Global Pharmaceutical SME

Flowserve; Austin (TX); On-site; USD 120,000 - 190,000; Full time

Job summary

Flowserve is seeking a Pharmaceutical Manufacturing and Regulatory Expert to lead regulatory strategy and market readiness for pharma applications in a global context.

The role focuses on translating pharmaceutical requirements into commercial priorities, building relationships with regulators, and guiding cross-functional teams to achieve launch readiness and compliance across life sciences applications.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or Business required; advanced degree preferred.
• Experience with regulatory bodies and health authorities is preferred.
• Ability to translate regulatory requirements into product priorities and roadmaps.

Responsibilities

• Voice of the customer translating pharmaceutical needs into priorities.
• Advise on cGMP, validation, supplier qualification, and documentation.
• Contribute to product roadmaps and market strategies.
• Develop market strategies for pharmaceutical and bioprocess applications.
• Engage with manufacturers, labs, OEMs, and industry partners.
• Collaborate with cross-functional teams on go-to-market plans.

Skills

Regulatory Affairs

Quality Systems

cGMP

Market Strategy

Education

Bachelor’s degree in Engineering

Bachelor’s degree in Life Sciences or Business

Job description

Company Overview:

Flowserve is a global manufacturer of pumps, valves, seals, and aftermarket services, delivering comprehensive flow control solutions that support essential industries such as energy, clean water, and pharmaceuticals. If you're looking for a culture built on ingenuity, innovation, and excellence, Flowserve offers the opportunity to put your experience in motion. Whether you're an individual contributor or a people leader, you'll find meaningful opportunities for professional growth, competitive rewards, and a workplace grounded in our core values: People, Safety, Integrity, Ownership and Ingenuity. At Flowserve, we're inspired by what we can achieve together—creating extraordinary flow control solutions that strengthen today's world while building tomorrow.

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.

Req ID : R-21040

Job Family Group : Sales

Job Family : SA Business Development

EOE including Disability/Protected Veterans. Flowserve will also not discriminate against an applicant or employee for inquiring about, discussing or disclosing their pay or, in certain circumstances, the pay of their co-workers. Pay Transparency Nondiscrimination Provision

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