Regulatory Specialist 2

Exalta Group• Remote, US,

88d•Remote

About The Position

This position is a subject matter expert in global medical device and quality system regulations and is responsible for regulatory strategy and planning, authoring and submitting regulatory applications, assessing product design, manufacturing, labeling and quality system changes, authoring change impact assessments, and ensuring product labeling documentation, labels, promotional material, and product claims are accurate and compliant with global regulations. The Specialist will ensure adherence to company policy and procedures and will assist in maintaining quality control processes. This position will help the organization maximize the number of patients served while maintaining a high level of quality and safety through the support of the business functions.

Requirements

A minimum of a bachelor’s degree in a scientific or technical discipline, preferably in regulatory, engineering, or biological science plus 3 or more years of relevant experience; in lieu of degree, 5 or more years of relevant experience may suffice.
Skilled with computers, takes advantage of new technology, learns new tools quickly, uses technology to enhance job performance
Understands facets of job, aware of duties and responsibilities, keeps job knowledge current.
Strong understanding of other functional items including product development, design controls and risk management.
Strong understanding of medical terminology, regulations, and guidelines related to medical devices and quality systems including FDA’s Quality Management System Regulation (QMSR), MDD 93/42/EEC, MDR 2017/745, and ISO 13485.
Information organized and accessible, maintains efficient workspace, manages time well
Knows product features, understands marketplace, shares expertise with others
Seeks to identify one’s self-improvement opportunities at work and takes appropriate action to address
Monitors status of projects, thoroughly deals with project details, holds project owners accountable, delivers clear, accurate depiction of status
Strives to eliminate errors, accurate work is a priority, seeks opportunities to improve product/services
Maintains understanding of technical processes/equipment, uses technology to increase performance/productivity
Adapts to change, open to new ideas and responsibilities
Communicates proficiently (written and verbal), delivers presentations, has good listening skills
Good listener, committed to finding solution to problems, works well with difficult people
Working cooperatively with internal and external customers in a manner that demonstrates a clear commitment to their needs and success
Able to reach decisions, takes thoughtful approach when considering options, seeks input from others, makes difficult decisions
Meets deadlines, works independently, accountable, maintains focus, punctual, good attendance record
High attention to detail
Honest, accountable, maintains confidentiality
Takes action, seeks new opportunities, strives to see projects to completion
Builds strong relationships, is flexible/adaptable, works well with others, solicits feedback
Strives to understands contributing factors, works to resolve complex situations
Manages workload, works efficiently, meets goals and objectives
Defines appropriate goals, works toward achieving goals, articulates vision and steps for achievement.
Working in a productive, dependable, and efficient manner to produce high quality results in accordance with deadlines and other expectations.
Looks for opportunities to increase knowledge, works to increase responsibility, strives to achieve personal goals
Meets deadlines, establishes appropriate priority, gets the job done in a timely manner, able to work under pressure
Works to establish and articulate visions, shows creativity when defining solutions
Demonstrating high levels of teamwork and ability to work cross-functionally
This position requires the use of personal protective equipment during various tasks/activities including but not limited to scrubs, gloves, masks, safety glasses, and safety shoes.

Nice To Haves

RAC certification(s) a plus

Responsibilities

Provides regulatory support to product development and business teams including preparation of regulatory opinion documents, coordination of labeling activities, and review/approval of design control documentation, risk management reports, technical protocols/reports, clinical documentation and other outputs of product development.
Prepares/writes, submits, and manages global regulatory applications (including MDSAP markets, EU, and UK) as well as internal regulatory file documentation. Supports distributors and business partners in securing and maintaining regulatory clearances.
Maintains systems for tracking current projects and for projection of future activity loads.
Acts as company representative, developing and maintaining positive relationships with global regulatory agencies and business partners through oral and written communications.
Works professionally and cooperatively with cross-functional teams such as research and development, operations, quality, microbiology, packaging, medical affairs, and clinical affairs to ensure project success.
Assesses product design, labeling, quality system, manufacturing, and material changes for regulatory impact. Communicates changes effectively throughout the organization. Authors key portions of company responses to proposed standards, directives, policies and legislation regarding company products and systems.
Develops, processes, and maintains assigned departmental procedures, work instructions, and forms, and facilities training. Reviews and supports creation/updates of labeling procedures.
Supports the design, development, review, and approval of product labels, label items, advertising/promotional materials and product claims to assure accuracy, consistency and compliance to global regulatory requirements, as well as company and customer requirements. This includes verification of labels and advertising/promotional materials, and creation, verification, review, and processing of instructions for use.
Monitors and assesses changes to global regulatory regulations, directives, standards and guidance requirements (regulatory intelligence assessment). Manage project teams for completion of required activities to ensure compliance.
Supports regulatory aspects of the quality system and product non-conformities and leads assigned corrective and preventive action activities.
Front-room participation in internal audits. Back-room participation in external audits.