Dr Reddy’s Laboratories Ltd Hiring 2022 Dr Reddy’s Laboratories Ltd Notification full details below..Interested and eligible candidates can Apply Now.Dr. Reddy’s Laboratories is an Indian multinational pharmaceutical company located in Hyderabad, Telangana, India. The company was founded by Kallam Anji Reddy, who previously worked in the mentor institute Indian Drugs and Pharmaceuticals Limited.Dr. Reddy’s manufactures and markets a wide range of pharmaceuticals in India and overseas.
- Post Name: Production specialist (Downstream)
- Department: Biologics
- Qualification: Science Post Graduate
- Experienced: 01 to 4 Years
Job Description: Dr Reddy’s Laboratories Ltd Hiring For Production specialist (Downstream) !
Important Details :
- Post of date:09/09/2022
- Location: Hyderabad, Telangana, India
- Skills Required: Chromatography systems, TFF operations & filtration techniques, Autoclave operations, QMS
- Selection Process: The selection will be on the basis of Interview.
Roles and Responsibilities
|Execute unit operations within DS/UPS as per the BPR ; Conducts activities in support of production schedules; Obtains and stocks supplies as required and under supervision; Prepares media / buffers and solutions as required for the unit operation , Perform routine cleaning and support activities in GMP Manufacturing areas, including rotuine process area cleaning, autoclave operation, manual cleaning and sterilization of components and parts; Monitors processes and results and suggest methods to ensure process success ; Interfaces with process automation systems
IN ORDER TO execute unit operations as per the production specification and yield requirements
|Compliance & Documentation|
|Issues discrepancies and work with cross-functional departments to close the discrepancies and implement appropriate corrective actions; Comply with all relevant GMP, safety standards and SOPs of the operation of designated manufacturing equipment. Complete batch documentation in compliance with GMP. Collection and maintenance of data in accordance with cGMPs, company standards, policies and other regulatory requirements; Supports team in effective and timely completion of root cause investigations and CAPA
IN ORDER TO ensure effective and efficient production operations across all plants.
|Maintaining manufacturing equipment to ensure correct functionality and calibration compliance. Operation of manufacturing equipment and automated systems within the validated process parameters ; Support qualification and validation activities
IN ORDER TO ensure that the batch runs on a qualified equipment.
|Safety & Facility Inspection|
|Actively promote safety awareness and improvements; Proactively engage in continuous improvement activities; Adhere to the companys safety rules and conduct all work in a manner report all unsafe matters and near miss /accidents.
IN ORDER TO ensure safe and hazard free production operations
How to Apply :
Step 1: Click on below link and you will be redirected to Career Page of Recruiting Company or Career portal.
Step 2. Register on Career Page of the Company or Career Portal by giving log in credentials and other personal or education details .
Step 3.Upon successful registration .User need to log in with credentials.
Step 4.Once logged in, User need to fill the all relevant personal ,educational , Work experience details ,attach resume and submit application form.