JB-203 – Senior Executive, Corporate Quality Control
Rhydburg
- Location
- Dehradun, Uttarakhand, India
- Job type
- Full-time
About the role
Rhydburg
Website:
rplglobal.com
Job details:
This is a remote position.
Job Description
- Review technical documentation related to finished pharmaceutical products prior to regulatory dossier preparation.
- Draft and review product specifications and analytical test methods for finished formulations.
- Coordinate with external testing laboratories for analytical testing of regulatory samples.
- Arrange and monitor testing of samples required for regulatory submissions.
- Review analytical data generated from external or internal laboratories for accuracy and compliance with specifications.
- Review batch manufacturing records and batch production records received from manufacturing sites.
- Verify quality control testing data and analytical reports generated during product analysis.
- Evaluate analytical documentation to ensure consistency with regulatory requirements and product specifications.
- Coordinate with manufacturing sites and quality control teams to resolve technical discrepancies in analytical data.
- Compile and organize verified technical documentation for regulatory dossier preparation.
Requirements
Requirements
- Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, or a related discipline is mandatory.
- Minimum two to three years of experience in Quality Control or finished formulation analytical testing within the pharmaceutical industry.
- Strong knowledge of pharmaceutical analytical testing, specifications, and laboratory practices for finished products.
- Experience drafting, reviewing, and understanding analytical methods and specifications.
- Ability to review batch manufacturing records, analytical reports, and technical documentation for regulatory compliance.
Benefits
Benefits
- Option to work from home or from office depending on operational requirements.
- Flexible working schedule with responsibility-based task ownership.
- Exposure to pharmaceutical analytical documentation and regulatory submission preparation.
- Opportunity to work with manufacturing sites and external analytical laboratories.
- Participation in technical compliance and regulatory preparation activities.
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