Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
1.Vacancy details:
- Department :Team Member – Packing
- Qualification:A Bachelor’s or Master’s degree in Pharmaceutical Sciences, Chemical Engineering, or a related field
- Experience – 7 years
- Salary: ₹ Not Disclosed
Job Description: Greetings from Wipro Ltd..!!
- Important Details :
- Location: Visakhapatnam
- Post of date:12/06/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Job Description
Job Summary
We are looking for a candidate to oversee manufacturing and production operations, managing equipment, process validation, handling change controls, deviations, incidents, and ensuring compliance with regulatory audits. Responsibilities include creating SOPs (Standard Operating Procedure), providing training, and applying expertise.
” Roles & Responsibilities
- You will be responsible for handling line operations, specifically production and manufacturing activities like CIP (Cleaning-in-place), SIP (Sterilizing-in-place), and batch manufacturing.
- You will be responsible for handling equipment like Steam Sterilizer, Dry heat sterilizer, HVAC (Heating, Ventilation, and Air Conditioning), water system, compressed air, Nitrogen system, etc.
- You will be responsible for process validation for Sterilization, Washing, Aseptic filling, and cleaning procedures.
- You will evaluate change controls, deviation, and incident, (OOS) out of specification, (OOT) out of trend, and risk management.
- You will prepare the production process SOPs (Standard Operating Procedures) and batch records.
- You will provide training on GMP (good manufacturing practices).
- You will apply knowledge of aseptic processes, Lean, OEE (Overall Equipment Effectiveness), and similar KPIs (Key Performance Indicators).
- You will respond to queries and questions regarding regulatory audits such as US FDA (Food and Drug Administration).
Qualifications
Educational Qualification
A Bachelor’s or Master’s degree in Pharmaceutical Sciences, Chemical Engineering, or a related field
Minimum Work Experience
7 years of experience in pharmaceutical manufacturing operations
Skills & Attributes Technical Skills
- Expertise in line operations, especially in manufacturing activities like CIP, SIP, and batch manufacturing.
- Proficiency in understanding equipment such as Steam Sterilizer, Dry heat sterilizer, HVAC, water system, compressed air, Nitrogen system, etc.
- Understanding of Process Validation for Sterilization, Washing, Aseptic filling, 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.
- Good understanding of GMP and good laboratories practice.
Behavioural Skills
- Capacity to provide training on GMP and other relevant areas.
- 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.
- Must have hands-on experience in sophisticated manufacturing machines and equipment.
- Effective communication and training skills for user departments and service providers.
Additional Information
About the Department – Global Manufacturing Organisation (GMO)
At 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. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. The World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future.
” Benefits Offered
At Dr. Reddy’s, we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.
” Our Work Culture
Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
For more details, please visit our career website at https://careers.drreddys.com/#!/
2.Vacancy details:
- Department :Team Member – QC Micro
- Qualification:BSC – Microbiology & MSC – Microbiology
- Experience – NA
- Salary: ₹ Not Disclosed
Job Description
- Follow SOPs for conducting QC operations as per requirements.
- Perform Environmental Monitoring (EM) activities in manufacturing areas and the microbiology laboratory.
- Prepare water trends and EM trends on a monthly, semiannual, and annual basis.
- Conduct microbial sampling for water for injection, purified water, potable water, and pure steam.
- Conduct sampling for compressed gases and nitrogen gases.
- Perform water analysis on water samples according to procedures.
- Decontaminate released media plates and biological indicators according to procedures.
- Operate steam sterilizers, decontamination autoclaves, and hot air ovens.
- Verify media stock and other lab consumables related to microbiology.
- Release microbial analysis plates and tubes (water analysis, environmental monitoring, bioburden, MLT, or any microbial activity plates and tubes) and update results in LIMS while compiling COAs.
- Perform daily calibrations of balances and pH meters.
- Prepare disinfectants and perform equipment cleaning and monitoring.
- Carry out Media Preparation, sterilization, and GPT for Ready To Use/in-house prepared media.
- Ensure that all equipment and instruments are in a validated and calibrated state.
- Participate in Media filled vial observations.
- Maintain media/cultures properly in the microbiology laboratory.
- Perform microbial examination of non-sterile products (Microbial Limit Test) and method validation.
- Conduct in-process bioburden testing, method validation, and cleaning validation samples.
- Enumerate and inoculate biological indicators (BI’s).
- Perform container closure integrity testing for media fill vials after release.
- Isolate, subculture, and identify environmental isolates using the Vitek 2 identification system.
- Escalate issues to Team Leader/HOD.
- Perform any other assignments given by the Team Leader/HOD.
Qualifications
BSC – Microbiology & MSC – Microbiology
