Process Validation Jobs

Key ResponsibilitiesAssist in qualification and validation activities including IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification).Prepare, review, and maintain validation protocols, reports, and supporting documentation.Execute validation tests and document results accurately.Support process, cleaning, equipment, utility, and computerized system validation activities.Ensure compliance with GMP, GDP, and applicable regulatory requirements.Participate in risk assessments, deviation investigations, and corrective/preventive action (CAPA) activities.Analyze validation data and prepare summary reports.Coordinate with Quality Assurance, Production, Engineering, and Maintenance teams.Maintain validation schedules and support periodic review activities.Assist during internal and external audits related to validation activities.

Hands-on experience in handling Plastic Injection Moulding Machines from 350T to 3500T forautomotive component moulding. Independently manage process setting, parameter optimization, cycle time reduction, rejectioncontrol, and productivity improvement. Expertise in handling Small to large Injection moulds of Bumpers & Instrument Panels etc. withHot Runner / Sequential Valve Gate Systems. Strong troubleshooting skills for moulding defects such as:o Sink Markso Flasho Short Mouldingo Warpageo Weld Lineso Burn Markso Tiger Markso Other process-related defects Experience with robot automation / take-out systems. Conducting mould trials, mould validation, and process approvals. Close coordination with Mould Assembly and Quality Engineering teams. Good knowledge of engineering resins and raw materials such as:PP, ABS, PC, ASA, PBT , Glass-filled / Mineral-filled materials, etc. Implementation of 5S, Kaizen, Lean Manufacturing. Capability to handle OEM audits, customer visits, and process discussions. Experience in export mould trials, sample approvals, and packaging support. Ensure full Safety Compliance on shop floor.

Company: Prasanna Venkatesh & AssociatesType: Full-TimeAbout UsWe are a Chennai-based auditing and compliance firm delivering structured, accurate, and end-to-end financial services in GST, Income Tax, accounting, incorporation, and ROC compliance. With a strong portfolio of clients across industries, we are committed to excellence in client service, statutory accuracy, and timely delivery.Role: GST Expert - End-to-End GST Compliance & Litigation HandlingWe are seeking a highly skilled GST Expert with a minimum of 5 years hands-on experience in an auditors office. The ideal candidate must have thorough working knowledge of all GST return forms, portal usage, refunds, reconciliations, LUT filings, and litigation handling. Youll take complete ownership of GST compliance for multiple clients and coordinate directly with clients and the GST department.Key Responsibilities Prepare, file, and manage all GST returns: GSTR-1, GSTR-2A/2B reconciliation, GSTR-3B, GSTR-4, GSTR-5, GSTR-6, GSTR-7, GSTR-9, GSTR-9C Perform monthly/quarterly ITC reconciliation and supplier mismatch resolution Handle GST Refund Applications - for export, inverted duty, excess cash ledger, etc. Apply for and manage LUT filings (fresh and renewals for exporters/service providers) Prepare and file DRC-03, handle Show Cause Notices, respond to queries from GST officers Ensure timely uploads, validations, and issue resolution via GST portal & offline utilities Coordinate with clients to gather invoices, input data, HSN summaries, etc. Guide and support the internal team on complex GST rules and changes Stay updated with GST circulars, amendments, due date changes, and compliance risks Provide support during GST department audits and assessmentsRequired Qualifications & Skillset B.Com / M.Com / CA Inter / CMA Inter / MBA (Finance) 5+ years of GST experience in an auditor/compliance firm Complete hands-on experience in preparing & filing all GST returns listed above In-depth knowledge of: Input Tax Credit rules (including blocked credits, RCM, ineligible ITC) Refund filing process (RFD-01, refund tracking, deficiency memos, bank validations) GST Notices - SCNs, DRC-01, DRC-03 replies Portal proficiency: GST Portal, ICEGATE (for exporters), E-Invoice Portal Strong command over Tally ERP / Prime, Excel (vlookup, pivot, ITC reconciliation formats) Able to read and interpret GST Acts, circulars, FAQs, and departmental advisories Proficient in English and Tamil - for both written communication and verbal coordination with clients and officers Ability to manage deadlines for multiple clients independentlyPreferred Add-Ons (Not Mandatory) Knowledge of customs-related refunds, ICEGATE errors, or SEZ-related GST exemptions Experience consulting on high-value or complex GST planning Hands-on with Zoho Books, QuickBooks, or cloud accounting softwareWhy Join Us? Lead full-cycle GST compliance and advisory work Work with a variety of clients across industries Handle refund and litigation workflows from start to finish Join a growing, professional team with structured processesOffice location: (Opp. to Kilambakkam New Bus Stand)Take the next step in your GST career with a firm that values technical mastery, ownership, and impact.Job Types: Full-time, PermanentBenefits: Cell phone reimbursement Flexible schedule Internet reimbursement Leave encashment Paid sick timeWork Location: In person

Prospect database development involves building and maintaining high-quality lists of potential B2B leads, a key process in your role at aMarketforce for demand generation. This aligns with your team's focus on accurate data for cold outreach Prospect database development Email id generation and research Calling and verification List management on MS Excel Sheet Reporting

Post: Supplier Quality Engineer / Senior EngineerJob Location: FaridabadCompany: Aktive Technologies Pvt. Ltd.Support regulatory compliance related to ISO 13485, MDR, and customer-specific requirements.Required Candidate profileEnsuring all supplied materials, components, and services meet Aktiv Technologies quality, compliance, and regulatory standards.Experience with medical devices, automotive, aerospace industry.

