Responsibilities Initiate Master Manufacturing Records (MMaRs) & Master Packaging Record (MPaRs) Initiate Placebo and Optimization batch record for trails. Initiate Change Controls in QMS Track Wise for New Launch / Site Transfer / Submission batch / SOPs / Formats and commercial batch documents. Ensure QMS Change control closure within the stipulated timeline. Ensure support for timely completion of Investigations for document related deviations and document revision based on CAPA. Initiation of batch documents , SOPs and Formats in Content server. Check Monthly Schedule to ensure document readiness. Ensure all changes are aligned with cGMP regulations and corporate SODs. Perform all work in accordance with established regulatory, compliance and safety requirements. Coordinate with NPL and RA regarding Deficencies from Regulatory Agencies and Clarifix. Develop and maintain effective working relationships with internal and external customers.Qualification & ExperienceMinimum Bachelor of Pharmacy / Science or any equivalent degree. Experience Minimum 1 year of experience in GMP regulated pharmaceutical industry.  Knowledge, Skills and Abilities Adequate knowledge in handling QMS Trackwise tool, Content server tool. People management skillset Adherence to cGMP Exhibit Perseverance in all the tasks performed Problem solving skills

Responsibilities Preparation of various master documents required for the submission batch execution and supports the product development by preparation of documents like master production records, Master Packing records and various reports like Exhibit Batch Summary Reports, Hold Study reports, Photo stability Reports, Transportation worthiness study report, Bulk product Stability Reports, SOPs and other miscellaneous reports. Responsible for Maintenance & updating of proper inventory of all the change parts and accessories for the equipments and Instruments. Indenting the punches, dies & machine change parts for the development and submission batches. Issuance of Logbooks for the new equipments, instruments, punches and dies. Preparation of Purchase indents in SAP for the procurement of raw and packing materials. Supporting the other sub-ordinates in learning of the equipments, system and process. Perform all work in accordance with established regulatory, compliance and safety requirements. 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 related to Docuemntation & change controlQualification & ExperienceUniversity / College degree in Chemistry, Pharmaceutical Technology, or related science preferable B. Pharm/ M Pharm (Pharmaceutics) Knowledge, Skills and Abilities Should have good communication knowledge of English (Speaking, Reading and Writing). Should have skills in Microsoft Word, Excel and working knowledge in SAP. Knowledge of the Pharmaceutical manufacturing Process and cGMP is desirable. Should have the attitude of performing the allotted activities in compliance with all the established procedure with an aim to develop Quality Pharmaceuticals. Should take ownership for quality in the job, support our corporate values of Collaboration, Courage, Perseverance, and Passion. Experience Should have minimum 5 years experience in Technical Writing in the pharmaceutical industry/ GMP environment and overall 8-10 years working knowledge of Formulation Development, Manufacturing process in pharmaceutical industry.

Responsibilities To involve in execution of operation and cleaning of Sifting, Blending, Bin Docking, Compaction, Granulation & Dispensing and other general activities in Compounding. To handle and perform Operation, Cleaning & Calibration activities of equipments like, Vibro sifter, Quadro Comill, Bin Blender and Cage blenders, Roller Compactors, LAF in Dispensing and other portable & Non portable equipments and Accesssories etc.,which ever are used in (Compounding) production deparment. To keep update in all training activities and other cross functional departments trainings (as and when assigned) in learning plan. To be a Qualified Operator and Visual inspector as per Qualification for cleaning activities in Compounding. To work inline with the cGMP requirements like (But not limited to) Status Labelling, In-Process test execution, on line documenting of environmental conditions and pressure difference monitoring, Weighing and Calibration activities to be followed. To follow Good Documentation Practices. To execute batch as per instruction given in batch document (MMaR and Protocol). To involve in equipment/area qualification activities as per the requirement and/or product / systems associatred with all regular activities directly / indirectly supporting the entire product life cycle. To execute/Support and escalate to supervisor in case of equipment break down due to power failure, critical / unknown alarms, movement of equipments, material and parts in order to avoid incidents. To follow health and Hygiene practices and adhere to safety and compliance aspects in all the steps in the production area. To perform all other duties, documentation and execution activities assigned by respective supervisor based on business and compliance requirement. Works in a safe manner collaborating as a team member to achieve all outcomes. Performs all work in support of our Corporate values. Demonstrates strong and visible support of our values. 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 & ExperienceMinimum degree in B.Sc/D.Pharm/Diploma/ITI/SSLC. 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 5 years of experience in the production process

Qualification & Experience                           Required Experience : 2-5 years                                                               

Qualification & Experience                            Required Experience : 2-5 years                                                              

Qualification & Experience                                    Required Experience : 2-5 years                                                                            

ExperienceCandidates with 1–5 years of experience are invited to apply. The ideal candidate should possess strong clinical knowledge, patient care skills, and the ability to work in a fast-paced hospital environment.

Qualification & Experiencecurrently seeking a DNB/MD Radiologist with 0-5 years of experience

ResponsibilitiesUndertaking patient assessments like speech and language disorder like Dysarthria, Aphasia Planning and providing appropriate treatment Giving advice and support to patients, family members and teachers Writing reports Maintaining records and case notes Liaising with doctors, physiotherapists, teachers and family members. And performing controlled therapy sessions with individuals, groups and/or families. Some therapists work with people who have difficulties swallowing or eating. Qualification & ExperienceAble to work accurately and with minimal supervision. Ability to comprehend written instructions given by the related departmental personnel. Ability to plan & organize ones 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. Enthusiasm. excellent interpersonal skills Organizational skills Initiative Flexibility Adaptability Patience Open-mindedness.

ResponsibilitiesReview & Verification: Check patient demographics, insurance eligibility, benefits, and coverage for specific medical procedures or medications. Submission to Insurance: Prepare and submit authorization requests with complete clinical documentation (e.g., medical necessity) to insurance companies. Communication & Follow-Up: Act as a liaison, contacting providers for more info and following up with insurers on pending approvals. Documentation: Accurately log all communications, authorization numbers, and outcomes in the system, adhering to HIPAA.  Qualification & Experience5+ years experience working in US Healthcare Pre-authorization / Benefit check Strong attention to detail and organizational skills. Excellent communication (written and verbal) and interpersonal abilities. Knowledge of medical terminology and healthcare coding (e.g., CPT, ICD-10). Familiarity with HIPAA regulations and insurance policies. Proficiency with Salesforce and EHR software. Ability to work efficiently under pressure, meeting turnaround times.