- 1203
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Active Jobs Found
(Last Updated: Jun 04, 2026)
- 2+ years
- Not Disclosed
- Mangalore, Karnataka, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
- 2+ years
- Not Disclosed
- Mangalore, Karnataka, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
Qualification & ExperienceExperience Required : Minimum 2-3 years experience in the health care sectorQualification Required : • M. Sc/ B. Sc or PG Diploma in Diet
- Others
- 8+ years
- Not Disclosed
- Cuttack, Orissa, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
- 8+ years
- Not Disclosed
- Cuttack, Orissa, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
Qualification & ExperienceThe Deputy Nursing Superintendent supports the Nursing Superintendent in managing nursing operations, supervising staff, maintaining patient care standards, and ensuring compliance with nursing protocols. Experience: 8 - 10 Years Education: UG: B.Sc in Any Specialization
- Nurse
- 2+ years
- Not Disclosed
- Cuttack, Orissa, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
- 2+ years
- Not Disclosed
- Cuttack, Orissa, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
Qualification & ExperienceWe are hiring a Critical Care Intensivist (MBBS) with minimum 2 years of ICU experience to manage critically ill patients, monitor vitals, handle emergencies, coordinate with teams, and ensure timely documentation and patient care.Experience: 2 - 5 Years Education: UG: MBBS in Any Specialization
- mbbs
- 2+ years
- Not Disclosed
- Nalagarh, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
- 2+ years
- Not Disclosed
- Nalagarh, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
ResponsibilitiesResponsible for verification of receipt documents and vehicle, de-dusting of materials and physical verification of materials and GRN preparation. To update status labelling on materials. All time readiness for any audit conducted for warehouse. Responsible to store the materials as per their storage conditions. Responsible for arrangement of materials as per their status i.e. Quarantine, Approved, Re-test, Rejected and expired (but not limited to). To perform preparatory work for dispensing i.e. Line clearance of dispensing area and verify to be dispensed materials as per request/process order. To dispense right material with right quantity as mentioned in request/process order. To perform palletization activity and placement of data logger as per market requirement. To perform vehicle verification, loading and dispatch of finished goods. To issue, handle, storage and retrieval of warehouse documents. To perform authentic documentation at every point of time as per cGMP. To perform operation & cleaning of warehouse related equipment's as available i.e. weighing balance, RLAF, Vacuum cleaner, Order picker, stacker, rack, mobile LAF, freezer, refrigerator (but not limited to) as per SOP. To develop, implement new process and system in the warehouse as per cGMP for smooth working. Responsible for safety in department, also encouraging others for "be safe and keep safe" and reporting of near miss and accident.
- Quality control
- clinical research
- Operations
- Management
- 10+ years
- Not Disclosed
- Chhatrapati Sambhajinagar, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
- 10+ years
- Not Disclosed
- Chhatrapati Sambhajinagar, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
ResponsibilitiesResponsible for maintaining Microbiology laboratory in a State of All time Audit readiness. Responsible for Review of GLP documents like List of instruments, Calibration Schedule, AMC schedule, Trends, Annual summary but not limited to in both microbiology laboratories. Initiation & Investigation of Microbial Excursions, OOS, deviation, change control, Incident related to QC- Microbiology and cross functional Team. To ensure & testing, reporting & timely release of Microbiological samples like SFG, FG, Raw materials, In process, Intermediate, stability and packing materials, compressed air, swab samples of OSD facility, Inhaler & foam facility and Nasal facility. To ensure Periodic requalification of instrument/ equipment. Execution of Microbiological method validation verifications/ Miscellaneous studies. To ensure the working area / instruments cleanliness, and proper filing of documents and storage of the same at the respective place. Up keeping the all documents of with online entries. Maintain the ATR in Microbiology laboratory. Procurement, receipt, revival and maintenance of standard cultures. Identification and maintenance of isolated microbial cultures. Up keeping of all the documents with online entries. Review of all analytical and related documents like logbooks, TDS, protocol, report but not limited to. Review of all analytical and related documents like logbooks, TDS, protocol, report and SOPs but not limited to. Responsible to face internal and external inspection and provide compliance to audit observations. Act as an SME for Microbiology related events. Responsible to impart technical trainings to concerned staff related to Microbiology topics.Qualification & ExpeirenceM. Sc.Years of experience: 15 to 20 Years
- Quality control
- clinical research
- Operations
- Management
- 10+ years
- Not Disclosed
- Mumbai, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
- 10+ years
- Not Disclosed
- Mumbai, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
