ResponsibilitiesSets, Operates and monitors primary packing machines such as Pharmapack, CVC, Parle makes and associated machines like unscrambler, canister filling, cotton inserters and conveyors Ensure calibration of balances, correct machine settings, batch start up and challenge and inprocess checks Performs minor troubleshooting of packing machines Quality Compliance Perform in process checks like bottle quality, tablet appearance, counting accuracy, etc as per BPR Monitor rejections and ensure minimal rejection and losses during batch run Carry out cleaning activities and line clearance as per SOP before and after batch Maintains hygiene and discipline in packing area Documentation and Compliance Maintain accurate and timely records for BPRs and log books including equipment usage logs Report deviations, machine malfunctions or breakdowns to supervisors promptly Fills BPR and logbooks online during start up and while in operation for in process. Assists in reconciliation and rejections of in process and finished bottles. Teamwork and Coordination Coordinates activities of contractual staff for smooth functioning of line Train junior operators, contractual as and when requiredQualification & ExpeirneceITI, Diploma in Pharmacy, Diploma in Engg, B.sc. Total experience of 4 - 7 years in Operation of Packing Machine. Must be able to work in shifts as needed

ResponsibilitiesAccountable for developing regional operational strategy for assigned clinical studies. Contribute to the translation of CDP into an optimal operational strategy and plan. Lead assessment of various scenarios operational for optimal execution of CDP. Collaborate with key investigators to reflect feasible and realistic operational inputs to CDP and ensure timeline and quality of studies meet the needs of CDP. Provide subject matter expertise and operational input into protocol synopsis and protocol, obtaining opinions in terms of study execution from key investigators, as appropriate. Challenge study team to ensure that operational feasibility, inclusive of patient and site burden and that timelines meet the needs of CDP. Validate budget and ensure impacts are adequately addressed. Participate in site selection process, with a focus on providing country insights, and therapeutic expertise to ensure alignment between study execution plan and program strategy. Responsible for clinical study budget planning and management, and accountable for external spending related to clinical study execution. Works closely with relevant stakeholders (strategic CRO partners, other vendors, CSM, COPL, and Program Management, Outsourcing, and Finance) to ensure the accuracy of budget spending on a regular basis. Oversee strategic CRO partners and other vendors to ensure the overall operational execution and delivery of the assigned clinical studies in compliance with quality standards (including ICH GCP, local regulations and Takeda SOPs), on schedule and on budget. Oversight includes but is not limited to Review and approval of key risk-based monitoring documents/plans, periodic review of outputs, decisions, and actions related to risk-based monitoring. Documented review and monitoring of issues, risks and, decisions at the study level. Support the identification of trends across sites and/or the study. Review and provide clinical operations expertise into clinical documents related to the drug development process Creation and maintenance of clinical trial materials, such as Investigator Brochures, study synopsis & protocols, clinical study reports, etc. Preparation of key regulatory meetings, as appropriate. Collaborate with cross-functional counterparts and strategic CRO partners/other vendors to ensure inspection readiness and lead Clinical Operations aspects of inspection readiness activities and act as subject matter expert during regulatory inspections.Qualification & ExpeirenceBachelor’s Degree or international equivalent required, Life Sciences preferred. Innovate and challenge peers and teams to think and work differently; Work independently, excel at solving issues without the need for support, but is effective at enlisting support for specific asks when necessary. Participate and lead clinical operations in cross-functional initiatives and workstreams that affect clinical operations; Adapt ways of working to the function’s current state and formulate strategic plans to work within the existing framework. Capable of assessing gaps cross-functionally and can take a supportive role in leading changes that benefits the function as it related to clinical trial execution and study management.

ResponsibilitiesResponsible for formulation and process development of oral dosage forms, including oral solid and liquid formulations. Troubleshooting and problem-solving of unresolved or new formula issues. Design and execute formulation trials and evaluate stability data to finalize formulation composition. Develop manufacturing processes for R&D formulations so that the technical transfer is successful for large scale batches. Assist to alternate vendor development formulation activities along with product development of site transfer project. Write/review master formulas, manufacturing procedures, SOPs, stability protocols/reports, process validation protocols/reports, Product Development Reports, QOS etc. Support the manufacturing of exhibit/submission batches per regulatory requirements. Support technology transfer for manufacturing processes from laboratory scale to production scale. Works with Analytical Method Development, Regulatory Affairs, Quality Control, Quality Assurance, Inventory Control, etc. to expedite the development and approval of new products by FDA. Assure that all formulation and process development activities are documented in the notebook as per company procedures and cGMPs. Qualification & ExperienceMinimum master’s degree in pharmaceutical sciences with 2+ years relevant experience. Candidate should have hands on/practical experience in development, technology transfer and ANDA submissions for solid/liquid oral dosage forms (solutions, suspensions, tablet, capsules) for regulated and semi-regulated markets like US, Europe and ROW. Broad knowledge base of pharmaceutical sciences and processing in the Pharma industry. Candidates with prior site transfer and AVD project development experience may be preferred.

