Average salary: Rs335,542 /yearly
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- ...Cross-Functional Collaboration : Work closely with internal teams (e.g., R&D, Quality Assurance, Manufacturing, Legal) to collect and review the necessary technical documents, clinical trial data, product specifications, and test reports for regulatory submissions. Assist...SuggestedFull timeLocal area
- ...and Finance teams for invoice and GST‑related clarifications. Maintain GST workings, reconciliations, and backup files for internal reviews and audits. Education Qualification & Experience ~ BBA/ BCom/ MCom/ MBA Finance ~1 - 5 years of relevant experience in any...Suggested
schott poonawalla
Vapi2 days ago - ...Responsibilities: Manage the end-to-end procurement cycle from receipt of Purchase Requisition (PR) to Purchase Order (PO) issuance. Review pending purchase requisitions and prioritize procurement based on operational and project requirements. Float enquiries, obtain...Suggested
schott poonawalla
Vapi2 days ago - ...requirements. • Define wall thickness, draft angles, ribs, bosses, snap-fit features and parting lines. • Participate in mold design reviews, tool trials (T0/T1/T2) and design modifications. • Identify and resolve moulding issues including warpage, sink marks, shrinkage...Suggested
MERIL
Vapi4 days ago - ...data quality, and adherence to clinical and regulatory requirements. 2. Clinical Documentation & Protocol Development • Develop, review, and finalize study protocols, investigator brochures, CRFs, and SOPs. • Ensure clinical documentation meets internal quality standards...Suggested
MERIL
Vapi4 days ago - ...target by visiting customers/ performance against set parameters and provide regular updates and providing proper guidelines. Milestone reviewing and legal guidelines are complied with while repossessing with the do timely allocation of the cases of the team be Profecient in...SuggestedFull time
Bajaj Finance Limited
Vapi27 days ago - ...EDQM, and the FDA of Russia, China, Japan, Mexico, Brazil, the UK, Australia, and Canada. Job Responsibilities: • Compilation and review of regulatory dossiers (CTD, ACTD, eCTD) for CIS, LATAM (especially Brazil & Mexico), African, and EU regions. • Handle full...SuggestedPermanent employmentFull timeWorldwide
- • Prepare, review, and maintain regulatory dossiers and technical documentation for domestic and international markets. • Support submissions for EU IVDR, WHO PQ, ANVISA, and other applicable regulatory frameworks. • Coordinate with QA, R&D, Manufacturing, and Marketing...SuggestedFull time
- ...Pipelines: Validate datasets and monitor training runs to benchmark model performance. 3. Quality Ownership & Engineering Code Review: Review frontend and backend code from a testability perspective, identifying anti-patterns and suggesting better error handling....SuggestedWork at officeLocal area
MERIL
Vapi4 days ago - ...Phototherapy light intensity measurement CPAP pressure and flow control electronics 3. Process Engineering & Documentation • Prepare, review, and maintain DHF, Risk management, R&D QMS. • Ensure implementation of ECO/ECN changes related to electronics hardware, firmware...Suggested
MERIL
Vapi4 days ago - ...the team to meet daily work demands. Work with a multi-functional team to execute Projects within allotted timelines & budget. Review flow diagrams, P&IDs, material & energy balance Review equipment list, equipment drawings and datasheets, Technical bid analysis (TBA...Suggested
jay finechem private limited
Vapi14 days ago - ...safety practices and emergency preparedness. Investigate and report any incidents involving radiation exposure or non-compliance. Review safety measures periodically and recommend improvements to enhance radiation protection. 4. Quality and Documentation Maintain...Suggested
MERIL
Vapi4 days ago - ...groups to ensure on- time completion of work activities and the implementation of project control procedures. Hands on experience of reviewing and closely monitoring of project schedule and costs. Should be able to provide project oversight, control, and Value Improvement...SuggestedFor contractorsLocal areaWorldwide
Bayer
Vapi4 days ago - ...teams Debug, test, and enhance existing backend systems Write clean, maintainable, and well-documented code Participate in code reviews and follow best practices Required Skills & Qualifications ~2+ years of hands-on experience in backend development using...Suggested
MERIL
Vapi4 days ago - ...and manpower Ensure all the processes are carried out as per cGMP guidelines in coordination with Quality Assurance Department Review the filled BPR after completion of batch Review the BPR, SOP, validation protocol, and other production related documents Initiation...SuggestedFull time
aarti pharmalabs ltd. (apl)
Vapi8 days ago - ...Ensure all products meet design, safety, and performance specifications as per ISO 13485, BIS 13450, and IEC 60601 standards. Review and approve quality control data, test results, and inspection reports before product release. Coordinate with the Production and...