ResponsibilitiesHead the Safety Evaluation And Risk Management Team Author/review/approve safety reports and maintain oversight Contribute to the development and implementation of Risk Management Plans including authoring/review/approval Review and oversight of Signal detection and evaluation activities Liaise and collaborate with other GPV functions, Global Glenmark affiliates and external business partners Review draft responses to regulatory authority/healthcare professionals queries as applicable Review literature search results for ICSRs and articles for inclusion in safety reports Participate in governance meetings Support product labelling activities Support audits, inspection and CAPA management relating to SERM activities Support assessment and implementation of regulatory intelligence impacting SERM activities Provide technical guidance in the development and maintenance of procedural documentation Support organizational initiatives in driving global operational excellence in Pharmacovigilance Support the QPPVsQualification & ExperienceMD/MBBSYears of experience: 16-18 years
- mbbs
- MD
- hospital management
- 10+ years
- Not Disclosed
- Mumbai, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
- 10+ years
- Not Disclosed
- Mumbai, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
Responsibilities Facilitate the implementation and support of SAP Quality Management for SUN Pharma entities operated in SAP - ECC and S4 HANA including 3rd Party System Integrations. Perform detailed analysis of complex business process requirements and provide appropriate system solutions; identify, interpret, validate and document customer requirements. Facilitate workshops to collect business requirements. Map client business requirements, processes and objectives; develops necessary product modifications to satisfy customer’s needs. Design, customize, configure and testing of the module. Identify gaps, issues and work around solutions. Act as liaison with internal customer for troubleshooting: investigate, analyse, and solve software problems. Handle changes or emergency transports as needed for high priority issues; Document functional designs, test cases and results. Proactively identify and propose business process and/or system enhancements. Provide consulting services on both new implementations and existing support projects. Act as a liaison between the business functions and the technical team. Provide ad-hoc training and user support as required. Work self-directed and independently; may act as subject matter mentor to more junior members.
- Quality control
- Inspection
- Management
- 3+ years
- Not Disclosed
- Tandalja, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
- 3+ years
- Not Disclosed
- Tandalja, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
ResponsibilitiesLiterature search and study designing of Bioavailability and Bioequivalence studies of oral & non-oral products towards different regulatory submission. Review of BA/BE study protocol and provide Pharmacokinetic (PK) inputs into the study protocols Coordinate with the CRO for finalizing pilot and pivotal biostudy protocol for DCGI BE application. Develop protocol for patient based BA/BE studies & PD end point study for complex generics. Perform PK and Statistical analysis of in-vivo data obtained from BA/BE and pharmacokinetics studies using Phoenix Software. Use modeling & simulation tools for study optimization. Respond to regulatory queries related to PK analysis and study interpretation. Qualification & ExperienceGraduate : M.Pharm /Pharm D Experience Tenure : Minimum 3 years of relevant experience
- Drafting
- Management
- Communication
- 4+ years
- Not Disclosed
- Chennai, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
- 4+ years
- Not Disclosed
- Chennai, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
ResponsibilitiesPerform various tests and analyses related to Hematology in a laboratory setting. Support the Clinical Development team with scientific expertise for oncology and hematology projects. Provide application support for Hematology products and assist with biochemistry roles. Qualification & ExperienceBachelor's degree in a related field. 4-5 years of experience in Hematology or a similar role. Strong knowledge and experience in Hematology testing and analysis. Excellent communication skills and ability to work in a team. Ability to provide scientific support to cross-functional teams.
- clinical research
- mpharm
- Communication
- 3+ years
- Not Disclosed
- Chennai, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
- 3+ years
- Not Disclosed
- Chennai, India
- Post Date: May 19, 2026
- End Date: Jul 19, 2026
ResponsibilitiesProvide direct patient care in the operating room setting. Assist the surgical team throughout the perioperative process. Maintain a sterile field and ensure the readiness of surgical equipment. Monitor patients' vital signs and assist with anesthesia. Collaborate with the multidisciplinary team to deliver high-quality patient care. Follow hospital policies and procedures to uphold a safe environment.Qualification & ExperienceProven experience working as a Staff Nurse in the operating room. Valid RN license and BLS certification required. Strong understanding of surgical procedures and protocols. Excellent communication and interpersonal skills. Ability to work effectively in a fast-paced, high-pressure environment. Commitment to upholding the highest standards of patient care.
- clinical research
- mpharm
- Communication
- Nurse

