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12.0 - 17.0 years

9 - 12 Lacs

Valsad, Vapi, Daman & Diu

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Role & responsibilities 01 Quality Control Functions: 1.1 To ensure that the laboratory carrying out its testing, calibration, validation and all other technical activities in such a way to meet GLP requirements. 1.2 To carry out all technical activities and implementation of documented quality system. 1.3 To plan, schedule and monitor analysis of Raw Materials, Premix, Packing Materials, In-process materials, Finished products, Microbiological analysis, Water analysis and ensure that they meet defined relevant quality standards. 1.4 Periodically review logbooks, reports and test protocols related to Raw Materials, Premix, Packing Materials, Microbiological analysis, In-process and Finished products for proper entries, accuracy and completeness and ensure that they meet defined relevant quality standards. 1.5 To handle Quality management events according to SOP and complete its documentation with corrective and preventive actions. 1.6 To ensure that updated Specifications, Standard Testing Procedure, Test protocol and documents are available for use. 1.7 To review the resources of Manpower, Instruments, Equipment, Material and advise Management on the provision with justification. 1.8 To train the personnel in the department regarding Chemical Testing, Instrument qualification & current regulatory guidelines. 1.9 To establish effective communication systems with other departments including Commercial departments to achieve effective and efficient service from Quality Control Department. 1.10 To ensure implementation of cGMP in laboratory. 1.11 To ensure Qualification, Annual Maintenance and Calibration of QC instruments. 1.12 To ensure Management of Standards, Chemicals, Reagents and Glasswares. 1.13 To Review and approval of new or revised SOPs. 1.14 To handle instrument troubleshooting and interact with service Engineer in case of instrument breakdown. 1.15 To ensure compliance of Laboratory safety practices and firefighting devices. 2.0 General function 2.1 To provide compliance of Audit observations. 2.2 To take adequate measures to ensure updating of information and knowledge of the key people in the Quality control. 2.3 To provide support to planning, production, finish product for timely release of the goods for dispatch. 2.4 To monitor the microbiological analysis and ensure that all testing is carried out. 2.5 To create SOP awareness by continuous training. 2.6 To ensure good housekeeping of laboratory and up-keep of laboratory. 2.7 Self-updation of current regulatory guidelines. 2.8 Self inspection of other departments, as and when scheduled. . 2.9 Take necessary measures to prevent accident/incident and help in accident/incident Investigation. 3.0 Adherence and compliance to cGMP requirements. 3.1 Undertaking any other work, either for this department or any other department which the organization, which may be requested by the Plant Manager, for which training and/or an explanation has been provided and understood.

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4.0 - 9.0 years

3 - 5 Lacs

Hyderabad

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Experienced Candidates in QA as per ISO 13485 review batch records, handle deviations, CAPA, and audits; support validations; write and maintain SOPs; coordinate with cross-functional teams, documentation, and Compliance with regulatory standards. Required Candidate profile Graduate / Post Graduate in biotechnology / bio medical / Microbiology / Chemistry with strong hands on experience in QA operations in any Pharma or medical devices company.

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3.0 - 6.0 years

4 - 6 Lacs

Chengalpattu, Tambaram, Chennai

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We are seeking an experienced QA professional to oversee and ensure the implementation and maintenance of quality systems across operations including tissue processing, cryopreservation, cleanroom monitoring, inventory management, documentation, and regulatory compliance. The role involves cross-functional coordination, audit readiness, and driving continuous improvement initiatives. Role & responsibilities Supervise day-to-day QA operations across processing, quality control, cryopreservation, and allied functions. Review environmental monitoring and batch processing records; ensure regulatory and SOP compliance. Lead deviation handling, CAPA, root cause analysis, and trend analysis. Manage internal audits, vendor audits, and ensure readiness for regulatory inspections. Drive document control, change management, and quality risk assessments. Coordinate validation activities, training programs, and management review meetings. Oversee equipment qualification, material sampling, and calibration compliance. Support inter-branch QA coordination and provide QA coverage in team absence. Prepare and submit Annual Product Quality Review (APQR) and other compliance reports. Preferred candidate profile Bachelors or Masters degree in Life Sciences, Pharmacy, or related field. 3.5 - 7 years of relevant QA experience in healthcare, biotech, or tissue banking. Strong understanding of GMP, GLP, ISO standards, and regulatory frameworks. Experience with audits, validations, and QA documentation. Contact : HR Vaishnavi Phone: 7397274599 (call or whatsapp) How to apply : Email: vaishnavi.g@lifecell.in (Share your resume to this mail ID) Company Location: Kelambakkam (opp to VIT) https://maps.app.goo.gl/oCg3GhtsPwctTDQT6 https://forms.gle/U9ejBEqDZDaBZYfj6 - Apply here (Our HR team will call you Immediately as possible)

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4.0 - 7.0 years

2 - 5 Lacs

Pune

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Role & responsibilities Manage end-to-end HR operations, including recruitment, payroll, and compliance. Oversee contractual manpower deployment, vendor coordination, and SLAs. Ensure labor law compliance (ESIC, PF) and handle audits. Lead employee engagement, performance appraisals, and training programs. Supervise office administration, facility management, and workplace security. Preferred candidate profile Strong knowledge of HR practices in returnable packaging or related industries. Experience in third-party manpower handling & labor laws. Excellent leadership, negotiation, and communication skills. Proficiency in HRMS, MS Office, and compliance management.

