75 Coa Jobs

Responsibilities: * Prepare regulatory dossiers for product approvals * Collaborate with cross-functional teams on dossier updates * Ensure compliance with drug regulations according to NAFDAC standards. * Manage LOAs, COAs & BDNAF submissions

As a Quality Control Executive/Sr. Executive - Documentation Reviewer at Cadchem Laboratories Ltd., your role involves reviewing data of reaction monitoring, raw materials, intermediates, and finished goods to ensure timely release of samples. You will also be responsible for reviewing working standard COA and raw materials, as well as verifying and reviewing all inward and instrument usage log books. Key Responsibilities: - Review data of reaction monitoring, raw materials, intermediates, and finished goods for timely sample release - Review working standard COA and raw materials - Verify and review all inward and instrument usage log books Qualifications Required: - Bachelor/Master Degree ...

Role & responsibilities Analyze incoming materials by confirming specifications and conducting visual/dimensional tests Evaluate supplier performance for incoming materials Address internal customer complaints related to incoming materials Participate in product and process improvement initiatives Prepare data for Zero Defect Process Indicators Maintain records as per documented procedures Validate clean rooms and sterilizers Handle all incoming material responsibilities Calibrate measuring and monitoring devices Manage TRF for new incoming materials Analyze non-conforming products and implement CAPAs Preferred candidate profile Hiring: Assistant Manager Analytical Chemist Location: Plot No....

Position: QC Chemist ( Only Male) Job Location: Nerul, Navi Mumbai Industry: Ayurvedic / Herbal Pharmaceuticals Qualification: B.sc/ Msc ( Botany) Mandatory Experience: 0-2 Yrs Experience ( Freshers also can apply) Designation & Salary: Commensurate with industry experience and expertise. Working Days And Time: 8:00 AM to 5 PM / 6 Days week / Sunday fixed Off. Key Responsibilities: Smooth functioning and timely analysis & approval of FG, RM,PM & intermediate which is finally approved from Q.C. COA preparation for Export purpose & other documentation whenever required.Monitoring of Control sample observation register: RM & FP Monitoring of Control sample and maintaining destruction record For...

Job Title: ESO QA Specialist Location: Ankleshwar, Gujarat, India Seeking experienced QA professionals with 5+ years in GMP environments. Responsible for quality lifecycle management, audits, CAPAs, change control, and regulatory compliance.

Sample registration through LIMS, Sample management(Control & returned). Preparation of ROA/COA. Post analysis data entry in LIMS. Preparation of template in LIMS. Candidate should have good hands on experience in handling LIMS & sample management. Required Candidate profile It is on the rolls of Cotecna Life Sciences India Pvt Ltd(Erstwhile Geochem Laboratories)

Position: QC Chemist ( Only Male) Job Location: Nerul, Navi Mumbai Industry: Ayurvedic / Herbal Pharmaceuticals Qualification: B.sc/ Msc Experience: 0-2 Yrs Experience ( Freshers also can apply) Designation & Salary: Commensurate with industry experience and expertise. Working Days And Time: 8:00 AM to 5 PM / 6 Days week / Sunday fixed Off. Key Responsibilities: Smooth functioning and timely analysis & approval of FG, RM,PM & intermediate which is finally approved from Q.C. COA preparation for Export purpose & other documentation whenever required.Monitoring of Control sample observation register: RM & FP Monitoring of Control sample and maintaining destruction record Formats up-gradation fo...

Position title: ESO QA Specialist University degree in Pharmacy, Chemistry, Biology, or relevant Life Science Minimum of 5 years in a similar role or equivalent experience in a GMP-related environment Job location - Ankleshwar, Gujarat, India MISSION STATEMENT To ensure the quality lifecycle management for dedicated, subcontracted, product portfolio. Qualified auditor. Main Accountabilities And Duties Operational skills Operational quality management of a dedicated product portfolio which includes: Quality management of deviation and complaint records and their related CAPAs Assessment and management of change controls Edition of QA Agreements with Zentiva third parties and subcontractors Co...

