Description In compliance with FDA, European MDD/MDR & ISO regulations, the Sr. Quality Systems Specialist will perform work under general supervision. The general scope of this position is to assist in maintaining quality compliance, managing new geographies Quality Compliance Assessments, managing actions for the audit findings and CAPAs, assisting with External Standards management process, supporting audit activities and compiling quality metrics. This position requires frequent use and general knowledge of industry practices, techniques, and standards. You will assist the Principle Quality Specialist with the following: o Ensure Quality Management System procedures are established and maintained in compliance to International, National and Local regulatory requirements and company’s policies. o Identify changes to relevant regulatory requirements and industry standards o o Undertake gap assessment activities to newer regulatory requirements o o Work cross functionally to address the identified system gaps and implement changes o o Train the organization to ensure the new requirements are communicated internally o Develop and implement Standards and Regulation tracking and information collection tools, maintain Standards logs with current revisions of the standards, and report on progress of implementation o Provide QA support for International Product Registration o Ensure regulatory compliance to US, Europe and other international regulations to ensure market access and support commercialization efforts o Compile Quality records to support international regulatory submissions o Assist with Internal and External Audit Activities Skills Audit, Medical Device, quality systems management, Gap assessment, Regulatory, Data entry, Quality assurance, Regulatory compliance, Gmp, NCR, Compliance Top Skills Details Audit, Medical Device, Quality systems Management, Gap Assessment, Regulatory Additional Skills & Qualifications o Bachelor’s degree and 4+ years of related experience performing Quality System related activities in the medical device industry. o Working knowledge of cGMP, FDA 820 QSR and ISO 13485 or other Quality Systems. o Proficiency in data compilation, analysis, presentation, and document writing skills. o Excellent written and verbal communication skills. o Excellent organizational skills. o Experience with computer-based applications (MS Word, MS Excel, QAD). o Strong time management skills and the ability to multi-task in a fast-paced environment. o Operate as a team and/or independently while demonstrating flexibility to changing requirements. Pay and Benefits The pay range for this position is $45.00 - $59.00 Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • 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 Santa Clara,CA. Application Deadline This position will be accepting applications until Dec 27, 2024. 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.