Veristat International, Ltd is hiring a Senior Quality Control Associate to ensure the quality of critical documents for product development. Reporting to Medical Writing management, you will provide a meticulous quality control review to support regulatory submissions and medical communications.
What You'll Do
- Provide a thorough quality control review of regulatory documents and medical communications to support all phases of product development.
What We're Looking For
- A Bachelor’s degree is required.
- A minimum of 3 years of experience in a life science or clinical research environment, preferably in a CRO or pharmaceutical/biotechnology setting.
- Medical/technical writing experience and/or experience in a QC function is essential.
- Excellent command of the English language, including grammar, spelling, usage, and punctuation.
- Ability to focus and maintain a high level of attention to detail.
- Strong interpersonal and communication skills.
- Ability to function collaboratively in a team environment.
- Experience with Microsoft Office Suite is essential, including advanced Microsoft Word proficiency.
Nice to Have
- A Bachelor’s degree in a science-related field.
- Familiarity with medical terminology and statistical concepts.
Technical Stack
- Microsoft Office Suite
- Microsoft Word
Team & Environment
This role reports to Medical Writing management.
Work Mode
This is a hybrid position within a flexible and inclusive culture supported by a 70% remote workforce and 66% women-led teams.
Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
