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 met Provide effective Quality leadership during internal, customer and Health Authority inspections Ensure that Quality KPIs are meeting pre-defined targets, Ensures CAPA commitments are implemented in a timely manner and its effectiveness is monitored periodically Plans, manages and monitors the annual Quality Operations budget and all its resources and employees. Ensure the performance and utilization of resources to provide maximum efficiency to the organization. Qualification & 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, 

ResponsibilitiesManage and investigate product quality complaints received from the market in line with pharma regulations and Amneal’s established procedure. Perform detailed analysis of complaints and conduct root cause investigations using appropriate quality tools and prepare Report. Coordinate with cross-functional teams (Quality Assurance, Manufacturing, Regulatory, etc.) for effective resolution and investigation of complaint, Ensure timely closure of complaints as per defined timelines and regulatory requirements. Maintain accurate, complete, and audit-ready documentation of all complaints and investigations. Monitor, track, and trend complaint data to identify recurring issues and potential risks. Support continuous improvement initiatives to enhance product quality, safety, and compliance. Contribute to improving patient safety and customer satisfaction through effective complaint handling. Ensure full compliance with company SOPs, GMP guidelines, and regulatory standards (e.g., FDA, EMA). 

Qualification & Experience     Qualifications for Full-Time Nurse Incharge:           GNM / BSC - 5-/yrs experience.          

Qualification & Experience           Qualifications for Full-Time Staff Nurse:              GNM / BSc - 0-5yrs experience.           

Qualification & Experience     Qualifications for Full-Time Nurse Supervisor:            GNM / BSc - 10-15yrs experience.        

Qualification & Experience   Qualification: Any Graduate   Type: Full Time        Experience Required: -1-2 Years   

Qualification & Experience              Qualification:-MBBS, MHA/MBA                               Experience:-0-1 Year        

Qualification & Experience   Qualification: DMLT/BMLT        Type: Full Time         Experience Required: 3-4 Years      

Qualification & Experience                   Department : Psychiatry Department    Qualification : PhD /M.Phil in Clinical Psychology with 3 to 5 years experience   

Qualification & Experience                   Qualification : MBBS -Fresher / 1-2 years Experience