196 Regulatory Audits Jobs - Page 3

Job Title: Head Regulatory Affairs Location: Daman About the client: PSS has been mandated to hire a Head of Regulatory Affairs for a leading R&D backed, manufacturing women's health organization with operations in over 140 countries worldwide. It is the world's largest manufacturer of Contraceptives devices. Job Purpose The Head of Regulatory Affairs will lead global regulatory strategies for medical devices and contraceptive solutions. The role will ensure compliance with domestic and international regulations (and support product approvals, quality assurance, and market expansion. Key Responsibilities Regulatory Strategy & Compliance: Develop and implement regulatory strategies for medica...

Role Overview: As an experienced Internal Auditor with a strong background in construction and technical audits, you will be responsible for conducting audits of the technical teams to ensure compliance with internal policies, industry standards, and regulatory requirements. Your role will involve evaluating processes, identifying risks, and recommending improvements to enhance operational efficiency and technical accuracy across large-scale construction projects. Key Responsibilities: - Plan and conduct internal audits of technical teams, including engineering, design, procurement, and project management, ensuring compliance with project timelines, budgets, and quality standards. - Assess t...

As a Team Lead of Credit Compliance for WBG and Working Capital Business segment of the Bank, you will be responsible for managing and leading a team of professionals who support Business Groups in maintaining an effective control framework and ensuring compliance with all relevant RBI regulations, internal codes, and policies. Your key responsibilities will include: - Reviewing all credit proposals that go into the Credit Committee (Level E2) and identifying any regulatory inconsistencies. - Reviewing credit-related products, policies, and processes, providing feedback and advice to ensure comprehensive and compliant bank processes. - Advising the business/credit function of the bank on all...

Role Overview: You will be responsible for initiating, reviewing, and approving various quality management systems such as Change Controls, Deviations, Investigations, CAPA, OOS, and Complaints. In addition, you will handle Return Goods and ensure the proper functioning of the quality system by performing risk assessments as needed. Conducting regular internal audits will also be part of your duties. Key Responsibilities: - Review and approve all documents including SOPs, Spec & STPs, Forms, protocols, and reports to ensure compliance. - Review annual product quality review reports and provide training on cGMP topics to employees at the site. - Support customer audits/visits and regulatory a...

You will be joining HP & ASSOCIATES LLP, Chartered Accountants, a professional services firm specializing in Audit, Tax, and Advisory services. As part of the dynamic team, you will have the opportunity to work on various projects aiming to create, preserve, and transform value for clients. The sector-first approach ensures high-value solutions for clients to adapt seamlessly to industry changes. Your main responsibilities will include: - Assisting in audits, tax preparations, financial reporting, and compliance checks - Working on direct and indirect taxes, corporate finance, IT advisory, and risk management services - Participating in regulatory audits and providing advisory services to cl...

As a Manufacturing Engineer at this company, your primary role is to execute Manufacturing Engineering activities focusing on high-quality Process Verification & Validation. Your responsibilities include sustaining and improving processes, tools, and equipment of the Manufacturing systems to ensure predictable, reliable, stable, and efficient production processes. You will also support troubleshooting activities, new product industrialization projects, and manufacturing transfers for the site. Key Responsibilities: - Drive meaningful and innovative Process Validation - Suggest improvements in the process to enhance quality and reduce costs - Support Process Verification, Validation, IQ, OQ, ...

As a Senior AI & Emerging Technologies Leader, you will be responsible for architecting innovative solutions, leading high-performing teams, and driving end-to-end delivery of AI-powered digital transformation initiatives across industries such as BFSI, Telecom, Healthcare, and Public Sector. Your primary responsibilities will include: - Lead the design, development, and deployment of AI/ML and GenAI solutions such as LLMs, RAG architectures, vector databases, and orchestration frameworks. - Drive enterprise-scale AI adoption across business functions including AML compliance, customer experience, predictive analytics, and intelligent automation. - Architect and implement cloud-native AI sol...

Role Overview: As the Head of Risk and Compliance at ISG, you will be a senior level Risk & Compliance thought leader, subject matter expert, and portfolio lead with extensive experience in managing Risk & Compliance system development and product implementation projects. Your role will involve leading a Risk & Compliance industry solutions portfolio, owning thought leadership discussions, presenting product alliances, and providing presales support. Additionally, you will be responsible for leading the delivery effort for multiple accounts, building relationships with clients and service lines, and championing innovation in the risk & compliance portfolio. Key Responsibilities: - Lead a Ris...

