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    Pharma Jobs in Hyderabad: Dr. Reddy’s is Hiring a Process Engineering Specialist – Apply Now

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    Pharma Jobs in Hyderabad: Dr. Reddy’s is Hiring a Process Engineering Specialist – Apply Now

    Are you actively looking for Pharma Jobs in Hyderabad?
    Dr. Reddy’s Laboratories, a global leader in pharmaceuticals, is hiring a Process Engineering Specialist for its Hyderabad location. This on-site, full-time role offers an opportunity to work with advanced inhalation and injectable formulations, focusing on Quality by Design (QbD), process optimization, and technology transfer. Ideal candidates will have a strong background in pharmaceutical formulation development, process scale-up, and manufacturing readiness within a reputed pharma organization.

    About the Company:

    Founded in 1984, Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company driven by the mission to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. With more than 24,000 employees and a presence in 66 countries, the company stands for access, affordability, and innovation. Its strategy—The Next and the New—focuses on building a sustainable future by combining scientific excellence with responsible corporate governance. Dr. Reddy’s promotes diversity, equity, and inclusion, maintaining a workplace free from discrimination and fostering equal opportunities for all.

    Job Details:

    • Job Title: Process Engineering Specialist in Inhalation/Injectable formulations
    • Location: Hyderabad, Telangana, India
    • Job Type: Full-Time, On-site

    Roles & Responsibilities:

    • Deliver inhalation/injectable and other product types by combining formulation development with process understanding.
    • Collaborate with the manufacturing team for plant readiness and execution of manufacturing trials.
    • Apply expertise in QbD, process optimization, and dosage form development.
    • Analyze material characteristics and their impact on stability and manufacturability to design validation experiments.
    • Partner with R&D for process robustness, scalability, and cost efficiency.
    • Prepare technology transfer documents, safety files, and batch records, and review validation reports.
    • Ensure facility preparedness, batch execution, and troubleshooting at the plant and vendor sites.

    Qualifications:

    Master’s in Pharmaceutical Sciences / M.Tech in Chemical Engineering.

    Experience:

    3–8 years in pharmaceutical companies focusing on injectable formulations.

    Skills & Attributes:

    • Expertise in formulation development, QbD, process optimization, scale-up, and technology transfer.
    • Knowledge of GMP and GLP standards.
    • Strong communication, analytical, and problem-solving skills.
    • Ability to work collaboratively across teams.

    CLICK HERE TO APPLY

    Apply now

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