ResponsibilitiesMonitoringofDP,RHandtemperatureintheirComponentpreparationandsterilizationarea(Autoclave area). ResponsibleforMaintenanceandcleaningofComponentpreparationandsterilizationarea(Autoclave area). TomaintaintheBMRsandotherlogbooksintheComponentpreparationandsterilizationarea (Autoclave area) as per cGMP and SOP. OperationandcleaningofdynamicpassboxinComponentpreparationandsterilizationarea(Autoclave area). CleaningandsanitizationofdrainpointsinComponentpreparationandsterilizationarea(Autoclave area). Preparation,filtrationandissuanceofdisinfectantanddeactivationsolutionstoallthesectionsinthe production area. Operation and cleaning of glove and filters integrity testers Responsible for cleaning and storage of all the filling machine accessories and change parts. Operation and cleaning of table mounted LAF and Ceiling mounted LAF. Operation and cleaning of steam sterilizer and HPHV steam sterilizer. PreparationofloadsmeantforAutoclavinglikegarments,disinfectant,filling,filtration,rubberstopperand seals for sterilization as per the validated load pattern. Responsiblefortheco-ordinationwithcrossfunctionaldepartmentslikeQA,QC,warehouseEngineering, HR and administration for the day to day activities. ResponsiblefortimelycompletionofcalibrationsandvalidationsincoordinationwithEng.andQArelated to Component preparation and sterilization area (Autoclave area). TimelycompletionofSOPstrainingandonthejobtrainingsrelatedtoComponentpreparationand sterilization area (Autoclave area).

ResponsibilitiesDeveloping and executing validation plans, protocols, and reports for software, systems, and processes to ensure compliance with regulatory requirements. Collaborating with IT, QA, and operational teams to assess validation needs and establish best practices in validation methodologies. Conducting risk assessments and impact analyses to identify potential issues and recommend appropriate validation strategies. Documenting validation activities and maintaining accurate records to support audits and inspections. Providing training and guidance to junior analysts, fostering a culture of quality and compliance within the team.Qualification & ExperienceBachelor's degree in Life Sciences, Engineering, Computer Science, or a related field. Extensive experience in validation activities within the healthcare, pharmaceutical, or clinical research sectors. Strong knowledge of regulatory requirements (e.g., GxP, FDA, EMA) and validation best practices. Excellent analytical and problem-solving skills, with a keen attention to detail and accuracy.

ResponsibilitiesLead and execute complex scientific clinical data review at both trial and program levels. Collaborate closely with SRP/SRS to review data, resolve eDC queries, and ensure data accuracy and completeness. Oversee data flows and Data Management Plans while performing continuous, in-depth data review activities. Contribute to protocol design and provide input into eCRFs and data collection tools. Align data review expectations and timelines with SRP/SRS, GDM, CROs, and cross-functional stakeholders. Define data quality standards, conventions, and ensure timely delivery of all CDM milestones. Develop and maintain key documents such as the Integrated Review Plan, ensuring regulatory compliance. Ensure inspection readiness and actively support audits and health authority inspections. Provide program-level leadership by supporting DMLs in planning, resource allocation, and cross-functional collaboration. Drive quality and continuous improvement by implementing best practices and leading process, system, and tool enhancementsQualification & ExperienceBachelor’s degree in Life Sciences or related field with 5+ years of Clinical Data Management experience, including strong expertise in scientific data review. Solid experience in clinical drug development with deep understanding of data flows, data review processes, and ICH-GCP regulatory requirements. Proven leadership capabilities at study or program level, with experience in stakeholder and resource management. Strong collaboration skills with the ability to work effectively with physicians, scientists, CROs, and global cross-functional teams. Proficiency in eDC and clinical data systems, combined with strong analytical, communication, and problem-solving skills and a quality-driven, continuous improvement mindset.

ResponsibilitiesWorking independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required. Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff. Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.Qualification & ExperienceUniversity degree in medicine, science, or equivalent Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data Excellent written and verbal communication in English Good social skills enabling you to deal with queries in a timely manner Willingness to travel as required (approximately 60%) Oncology studies experience is must

