196 Regulatory Audits Jobs - Page 4

You will be joining BNP Paribas India Solutions as an AVP / VP Financial Control, a supervisory role ensuring the day-to-day operations are conducted with high levels of personal integrity. Your key responsibilities will include: - Drawing up accounts of the Company as per applicable regulations and basis IND AS - Providing ongoing guidance on Financial Accounting to the team - Assisting compliance and tax teams with sharing information related to statutory and regulatory compliance - Contributing to various projects, particularly automation and process improvement initiatives - Managing Nostro Reconciliation and ensuring timely closure of breaks - Ensuring smooth month-end closure and adher...

Role & responsibilities Manage regulatory audits and inspections Respond to regulatory queries Internal Audit Report co-ordination and submission Co-ordinate with various depts for data Improve the Compliance framework of the company Responsible for the Internal Audit report preparation and submission Responsible for Off-site, onsite and AP audits and inspections. Regulatory interaction and reporting. Timely submission of IAR Preferred candidate profile Good understanding of MS Office and inter departmental co-ordination Graduate in commerce or law or CS Interested candidates can share theior updated resume on swapnali.mendonca@sharekhan.com

PREFERRED INDUSTRYAPPLY ONLY Immediate Joiners JOB LOCATION: SOUTH GOA, GOA PREFERRED INDUSTRY: Solar, energy efficiency or regulatory sector Job Description: Audit and Compliance Executive Location: South Goa, India (Work from Office) Experience: Minimum 3 years in International process (must) Job Type: Full-time Job Timings: 6am - 3pm IST About Us Cogncise Business Services is a fast-growing business solutions company with expertise across energy efficiency, marketing, and customer engagement. We partner with leading energy providers to help households in Oceania region adopt renewable energy solutions from solar panels and batteries to state-driven energy efficiency upgrades. Position Ove...

Core expertise in IPQA, 21 CFR compliance, validation & qualification, E-BMR/E-Log, QMS, risk assessment; skilled in audits, regulatory compliance, team management, training, and digital quality systems. Required Candidate profile B/MPharma 7 - 10 years of experience

JOB DESCRIPTION OF SUPERVISOR GROUND OPERATIONS CONTROL CENTRE (GOCC) JOB PURPOSE The Supervisor in Ground Operations Control Centre will be an integral link between Ground Operations and OCC and is responsible for ensuring the smooth and efficient functioning of ground and freight operations at various airports across India. The individual will oversee compliance with all relevant regulations, manage staff duty rosters, coordinate with airport authorities, and maintain infrastructure at stations. Additionally, the role involves handling charter flights, overseeing regulatory audits, recommending policy revisions, as well as monitoring and managing financial activities, including expenses, i...

Exp. in IPQA, line clearance & digital documentation w/ E-BMR & E-Log. Equipment qualification & process validation, w/ an understanding of 21 CFR Pt. 11 & audits. Risk assessment, CAPA management & conducting internal & vendor audits. Tech Transfer Required Candidate profile 10-15 Yrs B. Pharma / M. Pharma

Exp. in IPQA, line clearance & digital documentation w/ E-BMR & E-Log. Equipment qualification & process validation, w/ an understanding of 21 CFR Pt. 11 & audits. Risk assessment, CAPA management & conducting internal & vendor audits. Tech Transfer Required Candidate profile 10-15 Yrs B. Pharma / M. Pharma

As a Senior Manager 2 in the Global Quality CMO department at Sun Pharmaceutical Industries Ltd, your primary responsibility will be to ensure that SUN Pharma Quality and Compliance Standards, along with global regulatory authorities requirements, are consistently met across all SUN affiliates, CMOs, Suppliers, and SUN sites/Operational Units. Your role will involve providing Quality Oversight, conducting Independent auditing, and implementing necessary Follow-up actions to achieve, maintain, and enhance the desired level of compliance. Your essential job functions will include participating in the evaluation of Contract Manufacturing Organizations (CMOs), overseeing and approving various Qu...

