Global Pharmaceutical SME

Corporate; Texas; Hybrid; USD 173,000 - 260,000; Full time

Job summary

Flowserve seeks a Pharmaceutical Manufacturing and Regulatory Expert to lead market strategy and regulatory engagement across global life sciences manufacturing. The role acts as a technical authority on CIP/SIP, cGMP, validation, and supplier expectations, shaping product priorities with customers and partners.

The candidate will drive market readiness, regulatory alignment, and technology adoption, collaborating with engineering, sales, and product teams to advance Flowserve’s pharma growth

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or related field.
• Advanced degree or equivalent relevant experience preferred.

Responsibilities

• Voice of the Customer: translate requirements into actionable priorities.
• Regulatory Guidance: advise on cGMP, validation, supplier qualification, documentation, traceability, quality-system maturity, and regulatory risk.
• Commercialization & Product Strategy: contribute to roadmaps and launch readiness.
• Market Execution: develop targeted market strategies for pharma and bioprocess apps.
• Stakeholder Engagement: build strategic relationships across manufacturers, labs, OEMs, and partners.
• Technical Evaluations: support trials, evaluations, and industry events.
• Cross-Functional Go-to-Market: collaborate with Sales, Product, Engineering, Operations, and Marketing.
• Market & Competitive Intelligence: conduct benchmarking and opportunity analysis.
• Channel & OEM Development: support early design-in opportunities and partner qualification.
• Executive Alignment: communicate priorities and risks to leadership.

Skills

Regulatory guidance

Voice of customer

Market strategy

Executive alignment

Education

Bachelor’s degree in Engineering/Life Sciences/Business

Advanced degree (MS/PhD) preferred

Job description

The Pharmaceutical Manufacturing and Regulatory Expert will provide industry-informed and regulatory-body expertise, market insight, manufacturing expectations, and customer credibility to support Flowserve’s pharmaceutical growth initiative. This role will lead pharmaceutical market strategy, cultivate strategic relationships across global pharmaceutical manufacturers and bioprocess 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 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.

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.

EDUCATION

Bachelor’s degree in Engineering, Life Sciences, Business, or a related field required. Advanced degree (Master's, MS, PhD) or equivalent relevant experience preferred.

The pay range for this role is $172,930.93 - $259,518.35 per year.