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Team Member - Documentation

Job in Lincoln, Lancaster County, Nebraska, 68511, USA
Listing for: Dr. Reddy’s Laboratories Ltd
Full Time position
Listed on 2026-08-02
Job specializations:
  • Business
    Data Analyst, Data Scientist
Salary/Wage Range or Industry Benchmark: 90000 - 120000 USD Yearly USD 90000.00 120000.00 YEAR
Job Description & How to Apply Below

Company Description

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. Asthepharmaceutical 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 Nextand 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.

Job Description
  • Preparation, Review and approval of Standard Operating Procedures (SOPs).
  • Preparation, review and approval of various protocols and reports, including:
    • Confirmatory Batch Protocol
    • Hold Time Protocol
    • Process Evaluation (Pre-validation) Protocol
    • Trial Protocol
    • Process Performance Qualification/Validation Protocol
    • Stability Protocol
  • Preparation, Review and approval of Master Production Records (MPRs) such as:
    • Master Formula Record (MFR)
    • Manufacturing Instructions (MI)
    • Production Order Raw Materials (PORM)
  • Team management and daily work plan assignments and monitoring of daily deliverables inline with the Plan / shopfloor requirements
  • Good process knowledge of Injectable processes
  • Designing of Master Batch Records (MBRs) in PASIX, ESP, GM , PVL, and PM  based on MPR/PIS/MPC for new products as well as site transfer products, following SOPs and GMP requirements.
  • Good decision making skills for
  • Document circulation to cross-functional teams (CFT), follow-up for review, corrections, and approval.
  • Creation and modification of Bill of Materials (BOM) and Recipes in SAP.
  • Follow-up for BOM and Recipe-related tasks for Exhibit, Validation, and Commercial products.
  • Creation of codes in SAP, such as:
  • Creation of reservations in SAP.
  • Inter and intra communication for sending BOM messages to CFTs.
Qualifications

B.Pharm/M.Pharm/M.Sc

MES Design Exposure good to have

Additional Information

Global Manufacturing Organisation (GMO)
dy'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. he World Economic Forum has recognised our largest…

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