Role Overview: As a Manager-II in the MSTG department at Dadra, your primary responsibility will be to provide support in the execution and monitoring of trial, scale up, and exhibit process qualification batches. You will be involved in preparing and reviewing new product documents such as material requirement sheets, master formula cards, bill of materials, risk assessment reports, sampling protocols, reports, exhibit batch manufacturing records, and exhibit protocols. Sharing process knowledge with cross-functional departments through presentations to facilitate smooth technology transfer will also be a key aspect of your role. Key Responsibilities: - Review and evaluate product history a...

Job Description: You will be a member of the ACG Associated Universal Capsules team, with your primary responsibility being to ensure that the Plant complies with the Quality Management System (QMS) guidelines. Your role will involve: - Strengthening the review mechanism of batch records - Conducting effective reviews of batch records - Releasing batches according to the daily plan in a timely manner - Ensuring compliance during internal, external, and regulatory audits To excel in this role, you should hold a degree in B. Pharmacy or B.E. Mechanical with relevant Quality Assurance (QA) experience. Your competencies in these areas will be critical to successfully fulfilling the responsibilit...

Key Roles and Responsibilities: Regulatory Compliance & Licensing: Lead and manage all regulatory approvals, licensing, and registration activities across relevant regulatory authorities to ensure timely approvals (FSSAI, Tea Board of India, MSME, Factory License, Trade License, etc.). Develop and oversee robust systems for regulatory compliance reporting (e.g., Whistleblower avenues). Establish and implement compliance frameworks aligned with food safety and regulatory guidelines. Provide proactive strategic advice on regulatory matters across domains including Health, Safety, Environment, Food Safety, Pollution Control, Customs, and Product Liability. Ensure up-to-date renewals and complia...

Role Overview: As a Senior Manager Supply Chain Management, you will be responsible for leading the end-to-end supply chain function for the Primary Pharma Packaging Plant in Gonde Nashik. Your role will involve ensuring the uninterrupted availability of raw materials, consumables, and services in compliance with stringent pharmaceutical industry standards. You will need to have expertise in Procurement, Stores, Logistics, Inventory Management, Vendor Development, and Materials Planning, with a focus on cost efficiency, timely availability, and compliance with CGMP, FDA, and regulatory standards. Effective coordination across functions will be essential in this role. Key Responsibilities: - ...

Role Overview: As a Raw Material Quality Control Analyst, your main responsibility will be to ensure that all raw materials (API & excipients) used in manufacturing are sampled, tested, and released according to pharmacopeial/in-house specifications and regulatory standards before they are utilized in production. You will play a crucial role in maintaining the quality and integrity of raw materials used in pharmaceutical manufacturing processes. Key Responsibilities: - Receive and verify raw material intimation from the warehouse. - Conduct GMP-compliant sampling using appropriate tools and in classified environments (if applicable). - Properly label samples and maintain sampling logbooks. -...

As an experienced CSSD Incharge at Apollo Hospitals Jabalpur, you will play a crucial role in overseeing the Central Sterile Supply Department (CSSD) operations. Your responsibilities will include: - Supervising and managing the sterilization, disinfection, and decontamination of surgical instruments and medical equipment. - Ensuring compliance with NABH, NABL, and hospital infection control protocols. - Overseeing the proper handling, packaging, labeling, and storage of sterilized equipment. - Maintaining sterilization records and reports for audits and regulatory compliance. - Implementing quality control measures to prevent cross-contamination and hospital-acquired infections (HAIs). - Mo...

B.Sc/M.Sc Chemistry, 1–8 yrs exp in API/Pharma QC. Must handle HPLC/GC/UV/IR, cGMP, stability, and docs. Local preferred Dahej. Only male candidates are required. Only pharma experience required.

As a Material Management Specialist, your role involves planning and controlling inventories of raw materials and packaging materials to meet production requirements. You will coordinate with Purchase and Quality Control teams to ensure timely availability and release of materials. Additionally, you will oversee the receipt, storage, and dispensing of materials in compliance with SOPs, MSDS, and safety requirements. It will be your responsibility to manage the return, rejection, and destruction of non-conforming materials following established procedures. Your key responsibilities include: - Planning and controlling inventories of raw materials and packaging materials - Coordinating with Pur...

