Intern, QA-doc Control

1 day ago

Tuas, Singapore Pfizer Full time

Internship Scope (Duties & Responsibilities)

The incumbent will support the site document management system and ensure the end-to-end process is in full compliance with GMP predicate rules and Pfizer's internal requirements.
- Follow the site procedures in document issuance, reconciliation and archival.
- Collaborate with cross functional teams on controlled issuance and reconciliation.
- Understand regulatory expectations.

Working with the site document management team on the end-to-end process on Document system and retention requirement ensuring compliance with the regulatory cGMP requirements
- SME deck development for the process and understand the regulatory expectation.
- identify continuous improvement opportunities and work with site users to improve the process.
- support the annual product review process and data collection activities.
- plant walk as part of QA oversight.

Skills to be Developed
- Basic cGMP and GDP on pharmaceutical manufacturing
- Knowledge on documentation structure and retention requirement, data integrity and prevention
- Soft skill: people interactions, engaging and negotiations skills
- Annual product review requirement
- Basic QA oversight

Qualification

Diploma/ Degree in science

Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

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