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\tEnsure Quality Management System procedures are established and maintained in compliance to International, National and Local regulatory requirements and company’s policies.

o\tIdentify changes to relevant regulatory requirements and industry standards o

o\tUndertake gap assessment activities to newer regulatory requirements o

o\tWork cross functionally to address the identified system gaps and implement changes o

o\tTrain the organization to ensure the new requirements are communicated internally

o\tDevelop 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\tProvide QA support for International Product Registration

o\tEnsure 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\tAssist with Internal and External Audit Activities

Skills:

Audit, Medical Device, quality systems management, Data entry, Quality assurance, Regulatory compliance, Gmp, NCR, Compliance

Additional Skills & Qualifications:

o Bachelor’s degree and 5+ years of related experience performing Quality System relatedactivities 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.

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 for other accommodation options.