Job Alert Sr. GM / Associate Vice President – Quality Control Location: North India Industry: API / Chemicals Manufacturing Salary: Open (Attractive hike on current package) Experience: 16+ Years | Age: 50 Years We are seeking a dynamic Quality Control leader for a reputed API Manufacturing organization . The candidate must have strong exposure to regulatory-driven companies with proven expertise in leading global regulatory audits (USFDA, EMA, MHRA, etc.) and managing large QC operations. Key Responsibilities: Head the Quality Control department ensuring compliance with cGMP & international regulatory guidelines. Lead a QC team of 150–200 employees , driving efficiency, compliance, and tech...

Compliance with SEBI regulations, stock exchange rules Internal Audits & Inspections Reporting & Filings Policy development & implementation Grievance Redressal Training & Awareness Surveillance & Monitoring Coordinate with regulators(NSE,BSE,SEBI)

Role & responsibilities Conduct Transaction Monitoring as per guidelines defined in the Process maps Prepare transaction monitoring reports and ensure timely and accurate reporting Participate in calibration exercises on a regular basis to ensure consistency in measurement. Conduct ongoing analysis of quality performance and recommend actions for improvement at associate / process level Update performance data to ensure timely and accurate reporting of SLAs Work closely with Client Trainer / SME and Operations team to conduct team huddles. Perform transaction processing as per defined policies and procedures Provide feedback to associates based on monitoring results if required. Preferred ca...

Role & responsibilities 1. Audit Planning & Execution: Assist in preparing the annual audit plan in line with hospital objectives and risk assessments. Conduct internal audits across departments such as Finance & Accounts, Billing, Pharmacy, Supply Chain, HR, IT, Clinical and Non-clinical operations. Review compliance with statutory requirements (Income Tax, GST, NABH/NABL standards, etc.). Perform surprise audits in critical operational areas (pharmacy, billing counters, cash management, stores, ICU/OT consumables) 2. Risk & Control Assessment: Evaluate internal control systems, identify gaps and suggest process improvements. Analyze financial data, operational processes, and clinical docum...

Role Overview: As a Manager in the Quality Assurance department at ZLL-SEZ Oncology Injectable (Alidac), your role will be critical in handling in-process Quality Assurance functions. You will ensure that defined and approved IPQA checks are followed and documented during Dispensing, Manufacturing, filling, capping, and Packing stages. Your responsibilities will include ensuring compliance with Current Good Manufacturing Practices and sterility assurance activities in aseptic product manufacturing. Additionally, you will review Smoke study protocol, report, and Video recording, and participate in regulatory audits. Key Responsibilities: - Handle in-process Quality Assurance functions by ensu...

Walk-In Drive for Development Quality Assurance - Formulation Department @ MSN R&D Center Pashamylaram on 20.09.2025 (Saturday ) Roles & Responsibilities 1. Issuing of Batch Manufacturing Records, Analytical Raw datas and maintaining the respective log books. 2. Issuing of registers and formats for all departments and maintaining of records for issuance and reconciliation. 3. Issuance approval, Issuance and Retrieval of the documents in eDMS. 4. Receiving, Issuing and reviewing the bio batches related executed Batch Manufacturing Records, Analytical raw datas and archiving. 5. Responsible for review of product development documents and analytical documents related to technology transfer. 6. ...

B.Sc/M.Sc Chemistry, 1–8 yrs exp in API/Pharma QC. Must handle HPLC/GC/UV/IR, cGMP, stability, and docs. Local preferred Dahej. Only male candidates are required. Only pharma experience required.

As an experienced candidate with 17-20 years of experience, your role as Engineering Department Manager will involve the following responsibilities: - Manage and lead the engineering department at the site, ensuring smooth operations. - Oversee operation and maintenance of HVAC systems and utilities. - Develop, implement, and monitor monthly planners and maintenance schedules. - Ensure readiness of the department for customer and regulatory audits; represent the department during audits. - Implement corrective and preventive actions (CAPA) and monitor their effectiveness. - Monitor and ensure compliance with process equipment and facility maintenance activities in line with cGMP requirements...

Job Summary Dispatch Achievement Verification of all Inwards & Outward material with correct documents, material code & qty etc. Stock Management Slow & non moving stock management 5s & Kaizan though implementation in ground operation Labor Management SOP compliance Minimum stock planing of Material & Packing material Working Language : - Hindi,Marathi,English