Posted:10 hours ago|
Platform:
On-site
Part Time
Summary of Key Responsibilities:
Responsibilities include adequate and accurate review of analytical data generated for regulatory submission.
Review documents of Validation reports, Analytical reports
Review of data generated for regulatory filing
Ensure data integrity through review
Ensure adequacy of documents with respect to ICH and regulatory guidelines
Complete documentation activities for review and approval of documents
Audit trail review for data reviewed
Review data in instrument applications like Empower
Minimum requirements
3 years of previous work experience in lab or QC, Minimum 2+ years of relevant experience in
document review
Bachelor’s /Master degree in Science
Ability to work collaboratively in a fast-paced, high energy organization
Report writing skill
Behavioral competencies
Work in Team
Communication skills
Willingness to learn
Sun Pharmaceutical Industries Ltd
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