About the role Artwork Proofreading, grammar & punctuation to provide quality output. Ensure Content adheres to all compliances (i.e. Mock-up & Permission copy) & guidelines of artworks. Take Final Artwork Approval from Client & Plant. After Approval from Both the side we verify in hard copy and make it with Red Stamp and send for barcode check. Barcode check & verification of artwork we make artwork final approval with green stamp. Fill the checklist of final artwork. Sent for verification to higher authority. Maintain product Artworks/ documents distribution record. Give Final Printing Approval received from printer. Follow up for mock-up & permission to plant Follow up for artwork approva...

As a Frontline Officer - Quality ECH, your role will involve the following responsibilities: - Expertise in operating Analytical Instruments like GC, GC-MS, ICP-OES, UV-VIS Spectrophotometer, TOC Analyzer & KF Titrator. - Troubleshooting knowledge of instruments, responsible for calibrations & performance of laboratory instruments. - Analysis of Raw material IP and Finished products of ECH plant. - Analysis of various samples for Trace metal contents by ICP/AAS. - Preparation of the Analysis report & reporting it to the concerned Department. - Filling the Customer Questionnaire related to ECH plant. - Clearance of Finished goods in SAP QA Module. - Issuing of Material from Stores & monitorin...

Job Opening: Graphic Designer Pharmaceutical Packaging Location: Pune, Maharashtra Employment Type: Full-Time Experience Required: 6 months to 1 year Industry: Pharmaceutical / Healthcare B.Pharm graduate (mandatory) Prior experience in import & export procurement (pharma/healthcare industry preferred) Knowledge of supply chain, vendor management, and logistics Familiarity with regulatory and compliance documentation for pharma exports (WHO-GMP, COA, COPP, etc.) Strong MS Office/Excel skills and comfort with digital procurement tools Excellent negotiation, communication, and coordination skills What you'll do: Manage supplier sourcing and negotiations for pharma and healthcare products Coord...

About Kennametal With over 80 years as an industrial technology leader, Kennametal Inc. delivers productivity to customers through materials science, tooling and wear-resistant solutions. Customers across aerospace and defense, earthworks, energy, general engineering and transportation turn to Kennametal to help them manufacture with precision and efficiency. Every day approximately 8,700 employees are helping customers in nearly 100 countries stay competitive. Kennametal generated $2.1 billion in revenues in fiscal 2023. Learn more at www.kennametal.com . Follow @Kennametal: Twitter, Instagram, Facebook, LinkedIn and YouTube. Job Title: Architect IT Applications-India Location: Bangalore In...

Project Analyst I Office Based India, Bangalore ICON plc is a world-leading healthcare intelligence and clinical research organization Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development, We are currently seeking a Project Analyst I to join the Language Services team, This role plays a key part in managing eCOA-related translation projects, with a focus on reviewing and validating clinical trial screenshots You will collaborate with global stakeholders and vendors to ensure the accuracy, quality, and compliance of language assets that directly impact patient-facing clinical t...

Role & responsibilities To be well versed about coordination and collaboration with Quality functions of third party manufacturing (CMO) sites and CMO team for compliance of product, facility, systems, procedures. and for documents required from third party for various purpose; review, RA submission etc. Must have knowledge and know how on regulatory pathway for registration of product as per third party and or loan license norms/rules and requirement of documentation for regulatory submissions. Incumbent is expected a good reviewer and investigator To know the function of oversight of CMO sites for batch/lot releases as applicable form the manufacturing (Feed supplements and Pharma products...

We are looking for a skilled AX Finance Functional Consultant with 7-10 years of experience to join our team in Bangalore, Hyderabad, Chennai, Pune, Gurugram, and Greater Noida/Kolkata. The ideal candidate will have expertise in End-to-End implementation, Dynamics 365 Finance & Operations, and knowledge of General ledger, AR, AP, Fixed asset, Budget, Cash and Bank management. Roles and Responsibility Implement and configure AX Finance modules, including General ledger, AR, AP, Fixed asset, Budget, Cash and Bank management. Provide functional expertise in Project accounting, COA, and project documentation. Conduct Fit gap analysis and provide recommendations for improvement. Collaborate with ...