The position of Sr. Manager Supply Chain Management will entail leading the end-to-end supply chain function for the Primary Pharma Packaging Plant located in Gonde Nashik. Your responsibilities will include ensuring uninterrupted availability of raw materials, consumables, and services in compliance with stringent pharmaceutical industry standards. To excel in this role, you must possess expertise in Procurement, Stores, Logistics, Inventory Management, Vendor Development, and Materials Planning, with a keen focus on cost efficiency, timely availability, and compliance with CGMP, FDA, and regulatory standards. Effective coordination across functions is also a key aspect of this position. In...

Job Requirements Role/ Job Title: Senior Specialist-IT Governance & Compliance (IT Compliance & Risk Specialist) Function/ Department: Information Technology Job Purpose The role entails the responsibility to be a part of IT Governance and Compliance Team of the bank and would be working towards GRC control function: Compliance & Regulatory reporting viz Cyber KRI, TRANCHE, ICAAP etc. Roles & Responsibilities Custodian of IT governance and IT process governance framework. Handling of Regulatory audits and submissions. To understand Indents from regulators, collated, review the data and timely submission. Responsible for IT policy creation, review, update, awareness, and monitoring. Administr...

As a Pharma Subject Matter Expert (SME) Trainer, you will be responsible for training candidates in various aspects of Quality Control (QC), Cell Culture Techniques, and Laboratory Procedures. Your role involves providing hands-on experience in analytical testing, microbiological testing, and pharmaceutical laboratory operations. It is essential to educate candidates on method validation, stability testing, and data integrity while ensuring compliance with FDA, USP, and cGMP regulations. Additionally, you will train individuals in utilizing HPLC, GC, UV-Vis, FTIR, PCR, ELISA, and Spectroscopy techniques. Your responsibilities include conducting mock interviews, assisting with resume preparat...

We are seeking a detail-oriented Deputy Manager Quality Assurance to support robust QA operations and also some Regulatory Affairs functions at Acharya Group's API manufacturing unit. This role focuses on maintaining our Quality Management System (QMS) for API production, ensuring cGMP and regulatory compliance for EU, USFDA, PMDA, and other Major Regulatory Regions. Key responsibilities include participating in batch release and continuous improvement; overseeing validation of API manufacturing processes, equipment, and analytical methods, managing deviations, conducting investigations, and implementing CAPA plans. Candidates must have prior experience in Quality Assurance within API manufa...

Coordinate technology transfer activities for (OSD) formulations from R&D to manufacturing sites, Support scale-up, exhibit, and validation batches, participate in investigations, deviation handling, and change control activities.

Lead end-to-end tech transfer of OSD products from R&D to commercial manufacturing sites, conduct scale-up and process validation activities, and provide technical support during regulatory audits and inspections.

Hi, Greetings from Avani Consulting . We are hiring for the below opportunity: Company: A leading Pharmaceutical API Unit Designation: Associate Engineering maintenance Process, WTP Experience: 3-5 year in API-Pharmaceutical Qualification: Diploma / BE in Mechanical Engineering Department: Engineering Location: Mysore Package 5-7 Lakh Roles & Responsibility: 1. Candidate should have Experience in Maintenance of Process equipments like Glass lined, SS Reactors, ANFD (Agitated Nutche filter & driers), RCVD, hot water system, Sifter, multi mill, Different process pumps like centrifugal, positive displacement with single and double mechanical seals etc. 2. Hands on experience in pumps, agitator ...

4+ Yrs of exp in Compliance audits,User Access Reviews,Data Analysis. Reviewing Access logs, Identifying discrepancies, Collaborating with DT & CDR teams to rectify access related issues. proficiency in data management & access management tools.

Job Description Manager / Sr. Manager (Contract Manufacturing & Quality Compliance) Location: Pune Department: Manufacturing & Quality Reports To: Head – Operations / Quality Role Overview We are seeking an experienced and proactive professional to manage and coordinate production activities at contract manufacturing sites. The ideal candidate will have strong expertise in production planning, quality systems, regulatory compliance, and cross-functional collaboration to ensure timely supply of high-quality products in alignment with business objectives and global regulatory expectations. Key Responsibilities Production & Planning Manage and oversee production planning at contract manufacturi...

