Medical Job at Bayer in US | Apply Now
This Medical Job at Bayer offers a high-impact opportunity in global Medical Affairs, focusing on medical devices and SaMD lifecycle strategy. Among leading Bayer jobs and competitive Medical jobs in the US, this role stands out for its strategic involvement in device development, global medical leadership, and cross-functional collaboration.
Job Details:
- Job Position: Medical Device/SaMD Medical Affairs Device Lifecycle
- Location: Indianola/Pittsburgh, PA
About the Company:
At Bayer, the mission is driven by solving the world’s toughest challenges and striving for a world where “Health for all Hunger for none” becomes reality. Innovation is powered by energy, curiosity, and dedication, continuously expanding capabilities and redefining what is possible in healthcare. Bayer jobs are recognized globally for offering meaningful career growth in healthcare innovation, making this one of the most strategic Medical jobs in the US within the medical device domain.
Job Description:
Responsible for global medical and scientific expertise regarding assigned product portfolio (device or digital) and engagement with R&D, RM, QA, etc., as per lifecycle and lifecycle NPD needs. Also responsible for supporting regional MA colleagues and collaborating with marketing and strategy teams related to the assigned product portfolio and clinically relevant expertise areas. This Medical Job is site-based, working from the Indianola/Pittsburgh, PA work location. A US Residence based option may be available for the selected candidate. This position is listed under Bayer jobs and is part of the growing Medical jobs in the US portfolio.
Qualifications:
- Medical qualification as MD or equivalent (D.O., M.B.B.S, etc.), or a Bioscience/engineering degree with relevant experience in the medical device area;
- Relevant experience with medical device development and initial knowledge in FDA, EU, ICH guidelines, initiatives, and regulations governing medical devices & SaMD;
- Medical device experience supporting development of brand plans, marketing campaigns, and related content;
- Capability to work collaboratively with management and peers to assess, evaluate, and implement business strategies aligned with global or appropriate regional activities;
- Strong communication and interpersonal skills with the ability to drive measurable outcomes with virtual teams;
- Desire and ability to work in a fast-growing, agile business environment;
- Willingness to travel internationally to global meetings and international congresses;
- Good writing skills and ability to analyze safety data;
- Fluent in English, both written and spoken.
Preferred Qualifications:
- Clinical experience is an advantage.
- 2-3+ years of experience with medical device development, initial knowledge in FDA, EU, ICH guidelines, initiatives, and regulations governing medical devices & SaMD.
Key Responsibilities:
- Consolidates existing medical-scientific expertise & activities between global product experts;
- Co-develops/aligns global medical strategy for the relevant brands;
- Completes evidence gap identification, publication planning, and opinion leader development;
- Improves dialogue, information exchange, and alignment between global/regions/countries;
- Serves as a member and medical lead for device development projects/studies within Product Squads;
- Co-develops, with marketing, the integrated brand strategy;
- Provides ongoing lifecycle support for the license to market.
- Co-Leads risk assessment for devices and provides health risk assessments (HRA) as required;
- Contributes to global communication strategy and campaigns reflecting disease management applicable to devices or SaMDs;
- Leads/supports global projects and adapts product offerings to critical industry trends and competitive activity;
- Contributes to the development and execution of the congress strategy and global standards development.
This posting will remain available for applications until at least 2-4-2026.
