ResponsibilitiesDevelop and apply image analysis, computer vision, and machine learning methods for digital pathology datasets. Design and implement analysis pipelines for whole-slide imaging (WSI), H&E, IHC, multiplex immunofluorescence, and spatial omics datasets. Build reproducible and scalable workflows using Python and modern ML/DL frameworks such as PyTorch or TensorFlow. Perform tissue segmentation, cell phenotyping, feature extraction, and spatial analysis using state-of-the-art computational approaches. Collaborate with pathologists and translational teams to interpret image-derived biomarkers and biological findings. Contribute to evaluation, validation, and benchmarking of image analysis algorithms and workflows. Support deployment and operationalization of computational imaging pipelines in cloud or high-performance computing environments. Stay current with advances in computational pathology, AI/ML, and spatial biology technologiesQualification & ExperiencePhD or MS in Computer Science, Biomedical Engineering, Computational Biology, Bioinformatics, Electrical Engineering, Applied Mathematics, or related quantitative discipline. Strong background in computer vision, image analysis, and machine learning/deep learning. Demonstrated experience working with biomedical imaging data (pathology preferred).

ResponsibilitiesPeriodic review and updates to quality agreements to ensure alignment to Amgen expectations and to address needs depending on material type. Documentation review and approval including: supplier manufacturing records, investigation reports, Amgen quality records, and validation records (process & analytical) . Evaluation and documentation of raw materials and devices for changes to incoming inspection profiles Oversight and completion of supplier assessments and documentation to support product complaints. Ownership of supplier metrics, performance assessments, and other key documents to inform the health of supplier relationships. Review and approval of change control records for supplier changes. Management of supplier audit records, ensuring on time completion and CAPA closeout activities are documented with appropriate closeout evidence. Prepare, review and approve SOPs and other GMP/GDP documentation in compliance with corporate and regulatory requirements, to ensure alignment with procedures, current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP) and other applicable regulations. Take part in operational and quality improvement initiatives, programs, and projects. Develop solutions that are thorough, practical, and consistent with functional objectives This role may require working in shifts or extended hours within the same shift to support global time zones.Qualification & ExperienceMaster’s degree with 10 years of experience in manufacturing and quality management systems or a related field OR Bachelor’s degree with 12 to 13 years of experience in quality management systems or a related field 

Responsibilities Manager - Quality AssuranceJob Description Candidate should have good communication skill Must have Regulatory Knowledge and audit handling exposure Must have working exposure of Cleaning Validation and respective work area's Must have sound knowledge of Non-sterile dosage forms Having work experience of preparation of Risk Management, Cross-contamination control strategy etc. Handling of Change Management system 

ResponsibilitiesResponsible for managing QA documentation, ensuring GMP compliance, and supporting quality systems through effective handling of SOPs, BMR/BECR review, validation and qualification activities. Oversees document control, vendor qualification, calibration and maintenance coordination, and ensures timely closure of deviations, change controls, and CAPAs while maintaining data integrity and audit readiness across all QA operations. Issuance, archival and retrieval of documents. Issuance of Control coples to respective dept. Destruction of the GMP documents once the retention term has passed and controlled coples of the obsolete GMP documents. Tracking of all QA documents. 5. Maintaining backup of QA softcoples. Maintaining SOP/s with proper indexing. Preparation and review of SOPs Management of QA Stationary (Controlled Coples and logbooks) Dispatch and line clearance activity.

Responsibilities Achieve monthly, quarterly, and annual sales targets for assigned products within the designated territory.  Develop and implement effective sales strategies and action plans to maximize market penetration and achieve business objectives.  Identify and cultivate strong relationships with key customers, including doctors, pharmacists, hospitals, and other healthcare professionals.  Conduct regular market visits to understand customer needs, gather market intelligence, and identify new business opportunities.  Promote and present Piramal Pharma's product portfolio to healthcare professionals, effectively communicating product benefits and features.  Organize and participate in medical camps, CMEs (Continuing Medical Education), and other promotional activities to enhance product visibility.  Monitor competitor activities and market trends, providing regular feedback to the sales management team.  Manage and optimize resource allocation, including promotional materials and samples, to ensure efficient sales operations.  Prepare and submit timely and accurate sales reports, forecasts, and other required documentation.  Ensure compliance with all company policies, ethical guidelines, and regulatory requirements.Qualification & Expeirence Bachelor's degree in Pharmacy, Science, or a related field.  Minimum of 2-4 years of proven experience in pharmaceutical sales, preferably in a similar role.  Strong understanding of the pharmaceutical market and healthcare industry dynamics.  Excellent communication, presentation, and interpersonal skills.  Demonstrated ability to build and maintain strong customer relationships.