ResponsibilitiesTechnology Transfer Leadership  Lead end-to-end technology transfer of formulations (OSD / semi-solids as applicable).  Plan, review, and approve Technology Transfer Protocols (TTP), Reports (TTR), and risk assessments.  Coordinate transfers from R&D, pilot plant, contract manufacturers, or global sites.  Ensure readiness of manufacturing processes, equipment, and documentation. Process Scale-Up & Validation  Lead scale-up, exhibit, and PPQ batches.  Define and monitor CPPs, CQAs, and control strategies.  Support and review process validation, cleaning validation, and hold time studies.  Drive process optimization and yield improvement initiatives. Cross-Functional Coordination  Act as a technical interface between R&D, Production, QA, QC, Engineering, Supply Chain, and Regulatory Affairs.  Provide technical inputs for regulatory filings, queries, and variations.  Support new product introduction (NPI) and site transfer projects. Compliance & Regulatory  Ensure all activities comply with cGMP, ICH, USFDA, EMA, WHO, and other applicable guidelines.  Lead and support regulatory inspections, customer audits, and internal audits related to tech transfer.  Handle deviations, change controls, CAPA, and risk management for transferred products.Qualification & ExperienceEducation: B. Pharm / M. Pharm  Strong expertise in pharma formulation processes and scale-up.  Hands-on experience with process validation and regulatory batches.  Sound knowledge of QbD, risk assessment tools (FMEA, Ishikawa).  Experience handling regulated markets (US/EU).

ResponsibilitiesCreate, review, and approve test method transfer and validation protocols, reports, and equipment qualification records. Maintain compliance with Current Good Manufacturing Practices in Quality Control and Stability laboratories. Support media preparation, Bio ball culture handling, and conduct microbiology-related investigations. Perform testing on various samples, manage Laboratory Information Management System builds, and review laboratory data. Serve on cross-functional teams, conduct safety inspections, participate in investigations, recommend corrective actions, and train junior colleagues. Qualification & ExperienceHigh school diploma (or equivalent) with 8+ years of experience or associate’s degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience Strong technical skills in method validation and testing Experience in microbiological testing of water Deep understanding of pharmaceutical manufacturing, packaging, and quality assurance operations Detail-oriented with robust knowledge of quality systems Familiarity with research unit clinical and analytical laboratory environments Effective written and verbal communication, as well as interpersonal skills

ResponsibilitiesLead report preparation from prep to submission with key stakeholders/contributors within Clinical, Regulatory, Safety, DevOps, Submissions, etc. Review data to ensure consistency between various contributors. Compile the information for reports using various electronic tools and document management system. Coordinate the review and approval of the report and address review comments. Ensure reports are completed prior to regulatory due date to meet compliance. Provide guidance to contributor regarding report requirements. Participate in projects or subject matter tasks that support the group and deliverables. Participate in developing and performing User Acceptance Testing (UAT) as required. Complete training in accordance with Pfizer’s and WSR Safety information Management curriculum. Qualification & ExperienceBachelor’s Degree in life sciences, healthcare, or pharmaceutical discipline required. Experience in the pharmaceutical industry, clinical research, or healthcare related field is preferred. Excellent English verbal, written communication and presentation skills required. Must be detailed oriented. Strong project management and issue resolution skills required. Demonstrated ability to perform in a cross-functional environment. Knowledge of regulatory/safety regulations and guidelines desired. 

ResponsibilitiesStrategic/ Policy Ensure achievement of Sales budgets for the assigned geographical territory Develop a clear understanding of his/her role as a responsible Officer of the Company and apply the knowledge, experience and skills to achieve the defined objectives for the position and the team.  Review and discuss his/her plans for the achievement of territory’s sales budget each month (overall and product wise). Seek the assistance of the District Manager in formulating sales strategy. Conduct sales analytics to identify areas / stakeholders to be focused upon for driving business growth in the territory Provide inputs to the District Manager to help him validate the sales forecast or the rolling sales plan as per the defined frequency Provide inputs to the District Manager to help him manage salvage net to maintain it at an acceptable level Jointly with the District Manager, classify the medical practitioners in his/her territory in three categories A, B and C in the descending order of importance, A being the most important and C the least. . 

Qualification & Experience                          Qualification: B.SC NURSING/ GNM WITH RELEVANT EXP. OF 1-5 YRS. IN ANY NABH HOSPITAL                            

Qualification & Experience                                              Qualification: B.SC. IN CARDIAC CARE TECHNOLOGY WITH RELEVANT EXP. OF 2-5 YRS. IN ANY NABH HOSPITAL.             

Qualification & Experience                            Qualification: B. PHARMA WITH RELEVANT EXP. OF 2-5 YRS. IN AN NABH HOSPITAL.