Description Thomson is looking for a Senior Specialist in Quality Assurance to join our dynamic and growing team. This role is crucial for maintaining our high standards of quality and ensuring compliance with ISO certifications. The ideal candidate will be a seasoned professional with a strong background in quality assurance, documentation control, ISO/GMP certifications, and audits. Additional Skills & Qualifications • Act as the primary liaison between the Quality Control Manager and Documentation Control during audits, focusing on ISO certifications for non-manufacturing processes. • Oversee and manage documentation control, ensuring thorough preparation and compliance for audits. • Assume responsibility for processes that have been divided among multiple roles, streamlining and improving efficiency. • Lead the organization through audits as a certified auditor, drawing on experience from large organizations like Thomson. • Work closely with the Compliance and Quality Manager during internal ISO audits. • Direct project activities, providing guidance and support without direct management responsibilities. Qualifications: • • Open to candidates with various educational backgrounds, including those with extensive experience in lieu of a degree. • Preferably someone with significant experience, who has managed and navigated similar processes. • Strong analytical skills, attention to detail, and precision. • Experience with ERP systems, CAPAs, and detailed documentation. • Familiarity with ISO 9000 and ISO 13485 regulations. • Experience in the medical device, pharmaceutical, or biotech industries is acceptable. Pay and Benefits The pay range for this position is $37.00 - $47.00/hr. • Medical, dental & vision• Critical Illness, Accident, and Hospital• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available• Life Insurance (Voluntary Life & AD&D for the employee and dependents)• Short and long-term disability• Health Spending Account (HSA)• Transportation benefits• Employee Assistance Program• Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Carlsbad,CA. Application Deadline This position is anticipated to close on Feb 10, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.