Responsibilities Responsible to monitor the Analytical data review performed by review team. Responsible to monitor the investigations performed by QC investigation team. Review & Approval of Lab events, Out of specification results (LIRs), Out of trend (OOTs), Deviations, Anomalous results Investigation reports. Coordination with cross functional departments for smooth functioning of analytical activities. Review and approval of deviations in Track wise. Review and approval of Certificate of analysis (COAs). Review and approval of Specifications in LIMS and approvals of SOPs and STPs. Monitoring of stability studies activities, Review and approval of shelf life certificates & Protocols. Approval of protocols & reports of analytical method validations, verifications, Transfers and risk assessment reports. Approval of certificate of analysis of reference standards & Impurity standards. Preparation/Approval of SOPs and forms related to analytical activities. To perform Change control impact assessments and approvals in Trask wise. To perform un-announced Realtime checks and Internal audits as per the Schedule. Managing of Customer Request Samples activities. Coordination and providing the support for Business development and regulatory affairs activities. Batch release in SAP for Raw material, Solvents, Operational supplies (Packaging Materials, Filter bags etc..). Participate and lead performance conversations with employees, including monthly one on ones, to connect on performance; check in on employee's progress toward achieving Objectives, offer support and remove barriers; and, communicate and revisit performance expectations to reinforce and encourage high performance culture and a safe working environment for all employees. Utilize open, honest, two way communication to build trust-based relationships with employees, business partners .and direct leader while continuously improving leadership capabilities by personally seeking feedback and development. Create a culture which values trust and provides the opportunity for Employee development and growth in pursuit of our purpose and demonstrating our core Values - Collaboration, Courage, Perseverance and Passion. Utilize your networks to attract and hire talent in a comprehensive, differentiated and consistent manner essential to our continued growth; then, onboard new employees by providing a consistent experience that reflects the values and commitments made to candidates during the hiring process.Qualification & ExperienceM.Sc./ M. Pharma Experience 10 to 12 year experience, with demonstrated skill in preparation of protocol and reports, monitoring of process validation, etc.

Responsibilities Initiate Master Manufacturing Records (MMaRs) & Master Packaging Record (MPaRs) Initiate Placebo and Optimization batch record for trails. Initiate Change Controls in QMS Track Wise for New Launch / Site Transfer / Submission batch / SOPs / Formats and commercial batch documents. Ensure QMS Change control closure within the stipulated timeline. Ensure support for timely completion of Investigations for document related deviations and document revision based on CAPA. Initiation of batch documents , SOPs and Formats in Content server. Check Monthly Schedule to ensure document readiness. Ensure all changes are aligned with cGMP regulations and corporate SODs. Perform all work in accordance with established regulatory, compliance and safety requirements. Coordinate with NPL and RA regarding Deficencies from Regulatory Agencies and Clarifix. Develop and maintain effective working relationships with internal and external customers. 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 & ExperienceMinimum Bachelor of Pharmacy / Science or any equivalent degree. Experience Minimum 1 year of experience in GMP regulated pharmaceutical industry.  Knowledge, Skills and Abilities Adequate knowledge in handling QMS Trackwise tool, Content server tool.

Responsibilities Sampling of Raw Materials, Packing material, Intermediates and Finished Products. Execution of Method validation / Method transfer activity. Maintaining & monitoring of all the analytical method validation, cleaning validation and method transfer documents. Preparation and standardization of volumetric solutions. Calibration of all analytical instruments on need basis. Raw Materials, In-Process, packing materials, Intermediates, Finished Products and stability samples analysis on need basis. Performing Recertification of standards and impurities as required. Upkeep of laboratory cleanliness, ensuring compliance to good laboratory and safety practices. Coordination with other departments for smooth functioning of activities. Documentation of all works as required as per relevant Standard Operation Procedure (SOP).Qualification & ExperienceMinimum M. Sc. in Chemistry Knowledge, Skills and Abilities Demonstrated ability to solve and trouble shoot problems based on the analysis, experience and judgement. Excellent understanding of business and supporting technology related to the Pharmaceutical industry. Excellent Knowledge and Experience with regulatory Compliance. Strong motivational skills allowing to function independently as well as a proven ability to motivate others. Knowledge on LIMS/ Trackwise / SAP. 

Responsibilities Achieve monthly, quarterly, half yearly and yearly sales target by promoting company's products ethically to customers as per the business plan, also ensure Doctor / Customer Call average as per the customer management plan of the division  Organizing Camps (CME) as per the division strategy and customer needs  Facilitate the process of successful new product launch.  To create and update customer list as per the therapy and product of the division.  Ensure Ipad adoption (if applicable) as per division norms and adherence to CLM callsQualification & ExperineceBSc/ B. Pharm or Any Graduate with minimum 2 years of prior experience as a Medical Representative

Responsibilities Achieve monthly, quarterly, half yearly and yearly sales target by promoting company's products ethically to customers as per the business plan, also ensure Doctor / Customer Call average as per the customer management plan of the division  Organizing Camps (CME) as per the division strategy and customer needs  Facilitate the process of successful new product launch.  To create and update customer list as per the therapy and product of the division.  Ensure Ipad adoption (if applicable) as per division norms and adherence to CLM callsQualification & ExperineceBSc/ B. Pharm or Any Graduate with minimum 2 years of prior experience as a Medical Representative