Qa Senior Specialist

MOBS Lab

Base: $106,200.00 - $167,200.00; bonus/equity: ann...
**
Cgmp compliance
Regulatory requirements
Quality systems management
** MOBS Lab is seeking a Senior Quality Specialist to ensure compliance with cGMPs and regulatory requirements through quality oversight in manufacturing operations. The role involves managing quality systems, conducting audits, and collaborating with various teams to implement continuous improvements. **

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 successful candidate will be eligible for annual bonus and long-term incentive, if applicable, and a comprehensive package of benefits including medical, dental, vision, retirement benefits, paid holidays, vacation, and compassionate and sick days.

Matching Summary

Match Score: 75

** MOBS Lab is seeking a Senior Quality Specialist to ensure compliance with cGMPs and regulatory requirements through quality oversight in manufacturing operations. The role involves managing quality systems, conducting audits, and collaborating with various teams to implement continuous improvements. **

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 (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.

Skills & Requirements

Must-have

  • cGMP compliance
  • regulatory requirements
  • quality systems management
  • GMP walkthroughs
  • batch record review
  • SOP review

Nice-to-have

  • continuous improvement initiatives
  • team-based environment
  • validation activities
  • process simulation 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
  • Understanding of cGMPs and regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter