75 Coa Jobs - Page 3

As an Oracle Functional Consultant, you will be responsible for successfully executing a minimum of two end-to-end Fusion Finance implementations, upgrades, lift & shift, and support projects. Your expertise in Oracle Cloud (Fusion) Financials Functional modules such as GL, AP, AR, FA, Cash Management, FAH, Intercompany, Expenses Management, RMCS, and Procurement will be crucial in meeting business requirements. Your key responsibilities will include understanding business requirements, conducting fit-gap analysis, and preparing functional design documents. You will independently manage the Finance track, interact with clients, and lead business requirements and training sessions. Additional...

Role & responsibilities Responsibilities Preparation of SOPs, Protocols, Quality Documents Etc. Document Quality Assurance activities and create Audit reports Artwork checking & Approval Preparation of regulatory documents Draft preparation for product permission COA preparation Raw material, finish TR preparation All validation document prepn. All calibration documents prepn. AMV prepn. Specification & STP Prepn. As per Pharmacopoeia . Address and discuss issues and proposed solutions with superiors. Requirements and skills Proven work experience as a Quality Assurance officer or similar role Working knowledge of tools, methods and concepts of quality assurance Solid knowledge of relevant r...

MES Consultant --> --> Location, Designation --> LocationRemote DesignationMES Consultant Experience4 - 6 Years : Assist in shop floor/Camstar software requirements analysis and implementation of changes to existing and/or new modules as well as related 3rd party solutions to support changing business needs. Manage MES systems documentation, Prepares technical and user documentation and conducts system training Work closely with cross functional team to provide stable MES to business users Manage Camstar administration tasks. 4+ years of strong programming experience with Integration projects Support for system integration between Camstar MES and other applications. Manage MES services in De...

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...

Technical Documentation Must have documentation experience in COA, MSDS, VQ Filings, APQR, MOA, DMF, Stability data

Candidate should have experience of Customer Liaison (Domestic & International), Export/Import, GST & Compliance Knowledge, Sales Documentation (Export & Domestic), COA/COO Understanding, Collection Monitoring, Required Candidate profile Proficient in D-365 / ERP, Strong English Communication Skills

Must to have experience in COA/ Certificate of Analysis, MSDS, Specifications/ TDS, Method of Analysis, Stability Data, DMF/ Drug Master File. Must have knowledge of Pharmacopoeias, ICH guidelines.

Must have knowledge of documentation (COA, MSDS, VQ Filings , APQR, MOA,DMF) COA/ Certificate of Analysis • MSDS • Specifications/ TDS • Method of Analysis • Stability Data • DMF/ Drug Master File • Declarations Required Candidate profile Intrested Candidate Can share your CV in Whatsapp : 91-9724346949 / 9327657730

QC Daily Analysis Conducted tests Assay and Dissolution KF ,PH Preparation of solutions for HPLC Analysis Documentation preparation like SOP,MOA,MSDS,STP

Position- Python Openstack (consultant) Exp- 5 to 8 years Location-Gurgaon Job Summary: We are seeking a skilled OpenStack and NFVI Engineer to design, implement, and manage cloud-based infrastructure solutions. The ideal candidate will have hands-on experience in deploying OpenStack environments and expertise in NFV, virtualization, and network functions. Key Responsibilities: Design, deploy, and maintain OpenStack-based private or hybrid cloud environments. Configure and optimize NFVI for high availability and performance to support VNFs (Virtualized Network Functions). Implement and manage virtualization technologies like KVM, VMware, or similar. Automate deployment, scaling, and maintena...

We are hiring a Sr SAP PP QM Consultant for a 6-month full-time onsite contract role in Ahmedabad. The candidate must have 610 years of experience in SAP PP & QM support, with expertise in data modeling, RICEF developments, QM configuration, production planning, order management, and vendor evaluation processes. Responsibilities include working with SAP add-on technologies, SDLC for RICEF objects, cross-functional solution design, and CAPA management workflows. Strong hands-on in Quality Planning, Quality Notifications, Process Orders, Batch Management, and integration with LIMS. Immediate joiners only.

We are hiring for the role FSQA Specialist Roles and Responsibilities: Inspect incoming rice and other food products for quality parameters such as moisture content, foreign matter, broken grains, and discoloration . Ensure strict compliance with internal quality standards , customer specifications, and regulatory requirements (USDA, FSSAI, etc.). Monitor and maintain food safety programs including HACCP, GMP, and sanitation protocols . Review and validate supplier documents like Certificates of Analysis (COA), test reports, and compliance records. Maintain accurate quality inspection reports , non-conformance records, and documentation logs. Collaborate with procurement and supplier teams t...

