QA Specialist

**Work mode**:Hybrid

**Onsite Location(s)**:Lima, Peru

**Additional Locations**: N/A

**Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance**
- At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing - whatever your ambitions.

**Your Responsibilities will include**
- Coordinate and maintain Quality system data to assist QA Latam teams in making critical assessment of the health of the quality system by executing the required elements: including data collection, data base population and updating, logging and tracking of issues/action items, conducting analysis, generating reports, creating presentations, participating in core team meetings, and documentation through meeting minutes or released quality documents. Verify compliance with local health regulations.
- Create summary presentations of the analysis for review by a variety of key stakeholders.
- Work with QA and other leaders to identify areas within the quality system in need of improvement and execute NCEPs and Corrective and Preventive Actions as appropriate.
- Assist in the Quality Systems portfolio management by monitoring, tracking, and providing data to management around the quality system for review in templates and presentations.
- Provide data to project/department managers on status of project metrics for their assigned project including tracking milestones, budget attainment, and other relevant metrics.
- Ensure that improvement project deliverables meet regulatory and corporate standards. Assist in the execution of assigned project plan and changes to business practices.
- Ensure that the quality assurance system in the stages of reception, storage, and distribution guarantees the conservation, stability, and quality of pharmaceutical products, medical devices, and health products, and for controlled products, their custody.
- Control that the commercialization of products is carried out exclusively to pharmaceutical establishments, commercial establishments, or the final consumer, as appropriate.
- Support local strategies for regulatory approval in collaboration with Marketing, Planning, Regulatory and International Division teams.
- Coordinate the localization process to ensure compliance with Peru´s labeling requirements.
- Foster positive relationships with regulatory agencies and industry associations through verbal and written communications, acting as the focal point for regulatory advocacy in Peru.
- Order the withdrawal from the market of products or devices from batches, series, or identification codes, when necessary, and communicate the fact, when appropriate, to the National Authority of Pharmaceutical Products, Medical Devices, and Health Products.
- Authorize the marketing of products or devices after verifying their compliance with the specifications approved in the sanitary registration.
- Verify that official books or electronic data records are kept up to date and remain in the establishment.
- Train and supervise assistant and technical staff in the correct performance of their duties.
- Ensure the accuracy of the statements, documentation, and information submitted to request the Sanitary Registration or its modification.
- Notify suspected adverse reactions and adverse incidents of pharmaceutical products, medical devices, or health products in the authorized format (physical or electronic) validated and within the deadlines established in local regulations if stricter than BSC, while maintaining the confidentiality of these notifications.
- Report to the National Authority of Pharmaceutical Products, Medical Devices, and Health Products (ANM) the quality control analysis protocols or quality control test reports of the batches entering the market, as established by local regulations.
- Verify that the promotion and advertising produced and disseminated in drugstores comply with current regulations.

**What we are looking for in you**

Required Qualifications:

- Bachelor's Degree in Pharmacy, licensed to assume Technical Direction.
- Minimum 3 years of experience in the medical device Quality & Regulatory Affairs field.
- Knowledge of DIGEMID regulations.
- Advanced proficiency in English.
- Experience in interactions with regulators: Regulatory Intelligence, Advocacy, and/or Policy.
- Ability to read, analyze, and interpret general, scientific, and business periodicals, as well as governmental regulations.
- Excellent attention to detail with the ability to identify trends and gaps.
- Ability to manage databases in software and systems.
- Effective communication of complex ideas, both verbally and in writing, good drafting skills.
- Team player with excellent interperson