JT177 - QUALITY SYSTEMS SPECIALIST
San Juan, Puerto Rico
Temporary
Medical Device
Mid Level
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA
Responsibilities:
- Provides oversight for the development and maintenance of quality programs, systems, processes and procedures that ensure compliance with policies and that the performance and quality of services conform to established standards and agency guidelines.
- Provides expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and agency guidelines to assure compliance.
- Works directly with operating entities to provide process analyses oversight on a continuing basis to enforce requirements and meet guidelines.
- Leads audit and inspection preparation, resolution of audit and inspection findings and liaises with auditing groups and inspectors through all stages of the audits.
- Coordinates legal requests in support of government investigations or litigations.
- Ensures the quality assurance programs and policies are maintained and modified regularly.
- Facilitates uniform standards worldwide and enables best practice sharing, thereby fostering the achievement of company's mission globally.
Qualifications:
- Bachelor’s degree in Science, Engineering, or related field required with a minimum of 2 years of Quality Management Systems and medical device experience
- Strong understanding of global regulatory requirements for medical devices, including FDA regulations (e.g., 21CFR Part 820), ISO 13485, Medical Device Directive, and European Medical Device Regulation.
- Experience defining, driving, and implementing process improvement and functional excellence efforts.
- Strong organizational skills and time management skills
- Ability to multitask, support multiple projects, function globally, prioritize, conduct team meetings, and meet project deadlines.
- Proven experience in achieving results through influence management and motivating teams.
- Good communication (oral and written), presentation, and interpersonal skills. (Bilingual)
- Exhibits high degree of initiative and good judgment.
- Experience working with Change Control, CAPA, documentation, audit and/or training.
Trackwise and MAP Agyle tools knowledge
- Availability for 1rst shift
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
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