Pharma Quality Officer Vacancy 2022 - Apotex - Apply Online

Pharma Quality Officer Vacancy 2022 – Apotex – Apply Online

Quality officer vacancy. Pharma senior quality officer vacancy. B Pharma job opening 2022. Candidates with bachelor’s degree in pharma and MSc degree may apply for the job vacancy at Apotex. Apotex job opening 2022. Pharma job. Check out all the details on the same below:

Job Title: Senior Officer, Quality Cnt-ARPL-QCST AR

Location: Bangalore, KA, IN, 560099

Eligbility Criteria:

MSc/B Pharm or any equivalent degree.

Knowledge, Skills, and Abilities

  • Command on Microsoft Office (Word, Excel).
  • Able to prioritize the tasks.
  • Best in effective planning of work activities to meet the timelines.
  • Able to perform multi-parameter analysis on HPLC instrument.

Experience:

Minimum 2 to 4 years of experience in GMP regulated Pharmaceutical Industry.

Job Summary

Method verification/validation of compendia/pharmacopeial updations, Method verification of SDC’s (Supplier Driven Changes) method. Method validation of cleaning verification, Preparation of method verification and validation protocols and reports, Evaluation of SDC, compendial/pharmacopeial updations, Preparation of In-House method, and Specification. Analysis of raw material and excipients.

Job Responsibilities

  • Analysis of Compendia, raw material samples, Analytical method transfer samples as per the method of analysis by adhering to the regulatory procedures.
  • Preparation and review of Memo, Method Verification/ Method validation protocols, Method Verification/Method validation reports, and Method transfer summaries.
  • To involve in investigations and excursions as per SOP, to provide technical support during investigations of OOS/OOT results, and to identify assignable causes.
    Compendia changes review and method verification.
  • To perform the cleaning validation as per the protocol.
  • Perform all work in accordance with all established regulatory and compliance and safety requirements.
    Responsible for preparation and updating of specification and method of analysis as per regulatory requirements and compendia requirements.
  • To be responsible for all activities in the Quality control Laboratory, including cGLP, documentation, and implementation of the departmental quality system as and when required.
  • To generate and maintain records related to laboratory samples.
    Works in a safe manner collaborating as a team member to achieve all outcomes.
  • Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.
  • Ensure personal adherence with all compliance programs, including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
  • All other relevant duties as assigned.

Apply Online

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