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    Team Member Quality Control - Visakhapatnam, India - Dr Reddy's Laboratories Limited

    Dr Reddy's Laboratories Limited
    Dr Reddy's Laboratories Limited Visakhapatnam, India

    Found in: Talent IN C2 - 1 week ago

    Default job background
    Full time
    Description
    Job Description


    Job summary

    We are seeking an individual to test samples and complete within window period for stability batches, adhering to GMP (Good Manufacturing Practices).

    This role involves calibrating and maintaining assigned equipment within departmental and organizational guidelines, processes, and procedures. The primary objective is to ensure accuracy in results provided within timelines.


    Roles & Responsibilities

    • Your responsibilities encompass testing assigned samples and releasing data within defined timelines, ensuring absence of executional errors against established procedures. You will be responsible for preparing required reagents and buffers in alignment with the testing plan and ensuring the availability of equipment for analysis.
    • Your role involves documenting activities contemporaneously, adhering to Good Documentation Practices and compliance expectations, and conducting self-checks post-analysis to ensure accuracy.
    • You will promptly inform the supervisor about risk actions, providing necessary data and analysis to support the investigation process. You will adhere to QMS (Quality Management systems) and closure timelines, actively participate in laboratory investigations and discrepancy closures, fulfilling defined roles in audits.
    • Your responsibilities also include ensuring lab cleanliness, proper sample storage, chemical labeling, removal of expired material, usage of calibrated equipment, equipment calibration, maintenance, and qualification.
    • You will address instrument-related issues and conduct root cause analyses (RCAs) for unknown problems, and play a crucial role in training new team members on analytical techniques.
    Qualifications


    Educational qualification:
    An M.Sc., M.Tech. or B.Tech. in Microbiology, Biochemistry, or Biotechnology


    Minimum work experience: 2 years


    Skills & attributes:

    Technical Skills


    • Basic understanding of the Analytical skills in pharma labs, including processes, regulations, and trends.
    • Hands-on experience in High-Performance Liquid Chromatography (HPLC) techniques, including Size Exclusion, Reverse Phase, Ion Exchange chromatography, and Peptide mapping analysis, especially within the context of Analytics.
    • Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP).
    • Basic knowledge in protein chemistry, including an understanding of protein structure, function, and relevant analytical techniques.
    • Basic knowledge and hands-on exposure to Microbiology techniques, particularly relevant for individuals working in Microbiology Labs.

    Behavioural skills

    • Prioritizes effective communication and demonstrates a performance-oriented mind-set.
    • Effective verbal and written communication skills.
    • Performance-oriented approach, consistently striving for high standards.
    • Demonstrates flexibility in working shifts and a clear understanding of team dynamics.
    Additional Information


    About the Department
    Biologics

    Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon.

    With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities.

    Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products.

    With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation.

    Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs.
    We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure

    Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date.


    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

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