Responsibilities Develop and implement strategic sales plans to achieve and exceed assigned sales targets for a specific product portfolio.  Identify and cultivate new business opportunities with healthcare professionals, including doctors, pharmacists, and hospitals.  Maintain and strengthen existing customer relationships through regular visits, effective communication, and product presentations.  Educate customers on product features, benefits, and clinical data, addressing their inquiries and concerns effectively.  Monitor market trends, competitor activities, and customer feedback to identify opportunities and challenges.  Prepare and submit regular sales reports, forecasts, and expense reports accurately and on time.  Collaborate with marketing and medical teams to ensure effective product promotion and support.  Participate in sales meetings, training programs, and medical conferences as required.  Adhere to all company policies, ethical guidelines, and regulatory requirements.Qualification & Expeirence Bachelor's degree in Pharmacy, Science, or a related field.  1-3 years of proven sales experience in the pharmaceutical industry.  Demonstrated ability to achieve and exceed sales targets.  Excellent communication, interpersonal, and presentation skills.  Strong negotiation and persuasion abilities.  Ability to work independently and as part of a team.  Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

ResponsibilitiesLead and execute process validation activities, including protocol generation, execution, and report writing for new and existing products. Provide technical expertise and troubleshooting support for manufacturing operations, resolving deviations, and implementing corrective and preventive actions (CAPAs). Participate in technology transfer activities for new products and processes from R&D to commercial manufacturing. Conduct process optimization studies to improve yields, reduce cycle times, and enhance product quality. Collaborate with cross-functional teams including Production, Quality Assurance, Quality Control, and R&D to ensure seamless execution of projects. Prepare and review technical documents, including batch records, specifications, and standard operating procedures (SOPs). Support regulatory submissions by providing necessary technical data and documentation. Stay updated with industry best practices, regulatory guidelines (e.g., cGMP, ICH), and new technologies in pharmaceutical manufacturing. Participate in investigations of critical quality events, out-of-specification (OOS) results, and customer complaints.Qualification & ExperienceBachelor's degree in Chemical Engineering. 5-8 years of experience in a Technical Services, Process Development, or Manufacturing role within the pharmaceutical industry. Strong understanding of pharmaceutical manufacturing processes (e.g., solid oral dosage forms, sterile injectables, APIs). Proficient in process validation, technology transfer, and process optimization principles. Familiarity with cGMP, ICH guidelines, and other relevant regulatory requirements.

ResponsibilitiesIssuance, 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. Review of BMR/BECR Perform Qualification for new Equipments/Existing Equipments Ensure & Co-ordination of area validations. Reviewing of calibration /PM Schedules. Preparation of VMP &validation Documents Handling of Vendor Qualification Activities. Any other work assigned by HOD/Second line.

ResponsibilitiesResponsible for tech-transfer of injectable and ophthalmic formulations from R&D to commercial scale Gap analysis - To evaluate the product feasibility, technology feasibility at manufacturing site along with gap analysis with available technology for site readiness Documentation – Onsite documentation, and timely execution of scaleup, exhibit and validation batches Risk assessment – To carry out the risk assessment to identify the impact of critical process parameters and critical material attributes To design and review the sampling plan for scaleup, process optimization and submission batches To study and verify the parameters established during development are still with in the determined design space in scaleup and exhibit batches To coordinate with other departments at plant in completing scaleup and exhibit batch related activities In coordination with CMO and PM, ensure the availability of raw materials, packaging materials, filters, tubings etc. required for scale-up, exhibit and commercial batches before initiation of execution Compile the batch orsevations and prepare the report of scale-up, EB and commercial/PV batches To ensure smooth technology transfer of products developed at Apotex to CMO Technical support to formulation development team Involve in formulation development activities and assist in development of scaleable manufacturing process Review and compilation of the developmental plant scale batches data and stability results Coordination with different cross-functional teams like AD, procurement, QA, packing, regulatory affairs, project management for smooth execution of scale-up batches Coordination with external labs for successful completion and receipt of studies data performed for plant scale batches Review of MFR, BMR, BPR, stability protocols, study protocols and reports, Executed BMR, BPR, Issuance, maintenance, writing, review of raw data, completeness check and archival of laboratory notebook Coordination with vendor and internal service engineer for installation, calibration, maintenance and trouble shooting Report to next level manager regarding day to day activities. Preparation of SOPs and ensure compliance as per SOP Take up any other work as allottedQualification & ExperienceD /M Pharma in Pharmaceutics/B.Pharma. Knowledge, Skills and Abilities Must have experience in development and tech-transfer of injectable and ophthalmic and complex drug products Effective command over verbal and written communication with good interpersonnel skills. Engage with CMO partners and support the group submission plans Proficient in MS office and advanced software tools. Having well versed knowledge on regulatory guidelines Able to priortise the task, best in effective planning of work activities to meet the timelines. Experience Minimum 6 to 10+ years of experience in Injectable and Ophthalmic dosage forms in area of Development, Manufacturing and technology transfer expertise for CMO.

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 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