ResponsibilitiesAnalysis of packing material, raw material samples as per method of analysis by adhering to the Regulatory Procedures. Sampling and analysis of water as per the procedures defineded. Works as a member of a team to achieve all outcomes. Performs all work in accordance with all established regulatory and compliance and safety requirements. Any other Responsibilities / Duties assigned by the Head of the Department / Designee as and when required. Performs all work in support of our Corporate values of perseverance, passion, collaboration and courage. Performs all work in accordance with all established regulatory and compliance and safety requirements. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned.Qualification & ExperineceMinimum Msc/Bpharm or any equivalent degree. Knowledge, Skills Abilities Effective command over verbal and written communication with good interpersonal skills Command on Microsoft-office (Word, Excel) Able to perform all the allocated tasks Well expertised in cGDP and cGLP. Best in effective planning of work activites to meet the time lines Experience: Minimum 3 to 6 years of experience in GMP regulated Pharmaceutical Industry

ResponsibilitiesQuality system management Implement and maintain a local quality system applying primarily to SwissMedic-regulated activities related to the import and distribution of products and controlled substancesAssure compliance with local regulations in Switzerland, international GDP / GMP requirements and the companyWrite SOPs and relevant documents, manage them in eDMS (electronic Document Management System) and support in implementation by training employeesQA GMP, systems: GMP and process trainings, personal file maintenanceProviding support to ensure inspection readiness and participation on internal audits and HA inspectionsQA POs executions in FioriProduct Quality ManagementPreparation of Market release of purchased or repacked products for Swiss Market:

ResponsibilitiesPerforming timely sampling and analysis of raw material, bulk product, intermediates, finished goods and other samples for Pharmaceuticals. Performing analysis of market complaints, Stability, process validation samples, Cleaning Validation of Pharmaceuticals. Good Laboratory Practice Performing calibration & maintenance of lab. Equipment and assisting for the qualification of laboratory equipment. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining record. Participating in Investigation of out of specification results, performing retesting. Maintaining laboratory raw data related to testing activity.Qualification & ExperienceEducation / Experience: Post Graduate in Science (Organic or Analytical Chemistry) 1 - 5 years in chemical & instrumental testing laboratory with exposure to GMP, GLP.

ResponsibilitiesReview of Master Documents Review and maintain Master Batch Manufacturing Records and Master Batch Packing Records to ensure accuracy, regulatory compliance, and alignment with approved specifications and process related changes. Coordinate with Production, QC, and Regulatory Affairs for timely updates and approvals. Annual Product Quality Review (APQR) Prepare, compile, and review Annual Product Quality Reviews (APQRs) in line with regulatory expectations. Support identification of improvement opportunities and follow-up of CAPAs arising from APQR findings. cGMP Training Coordination Coordinate and monitor cGMP and quality-related training programs for site personnel. Maintain trainingschedules, records, and effectiveness assessments.Qualification & ExperienceBachelor’s or master’s degree in pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline. Experience 1–5 years of relevant experience in Pharma Quality Assurance / Documentation

Responsibilities Planning and Execution of all Microbial and mammalian upstream related processes and lab activities.  Designing and executing experiments for yield and Quality improvement and process intensification of current commercial microbial and mammalian products and protocol based batches execution.  An executive with extensive expertise in Biologics (Upstream) Development & Manufacturing: Product Technical Life Cycle Management.  Collaborate with cross-functional teams to facilitate the transfer of upstream processes from development to manufacturing.  Provide technical expertise in upstream bioprocessing, to optimize manufacturing processes.  Work closely with development teams to gather and document critical process parameters and data for successful transfer.  Collaborate with Quality Assurance to ensure compliance with cGMP and other regulatory standards.  Participate in process validation activities and support the resolution of deviations or discrepancies.Qualification & ExperienceEducation: Master’s in Biotechnology, or related field. Relevant professional / Educational background 3+ years in biopharma manufacturing in MSAT or process improvement roles.

Responsibilities Achievement of set targets. Maintaining set call Average/coverage. Complete use of allotted resources. Increasing prescriber base Focus on target customers. Maintaining call average and customer coverage Increasing PCPM. Timely reporting. Ensuring ROI  Relationships around the role  Reporting to (Business) Regional Sales Manager / Sr. Regional Sales ManagerQualification & ExperienceDesirable - B.Pharm / D.Pharm / BSc. + MBA Essential - Graduates in any discipline Experience: 6 Months. to 2 years as a Medical Rep in a reputed organization.

ResponsibilitiesMaintaining set call Average/coverage. Complete use of allotted resources. Increasing prescriber base Focus on target customers. Maintaining call average and customer coverage Increasing PCPM. Timely reporting. Ensuring ROIQualification & ExperienceDesirable - B.Pharm / D.Pharm / BSc. + MBA Essential - Graduates in any discipline Experience: 6 Months. to 2 years as a Medical Rep in a reputed organization.

Qualification & Experience          Department : Critical Care Qualification : MD/DNB in Anesthesiology             Experience : 0-3 Years

Qualification & Experience          Qualification : MBBS (FMGE Qualified) / B.Sc Physician Assistant Course                         Experience : Freshers / Experienced        

Qualification & Experience               We are hiring for a Nephrologist (DM/DNB) at JEEVAN REKHASUPERSPECIALITY HOSPITAL