and regulatory compliance. With the MCPL GMP facility and controlled lab stores coming up, dedicated personnel are essential for seamless...RegulatoryImmediate start
- ...manpower efficiently. Maintain accurate production records, including batch reports, consumption, output, and wastage. Ensure strict compliance with SOPs, quality parameters, and regulatory requirements. Coordinate with QC, R&D, Packaging, and Inventory teams for timely...RegulatoryShift work
- ...inspections to ensure conformance to product specifications and regulatory standards. ● Track defect rates, analyze performance data, and... ...preventive action implementation. ● Prepare and present management reports linking quality metrics to business outcomes and recommending...Regulatory
- ...incumbent will assure individual compliance with all concerned regulatory requirements, GxP's and applicable department programs, including... ...qualification, analytical method transfer, validation protocol and reports for accuracy, completeness and traceability as well as adherence...RegulatoryContract work
- ...Location: Vapi, Gujarat / Field-based (as per requirement) Reports To: Senior R&D Engineer / R&D Manager – Surgical Robotics... ...Cross-Functional Collaboration • Work closely with R&D, Clinical, Regulatory, Quality, and Manufacturing teams to support cross-functional projects...RegulatoryInternship
- .../ On-site (with frequent travel to hospitals & demo sites) Reporting To: Head – Autonomous & Surgical Robotics Position Overview... ...training, service logs, usage patterns, and case reports. Support regulatory, clinical evaluation, and quality teams with data inputs as...Regulatory
- ...that all production activities are carried out in compliance with regulatory standards and company protocols, aiming to enhance product... ...and receive the materials from stores. Preparation of Daily report, formats and BMRs as and when required. Online BMR entries to...RegulatoryLocal areaShift work
- ...Senior Officer / Executive – MSTG Orals Business Unit R&D1 Regulatory Affairs Job Grade G12A/G12B Location Dadra At Sun... ...sheet, master formula card, bill of material, risk assessment reports, scale up protocol and reports, exhibit/ trial batch manufacturing...Regulatory
- ...– Software & Embedded Systems Location: Vapi, Gujarat. Reports To: Manager / Senior Manager – R&D (Software & Embedded Systems... ...compliance with internal engineering standards and external regulatory norms relevant to medical diagnostic devices. Maintain version...RegulatoryFull time
- ...role involves servicing walk-in customers, generating leads, cross-selling financial products, and ensuring strict compliance with regulatory and audit requirements. The Authoriser will also act as a key custodian and play a pivotal role in maintaining service quality and team...Regulatory
- ...manufacturing operations including compression pellet coating capsule filling and packaging. Ensure compliance with GMP SOPs and regulatory requirements throughout all production activities. Maintain accurate and timely documentation using e-BPR and e-log systems. Collaborate...RegulatoryFull time
- ...production. Ensure compliance with SOPs, batch records, and regulatory requirements. Monitor in-process checks (weight, hardness, thickness... ...standards in compression area. Prepare daily production reports and escalate issues to management. Qualifications ~...RegulatoryShift work
- ...Job title Regulatory & Compliance Manager Ensuring that our master batch and additive solutions meet or exceed the compliance expectations of customers, certifying bodies, and regulatory agencies in both domestic and international markets Roles and Responsibility:...RegulatoryLocal area
- ...validation activities across manufacturing and testing processes. Conduct internal and external audits to ensure compliance with GMP and regulatory requirements. Investigate and resolve quality deviations, CAPAs, and out-of-specification results. Collaborate with cross-...RegulatoryFull time
- ...Job Purpose To ensure compliance with cGMP, USFDA, and other regulatory requirements by implementing and maintaining Quality Management... ...investigate production-related deviations. Prepare investigation reports and implement corrective and preventive actions. Training &...Regulatory
- ...RESPONSIBILITIES: • Responsible for stable product specifications from local production • Resolves quality issues, supply bottlenecks, regulatory changes (reasons for LTO projects) • Maintain market conformity of products (e.g. regulatory changes, systematic complaints) • (...RegulatoryLocal area
- ...Purified Water, and related utilities, through systematic monitoring, preventive maintenance, and strict adherence to GMP, quality, and regulatory requirements. Responsibilities: Ensure smooth operation & preventive maintenance of WFI, purified water, PSG, HSRO & CSRO...Regulatory
- ...customer clients through the loan application process addressing any questions or concernsStay updated on market trends loan products and regulatory changes to provide informed advice to clientsConduct follow-ups with clients pre-closure and post-closure to ensure satisfaction and...RegulatoryFull time
- ...machine utilization productivity and output efficiency. 2. Regulatory & Quality Compliance Ensure full compliance with ISO 13485... ...rejections and optimize cost control. 8. MIS & Management Reporting Prepare and present daily weekly and monthly plant performance...RegulatoryFull timeShift work
- ...procurement supply chain and sales teams. Provide regular MIS reports on production status material consumption and dispatch schedules... ...& Documentation Ensure PPIC processes comply with GMP regulatory and EHS standards. Maintain accurate documentation for audits...RegulatoryFull time
- ...preventive measures, while also maintaining root cause analysis reports to prevent recurrence. # Providing guidance to the QMS team for... ...block . # Desired candidate should possess exposure to regulatory audits, specifically with experience in USFDA audits. This...RegulatoryFull time
- ...manufacturers' products by allowing them to create differentiated packaging, protect against counterfeiting, and ensure governmental and regulatory compliance. From best before dates on eggs, to serialized identifying codes on medicines, to batch codes on electronic components,...Regulatory
