Remote Global Pharma Growth & Regulatory Lead

Flowserve Chile S.p.A.; United States; Remote; USD 150,000 - 210,000; Full time

Job summary

Flowserve Chile S.p.A. is seeking a Pharmaceutical Manufacturing and Regulatory SME to bring industry-informed regulatory expertise, market insight, and manufacturing expectations to Flowserve’s growing pharmaceutical business.

This remote role leads market strategy and builds strategic relationships across global pharma manufacturers and bioprocess OEMs. As a technical authority across bioprocess and cGMP compliance, you will drive market readiness, regulatory alignment, and technology adoption

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, Business, or related field.
• Several years in pharmaceutical, biopharmaceutical, biotech, or regulated life-sciences.
• Knowledge of FDA/EMA expectations and global pharmaceutical regulations.
• Strong understanding of pharmaceutical manufacturing requirements.
• Experience translating market needs into product or operations requirements.

Responsibilities

• Translate regulatory and market requirements into actionable product priorities.
• Advise cross-functional teams on cGMP, validation, and supplier qualification.
• Develop market strategies for pharma and bioprocess applications.
• Identify strategic relationships with pharma manufacturers and OEMs.
• Support go-to-market plans with sales and marketing teams.
• Communicate priorities to executive leadership.

Skills

Regulatory knowledge (FDA/EMA)

Cross-functional collaboration

Stakeholder engagement

English fluency

Education

Bachelor’s degree in Engineering or Life Sciences

Advanced degree preferred

Job description

Flowserve Chile S.p.A. is seeking a Pharmaceutical Manufacturing and Regulatory SME to bring industry-informed regulatory expertise, market insight, and manufacturing expectations to Flowserve’s growing pharmaceutical business.

This remote role leads market strategy and builds strategic relationships across global pharma manufacturers and bioprocess OEMs. As a technical authority across bioprocess and cGMP compliance, you will drive market readiness, regulatory alignment, and technology adoption