Average salary: Rs360,000 /yearly
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Rs 2 - 3.5 lakhs p.a.
...Description We are seeking detail-oriented Documentation Executives to join our student support team in India. The ideal candidate will manage application forms, documentation and verification for students applying to medical colleges in India and abroad. Medipedia...SuggestedLong term contractOverseas- ...experienced Sr. Technical Writer with 8+ years experience to join our organization who will be the evangelist in crafting elegant technical documents that can be easily understood by a wide range of audience. You must have a passion to understand how Payments software products work...SuggestedFull time
Rs 3 - 6 lakhs p.a.
..., Hyderabad(Vizag) Experience: 35 Years Department: Computer System Validation (CSV) Required Skills: LIMS Validation CSV Documentation LabSolution Software Validation IQ, OQ, PQ Execution Manufacturing System Validation Good knowledge of validation protocols...SuggestedImmediate start- ...other GEA granulation line equipment. Responsible for recording of activity in logbooks, Batch manufacturing record & complete documentation as required in the manufacturing of product and the cleaning of facilities and equipment, following cGMP's and good documentation...SuggestedImmediate start
- ...Quality Control, and Maintenance teams for smooth shift operations. ~Ensure correct chemical and dye dosing, material handling, and documentation. ~Manage manpower allocation, productivity, and machine utilization during the shift. ~Maintain records for batch processing,...SuggestedFull timeShift work
- ...faculty at the Baddi Campus Counsel and assist students individually at the Office of International Affairs Maintain accurate documentation, data records, and submit monthly reports (hard copy and electronic) Maintain and update the OIA office space with relevant...SuggestedWork at office
- ...management in inventory/Information management software of QC like LIMS software. Having adequate knowledge of preparation of the QC documents like SOPs, Protocols and general documentation. Having adequate knowledge of Pharma Industry Guidelines and Pharmacopoeias....Suggested
- ...reagents and buffers in alignment with the testing plan and ensuring the availability of equipment for analysis. • Your role involves documenting activities contemporaneously, adhering to Good Documentation Practices and compliance expectations, and conducting self-checks post...SuggestedRelocation packageShift work
- ...cross-functional teams such as Quality Assurance and Regulatory Affairs. The role also involves mentoring junior staff, maintaining documentation, and staying current with emerging industry trends. Qualifications Expertise in formulation development, process...SuggestedFull time
- ...verification & labelling. # Routine calibration and verification of all instruments. # Logbooks verification. # To ensure that the documentation done is online and error free. # To ensure the correctness of the document before submitting it for the review of Group Leader/...Suggested
- ...relations. Ensure statutory compliance as per labor laws and USFDA regulatory expectations. Handle audits, inspections and documentation related to HR compliance. Manage payroll coordination, compensation benchmarking and HR budgeting. Lead learning & development...Suggested
- ...analytical testing for water and effluent parameters. ~Hands-on experience with ETP instrumentation and chemical handling. ~Good documentation and reporting skills. ~Awareness of environmental and pollution control norms. ~Teamwork, attention to detail, and safety-...SuggestedFull timeShift work
- ...down options: Ability to view department-specific or batch-specific data for detailed analysis. 10. Regulatory Compliance and Documentation: • Ensure production schedules are compliant with regulatory requirements. • Maintain records of planned vs. actual production...SuggestedShift work
- ...identified spares procurement for machines and equipment. Review of root cause analysis for major breakdowns. To ensure good documentation practices in department. To ensure cGMP compliance at workplace. To prepare and review reports and MIS data. Vendor...Suggested
- ...URS), Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) documents for: Facility and utility systems (HVAC, water systems, compressed air, etc.) Manufacturing and laboratory equipment...Suggested
Rs 11.5 - 19 lakhs p.a.
...preventive maintenance for all production equipments and instruments with engineering / QA / QC & outside agencies. To carry out routine documentation as per Regulatory Requirements. To work within the specified working hours. To ensure maintenance of production area and...- .... . Identify and address recurring problems either with the quality of the product or the reliability of testing procedures. . Document quality issues and performance measures for management review. . May liaise with external vendors. QUALIFICATIONS Education...Shift work
- ...Oversee complete ZLD operation including RO, MEE, ATFD, etc. Maintain daily records of chemical consumption and water balancing. Document treated water results and ensure compliance with statutory norms. Support audits, inspections, and environmental compliance...Full time
- ...Firefighting and emergency equipment. Ensure smooth operation of ETP meeting statutory compliance. Compliance of the all related QMS documents. Assure all-time readiness at sites for inspections and appropriate implementation of corrective actions regarding observations made...
- ...experience with GAMP, 21 CFR Part 11, GxP, IQ/OQ/PQ, and validation of manufacturing systems (SCADA, HMI, PLC, etc.). Conducting and documenting Computer System Validation (CSV) activities in pharmaceutical/life sciences environments. Prior experience working with...Immediate start
- ...Computer System Validation (CSV) activities as per GAMP-5 and 21 CFR Part 11 Preparation and execution of URS, FS, DS, IQ, OQ, PQ documents Validation of PLC, SCADA, DCS, MES and LIMS systems Risk assessment, impact analysis and change control documentation Review...Immediate start
- ...To ensure the availability of current versions of the Specifications, Standard test procedures & work sheets are available in Documentation section. Drive continual improvement in business process/ operations with focus on business plan/ strategies. To identify the...
Rs 4 - 12 lakhs p.a.
...performance across devices. • Adapt animations based on feedback and project requirements. • Maintain organized animation assets and documentation. Mandatory Key Skills • animation • 2d animation • game design • special effects • 2d • game engine •...- ...completion of new initiatives. Champion energy conservation and sustainable practices within plant operations. Ensure proper documentation, QMS compliance, and ERP/SAP system usage across departments. Maintain and present MIS reports on monthly, quarterly, and...Full time
Rs 4 - 20 lakhs p.a.
...audio assets for spins, wins, bonuses, UI interactions, and special features Optimize audio for performance across platforms, including mobile and desktop Participate in audio testing, mixing, and troubleshooting Maintain organized audio libraries and documentation....- ...team responsible for conducting sampling and analysis of packaging and raw material samples. The role involves ensuring accuracy in documentation, adherence to safety procedures, reporting discrepancies, and maintaining lab safety. ' Roles & Responsibilities You will be...Relocation package
- ...Higg FSLM (Facility Social & Labor Module). Ensure all relevant certifications (e.g., GOTS, GRS, OCS, RCS) are up to date, and documentation is complete for renewals and surveillance audits. Support internal teams in meeting sustainability performance targets and continuous...Full time
Rs 2 - 9 lakhs p.a.
...standards. Collaborate with cross-functional teams to address quality issues and implement solutions. Prepare and maintain documentation related to quality assurance activities. Analyze testing results and provide feedback to improve product quality. Stay updated...- ...respect to Abbott Quality guideline, other applicable regulatory guidelines and standard operating procedures at site. Ensure that Good Documentation Practices shall comply during the production process. 5. To check/ review/verify operation of manufacturing machine as per...
- ...Approve job descriptions, assign responsibilities, and develop QC team members through training. # Review and approve analytical documentation ensuring cGMP, cGLP, ALCOA++ compliance, and data integrity. # Prepare, review, and approve QMS activities including OOS, OOT,...