In this role, you will have the opportunity to work in critical areas of Compliance and Governance for BharatPe alongside some of the brightest minds in the industry who are dedicated to building #bharatpeforbharat. Your responsibilities will include maintaining oversight of developments in the BFSI and Fintech regulatory environment, particularly focusing on Anti Money Laundering (AML). You will be responsible for developing internal procedures to prevent money laundering, building new scenarios/rules, creating BRDs, and evaluating exception reports and alert closures. Additionally, you will review policies and procedures in the AML program (KYC/CDD/EDD) to ensure information consistency wi...

Role Overview: We are seeking an experienced professional to lead the KYC Concurrent Audit function. The role involves real-time audits of customer onboarding and KYC documentation, ensuring compliance with RBI, PMLA, and internal guidelines. The ideal candidate will have strong regulatory knowledge, leadership skills, and proficiency in MS Office for reporting and dashboards. Key Responsibilities: Lead concurrent audits of KYC processes across branches and digital platforms. Review onboarding files for completeness and compliance with RBI/PMLA norms. Identify gaps, escalate critical issues, and ensure timely closure of observations. Supervise audit team members and maintain consistency in e...

The Sta Accountant role requires you to utilize established procedures to efficiently and effectively complete daily tasks. Your responsibilities will include verifying, entering, and processing invoices promptly, researching and resolving vendor disputes over the phone, as well as retrieving and maintaining vendor W-9s as needed. Additionally, you will assist in accounts receivable billing, collections, and posting processes, monitor tax compliance, and file sales/use and hotel taxes on a monthly basis. You will be expected to review month-end closing submissions, make necessary corrections before finalization, troubleshoot mis-postings in property management systems, complete bank reconcil...

The Sta Accountant is responsible for utilizing established procedures to efficiently and effectively complete daily tasks. This includes verifying, entering, and processing invoices in a timely manner, as well as researching and resolving vendor disputes over the phone. The role also involves retrieving and maintaining vendor W-9s, assisting in accounts receivable billing, collections, and posting processes, and monitoring tax compliance while filing sales/use and hotel taxes monthly. Additionally, the Sta Accountant is expected to review month-end closing submissions, make necessary corrections, and review a high volume of transactions to troubleshoot mis-postings in property management sy...

Job Description : Responsible for the overall operations and activities of the Drug Product Plant. Oversee production and manpower planning for the Drug Product Plant. Ensure products are manufactured and stored as per approved procedures and documentation to maintain quality standards. Review and ensure execution of Batch Production Records (BFR, BPR, etc.) as per cGMP requirements. Ensure qualification of equipment and instruments is carried out as per schedule. Ensure product validations are conducted in line with regulatory requirements. Monitor and maintain minimum stock of consumables, logbooks, and status labels. Ensure preventive maintenance of equipment as per the defined schedule. ...

Role Description: Quality control executive Location: Mil Laboratories Pvt. Ltd. 541, GIDC, Manjusar, Ta. Savli, Dist. Vadodara - 391775 Experience: 5 to 6 years Roles Responsibilities:- To perform all the testing related to RM, bulk, FP and stability samples To perform all the testing of packaging materials Handling of QMS documents like SOP, CAPA, repeat analysis, Deviation etc. To manage and lead the team To perform analytical method validation To prepare specifications for different materials New vendor approval Should have working experience of HPLC, GC, UV spectrophotometer, centrifuge etc. What will you need to be successful Preferred experience in sterile pharma plant. Extensive unde...

As a Quality Assurance professional in the Pharmaceutical & Life Sciences industry, your primary responsibilities will revolve around the review and approval of Supplier Qualification documents, including NSQR, VQ Documents, etc., from Raw material / Packing material manufacturers and external service providers. You will be tasked with preparing and distributing corporate approved supplier lists, New product tentative approved supplier lists, and Tentative approved supplier lists to all SQAs. Your role will also involve providing support to site QA for regulatory audits and Customer audits, reviewing vendor notifications, and coordinating with RA & SCM for further requirements. Additionally,...

Ensures Products meet established standards by developing and implementing quality control procedures, conducting audits, monitoring performance metrics, and resolving quality issues. Maintain documentation, Ensure compliance with Pharma regulations Required Candidate profile M.Sc - B. Pharma - M. Pharma - BE - Chemical Good knowledge Of Quality Assurance Good Command over English And Computer Must be ready to face customers Inquiries And Local And US FDA Authority