Medical Safety Specialist II

Location: Center Valley

** Working

Location:

NATIONWIDE; PENNSYLVANIA, CENTER VALLEY*
* ** Workplace Flexibility:
Remote*
* ** _For more than 100 years, Olympus has focused on making people's lives healthier, safer and more fulfilling. ​_*
* ** _​_*
* ​

Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can fulfill their desires, dreams, and lives.

​

Our five Core Values empower us to achieve Our

Purpose:

** Patient Focus, Integrity, Innovation, Impact and Empathy.*
* Learn more about Life at Olympus:
.

** Job Description*
* As a Medical Safety Specialist II (MSSII) you will have an integral role in the day-to-day functioning of the global medical safety organization. In this vital role, you will execute upon medical safety processes globally (specifically for the Japan business)  an individual contributor you will influence the science and practice of all medical safety activities related to the detection, assessment, understanding of product risks and their effective mitigations to protect patients worldwide.

You will demonstrate the ability to apply your solid clinical experience, product expertise, and medical safety domain knowledge to collaborate and influence patient safety in activities being performed cross-functionally across the product lifecycle for all Olympus therapeutic areas.

You will report directly to the Senior Director Medical Safety as a member of the global medical safety team. You must be adept at cultivating strong collaborative relationships across Medical & Scientific Affairs as well as Infection Prevention & Control, Quality Affairs & Regulatory Affairs, Research & Development, Legal, and Health Care Compliance.

** Job Duties*
* + Complaint Assessment:  Uses tools created for consistency and SOPs to medically assess causality and severity of adverse events reported to Olympus.  Provides recommendations for escalation.

+

Risk Management:

Develops expertise of the risk management file documents for assigned products with responsibility to provide information related to observed and potential patient harm, severity, and mitigations to reduce potential for harm.

+ QARA Processes:  Develops an understanding of medical safety's role in QARA processes across the product life cycle and provides Medical Safety review and approval for PMS documentation, labeling/IFU creation, Clinical Evaluation Reports, developing responses to inquiries from regulators, Human Factors Engineering reports, non-conformance dispositions, and CAPA.

+ Cross-functional meetings:  Uses Medical subject matter expertise to represent Medical Safety in cross-functional meetings related to HHA, FCA, trending, and complaint review boards; internally aligns on and contributes to escalation of key events or issues with potential for safety impact.  Engages more experience team members if additional data or information is needed to facilitate medically sound decisions related to patient safety.

+ Medical Safety or cross-functional projects:  Plays an active role in contributing to Medical Safety priorities and initiatives, aligning goals and performance with business and functional objectives.

+ Uses clinical knowledge and experience to serve as a medical safety expert contributor to assess and understand product risk and influence and advise on mitigation strategies.

+ Searches, reviews, trends, understands, and interprets adverse event data, literature, and other safety-relevant data for the purpose of signal detection.

+ Demonstrates knowledge and experience working with:

+ Various regulations (HIPPA, EU-MDR, FDA 21 CFR Part 803, 806, 820)

+ Various standards (GCP, ISO 13485, ISO 14971)

+ Regulatory filings (FDA IDE, 510K, EU-MDR CERs, SSCP, PMCFs, PSURs)

+ Corrective Actions - Preventative Actions (CAPAs)

+ Health Hazard Assessment & Field Corrective Actions

+ Resolving product non-conformances

+ IMDRF dictionary terms and proficiency in adverse event coding and reporting

Post market surveillance, escalations, and mandatory safety reporting requirements.

+ Endoscopic diagnostic and therapeutic procedures in the following therapeutic areas:
Gastroenterology,…