ResponsibilitiesCare for critically ill patients Monitor vitals and ICU equipment Assist in emergency procedures Maintain detailed patient recordsQualification & ExperienceQualification: GNM / B.Sc Nursing Experience Required: 2–5 years ICU experience

ResponsibilitiesSupervise nursing staff and patient care Manage duty rosters and staff allocation Train and guide nursing team Ensure nursing protocols and standardsQualification & ExperienceQualification: B.Sc Nursing / GNM Experience Required: 5+ years (Minimum 2 years in supervisory role)

ResponsibilitiesEstablishing lab infra at Pune location Procurement of instruments and lab setup Calibration of instruments updating of master list and storing in EDMS preventive maintenance of devices in the lab preventive and annual maintenance of environmental and altitude chambers, qualification of labs Regular data entry of environmental data at various labs at Pune (Baner 6th floor, 5th floor and Chakan lab) Establish Chinchwad lab (move existing infra to this site) Add supplier to ASL as per the need Facilitate instruments transfer from outside India to Pune labs following established government regulations and be compliant with the process Maintain inventory of devices and accessories at central warehouse for S&RC BU Movement of devices, instruments and accessories between warehouse and labs within Pune Calibration of instruments with respective calibration agencies within India and abroadQualification & ExpeirenceBachelor's / Master's Degree in Mechanical Engineering, Minimum Required Experience Minimum 2 years of experience in medical devices lab admin and total of 6 years of experience as minimum in similar experience

ResponsibilitiesProvide Guidance and Leadership on mechanisms to optimize product development and regulatory approvals. Develop the international regulatory strategy and contribute to Global regulatory plans. Support regulatory product compliance (e.g. RIM, PMCs, ESC levels, and agency commitments). Support and advise on the local label strategy and alignment to cCDS/reference label. Build effective relationships and communication paths across global, regional, local and functional organizations. Enable efficiencies and seamless execution across the international countries. Contribute to process improvement projects, as assigned.Qualification & ExperienceDoctorate degree and 6 years of directly related experience OR Master’s degree and 8 years of directly related experience OR Bachelor’s degree and 10 years of directly related experience Education & Experience (Preferred) Degree and in-depth regulatory experience and/or related to the region. In-depth knowledge of regional countries legislation and regulations relating to medicinal products.

ResponsibilitiesSupervising medical content operations, including monitoring content creation, review, approval, and publication processes to ensure timely execution and alignment with medical, regulatory, and compliance requirements.  Monitoring compliance procedures and documentation related to scientific publication lifecycles, proactively identifying process gaps and risks, and supporting the preparation of compliance reports, dashboards, and operational insights for leadership review. Coordinating project management activities – including planning, execution, change management, deployment, training, and reporting – contributing to the successful execution of the SciComm strategic communication plan. Driving user acceptance testing for new technology builds and enhancements. Proactively communicating with stakeholders across functions and geographies to ensure strategic alignment and to seek opportunities for increased efficiency and innovation. Serving as business authority, advocate, and point of contact on technology & process related issues within Global Scientific Communications in India. Facilitating and participating in key governance forums and project sponsor meetings. Collaborating with analytics leads to identify, implement, and managing key performance indicators, impact metrics, dashboards, and other analytic needs. Continually assessing the landscape and proactively identifying opportunities to improve, standardize, or streamline business processes. Partnering with the appropriate training experts and establishing pathways to assess and understand the educational needs of the capability audience Supporting recruitment, coaching, mentoring, and development of operations team members as appropriate Qualification & ExpeirenceMasters in Science field with 8-13 years of directly related industry experience along with good work experience in project management (PMP or DASM certification preferred)

