Qa Senior Specialist

med-in.at

Base: $106,200.00 - $167,200.00; bonus/equity: ann...
Hybrid (3 days on-site, 1 day remote)
Cgmp compliance
Regulatory requirements
Quality systems management
The Senior Quality Specialist at med-in.at is responsible for ensuring compliance with cGMPs and regulatory requirements through quality systems and auditing activities. The role focuses on managing quality systems, conducting inspections, and supporting internal and external audits within a hybrid work environment

Job Summary

  • The Senior Quality Specialist is a key leader in ensuring site-wide compliance with cGMPs and regulatory requirements through robust quality systems and proactive auditing activities.
  • This role provides quality oversight for manufacturing operations, with primary responsibility for managing and executing critical quality systems (e.g., change control, deviation management, and document control), conducting GMP walkthroughs, and supporting internal and external inspections.
  • The salary range for this role is $106,200.00 - $167,200.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Medical, dental, vision healthcare and other insurance benefits, retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.

Matching Summary

Match Score: 85

The Senior Quality Specialist at med-in.at is responsible for ensuring compliance with cGMPs and regulatory requirements through quality systems and auditing activities. The role focuses on managing quality systems, conducting inspections, and supporting internal and external audits within a hybrid work environment.

Salary

Base: $106,200.00 - $167,200.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Medical, dental, vision healthcare and other insurance benefits, retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.

Skills & Requirements

Must-have

  • cGMP compliance
  • regulatory requirements
  • quality systems management
  • batch record review
  • SOP review and approval
  • deviation management

Nice-to-have

  • continuous improvement initiatives
  • team-based environment
  • proactive auditing activities
  • risk management

Key Requirements

  • Associate degree with five years experience
  • Bachelor's degree with three years experience
  • Familiarity with GMP documentation review
  • Leadership skills
  • Oral and written communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter