Global Principal Business Development Manager Pharmaceutical Industry (m/f/d) -
# Global Principal Business Development Manager Pharmaceutical Industry (m/f/d) - **Flowserve** · United Kingdom · `Remote` · `Full Time` 💼 **Уровень роли:** `Senior` 🕒 **Статус:** *Опубликовано: сегодня* · *Источник: Himalayas (JSON API)* --- ### Top Skills & Match 🎯 **Ключевой стек роли:** `[Business-Development-Manager]` `[Regulatory-Affairs-Specialist]` `[Pharmaceutical-Consultant]` `[Subject-Matter-Expert]` `[Life-Sciences-Manager]` `[Global-Business-Development-Manager]` `[International-Business-Development-Manager]` `[Pharma-Business-Development]` `[Pharmaceutical-Business-Development]` --- ### About the Role Your Role and Impact The Pharmaceutical Manufacturing and Regulatory Subject Matter Expert (SME) will provide industry-informed and regulatory-body expertise, market insight, manufacturing expectations, and customer credibility to support Flowserve ’s pharmaceutical growth initiative. This role is a remote role and will lead pharmaceutical market strategy, cultivate strategic relationships across global pharmaceutical manufacturers and bioprocess Original Equipment Manufacturers (OEMs), and translate rigorous pharmaceutical-market requirements into commercial and product priorities. Serving as a key technical authority across life sciences manufacturing, clean-in-place/steam-in-place (CIP/SIP) applications, and current Good Manufacturing Practice (cGMP) compliance , this subject matter expert drives market readiness, regulatory alignment, and technology adoption across Flowserve ’s global customer base. Ideal candidates bring extensive experience with a regulatory body, health authority, notified body, or senior regulatory-quality leadership role involving pharmaceutical manufacturing, inspection readiness, quality systems, validation, supplier expectations, and regulatory engagement and are located in Ireland. Key Responsibilities - Voice of the Customer: Serve as the primary voice of the customer, translating pharmaceutical application, quality, regulatory, and operational requirements into actionable business and product development priorities. - Regulatory Guidance: Advise cross-functional engineering, sales, and operations teams on pharmaceutical and regulatory-body expectations, including cGMP, validation, supplier qualification, documentation, traceability, quality-system maturity, regulatory risk considerations, and change control. - Commercialization & Product Strategy: Provide critical input to product-development roadmaps and commercialization plans based on customer feedback, market trends, and launch-readiness requirements. - Market Execution: Develop and implement targeted market strategies for pharmaceutical, biopharmaceutical, and bioprocess applications. - Stakeholder Engagement: Identify and nurture strategic relationships with pharmaceutical manufacturers, drug-development laboratories, bioprocess OEMs, skid integrators, universities, and industry partners. - Technical Evaluations: Support customer trials, technical evaluations, reference installations, industry conferences, and global roadshows. - Cross-Functional Go-to-Market: Partner with Sales, Product Management, Engineering, Operations, Supply Chain, and Marketing to develop go-to-market plans, sales enablement materials, and customer-value propositions. - Market & Competitive Intelligence: Conduct competitive benchmarking and market analyses to identify emerging growth opportunities, target segments, priority accounts, and strategic partners. - Channel & OEM Development: Support OEM and channel partner development, focusing on early design-in opportunities and partner qualification. - Executive Alignment: Communicate strategic priorities, progress, risks, and recommendations directly to executive leadership and cross-functional stakeholders. Required Qualifications - Bachelor’s degree in Engineering, Life Sciences, Business, or a related field required. Advanced degree (Master's, MS, PhD) or equivalent relevant experience preferred. - Several years of experience in the pharmaceutical, biopharmaceutical, biotech, bioprocess, or regulated life-sciences industry. - Knowledge of FDA/EMA expectations and global pharmaceutical regulations. - Strong understanding of pharmaceutical manufacturing requirements and regulatory expectations - Demonstrated experience translating customer and market needs into product, commercial, or operational requirements. - Experience working cross-functionally. - Proven ability to engage credibly with technical and commercial stakeholders at pharmaceutical manufacturers, OEMs, system integrators, and other industry partners. - Strong knowledge of the pharmaceutical / biopharmaceutical market, including customer decision drivers, operational challenges, and application requirements. - Ability to develop and communicate market strategies, value propositions, and go-to-market recommendations. - Fluent English and willingness to travel internationally. Preferred Qualifications - Existing network in pharma, biotech, Contract Development and Manufacturing Organization (CDMO), or bioprocess markets What We Can Offer You At Flowserve , you'll find a range of options to fit your, and your family's, needs. We want to provide our team with the right resources to invest in your physical, mental and financial well-being no matter where you sit or what stage of life you're in. Originally posted on Himalayas
- Business-Development-Manager
- Regulatory-Affairs-Specialist
- Pharmaceutical-Consultant
- Subject-Matter-Expert
- Life-Sciences-Manager
- Global-Business-Development-Manager
- International-Business-Development-Manager
- Pharma-Business-Development
- Pharmaceutical-Business-Development
Наблюдалась 2026-10-16, впервые 2026-10-16, источник — Himalayas (JSON API).