ResponsibilitiesGenerate and execute of global and country-specific regulatory strategies Provide CMC regulatory strategy for assigned projects by defining minimal regulatory filing requirements, submission strategy, and regulatory risk assessments Develop global dossiers for CMC content for initial submissions, variations and amendments Support change management activities Develop response strategy and respond to health authority questions Liaise with other functions in development, operations and commercial to ensure alignment of global regulatory strategies, timing, execution and supply plans Liaise with local regulatory teams to align on filing strategy Monitor and, as necessary, provide data to be entered into tracking systems for department deliverables and ensure information is current. Maintain submission information according to the Regulatory Information Management (RIM) system Follow established department regulatory processes to ensure cross-product alignment Qualification & ExpeirenceCMC- specific regulatory knowledge & experience Education & Experience (Basic) Bachelor’s degree and 8-13 years of directly related experience Experience in manufacture, testing (QC/QA or clinical), or distribution Regulatory CMC experience

Responsibilities The Supervisor, Coding Quality Assurance plays a crucial role in ensuring the accuracy and compliance of medical coding processes within a healthcare organization. This position involves overseeing and leading a team of medical coders, conducting quality assurance audits, providing feedback, and implementing improvement strategies to enhance coding accuracy and efficiency. Essential Functions And Tasks Team Leadership:  Lead and manage a team of medical coders.  Provide guidance, support, and mentorship to coding staff.  Foster a collaborative and positive work environment.  Conduct regular team meetings to discuss updates, challenges, and training opportunities. Quality Assurance:  Develop and implement a comprehensive medical coding quality assurance program.  Conduct regular audits of medical coding work to ensure accuracy and compliance with coding guidelines, regulations, and organizational policies.  Provide constructive feedback to coding staff based on audit findings.  Collaborate with coding educators to address training needs identified during QA audits.Qualification & Expeirence Bachelor's degree in any Life Science field.  Certified Coding Specialist (CCS) or Certified Professional Coder (CPC) certification.  Minimum of 6 years of experience in medical coding. 

Responsibilities The Coding Quality Assurance (QA) Specialist is primarily responsible for determining the appropriate CPT and ICD-10 codes to be applied to patient accounts for billing purposes based on providers’ documentation in the patient’s medical record. Essential Functions And Tasks  Assigns appropriate billing codes to patient accounts. Performs ongoing analysis of medical record documentation for completeness.  Provides feedback to Coders on coding discrepancies.  Provides feedback to Coding Supervisor on documentation deficiencies.  Performs special projects and other duties as assigned. Qualification & Expeirence High School Diploma or Equivalent.  Four (4) years of Emergency Department (ED) and Hospitalist Medicine coding experience.  Certified Professional Coder (CPC), or equivalent, preferred. 

Responsibilities The Regulatory Affairs Specialist provides cross?specialty administrative, compliance, and quality reporting support for Radiology, Anesthesia, Emergency Medicine, Hospital Medicine, and additional service lines as assigned. Reporting to the Healthcare Quality Director, this role assists in organizing, auditing, and maintaining the company’s regulatory and quality programs—ensuring accuracy, compliance, and readiness for internal and external review.  The Regulatory Affairs Specialist plays a key role in auditing documentation and coding, preparing regulatory materials, updating internal resources, and supporting the operational execution of quality programs such as MIPS (Merit?Based Incentive Payment System). This position collaborates closely with Operations, Coding, and Business Intelligence  A current Certified Professional Coder (CPC) credential and three years of experience with the MIPS program is required. Qualification & Experience High school diploma or equivalent required; associate or bachelor’s degree preferred.  Current Certified Professional Coder (CPC) credential required.  Minimum of three years working with the MIPS program is required.  Minimum of two years administrative experience.  Familiarity with Radiology, Anesthesia, Emergency Medicine, or Hospital Medicine coding is a plus but not required.

ResponsibilitiesValidation & Qualification Management Preparation, review, and approval of: User Requirement Specifications (URS) Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) Computer system validation (CSV) Quality Control laboratory equipment qualification SOP and Protocols preparation; review and approval Execution of FAT/SAT and commissioning supportExpeirenceBachelor / Master of Pharmacy / Master of Science 07 to 09 years