Medical Writing Operations Specialist II

This role will perform quality review of regulatory documents to ensure content accuracy and consistency. The ideal candidate will have a strong working knowledge of drug development process, regulatory guidelines, industry standards, and best practices.

Requirements

• BS/BA degree in a related discipline
• 5+ years of experience in Biotech/Pharmaceutical industry
• 3-5 years of quality assurance, clinical development, or laboratory experience
• BELS certification is a plus

Benefits

• Comprehensive employee benefits package
• 401k plan with generous company contributions
• Group medical, dental and vision coverage
• Life and disability insurance
• Flexible spending accounts
• Discretionary annual bonus program
• Sales-based incentive plan
• Opportunity to purchase company stock
• Long-term incentives
• 15 accrued vacation days in the first year
• 17 paid holidays
• Up to 10 sick days throughout the calendar year