ResponsibilitiesSupports assessment of regulatory requirements, stakeholder expectations, and emerging regulatory trends, and highlights potential impacts to regulatory teams.Contributes to execution of regulatory strategies by supporting global, regional, and multi-country submission activities Assists in identifying regulatory pathways for product changes and supports documentation required for submissions. Supports evaluation of regulatory requirements for product lifecycle activities, including design, labeling, and manufacturing changes Coordinates preparation, compilation, and submission of regulatory dossiers (e.g., FDA 510(k), EU MDR Technical Files, emerging market submissions).Ensures completeness, accuracy, and compliance of submission documentation in alignment with regulatory requirements Maintains and updates regulatory information management systems (RIM) to track submissions, approvals, and renewals. Supports change control processes by coordinating regulatory impact assessments and associated documentation Collaborates with cross-functional teams (R&D, Quality, Clinical, Marketing) to gather required inputs for regulatory deliverables.Tracks submission timelines, dependencies, and deliverables to ensure on-time execution Supports responses to regulatory authority queries by compiling and organizing required documentation. Maintains regulatory documentation, technical files, and dossiers in an audit-ready stateQualification & ExperienceBachelor’s degree in Engineering, Life Sciences, Pharmacy, or related field; advanced degree preferred.Typically 3–6 years of experience in Regulatory Affairs, Regulatory Operations, or related function within medical devices/pharma Experience with regulatory submissions, documentation, or publishing preferred Exposure to global regulatory frameworks (FDA, EU MDR, TGA, NMPA, PMDA, CDSCO, etc.) is desirable

ResponsibilitiesDevelop and maintain data management documentation, including study protocols, case report forms and data management plans. Design case report forms (CRFs) and electronic data capture (EDC) systems for data collection. Perform data entry and cleaning activities, including discrepancy management and query resolution. Conduct data validation checks and implement quality control measures to ensure accuracy and completeness. Conduct data review from other modules and vendors utilized for the study. Develop and execute standard operating procedures (SOPs) for approval, data entry screen design and testing, validation check testing and approval. Collaborate with study team members to resolve data-related issues and discrepancies. Generate and review data listings, summaries and reports for clinical study reports. Serve as a primary or backup resource for issues about data management. Ensure compliance with guidelines, Good Clinical Practice (GCP), CDISC standards and other relevant regulations.Qualification & ExperienceBachelor’s degree in a scientific or healthcare-related field. Minimum 5 years of experience in clinical data management or a similar role in the pharmaceutical or clinical research industry. Experience in medical devices company is preferred. Strong understanding of clinical trial processes, data management principles and regulatory guidelines.

ResposnibilitiesWork towards regional profitability through close monitoring of gross margin relative index. Successfully partner with internal teams and marketing team to achieve set targets. Implements and executes the launch strategies developed by the Sales and Marketing organization. Completes a thorough analysis of the territory, sales forecasting and planning. Generates and follow-up on sales leads. Build strong business relationships with key industry players whilst achieving sales goals and growth across allocated territories Provide solutions for customers and add value to the sales process through negotiations, resulting in winning business/orders and positive customer experience Qualification & ExpeirenceAt least 8 to 12 years sales and marketing experience (preferred from neuro/ interventional segment) with minimum 2-3 years or people manager experience Proven record in sales management, channel management and key account management. Proven track record of 3 years of consistent performer. Achievement in all 4 quarter targets

ResponsibilitiesExecute shift packing activity by managing available resources and reduces micro stoppage of machine to achieve shift target  Utilise shift resources optimally to get desired production output Regulate usage of consumables in the production process at optimum level to save cost Key Accountabilities (2/6) Review documentation related to packing activity and monitor standard packing parameters as per BPR to meet regulatory requirement  Review and monitor critical in-process parameters like NFD, camera challenge, RH temperature etc.  Review and perform all operations as per GMP and safety norms by reviewing all processes and documents for compliance  Maintain system integrity by updating online documentation Perform qualification and calibration of equipment as per schedule and update output of all activities in the systemQualification & ExperienceB. Pharm. / B. Sc. (Chemistry) Relevant Work Experience 1-5 years of experience in packing with knowledge of handling of QMS activity, qualification and other related documents

Responsibilities Analyse samples as per priority and work allocation  Review the data as per respective specification, Microbiological Methods and results obtained  Prepare, review and submit reports to Team leader within stipulated timelines in order to support individual sample release within stipulated timelines to achieve SLA  Review reports as per cGMP & GDP for compliance to GLP  Ensure no GMP / regulatory concern are raised by adhering to SOPs and following procedures 

