Team Member_Packing
- Production - Sterile
- Pydibimavaram
- GMO
This vacancy has now expired. Please see similar roles below...
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.
For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).
‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency
Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.
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• Execution of Qualifications/Validations of packing equipment
You will be responsible for documentation and execution of qualification activities. This includes preparation, review and execution of URS (User Requirement Specification), DQ (Design Qualification), FDS (Functional Design Specification), UTM (User Traceability Matrix), IQ (Installation Qualification), OQ (Operational Qualification), PQ (Performance Qualification), RQ and (Requirement Qualification) documents.
• Your responsibilities include review of miscellaneous qualification documents and preparation and review of risk assessments for equipment and systems.
• You will be responsible for new project related FAT (Factory Acceptance Test) and SAT (Site Acceptance Test).
• You will review and compile raw data, relevant certificates, analysis test reports and
• preparation and review of final summary report.
• You will be responsible for preparation and review of protocols and reports for media fill validation and cleaning validation.
• Your role involves initiation of relevant CRN (Change Request Number) for new or existing activity, timely closure of assigned action plans as per CRN, and CRN review and approval.
To ensure and adhere Organization Safety/Quality policies, Procedures, norms and its effective implementation from time to time.
Ensure the adherence of SHE standards and policies across the plant with respect to MSI.
To follow the personnel hygiene practices and discipline.
Maintaining cGMP practices in production area and report any discrepancies/incidents to immediate supervisor.
Educational qualification and work experience
Educational qualification: A B.Pharm/M.Pharma
Minimum work experience: 4 to 6 years of experience in qualification activities
Skills & attributes
Technical Skills
• Experience in working with sterile product facility related validations such as equipment validation, media fill, cleaning validation, process validation, area qualification, and other miscellaneous qualifications.
• Expertise in preparation, review, and execution of documents, including URS, DQ, FDS, UTM, IQ, OQ, PQ, RQ.
Behavioural skills
- Effective listening skills, ensuring a comprehensive understanding of information.
- A keen eye for detail, ensuring accuracy and precision in tasks.
- Awareness and sensitivity to deadlines, ensuring timely completion of tasks.
- Analytical skills and the ability to troubleshoot, enabling effective problem-solving.
- Strong interpersonal skills and the ability to work well in a team, fostering collaboration and positive team dynamics.
At Dr. Reddy’s, we actively help to catalyze your career growth and professional development through personalized learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards...
" 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...
For more details, please visit our career website at https://careers.drreddys.com/#!/
"
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