Dr. Reddy’s Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities..
- Important Details :
- Post of date:29/11/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Job Description : Greeting from Dr.Reddys Laboratories Ltd..!!!!
Vacancy details:
- Department: Team Member – Production – OSD (Granulation)
- Educational qualification: A Diploma or Bachelor’s degree
- Minimum work experience: 2-4 years of experience in pharmaceutical manufacturing operations, with a focus on batch manufacturing, and process validation
- Job Location: Visakhapatnam
Job Summary
We are looking for a candidate to oversee manufacturing operations related to all types of granulations and managing equipment.
Roles & Responsibilities
Adhere to the SOP’s and other laid down the procedures in the production area
Follow and adhere to the company safety norms, Company policies and procedures in the departments.
To ensure effective implementation of Company policies and Procedures in the departments.
Preparation and Review of alarm trending of equipment.
To ensure that the qualification, Validation, Calibration of equipment and process validation are done as per schedule and requirement.
Execution of M
Responsible for activities like Dispensing and Manufacturing (Granulation0 as per Production plan.
To perform on line entries in GMP documents like BMR’s, log- books etc. as per Good Documentation practice through manually or MES (Manufacturing Execution System).
To do operation & changeover of machine, their trouble shooting’s etc. as per SOP’s and instructions of seniors.
To fòllow the personnel hygiene practices.
To coordinate with the research and development and development and manufacturing sciences and technology team for planning and execution of the Exhibit Batches in the manufacturing Department.
To coordinate with the supervisor and other related departments for smooth functioning.
Preparation of disinfectant solution as per the schedule and respective SOP’s.
To ensure timely completion of calibration & Preventive maintenance activities of manufacturing equipment’s.
To coordinate with engineering department to reduce manufacturing breakdown time and ensure proper rectification of the problems occurred.
To ensure on time completion of assigned SOP trainings.
Review of area environment monitoring trends.
Review of Executed eBMR & workflows and ensure the submission to IPQA department on time.
Review the Audit trail reports of equipment.
To Perform any task/project assigned by HOD.
As part of all team area readiness, maintain to meet the current regulatory compliance & Norms
Skills & attributes:
Technical Skills
• Proficiency in understanding equipment such Granulation, Compression, Coating, Capsule Filling, Imprinting and Inspection etc.
• Understanding of Process Validation for Potent Oral Solid Product and cleaning procedures.
• Knowledge for evaluation of change control, deviation, incident, out of specification, out of trend, and risk management.
• Experience in preparing production process SOPs and batch records.
• Understanding and application of Aseptic processes, Lean, OEE, and similar KPIs.
• Hands-on experience in regulatory audits, particularly with agencies like the US FDA.
Behavioural Skills
• Capacity to provide training on good manufacturing practices and other relevant areas.
• Demonstrates a proactive approach to identifying and solving challenges in manufacturing processes.
• Exhibits a keen attention to detail in handling complex manufacturing activities, ensuring precision and accuracy.
• Collaborates seamlessly with cross-functional teams, promoting a cooperative and inclusive work environment.
• Efficiently manages time to meet production schedules and deadlines without compromising quality.
• Displays a willingness to stay updated on industry trends, regulations, and emerging technologies, contributing to ongoing professional development.
• Knowledge of working in regulatory environment like USFDA, MHRA, TGA.
• Should have good understanding of cGM, cGDP, and good laboratories practice.
• Must have hands-on experience in sophisticated manufacturing machine and equipment.
• Effective communication and training skills for user departments and service providers.