Perform accurate data entry and database management.Maintain and update records, files, and documentation.Handle internal communications and emails related to operations.Process invoices, purchase orders, and other financial documents.Assist in the preparation of reports and presentations.Coordinate with front office and other departments for smooth workflow.Maintain confidentiality of company information and sensitive documents.Schedule and coordinate meetings or internal events as required.Monitor and manage inventory of office supplies.Provide general administrative and clerical support.

I am looking for a business analyst to support lean six sigma implementation at manufacturing facilities. Knowledge of process consulting and experience with data analysis and chart creation in excel, dashboards and able to produce presentations in powerpoint in English

Job Opening: Quality Assurance (QA) Officer with IPQA ResponsibilitiesLocation: On-site Nalagarh, Himachal PradeshExperience: 3+ years mandatory experienceQualification: B. Pharm / M. PharmLanguage & Software Skills: Proficiency in English and Microsoft Office (Word, Excel, PowerPoint) MandatoryAbout the Role:We are hiring a knowledgeable and proactive Quality Assurance (QA) Officer to join our pharmaceutical manufacturing unit in Nalagarh. This role combines core QA responsibilities with In-Process Quality Assurance (IPQA) oversight on the production floor. The ideal candidate will ensure regulatory compliance, documentation accuracy, and continuous quality improvement throughout the production lifecycle.Key Responsibilities: Core QA Functions:Review and approve Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).Manage deviations, validations (mandatory), change controls, CAPAs, and maintain documentation as per regulatory norms.Conduct internal quality audits and assist in external audits by clients or regulatory agencies.Maintain and update SOPs, manuals, and master documents in accordance with current regulations.Oversee document control systems and archival processes.Train employees on cGMP practices and quality systems.In-Process QA (IPQA) Responsibilities:Monitor critical stages of manufacturing and packing operations to ensure GMP compliance.Line clearance before batch start-up and between changeovers.Sampling of in-process materials and verification of critical process parameters.Real-time review and recording of BMR/BPR entries during production.Ensure proper gowning, hygiene, and sanitation compliance on the shop floor.Immediate reporting and documentation of any deviation or non-conformance observed.Desired Profile:B. Pharm / M. Pharm with a strong academic and technical background.Minimum 3 years of QA experience in a regulated pharmaceutical manufacturing unit.Hands-on experience with IPQA activities and on-floor quality monitoring.Excellent written and spoken English communication skills MandatoryProficiency in Microsoft Office (Word, Excel, PowerPoint) MandatoryGood understanding of WHO-GMP, Schedule M, and other applicable quality regulations.Strong coordination skills, attention to detail, and documentation accuracy.Join a team committed to delivering excellence through quality-first manufacturing.If you're passionate about compliance, process integrity, and hands-on QA work we invite you to apply!#QualityAssurance #IPQA #PharmaJobs #QAOfficer #BPharmJobs #MPharmJobs #PharmaCareers #GMPCompliance #NalagarhJobs #QualityFirst #IndianPharma #HimachalPharmaJobs #AuditReady

Senior Quality Assurance OfficerExecutive: (Vapi) Job Location: VapiQualification: M.Sc. (Chemistry) or B.Pharm or M.Pharm. Experience: 5 to 7 years experience in a Cosmetic/API/Pharmaceutical Product manufacturing company. He has to review and prepare SOPs.He is responsible for deviation management.He is also responsible for change control management.He is responsible for CAP management.He has to prepare and review BPR & BMR.He is responsible for in process quality assurance.He has to prepare market complaint investigation report/He has to prepare annual quality product review.He has to prepare protocol and report for process validation.He is also responsible for qualification of equipments and manufacturing process.He has to conduct internal audits.Salary: Best in Industry.Share me resume on career.talenthunt.th@gmail.com / cv.talenthunt1@gmail.com Whatsapp me on 7016504771 / 9998137070.

QA validation qms microbiology chemist HPLC all b pharma m pharma b tech biotech candidate call us . Fresher and experienced both can apply for this job .

Develop project plans with accurate resourcing and work schedules. Develop method of work statements and processes for all projects undertaken. Develop Maintenance Philosophies. Develop Asset Registers, hierarchies and classifications from P&IDs, PFDs, single line drawings and other data sources. Prepare for and conduct Preliminary Criticality Analysis studies. Prepare for and conduct maintenance strategy analysis (Failure Modes and Effects analysis, RCM, criticality, etc.) using proprietary software. Develop maintenance strategies. Development of Planned Maintenance Routines for core discipline. Construction of planned maintenance program. Assist with workload smoothing and man-power projections. Perform spares analysis for critical equipment.

Thermal/ Equipment Validation Steam Quality Testing Compressed Air/ Nitrogen Gas Testing Plc Validation Hvac/ Clean Room/ Laf/ Rlaf Validation Calibration

Delhi, Delhi: Reliably commute or planning to relocate before starting work (Required)Candidates Having The Central Drugs Standard Control Organization(CDSCO) experience and similar with these organizations can apply .Informing strategic regulatory controls and providing the worldwide regulatory policy for product development, manufacturing, and registration: It aids the applicant in advancing a universally accepted product.Development of proper leaflets like a summary of product characteristics, patient information, etc.To complete record data of the companys products and maintain the records of therapeutic products in agreement with current regulations and guidelines.To prepare data about a new product for doctors and other healthcare professionals for harmless and effective practice of medicine and maintain records, and reports of post-marketing surveillance of the new product. It also helps to prepare the leaflets and advertising material for existing as well as new drugs.IMMEDIATE JOINERS CAN APPLY.

QA manager ,QA validation, Qms , Injection and osd both

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