More

    Quality Senior Specialist Job at TAPI – Join a Global API Leader

    Quality Senior Specialist – Build Your Future in Quality Assurance Jobs | Pharma Careers

    If you’re exploring growth-driven opportunities in quality assurance jobs and aiming to advance your journey in Pharma Careers, TAPI offers a powerful opportunity to contribute to global healthcare. As the world’s leading API manufacturer with 80+ years of expertise, TAPI provides a dynamic, compliance-focused environment where Quality Senior Specialists can make a meaningful impact in the pharmaceutical industry.

    Job Details:

    • Job Title: Quality Senior Specialist
    • Location :Not specified

    About The Company:

    At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies in various quality assurance jobs.

    Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence in our quality assurance roles. Join us and be part of a mission that transforms lives.

    Job Description:

    We are looking for a detail-driven Quality Senior Specialist with a strong foundation in GMP/GLP compliance and audit readiness to excel in quality assurance jobs.

    Key Responsibilities at This Quality Assurance Jobs:

    • Ensure on-time dispatch related activity like verification of any deviation/OOS/LIR & other related QMS elements in the batch or in its batch train.
    • Ensure review of all documentation (i.e. batch records, test results, deviation, LIR, OOS, CAPA, validation, COA, Change Controls, etc.) and perform disposition (release/rejection) of batches.
    • Ensure review of executed documents like batch record, analytical data, etc. and to ensure on-time compliance of error/deviations identified (if any).
    • Monitoring and follow-up of corrective and preventive actions (review, approval, and on-time closure of the CAPA) in order to resolve an event.
    • Review and approval Process/documentation (i.e. Protocol/report) of reviewing effectiveness to determine the effectiveness of a CAPA.
    • Involving in investigating, reviewing, and ensuring on-time closure of the investigation with resolution including CAPAs along with effectiveness determination.
    • Responsible for assuring/coordinating for timely shipment, delivery, and/or receipt to assure compliance with regulatory requirements.
    • Responsible for preparation of Annual quality review/periodic quality review.
    • Any task assigned by QA manager.

    Qualifications Required For Quality Assurance Jobs:

    The ideal candidate must have:

    • M Pharma with 3-5 years of experience.

    Skills

    • Good understanding of Pharmaceutical Quality System, GMP & GLP, which is essential for success in quality assurance jobs.

    CLICK HERE TO APPLY

    Related Articles

    LEAVE A REPLY

    Please enter your comment!
    Please enter your name here

    Stay Connected

    42,522FansLike
    21,523FollowersFollow
    32,000SubscribersSubscribe
    - Advertisement -

    Latest Articles