Meril
Vapi4 days ago - ...Clinical, R&D, Product Management, and Quality teams to gather feedback and refine XR modules. Participate in internal validation, UI/UX reviews, and prototype testing before feature releases. Provide technical insights supporting product development, engineering decisions,...
MERIL
Vapi4 days ago - ...technical and legal rules and with Company policies in the field of PCT Is responsible for creating preventive maintenance schedules; Reviews and adjusts them based on plant performance, equipment failure history and available best practices. Has responsibility for...Local areaWorldwideShift work
Bayer
Vapi4 days ago Rs 1 - 6 lakhs p.a.
...demonstration (FOD's) Development of agent prospecting habits, calling habits and work habits Work with agent on planning and reviewing of activities and goals Identify the training needs of the agent and work with Trainers to improve the same Meet Business Targets...Axis Max Life Insurance
Vapi20 days ago- ...Managing human and material resources to meet production targets and quality standards. Coordinating and supervising staff activities, reviewing performance, and initiating corrective actions as required. Ensuring Compliance adherence to safety, health, and environmental...Shift work
jay finechem private limited
Vapi14 days ago - ...Maintain and control quality-related documents and records in compliance with Good Documentation Practices (GDP). • Support preparation, review, and archival of quality documents such as SOPs, formats, logs, and reports. • Ensure document traceability, version control, and...
MERIL
Vapi4 days ago - ...materials, in-process samples, and finished products. Prepare and standardize reagents and solutions for various testing procedures. Review and evaluate test results, and compile reports documenting analytical data. Perform routine maintenance and troubleshooting on...Full time
- ...compatibility Write clean, maintainable, and well-documented code Debug, troubleshoot, and resolve frontend issues Participate in code reviews and follow best practices Required Skills & Qualifications ~2+ years of hands-on experience in frontend development ~ Strong...
MERIL
Vapi4 days ago - ...standards applicable to medical device manufacturing. Key Responsibilities: 1. Regulatory Documentation and Compliance Prepare, review, and maintain documentation for product approvals and certifications from BIS (Bureau of Indian Standards), AERB (Atomic Energy...Work at office
MERIL
Vapi4 days ago - ...devices and screen sizes. Collaborate with UI/UX designers to implement designs into functional mobile apps. Participate in code reviews and provide constructive feedback to peers. Optimize application performance and improve user experience. Keep up-to-date with...
xira infotech - digital marketing & software development age...
Vapi20 days ago - ...Functional Collaboration Work closely with XR developers, designers, industrial designers, and product teams. Participate in design reviews, prototyping sessions, and usability testing. Provide technical insights to improve XR realism, interaction quality, and...
MERIL
Vapi4 days ago - ...guideline. Initiating and timely closing of all QMS like change control, Deviation, Investigation, CAPA & SOP. Preparation and review of GMP documents needed. Keep plant all time ready for cGMP, Regulatory and Customer audit. Execute packing activities in right...Interim roleImmediate startWorldwideShift work
Bayer
Vapi4 days ago - ...count and physical inventory reconciliation Analyze variances and share reports with operations and management Prepare monthly review presentations and performance summaries Ensure data accuracy, consistency, and compliance across systems Support warehouse and operations...
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Vapi2 days ago - ...Design History File (DHF) & Design Control Develop and maintain complete Design History Files (DHF) including design inputs, outputs, review records, verification, validation, and design transfer documents. Establish and maintain traceability matrices linking design inputs...Immediate start
- ...Coordinate with testing teams for performance validation, safety compliance (AERB / BIS / IEC 60601), and regulatory testing. Document and review test results to ensure design integrity and compliance with design inputs. 4. Documentation & Compliance Prepare and maintain...
MERIL
Vapi4 days ago
