Qualification & Experience    To develop a systemic approach to the patient’s problem and decision-making skills in management. To develop and sharpen skills in examining and assessing patients with arthritis and related problems requiring joint replacement surgery. To attain basic surgical skills and techniques in primary and revision arthroplasty. To obtain experience in scientific data collection, analysis interpretation, publication, and surgical audit.

Qualification & ExpeirenceExperience: 1–5 Years Qualification: M.Sc / B.Pharma

Qualification & ExperienceQualification: GNM/BSc Nursing  Experience: 15 years’ experience including 3 years’ experience on same profile 

Qualification & Experience Qualification: GNM/BSc Nursing  Experience: 15 years’ experience including 3 years’ experience on same profile

Responsibilities  Ensure to preparation of all require forms and documents for submission projects for Health Canda.  Send it to peer review in within time line and respond to reviewer’s comments.  Create and update the RIMS record, CCR-QMS, LAMS-BLUE projects.  Compile all forms and documents and upload in DocuBridge to submission Health Canada.  Prepared Text Compare Reports for verification of Package Insert.  Verification of Labels through proof compare tools in BLUE for approval of Labels.  Effectively communicate and collaborating with team member for achive all outcomes.  Timely complete all assigned training in training portal.  Attained training, webinar, meeting which all are arranged by HR team, Department Laed, or Company.  To communicate and collaborate with GTA Team regarding projcets.  Works in a safe manner collaborating as a team member to achieve all outcomes.  Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.  Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.  All other relevant duties as assigned.Qualification M Pharmacy, B Pharmacy or Equivalent Degree  Knowledge, Skills and Abilities  Basic knowledge and/or understanding of regulatory requirements for filing labeling submissions in USFDA, Health Canada or ROW markets.  Good interpersonal communication skills 

Responsibilities  Creating SDTM and ADaM datasets for the studies conducted by Apotex using CDISC standards Annotation of CRFs for the clinical studies conducted by Apotex. Development and validate of in-house SAS programs in line with the quality standards and regulations. Ensuring the validation of software’s are done in line with the applicable company quality standards and regulations Validation and review of clinical trial data. Creation of Specifications for Define.xml, Validation and review of SDTM, ADaM, and Define.xml. Creating data sets, tables, listings and Procedural comparison, sorting of source data. Ensures that assigned work is performed in accordance with GCP, GLP, SOPs, regulatory requirements, best practices and established safety standards as applicableQualificationEducation Integrated Master’s Degree in science Knowledge, Skills and Abilities Expertise in area of statistical analysis, SAS and/or bio-statistics. Excellent communication and interpersonal skills. Flexible to work Experience At least 4-5 years of industry experience in clinical trials related submissions for different regulatory agencies.

Responsibilities To plan, organize and co-ordinate in the execution of operation and cleaning of compounding activities. To execute, review and supervise the below listed activities. Line Clearance. Area and Equipment cleaning verification. Initiation of swab request and any other applicable sample requests (As applicable). Initiation of equipment, instrument and area breakdown notifications. Review of executed batch records and equipment/area usage, calibration logbooks. Execution of SAP related activities. Execution and review of in-process tests at different stages of processing. To get the issued batch records, logbooks and to return the completed executed batch records, logbooks to QA.QualificationEducation Minimum qualification - B.Pharm/M Pharma. Knowledge, Skills and Abilities Proficient knowledge of Good Manufacturing Practices (GMPs) & Good Documentation Practices. Efficient communication, strategic thinking and problem solving skills. Adequate knowledge to understand the written procedures and policies. Experience Minimum 4 to 6 years of experience in the production process.

Responsibilities Develop and execute sales strategies to achieve and exceed assigned sales targets for pharmaceutical products.  Identify and cultivate new business opportunities within the assigned territory, including engaging with healthcare professionals, hospitals, and pharmacies.  Maintain and strengthen relationships with existing clients, ensuring high levels of customer satisfaction and retention.  Conduct regular visits to healthcare professionals to present product information, address inquiries, and provide solutions.  Monitor market trends, competitor activities, and customer feedback to identify opportunities and challenges.  Prepare and submit accurate sales reports, forecasts, and other required documentation in a timely manner.  Collaborate effectively with internal teams, including marketing and medical affairs, to support sales initiatives.  Participate in sales meetings, training programs, and product launches as required.  Ensure compliance with all company policies, industry regulations, and ethical standards. Qualification & Experience Bachelor's degree in Pharmacy, Life Sciences, Business Administration, or a related field.  1-3 years of proven experience in pharmaceutical sales, preferably in a similar role.  Strong understanding of the pharmaceutical market, product knowledge, and sales processes.  Excellent communication, interpersonal, and presentation skills.  Demonstrated ability to build rapport and establish strong relationships with diverse stakeholders.

Responsibilities Helps in demonstrating the operation in case of a new machine or a new pack-profile is implemented. - Preparation of protocol for validation/qualification pertaining to Process, Cleaning, Equipment and area/HVAC - Execution of validation/qualification activities - Coordination with different departments for performing validation/qualification activities - Compilation of data and report preparation - Maintaining documents as per Document control policy - Lessoning with FDA for manufacturing licenses and certificates.Qualification & ExperienceB.Pharma/M.Pharma/ B.Sc

ResponsibilitiesFormulation development of NCE projects, generic projects and line extension projects Preparation/review of literature summary and development report to the assigned product. Involve in execution and/or supervision of formulation development, process development and manufacturing of GMP batches of assigned product. Preparation/review of technical documents, which includes but not limited to MFC, BMR, BPR and Stability protocol following GDP. Representation in departmental audit Follow GxP (GMP, GDP etc.) for all processes and train the subordinates to follow the same. Execution and/or supervision of scale up/pilot scale batches in pilot plant under GMP condition. Preparation and/or review of technology transfer documents and technology transfer to manufacturing site, whenever required. Preparing/reviewing of QMS includes but not limited to change control, deviation, SOPs and OOS Communication with cross-functional team and client via mails, meetings and oral communication Provide training on but not limited to SOPs, technology, guidelines and project specific activities Performing and/or supervision calibration and maintenance of R&D instruments and equipmentQualification & ExperienceMaster of Pharmacy (M.Pharm)