Raw Material Inspection. Like Boards, Kraft, Liner, Adhesive, Coating, Film, Etc (Sampling, Testing, Reporting & Recording) In-Process Checking (Printing & Post printing) COA (Certificate of Analysis) making. Lab Instruments Calibration Required Candidate profile Customer Specification Analysis & Comparison Against Actual. Job Traceability (Forward & Backward) Creating Job file like Artwork, KLD, shade card, approved Dummy and Inspected incoming raw materials. Perks and benefits Accommodation, PF, ESI, Bonus

1. To prepare technical documents (Specification, MSDS, declarations, etc) for various products. 2. Will be a custodian of documents shared to customer. 3. To attend customer complaints and if necessary coordinate with factory QA team for addressing the issues. 4. To adhere to strict timeline to share customer related documents. 5. Master degree in related field in science 6. Should have prior experience in handling technical documents in botanical industries. 7. Should have basic knowledge about various medicinal plants and their contents 8. Should be a good team player

Dossier Preparation. Interact with Marketing, Quality Control, Product Development, R&D, & manufacturing units to collect necessary documents. MSDS of both Technical & formulation products. Discussions with regulatory team to improve knowledge. Required Candidate profile Must have exp in international regulatory affairs.

Job Title: Quality Control Executive Ayurveda Products Department: Quality Control (QC) Location: Kundli Job Summary: We are seeking a detail-oriented and experienced Quality Control Executive to ensure the quality, safety, and compliance of Ayurvedic products. The QC Officer will be responsible for implementing and maintaining testing protocols for raw materials, in-process samples, and finished products according to GMP and regulatory standards applicable to Ayurveda and herbal formulations. Key Responsibilities: Conduct routine quality checks and testing of raw materials, packaging materials, in-process samples , and finished Ayurvedic products . Ensure compliance with AYUSH regulations ,...

Dossier Preparation. Interact with Marketing, Quality Control, Product Development, R&D, & manufacturing units to collect necessary documents. MSDS of both Technical & formulation products. Discussions with regulatory team to improve knowledge. Required Candidate profile Must have exp in international regulatory affairs.

Position: Documentation Executive Analytical R & D Looking for candidates with 3+yrs of experience as Documentation Executive Total Experience: 3-6yrs Qualification: M Sc Location: Bangalore (Peenya 2nd Stage). Roles & Responsibilities Should have knowledge and exposure of SAP Software. Should be well versed with documentation procedures, preparation and review of Certificate of Analysis and specifications. Preparation and uploading of new finished product specifications, revision of existing finished product specifications, release of CoAs for finished products received from the units. Preparation of MSDS, work order requests, work order completion, and CoAs for samples tested for both inte...

Studying Legal Documents and collating info in a variety of formats. Ensuring compliance with regulations set by the Cosmetics & Perfumes Regulatory Agency as country wise Keeping up to date with changes in regulatory legislation and guidelines Required Candidate profile Well versed with US FDA, EU regulatory requirements Be well versed in the preparation of MSDS, COA, PIF and CPNP files Knowledge on Indian Drug & Cosmetic mfg Act especially on Schedule S Stds & GMP.

Reporting to Sr. Director - Regulatory Affairs Experience required: 5-8 Years Education: B. Pharm / M. Pharm Department: Regulatory Affairs Key Responsibilities: Prepare the status of all documents related to submission. Compile and review Regulatory submission documents required in line with the relevant guidelines. Coordinate with all stakeholders of the manufacturing plant for the collection of documents. Evaluation of change control: evaluate all post-approval changes. Review of specifications (API, Intermediate, FP, and Shelf life) executed BMRs, BPRs, COA, Method transfer report, Method verification, Analytical chromatograms intended for regulated or non-regulated market submission. Ge...

About Client Hiring for One of the topmost MNC!! Job Description Job Title: MES Camstar Developer Qualification : Any Graduate or Above Relevant Experience : 3 to 15 Years ROLES AND RESPONSIBILITIES Act as a Solution Architect for Camstar/Opcenter MES projects Lead and manage the design and development of CIO/MIO Maps and related workflows Gather and translate user requirements into functional specifications Responsible for the end-to-end implementation of MES solutions Coordinate with cross-functional teams and ensure timely delivery Manage and distribute work effectively across the development team Ensure adherence to regulatory and quality standards relevant to the industry Technical/Func...

About Client Hiring for One of the topmost MNC!! Job Description Job Title: MES Camstar Developer Qualification : Any Graduate or Above Relevant Experience : 3 to 15 Years ROLES AND RESPONSIBILITIES Act as a Solution Architect for Camstar/Opcenter MES projects Lead and manage the design and development of CIO/MIO Maps and related workflows Gather and translate user requirements into functional specifications Responsible for the end-to-end implementation of MES solutions Coordinate with cross-functional teams and ensure timely delivery Manage and distribute work effectively across the development team Ensure adherence to regulatory and quality standards relevant to the industry Technical/Func...

Preparation of Technical documents like below: COA/ Certificate of Analysis Specifications/ TDS Method of Analysis Stability Data DMF/ Drug Master File Declarations Preparation of Vendor Questionnaire Customer response for technical queries

Preparation & Review of dossier in CTD, ACTD, ETCD format Preparation of dossiers of stability Data, Analytical method validation Preparing the SPC/SMPC as per country guidelines Preparation and Reviewing of documents COA as per the country guideline

Responsibilities: Conduct regular audits on production processes Ensure compliance with regulatory standards Collaborate with R&D team for product improvement Review COA, artwork, labels, cartons & packaging materials