Responsible for Monitoring and support the Quality assurance of Vaccines under Development/Clinical/Technology Transfer To ensure the compliance of product manufacturing against pharmacopoeia, WHO and other applicable regulatory guidance documents. To monitor and ensure the shop floor compliance for manufacturing of clinical and Tech-Transfer batches. To monitor and ensure the compliance of cell bank management. Review of executed BPRs, testing reports, COA and EMP data for the development batches. Handling and follow up for timely closure of Change Controls, Deviations, OOS, Risk assessment and OOLs. Review & Approval of Protocols (PV,CV etc.), study reports, BPRs, MFRs SOPs and other docum...

As a Senior Consultant in Finance & Treasury at EIL Global IT Solutions and Services Pvt Ltd, a dynamic IT service provider headquartered in Adelaide, Australia, with a strong presence across Asia Pacific and EMEA, your role involves deep expertise in tools like Kyriba and familiarity with end-to-end finance processes. Your responsibilities include: - Defining future-state operating models - Standardizing workflows - Enabling scalable automation in alignment with regulatory requirements and business needs Your work directly contributes to strengthening financial governance, reducing operational risks, and increasing efficiency in financial transactions and reporting across global operations....

1. Machine Operation 2. Operating the machine according to daily Schedule 3. quality standards as per the COA 4. Daily check the preventive maintenance and troubleshooting of the machine 5. Daily check and load the raw materials into machine. Required Candidate profile 6 follow safety standards 7 Record production data report 8 check spare availability Compactor blade, DFC unit cutting blade filtration meshes 9 check chiller, stainer, disc filter & dewatering unit

• Assigning batch details • Preparing the batch CoAs • Keeping the entry of Inward and Outward details • Regulatory market review or our products and verify guidelines Required Candidate profile Candidates with excellent knowledge in COA, Batch Details, Batch Record, Vendor qualification, CAPA, Customer Query resolution.

GC, HPLC, UV, Malvern, LCMS | SOPs, MSDS, COA | 5S, NABL, GLP, IMS | Reports | Impurity Profiling Inventory, AMC, CMC & LIMS management. Monthly/Yearly report preparation. Audit exposure

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.

Job Title: Quality Assurance Executive Essential Oils Company: Aromaaz International Pvt. Ltd. Location: [Ghaziabad] Job Type: Full-time Key Responsibilities: 1-Ensure quality of essential oils, absolutes, carrier oils, and related natural products in compliance with international standards. 2-Conduct physical, chemical, and sensory evaluation of raw materials and finished goods. 3-Maintain GC-MS (Gas Chromatography-Mass Spectrometry) and other analytical reports for quality verification. 4-Develop, implement, and monitor SOPs for quality control and assurance across production and packaging units. 5-Coordinate with suppliers and vendors to ensure raw material quality. 6-Ensure adherence to ...

Responsible for follow the health, safety & environment norms as per company policy & procedure Responsible for follow the Good Laboratory practices & Good Documentation practices Maintain laboratory discipline Preparation of COA, Raw material trend Required Candidate profile Operate and calibrate instruments like Gas Chromatography, HPLC, Analytical balance, PH meter, GCMS Validity of instrument calibration, reagents, volumetric solutions, working standard

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.

The position of Oracle Fusion Finance Functional Lead requires a professional with 7+ years of experience in Oracle Fusion, including a minimum of 2-3 implementation projects in Oracle Fusion Financial Applications. As a candidate, you are expected to possess a sound understanding of financial business processes and concepts. Your role will involve hands-on experience in implementing Cloud Financial Modules such as GL, AP, AR, FA, CM, IC, and Tax. You should have proficiency in designing Chart of Accounts (CoA), Enterprise Structure, Multi-period Accounting, Allocations, Intercompany Elimination, and Consolidation. Additionally, you must be familiar with Translation and Revaluation processes...