ResponsibilitiesBe part of the Medicine Department and conduct OPDs on days assigned to you Admit patients under your care in the hospital and manage them independently Take part in any departmental activities for patients Coordinate with senior colleagues and the Director in following the departmental SOPs Maintain meticulous records of patients Ensure that patients are clearly instructed on follow-up visits Attend Departmental meetings and programs Adhere to the hospital guidelines for Associate ConsultantsQualification & ExperienceQualifications MD or DNB in Medicine Experience 5-7 years in a similar role

ResponsibilitiesProper pre donation counseling and taking of donor’s medical history. Pre donation medical examination. This work is complementary to the work of Staff Nurse. Phlebotomy Post donation care and manage post donation reaction. Verifying: a) The blood group donor, patient, done by Jr. Technician / Sr. Technician / Technical Supervisor. b) Cross match of donor’s blood with patient’s sample done by Technical Staff. c) Test results of HIV I & II, HBSAg, HCV, MP, VDRL, Atypical Ab, Haemoysin done by Technical Staff. Supervise discarding of reactive blood units and blood units which need to be discarded for any other cause and ensure proper documentation according to F.D.A. guidelines. Preserve and maintain the data of CMS. Supervise the proper preservation of donor sample for 35 days / 42 days depending on the expiry of the PCV/WB unit or for 8 days after the unit is issued whichever is earlier and patient’s sample for 8 days after received it. Supervise the tests performed on donor units that have cause post transfusion reaction and enter the cause of reaction if possible and guide accordingly. Supervise the Quality Control of the blood products, reagents and kits. Supervise issue of blood and blood components. Supervise issue of blood products as per expiry.Qualification & ExperienceMBBS MBBS + Dip in clinical pathology/ Pathology/ Bacteriology MBBS + Dip in Transfusion Medicine / Immunohematology/ Blood Transfusion MD pathology or DNB Pathology MD Transfusion medicine / DNB Transfusion Medicine/ MD Immunohematology and Blood Transfusion EXPERIENCE: 1 to 2 years Experience in licensed Blood Centre

ResponsibilitiesMaintain approved applications in compliance with FDA regulations for assigned ANDA Annual reports. Independently and proactively request documentation required for annual reports, compile, finalize and publish for managements review and subsequent dispatch to the Agency Independently work on supplements, compile and publish for managements review. Take a proactive approach for more complex submissions and contact internal stakeholders (when needed) to gain further insight on any given supplement. Convey findings to management and incorporate any.all applicable information in the submission to ensure a quality and a right first time submission. Assist management and proactively train Associate I’s and Associate II’s on guidance’s, internal processes, procedures, databases and trackers Other projects and duties as required/assigned. Process improvementQualification & ExperienceM. Pharma degree in RA/QA discipline, a plus. Minimum 5+ years pharmaceutical industry experience; Regulatory, Analytical, QA, laboratory or production experience preferred. Demonstrates an understanding of ICH and FDA guidelines Demonstrates the ability to evaluate regulatory documents and determine appropriate action.

ResponsibilitiesMaintain approved applications in compliance with FDA regulations for assigned ANDA Annual reports. Under minimal supervision, proactively request documentation required for annual reports, compile and publish for managements review. Under management’s direction/assignment, work independently on simple supplements, compile and publish for managements review. Assist management on more complex supplement to gain experience. Further educate oneself on FDA Regulations by reviewing any/all applicable post approval guidance’s to understand and accurately assess change controls. When needed, train Associate I’s on internal processes, procedures, databases and trackers. Other projects and duties as required/assigned Qualification & ExperienceM. Pharma degree in RA/QA discipline, a plus. Minimum four years plus pharmaceutical industry experience; Regulatory, Analytical, QA, laboratory or production experience preferred. Basic computer skills such as Word, Excel and familiarity with the internet Ability to work independently and on teams Good verbal and written communication skills Must be well organized, detail oriented, have the ability to multi-task and manage changing priorities

ResponsibilitiesLeads the Quality organization on site including Quality Control, Microbiology, Quality Compliance, Quality Systems and Quality Assurance Operations. Ensure a current Quality Management System is in place and continuously improved Ensure products are manufactured, released and distributed in accordance to cGMP requirements and registered specifications. Most senior professional and independent decision maker authority on product quality and potential market actions Assess and Mitigate Risks-- Identify quality risks and define proactive mitigations, to ensure the products are safe and effective before they reach the market. Work with the business to assure compliant and reliable supply Design and Implement the Site Quality Program—Collaborate with the Site GM and Corporate Quality to create, implement, monitor and update the site quality program. Manage Quality Data--Oversee the delivery of necessary data to site managers and supervisors, Corporate Quality and other internal and external stakeholders, to support the achievement of Quality objectives and ensure compliance Direct Quality Control-- Oversee the laboratory activity, including analytical site transfers, testing and approval or rejection of raw materials, packaging materials, in process materials and finished products for the site Promote a Sustainable Culture of Quality---Create, develop and maintain a culture of enhancing quality throughout the entire site operation. Create a space where people can speak openly and are encouraged to present new ideas to improve quality Maintain strong partnership with site leadership team Strategic partner in the site leadership team, with Supply Chain, Project Management, R&D, MS&T and Commercial to ensure project timelines and objectives are metQualification & ExperienceRequired – bachelor’s degree in chemistry, Biology, Pharmacy Preferred - Master or equivalent degree in Chemistry, Biology or Pharmacy Key Requirements Minimum of 10 years pharmaceutical manufacturing site quality operations and leadership experience, including: Deep knowledge of cGMP requirements of local and major international authorities like EMA and US FDA for products and process, 

Responsibilities Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report.  To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc.  Ensuring data integrity policy, GDP and its effectiveness up to compliance  To maintain the stability chamber and tracker.  To maintain the stability chamber and tracker.  To ensure charging and withdrawal of stability samples as per approved protocols.Qualification & ExperienceEducation :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs.

ResponsibilitiesCompetencies Collaboration Customer Centricity Developing Talent Innovation & Creativity Process Excellence Result Orientation Stakeholder Management Strategic Agility

Responsibilities  Manage Claims mailbox; including claims uploads and address customers’ inquiries  Validate & process commercial rebates, Admin fees, VIR, Indirect billback, Stocking allowance, and other fees posted by the customers. Maintain customer’s claim logs, navigate customer’s portals and download posted invoices.  Prepare customer reporting in line with contractual obligations.  Review and interpret contact terms to customer claims across assigned accounts.  Organize and stay on top of validation files and payment data.  Perform various Ad-Hoc analysis as needed to support other departments.  Work closely with Accounts Receivable in clearing outstanding deductions and discrepancies.  Assist in credit/debit applications, claim vs. payment reconciliations, provide data to support all disputes.  Analyze customer inquiries as needed, including sales and payment reporting.

Qualification & ExperienceMD Experience 3 years plus Department General Medicine 

Qualification & ExpeirenceQualification MS / MD / DNB in OBG Experience 2 - 5 years