ResponsibilitiesInterprets medical images (X-rays, MRIs, CT scans, ultrasounds) to diagnose and treat diseases. They produce detailed reports for referring physicians, guide image-based, minimally invasive procedures,Experience in interpreting X-rays, MRIs, CT scans, and ultrasounds Diagnose diseases, produce detailed reports, and guide image-based minimally invasive procedures

Responsibilities  Maintenance, Review and Ensuring Calibration of measuring and testing instruments/equipment's as per the schedule. Reviewing /verification of raw data, analytical results against the specifications and respective operating procedures. Review/Verification of instrument status labels/ status boards. Responsible to review and release the documents related to intermediates and Finished product within the stipulated time after review. Review the audit trails for the chromatographic and non-chromatographic systems. Responsible for the SAP activity. Responsible for the review of sampling activity. Review the Calibration and preventive maintenance data of analytical Instruments and equipment Responsible to investigate the Incidents, OOS, OOTs, OOCs and Deviations occurred across the lab during analysis.Qualification & ExperienceM.Sc Required Experience: 0 - 5 years

Responsibilities Responsible for sampling of RM, API as per respective specification. Testing of the product for MLT and bacterial endotoxin testing. Ensure sampling and testing meet the SLA. Perform the method validations for microbial limit test and the Bacterial endotoxin testing. Management of consumable for microbial testing. Involve in result entry and verifications. Performing activities in the Labware LIMS software. Involve in the media receipt, preparation and sterilization activities. Perform dry heat sterilization for sampling accessories. Cleaning and maintenance of sampling accessories Performing decontamination and disposable or Biological wastes. Performing area and equipment cleaning using approved disinfectant. Performing environmental monitoring of microbiology areas. Performing water sampling and testing Microbial identification using Vitek2 system. Qualification & ExperienceRequired Education Qualification: MSC Microbiology Required Experience: 01 - 05 years

Responsibilities Implementation of QMS and GMP regulations in accordance to the regulatory guidelines. Preparation and review of standard operating procedures in accordance to the regulatory guidelines. Ensure Data Integrity, adherent to policies and its implementation. Ensuring Preparation and review of Site Master File, Quality Manual and Organogram. Preparation and review APQR of the product under review and to initiate necessary changes based on the final recommendations. Document management and control - control of documents (master) and user copies of all master documentation. Labelling and Storage of master documents, validation documents and batch documents. Destruction of documents wherever applicable. Control on IOM, confidential documents and External documents. Issuance and control of batch records. Issuance, retrieval and storage of log-books. Responsible for obtaining licenses required for product manufacturing in coordination with regulatory affairs department. Responsible for handling Change controls, deviations, risk assessment and CAPA Management. Responsible for approval/rejection of change controls, Deviations, CAPA etc. Handling of failure investigations, market complaints and product recall and returns. Responsible to conduct and coordinate training on quality system procedures and CGMP across the facility. Evaluation of training questionnaires and certification of trainees. Review/approval of Trend analysis for quality system parameters Conducting Internal Audit as per the schedule and to ensure compliance action plans arising out of noted deficiencies.Qualification & ExperienceQualification: M.Pharma Required Experience: 12 - 18 years

ResponsibilitiesServe as an internal consultant for biostatistics analysis tools and methods Serve as a subject matter expert during client and vendor meetings for biostatistics analysis support Actively support business development in capabilities presentations to prospective and current clients Effectively manage assigned clinical study budgets for biostatistics analysis support Develop, coach and mentor junior biostatistics department personnel Act as the lead statistician on clinical research projects and help with SAS programming Provide statistical expertise for study design of clinical trial protocols Write statistical methods section of the study protocol, as needed Write statistical analysis plans ensuring appropriate regulatory requirements and study objectives defined in the study protocol are followed

ResponsibilitiesProvide management oversight and training to all direct reports within the Business Development team. Support SVP, Business Development in coordinating with Accounting, Operational Logistics / Project Management, and Business Development to prepare, maintain, and regularly communicate a forecast for all new business to include scope of work and project/contract timing. Support Sales Lead to coordinate with prospective and current clients/partners to understand the scope of work requirements for all new candidate projects and/or changes to current projects and prepare initial pricing and proposals that are responsive to the request. Review draft pricing and proposals as needed with SVP, Business Development Coordinate with Business Development team to ensure that all contracts, proposals, and other opportunities are updated and maintained via all available Business Development resources (Salesforce.com, KeyedIn, etc.) Oversee the preparation of Confidential Disclosure Agreements (CDAs), Master Service Agreements (MSAs), and associated Work Orders and Work Order Amendments Develop/maintain Business Development Operations processes. Proactively identify and coordinate with Business Development on resolution of problems/issues that may jeopardize winning new business. Ensure project scope of work, deliverable requirements, and project budgets are well coordinated with internal staff, helping to identify and communicate contract scope creep as early as possible. Coordinate with Accounting and operational departments to ensure all billing milestones are identified, tracked, and regularly reviewed. Communicate with support staff in a positive, proactive manner to ensure team objectives are met. Coordinate with SVP, Business Development to discern when to involve executive management to help reconcile problems/issues with internal staff members and/or clients/sponsors. Ensure the quality of all Business Development Operations deliverables prior to submission to clients/partners. Coordinate with SVP, Business Development, or other Executive Leadership to determine when outside legal review of documents is required. Support continuous improvement initiatives spearheaded by executive management and/or department heads. Comply with Statistics & Data Corporation’s data integrity & business ethics requirements.Qualification & ExperienceA bachelor’s degree, preferably in engineering, applied or life sciences or business is required. Four (4) years of experience in business development, account management, contracts management, or purchasing in the clinical trial industry is required.

Qualification & Experience                          Eligibility Criteria: To assist Senior Consultant in OPD & O.T                                                               

ResponsibilitiesThis role involves supervising and maintaining equipment, monitoring production processes and performing quality checksExperience1-2 years

Responsibilitiesnterview patients to learn their complaints and family medical histories. Conduct examinations and diagnostic tests. Analyze test results and discuss treatment options with patients. Confer with other medical staff to make diagnoses and design treatment plans. Prescribe medication and physical therapy. Take vital signs, draw blood, make injections, and administer anesthetics. Treat internal diseases, illnesses, injuries, and disorders.Qualification & ExperienceAble to work accurately and with minimal supervision. Ability to comprehend written instructions given by the related departmental personnel. Ability to plan & organize one’s work schedule effectively. Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel. Affinity to work in a team. Enthusiasm.

ResponsibilitiesEnsure preoperative checks are made on accepting the patient into the OT and prior to the administration of any anesthetics or surgical procedure along with the anaesthetist. Ensure that surgical policies and procedures are adhered to in relation to operations and correct procedures are followed in the checking of swabs, instruments, needles etc. Ensure that correct aseptic techniques are used at all times. Administer medicines in accordance with guidelines, Policies and Procedures. Undertake delegated responsibilities when needed to take charge of a shift without direct supervision. Correctly follow routine maintenance schedules and sterilization procedures for equipment. Administer drugs- oral, sublingual, intravenous, intra dermal, subcutaneous and intramuscular. Collect blood samples for blood investigation and monitoring blood glucose values with the use of glucometer. Provide clinical supervision and training in nursing procedures in the OT to staff nurses and CCA’s when required. BLS and PALS / NALS trained. To complete any other work assigned/ required from time to time basis.