Do you have an eye for detail and desire to get at the root causes of compliance problems? Whether you're skilled at seeing the impact of process inefficiencies in ineffectiveness, improving quality metrics, or leading critical projects, our Pharmaceutical & Medical Device clients are seeking experienced Compliance and Regulatory professionals who live to solve complex problems.
At PRP, our Recruiting Specialists listen to you, putting your goals and work/life balance needs at the center of our search efforts. Our main focus is your happiness, which we know comes from finding a job where you feel motivated and respected for the hard work you do every day.
You always know what to expect when entering a new position through PRP (the role, responsibilities, culture, etc.), and enjoy benefits such as medical, dental, vision, 401K Plan and life insurance. Oh, and did we mention the incentive bonuses based on client feedback?
Check out today's Quality & Regulatory Compliance jobs below — from the world's best Pharmaceutical & Medical Device organizations — and get in touch by applying!
See all Quality & Regulatory Compliance Jobs 
Project Manager for Project Management
This position is responsible for acting as the end to end project leader on change projects, following-up with all projects and design control tasks from concept through full implementation. Responsible for leading collaboration for project requirements and coordinating strategies within a cross functional team including Regulatory, Quality, R&D, Planning, Master Data, Engineering, and Product Management as required. Must be a Subject Matter Expert (SME) for Design Change Control Process.
Location: NJ | Apply
Project Manager (Remote)
Project Manager (PM) with experience designing & delivering project management materials and project management support to two projects. The PM will collaborate with project leads and subject matter experts to develop/ execute established plans/ timelines, as well as develop contingency plans, risk/mitigation, meeting minutes, action and decision logs for these projects. This is a remote role, with occasional travel for meetings in NYC.
Location: Remote + Some Travel | Apply
Lab Technician
The LabTechnician performs routine and complex operations for the GMP production of pharmaceutical products. The tech operates in accordance with environmental, health, safety, and cGMP guidelines. This role is responsible for the hands on execution of production activities and utilizes process knowledge to influence positive change during the review and revision of Standard Operating Procedures (SOPs) and other process documentation.
Location: MA | Apply
Research Associate
This is a a lab-based role. As a Research Associate, you will be working with senior formulation scientist daily basis in the lab. This role will prepare the protocols and assist Senior Formulation Scientist doing research at the cutting edge of nanoparticle synthesis and characterization
The primary responsibilities will include managing the everyday needs of the lab including helping senior members with routine protocols; ensuring proper maintenance of the laboratory equipment, buffers, stock solution and perform routine in vitro tests.
Location: NY | Apply
Design Verification Engineer
Participate in the execution of any 510 K remediation R&D. Assist in the development of DV protocols & reports. Assist in development of DV test plans. Assist in performing Test. Assist in root cause investigation of statistical or test failures. Assist with Test Method Development & validation. Assist in review of historical data and determining validity and / or establishing next steps. Assist in in gap analysis of Design History Files (DHF) content. Support Design Control and / or Change Control processes
Location: IN | Job Type: Contractor | Apply
Testing Engineer
The Testing Engineer develops test methods, solves various engineering problems, and performs testing studies for a wide range of medical devices across multiple strategic business units.
In this role will you will utilize engineering knowledge and technical expertise to create and refine test methods for various medical devices. The test engineer will work closely with Product Development and Production Engineering to assist in test method development and planning. You will also perform testing according to Good Laboratory Practice (GLP). Experience in communication and working with a wide variety of associates and excellent problem solving skills is needed to succeed in this role.
Location: IN | Job Type: Contractor | Apply
Regulatory Affairs Specialist
The main function of the RA Specialist coordinates the FDA regulatory submission process. The applicant may aid in authoring and/or publishing electronic submissions. He/she will also provide regulatory direction to development project teams as a core team member and develop regulatory plan for new products. The RA Specialist will also evaluate risk of regulatory strategies and offer solutions. The applicant will interpret and apply FDA regulations to business practices and will provide regulatory input, advice and guidance to the organization.
Location: IN | Job Type: Contractor | Apply
Quality Auditor
CQA – Certified Quality Auditors – Assisting Medical Device client with internal audits at their design centers.
Requirements:
This position requires travel to job sites nationwide.
Location: Nationwide | Apply
See all Quality & Regulatory Compliance Jobs HERE
Since 2012, Professional Resource Partners (PRP) has been honored to serve as a trusted source of quality and regulatory compliance consultants to the medical device and diagnostics industries. In 2017, we launched PRP Quality which specializes in Automotive Quality inspection, sorting, and containment. As an ISO:9001 Certified Business and a WBENC Certified Woman-Owned Business, our company is proud to deliver exceptional professional integrity and service to the many clients we support with our customized approach. It’s also the reason why, when PRP is involved, client expectations are not simply met, but they are consistently surpassed.
