Brooks Steriscience Hiring for AM / Manager – Lab QA Role

brooks-laboratories-limited-recruitment-job-vacancies
WhatsApp Group Join Now
Telegram Group Join Now
Instagram Group Join Now
    • Full Time
    • Anywhere

    Brooks Steri science, a reputed name in the pharmaceutical sector, is inviting applications for the position of Assistant Manager / Manager – Lab QA at their state-of-the-art facility located in Karjan, Vadodara, Gujarat. This role is ideal for professionals with 10 to 12 years of experience in Quality Assurance, particularly within laboratory settings, and holding a Master’s degree in Pharmacy (M. Pharm).

    This is a golden opportunity to work with an organization that emphasizes regulatory compliance, innovation, and quality excellence in pharmaceutical manufacturing.

    Job Overview: AM / Manager – Lab QA

    Job Location: Block No 61/62, Village Manglej, Nareshwar Road, Tal: Karjan, Dist: Vadodara, Gujarat – 391210

    Position: Assistant Manager / Manager – Lab QA

    Department: Quality Assurance

    Qualification Required: M. Pharm

    Experience: 10 to 12 Years

    Email to Apply: bharti.makwana@brookssteriscience.com

    Key Responsibilities

    As an AM / Manager in the Lab QA department, your responsibilities will include but are not limited to:

    Leading investigations for laboratory incidents such as OOS (Out of Specification), OOT (Out of Trend), OOC (Out of Calibration), microbial excursions, and deviations.

    Reviewing and approving equipment calibration records, preventive maintenance schedules, and working standards for laboratory instruments.

    Overseeing stability studies, including sample charging and withdrawal activities, ensuring alignment with regulatory expectations.

    Validating and reviewing analytical data for commercial and stability batches, ensuring data integrity and compliance.

    Reviewing and approving Analytical Method Validation (AMV) and Analytical Method Transfer (AMT) protocols and reports.

    Ensuring documentation such as STP (Standard Testing Procedure), specifications, and data sheets are prepared in line with pharmacopoeial standards and ICH guidelines.

    Conducting Good Laboratory Practice (GLP) training for QA personnel to reinforce best practices in data handling and compliance.

    Ensuring implementation of updated pharmacopeial standards and maintaining audit readiness.

    Maintaining robust compliance with regulatory bodies and ensuring lab readiness for inspections and audits.

    How to Apply

    Interested candidates are encouraged to email their updated resume, clearly mentioning Present and Expected CTC, to:

    Email: bharti.makwana@brookssteriscience.com

    You must sign in to apply for this position.


    You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.



    WhatsApp Group


    Join Now


    Telegram Group


    Join Now