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3.0 - 7.0 years

3 - 3 Lacs

Pune

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1.Cash and Bank Entry 2.Bank Reconciliation 3.Collection and Payment Entry 4.Provision Entry 5.Sales and Purchase register 6.PF ESI GST and Govt. Payments 7. Monthly and Year closing entries 8.Audit handling

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3.0 - 5.0 years

2 - 2 Lacs

Erode

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Location: Erode Experience Required: 3 to 5 Years Industry: Manufacturing Functional Area: Accounts, Finance, Tax, Audit Education: B.Com / M.Com / BBA / MBA (Finance) or any related UG/PG Degree Required Candidate profile Handle daily accounts in Tally, P&L, GST, TDS, PF/ESIC, audits, exports/imports, vouchers, payroll, and financial reports as per ROC norms. Good in Excel & statutory compliance.

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4 - 9 years

0 - 0 Lacs

Bengaluru

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Strategic: Representative for QMS activities in Drug product/ Drug substance area. Timely initiation and closure of QMS elements. Documentation related to Drug product/ Drug substance area. Training need identification for all the employees Assist the validations and routine validations of equipment and facility. Identify and implement the manufacturing and warehouse procedures with compliance to current GMP requirements. Coordination during customer and vendor audits. Coordinating with engineering and validation department for calibration and preventive maintenance. Coordination and implementation of software based QMS solutions like Track-wise, LMS, SAP etc. Operational: Initiation of change controls, deviations, Investigation and CAPAs and closure of the same. Tracking of QMS activities and coordinating with cross functional departments to complete the QMS activities like investigation for OOS, complaints, deviations. Identification, preparation and implementation of SOP’s. This position will prepare SOPs related to the machines which are undergoing commissioning and procedures which are proposed to implement in Drug product area. Preparation and review of URS, CLIA, SLIA, QRM, IQ and OQ documents. Involvement in the qualification activities of equipment and area in drug product area People: Champion the OneSource Core Values and lead by example by acting a member of a team to achieve organizational and common objectives. Identify business successors and coach, mentor, nurture and develop people towards leading the business as non-fungible assets in the organization with a succession and continuity plan. Preparation and execution of training modules on SOP’s in the department. Preparation and execution of QMS documents in the department. Preparation and execution of training modules on QMS and safety SOP’s in the department. Preparation and execution of training on soft skills to develop the team. Finance: Ensure activities, services and tasks engaged / managed meets or improves on budget, cost, volume and efficiency targets (KPIs) in line with business objectives. Ensure the availability / adequacy of resources to implement and maintain the pharmaceutical quality system and continually improve its effectiveness by applying resources to specific product, process or site.

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3 - 4 years

2 - 2 Lacs

Erode

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Location: Erode Experience Required: 3 to 4 Years Industry: Manufacturing Functional Area: Accounts, Finance, Tax, Audit Education: B.Com / M.Com / BBA / MBA (Finance) or any related UG/PG Degree Required Candidate profile Handle daily accounts in Tally, P&L, GST, TDS, PF/ESIC, audits, exports/imports, vouchers, payroll, and financial reports as per ROC norms. Good in Excel & statutory compliance.

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5 - 7 years

10 - 12 Lacs

Nagpur

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Company Name: Eshan Minerals Pvt. Ltd. Required Qualifications : Chartered Accountant with experience of 5-7 years (preferred- manufacturing industry) Should have supervised accounts, finance teams for at least 5+ years. Closely worked with CFO/Management for MIS/Financial controls and Funds management. Ability to discuss and resolve issues with Plant Heads and Department Heads. Roles and Responsibility : Supervise accounting team to ensure complete and proper recording of transactions in a timely manner. Ensure all tax compliances & payments are made timely and maintenance of supporting work papers. Ensure timely preparation of MIS and lead in preparation of management dashboards. Co -ordinate with Plant Head / Department Heads for seamless flow of information & proper documentation. Lead Internal & External Audit process & ensure books closing and maintenance of adequate working papers. Handle cash flows efficiently and supervise the payment process. Review accounting process to make them robust and efficient. Guide and motivate team and develop training programs for staff. Carry out all accounting / tax & financial activities as desired by Management & CFO. Assist in the preparation of the annual budget and periodic forecasts. Monitor budget performance and report variances. *Contact : 8799969317 *E-mail : hr1@eshanminerals.com

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7 - 12 years

9 - 14 Lacs

Bengaluru

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Do you have Fund Accounting experience, and are you seeking a new job? Apex Group is looking for an Assistant Vice President of Private Equity Fund Accounting, and the hybrid role comes with an attractive salary and benefits package. This full-time hybrid role comes with a favourable salary and some excellent company benefits. The successful Assistant Vice President candidate will join the Fund Services team as an AVP and will be closely working with Clients and Client Service Managers based in the APAC/UK/US region to perform duties related to the administration of Private Equity Funds. You will review and sign off the NAV and Financials of the Private Equity and Hybrid Funds, including recording Journal Entries, preparing monthly/Quarterly/Annual Financials, processing payments, preparing investor notices and various client reporting. Your key Assistant Vice President duties and responsibilities include: Review Capital Call and distribution workings along with notices and release to respective investors Manage end-execution of Private Equity Funds from other accounting applications to eFront Identify and implement process improvement techniques to improve process efficiency and team productivity. To apply for this Private Equity Fund Accounting role, you will need at least nine years of experience, preferably in PERE and Hybrid Funds. You will also require the following: Experience working on Investran, eFront and Macro-enabled workbooks Experience handling audit requirements and ad hoc client requirements in fund accounting Good conceptual knowledge of accounting principles and financial statement preparation Experience in handling client relationships and working on onboarding new clients, and developing reporting templates for the client's instruments.

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