Job Description

Rochester is a city on Lake Ontario, in New York State. Old industrial buildings cluster near the Genesee River's High Falls. A vast collection of toys and dolls forms the core of the Strong National Museum of Play. The George Eastman Museum, on the early-1900s estate of the Kodak founder, has photography exhibits, film archives, and gardens. Rochester Museum & Science Center has hands-on displays and a planetarium.

Details:

Full-time, locum position

Schedule is Monday through Friday from 8:30 am to 5:00 pm with variable weekend hours

100% inpatient caseload

Hospital setting with a full range of staff and care team

Benefits

We are proud to offer you a benefits package that includes:

Excellent pay rate

Convenient weekly direct deposits

Comprehensive malpractice insurance

Professional healthcare staffing experts that guide you through the entire locum process

Qualifications

Board Certified in Psychiatry

Valid New York medical license

Current, unrestricted DEA

MDstaffers Commitment to Excellence

We are committed to developing lasting relationships with our candidates. You are an expert at medical care, we are experts in healthcare staffing. Let us use our expertise and resources to find the right opportunity for you.

Our services are provided at no cost to our candidates

We have knowledgeable recruiters that cater to your career preferences

We assist with scheduling interviews and provide resources to simplify the licensing process

We facilitate the negotiation of your salary and terms of contract

Our experienced Support Services Department streamlines the credentialing process

To immediately speak with one of our Recruiters please call 866-90-STAFF ).

View more of our open positions by visiting .

MDstaffers is a proud member of NAPR and NALTO.

Job Reference: Job-14067

by Jobble

","

MDstaffers is seeking a qualified Adult Psychiatrist in Rochester, NY. For more information, please apply or c...","Psychiatric - Mental Health Physician","Full Time",[86],["B","3522307746"],"Work at MDstaffers","/jobs/3522307746-psychiatric-mental-health-physician","/jobs?keyword=MDstaffers","/jobs?keyword=Psychiatric+-+Mental+Health+Physician",{"_64":65,"_66":67,"_68":69,"_70":71,"_72":73},["D",1777305600000],"Eastman Kodak Company","We are hiring a Regulatory Affairs Lead within our Kodak Pharmaceuticals group in Rochester, NY. This individual is responsible for establishing, managing, and executing regulatory strategies to support a growing medical device organization as it evolves toward pharmaceutical and combination product development. This role provides hands-on regulatory leadership for FDA submissions, clinical studies, and product lifecycle management, while helping build scalable regulatory processes aligned with FDA medical device, drug, and combination product requirements.

Responsibilities:
Regulatory Strategy & FDA Submissions
• Develop and execute U.S. regulatory strategies for medical devices with alignment to future pharmaceutical and combination product pathways.
• Prepare, submit, and manage FDA 510(k) submissions, including traditional, special, and abbreviated submissions.
• Lead regulatory impact assessments for design changes, labeling updates, and manufacturing process changes.
• Manage FDA interactions including Q-Submissions, deficiency responses, meetings, and ongoing correspondence.
• Support regulatory submissions in global markets as required.

Clinical Studies & Development Support
• Provide regulatory oversight and support for clinical investigations, including IDE preparation, regulatory assessments, and FDA communications.
• Review and support clinical protocols, informed consent forms, and clinical study reports for regulatory compliance.
• Partner with Clinical, R&D, and Quality teams to ensure regulatory requirements are incorporated into study design and execution.

Combination Product & Early Pharmaceutical Readiness
• Support regulatory planning for combination products and future pharmaceutical development in alignment with FDA drug, device, and combination product regulations.
• Provide regulatory input on product classification, primary mode of action, and applicable regulatory pathways.
• Assist in establishing regulatory infrastructure and documentation practices suitable for drug and combination product development.

Quality System & Compliance
• Ensure regulatory compliance with applicable FDA requirements including 21 CFR Parts 820, 807, 803, 812, and applicable drug regulations as they emerge.
• Maintain regulatory documentation in alignment with the Quality Management System (QMS) and ISO 13485.
• Support internal audits, external audits, and FDA inspections as needed.

Cross-Functional Leadership
• Collaborate with Engineering, R&D, Manufacturing, Quality, Clinical, and Marketing teams to ensure regulatory requirements are understood and implemented.
• Review product labeling, promotional materials, and technical documentation for regulatory compliance.
• Provide clear regulatory guidance and risk-based recommendations to cross-functional stakeholders and leadership.

Process Development & Continuous Improvement
• Develop, implement, and improve regulatory processes, templates, and procedures to support organizational growth.
• Monitor changes in FDA regulations, guidance documents, and industry standards and assess impact on existing and future products.
• Mentor and support junior regulatory staff or project team members as the organization scales.

Qualifications (Education, Experiences and Skills):
• Bachelor’s degree in Life Sciences, Biomedical Engineering, Regulatory Affairs, or a related field required.
• 6–8 years of Regulatory Affairs experience within the medical device industry.
• Demonstrated hands-on experience preparing and submitting FDA 510(k) applications.
• Experience supporting clinical studies and IDE-related activities.
• Strong working knowledge of FDA medical device regulations and Quality System requirements.
• Exposure to pharmaceutical, drug device combination products, or early drug development strongly preferred.
• Excellent written, verbal, and interpersonal communication skills.
• Strong organizational skills and ability to manage multiple projects in a fast-paced, growing environment.
• Ability to think strategically while executing detailed regulatory activities.
","We are hiring a Regulatory Affairs Lead within our Kodak Pharmaceuticals group in Rochester, NY. This individual is responsible for establishing, m...","Regulatory Affairs Lead (Rochester)",[98],["B","3523235278"],"Work at Eastman Kodak Company","/jobs/3523235278-regulatory-affairs-lead-rochester","/jobs?keyword=Eastman+Kodak+Company","/jobs?keyword=Regulatory+Affairs+Lead+%28Rochester%29",{"_64":65,"_66":67,"_68":69,"_70":71,"_72":73},["D",1777428959000],"A leading imaging technology company is seeking an Electrical and Instrumentation Mechanic in Rochester, NY. In this role, you will provide skilled trade service to maintain and repair manufacturing equipment. Responsibilities include calibrating instruments, executing maintenance programs, and ensuring safety standards. The ideal candidate will have strong electrical skills, a detail-oriented approach, and the ability to work effectively in a team environment. Competitive pay estimated at $32 to $40 per hour based on experience.
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Mansueto Ventures is home to two of the most iconic and vibrant brands in business publishing: Inc. and Fast Company. Every day, the content, awards, and events produced help entrepreneurs and innovators succeed by providing useful insights, sparking essential conversations, and offering much-needed inspiration.

Inc. is the voice of the American entrepreneur, inspiring and documenting the risk-takers and ultra-driven go-getters who represent the most dynamic force in the American economy.
Fast Company is the world’s leading business media brand, focusing on innovation in technology, leadership, and design to inspire readers to shape the future of business.

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