ResponsibilitiesA Quality Manager ensures healthcare services meet rigorous safety, regulatory, and accreditation standards .Ensure all hospital operations and clinical practices align with regulatory requirements and accreditation standards (such as JCI, NABH, or ISO). Implement performance improvement initiatives to optimize clinical care, reduce risks, and enhance overall patient satisfaction QualificationsMasters in Hospital Administration or MBA , Familiarity with ISO 9001/17025 is essential, and certifications like Six Sigma are highly beneficial, NABH, NABL, JCIA Audits. Strong leadership, analytical, decision-making, and communication skills.

Responsibilities Checking and verification of Dispensing of materials and label generations as per approved procedures including Cross check of material identity and quantity Supervise dispensing activity to ensure compliance with Good Dispensing Practices and cross-contamination prevention measures. Coordinate with production and QA for line clearance and material reconciliation. Ensure all transactions are documented in e-logs and other software systems Ensure all transactions are done under controlled environment conditions including monitoring of daily environment records Ensure the cleaning of the area along with preparation of sanitation solutions and maintain proper records. Conduct calibration/daily verification of Weighing balances and other equipment as per SOP and schedule. Perform the dispensing of solvent materials. Perform QMS activity related to warehouse. Qualification & ExperienceQualification: -BSC /B. Pharm /D. Pharm or equivalent Experience of NLT 2 years Should have exposure to handling of SAP systems.

ResponsibilitiesWell versed in the analytical review which includes review of GLP, OOS, OOT, CAPA, Deviation, Incident and Change Control. Review of analytical documents and electronic records which include worksheet, chromatograms, AMT/AMV, FP/IP/Audit trails/Qualification data of instruments, Analysts. Preparation of Standard operating procedures and harmonization of the practices. To review and approve the Certificate of Analysis received from QC for Finished Product. Support batch release activities. Retention sample management.Qualification & ExperienceMust be qualified minimum in B. Pharm/M. Pharm/M.Sc.(Chemistry or relevant) Must have sound knowledge on handling HPLC, GC, KF, FTNIR, FTIR Exposure to regulatory audits from various regulatory bodies like US FDA, MHRA, TGA, ANVISA

ResponsibilitiesTo perform physical and chemical, instrumental analysis of Raw Material, packaging material, Water samples, In Process, Finished Product Samples and Stability Samples. The candidate should have experience on HPLC, GC UV, IR and Dissolution testing. To perform a Release testing, Dissolution profile study, challenge study ,Hold time study, RLD sample analysis, validation, verification, method transfer activity and API-Verification as when applicable. To perform instrument calibration and working standard qualification. Responsible to adherence of GLP and Health, Safety Environment system in Laboratory. To perform the task assigned by the supervisor/HOD as and when required. Should have good written and communication skill.Qualification & ExperienceBachelor / Master Degree of Science / Pharma. The candidate should have experience on HPLC / GC / UV / IR / KF / Dissolution etc. He should have exposure of QC working under GLP, GDP, GMP environment. The candidate having experience in US-FDA approved company is more preferable.

ResponsibilitiesAchieve sales targets in assigned territory Strengthen engagement with key healthcare professionals Deliver impactful scientific discussions Provide clinical insights to support evidence-based decisionsQualification & ExperienceBachelor’s in Pharmacy / Life Sciences 5–14 years pharmaceutical sales experience Must have Oncology field sales background Strong communication & relationship?building skills

ResponsibilitiesEvaluate and review clinical and commercial drug batches to ensure quality. Ensure product and process documents meet established specifications through rigorous sampling and statistical process control. Identify and address deviations from manufacturing and packaging standards. Approve investigations and oversee change control activities to maintain compliance with configuration management policies. Contribute to project tasks and milestones, organizing work to meet deadlines. Learn and apply basic team effectiveness skills within the immediate work team. Make decisions within limited options to resolve basic problems under supervisor's direction. Ensure manufacturing and packaging records conform to Pfizer policy and cGMP standards. Maintain inspection readiness, support regulatory and customer inspections, and improve quality assurance systems. Assist manufacturing/packaging staff in real-time compliance error detection and resolution, and lead or participate in Quality Risk Management assessments. Qualification & ExperienceBachelor's Degree in Sciences/ Pharmacy with Minimum 4-5 years in Pharma/ Biotech or Master's Degree in Sciences/ Pharmacy with Minimum 2 to 3 years in Pharma/ Biotech Experience in the pharmaceutical industry and Quality administered systems Sound knowledge of current Good Manufacturing Practices (part of GxP) Ability to work effectively in a team environment, both within one's own team and interdepartmental teams Effective written and oral communication skills

Qualification & Experience          Qualification: B.Sc in Cardiac Care Technology            Experience: Minimum 5 years         

Qualification & Experience    Qualification: M.Sc / B.Sc Nursing             Experience: Minimum 10 years             

Qualification & Experience           Qualification: B.Sc / Diploma in Operation Theatre & Anaesthesia Technology                        Experience: Minimum 5 years        

Qualification & ExperienceQualification: MPT (Cardiology) Experience: FreshersNote: Male Candidate is Preferred