Responsibilities Review the new/revised monograph as per current pharmacopoeia  Review the latest pharmacopeial updates and monitor its timely implementation to avoid any non-conformances  Intimate the concerned stakeholders to initiate and complete activities before effective date of pharmacopoeia  Escalate non-conformances timely to avoid any delays in operation  Maintain system integrity by updating documentations and deviations on CipDox while performing operations  Maintain all the online documentation and timely entries and supporting documents  Prepare new documents and update existing documents as per GMP requirement Qualification & ExpeirneceM.Sc. / B. Pharma. Relevant Work Experience 1-3 years of experience in QC department of a pharmaceutical organization with knowledge of latest regulatory standards and compliance norms

ResponsibilitiesTo execute analysis of finished goods / Stability samples / Raw materials / Packing materials In-process and cleaning samples along with relevant laboratory documentation Check all the instruments on the equipment required for the analysis are in working condition and are in calibrated state. Checking and ensuring proper status labels after confirming availability of all the requirements (as applicable) for analysis such as approved control procedure, analytical protocol, reference standards, chemicals, reagents, GC/HPLC Columns, glassware, water preparation equipment, water bath, sonication baths, mobile phase bottle etc. Ensure the online documents pertaining to day-to-day analysis are efficiently completed in timely manner. Reporting the activities daily to immediate supervisor.Qualification & ExpeirenceExperience: Minimum 3-5 years of experience in analysis of RM/FG/Stability/PM samples using various QC instruments (HPLC/GC/UV/IR/Autotitrator/Polarimeter etc.) Qualification: M.Sc. (Analytical/Organic Chemistry).

ResponsibilitiesManagement Role: Functions in a leadership role to other staff nurses. Responsible for assisting with supervision, direction and coordination of nursing Personnel. Makes appropriate room and care –giver assignments to optimize patient placement and workload balance throughout the shift.Develops objectives for the management of the unit. Ensure staff discipline. Works with the Head Nurse on improving patient care and customer satisfaction. Promotes environment of cooperation and mutual support to maintain focus on patient care; anticipates and supports needs of other staff. Must be able to communicate effectively, demonstrate delegation skill and develop good interpersonal relationship with patient, staff, physicians and visitors. Maintains quality of patient care including compliance with prescribed treatment and Hospital policy. Utilizes all personnel available to obtain maximum patient?care services. Evaluates work performed by all staff members and inform staff of information Necessary to the performance of their jobs. Investigates and identifies nursing problems and grievances and assist in their solutions, reports resolved and unresolved results to the Head Nurse.Assists on orientation of new personnel and participated in continuing educational program and clinical nurse training.Conducts regular staff meetings with the staff. Operates the unit within budgeted levels for staffing, supplies and equipment – recommends staffing patterns and standard of Nursing Care to the Nursing Manager.Reports and document all accidents / incident to patients, visitors or staff. Report promptly any unusual occurrence to the Nursing Manager. e.g. medication errors, complaint, VIP's or staff admitted, etcPerforms extra duties when called upon especially on an emergency. Maintains up?to?date knowledge and practice of nursing trends and new developments in the health field. Coordinates health education program in the unit. Supervises other no-nursing personnel. Conducts periodical survey to ensure nursing care standards. General Nursing Duties: Ensures patient?care services according to established procedures and policies. Assist doctors in procedures and other related duties. Attends to patients regularly to ensure maximum care and ascertain need for additional or modified services.Supervises maintenance of records of nursing and medical treatment and related services carried out by nursing personnel.Ensures proper utilization of supplies and power to avoid waste. Maintains adequate supplies and equipment for daily use and carry out periodic Inventory. Assists in the safekeeping of valuables. Safeguards patients' safety at all times. Ensures work place is always neat and clean. Acts promptly in emergency situation. Specific Unit Related Nursing Care: Clinical Management. Ensure that effective care and management are provided to patients within the ward. Provide support and direct care as required to patients with range of complex care requirements Ensure a problem solving approach in the delivery of patient care. Communicate and documents patient care requirements to all relevant members of the health care team. Insure patient care standards are meet and revised to incorporate the result of clinical findings and research to reflect advance in practice and technology. Insure nursing care is delivered in accordance with policy and procedure of nursing division, AHIL. Monitor and review standard of documentation of patient care. Ensure confidentiality of patient information is maintained. Participate in activities and development and evaluation of policies and procedures used in the delivery of patient care. Ensure safe custody controlled substance is maintained in accordance with best practice in hospital policy. Patient Care: Ensure the safe delivery of patient care. Provide safe patient environment and ensure patient incidents/ accidents are documented and investigated and action is taken to prevent the re occurrence. To develop & maintain the unit level orientation, in service and preceptor ship programme.  Develop and implement clinical competences relevant to your area and ensure that all staff is assed on a regular basis. To provide staff with progressive informal Feed Back on their performance and conducting formal and regular performance services. Acts to rectify unsafe or inappropriate behavior and practice Quality Improvement Initiate and develop quality improvement programme. Participate in JCI Accreditation.

Qualification & Experience                           Education : MBBS with Telangana Medical Registration              Experience : 0-5 Years             

Qualification & Experience                  Education : B.sc or M.sc Nursing    Experience : 3-5 Years