Overview:
TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV, hepatitis B, hepatitis C, and influenza, including Harvoni and Sovaldi.
Description:
- Collaborates with customers to ensure the correct and timely implementation of customer requests and document processing.
- Support the archival and submission of Quality Control related documents
- Supports the distribution, maintenance, and archival of GXP documentation.
- Scans, verifies and archives documentation as needed
- Recommends process improvements and proposes changes.
- Provides support with internal and regulatory audits/inspections as required.
- May participate in training users for electronic systems (as applicable).
- Supports the maintenance of periodic metrics. Trends relevant KPIs for various projects.
- Performs general word processing tasks and support.
- Checks format and conformance to document templates, verifies own work.
- Effectively utilize Microsoft Office and Adobe Acrobat in conjunction with daily tasks
- Provides additional support and assistance on tasks and projects as directed by management.
- Participates as required in training on issues affecting own department. Notifies manager of compliance questions and issues.
- Additional duties as assigned.
- These duties can be delegated to designated deputies of a satisfactory qualification level as needed.
- Exhibits a compliance-oriented mindset with a commitment to quality and integrity.
- Meticulous attention to detail required.
- GMP experience preferred.
TekWissen® Group is an equal opportunity employer supporting workforce diversity.
Job Types: Full-time, Contract
Pay: $20.00 - $22.00 per hour
Application Question(s):
- How many years of experience do you have in the implementation of customer requests and document processing?
- How many years of experience do you have with Quality Control related documents?
- How many years of experience do you have with GXP documentation?
Work Location: In person
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