Job Description

ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health challenges around the world. ELIQUENT is committed to serving clients’ needs with extensive expertise, unwavering integrity, and strategic insight in a manner that supports availability of safe, effective, and high-quality drugs, biologics, and medical devices. For more information, please visit our website at eliquent.com.

At ELIQUENT, we’re always looking to connect with experienced project managers who thrive in regulated life sciences environments. This pipeline posting is intended to identify qualified candidates for future opportunities across our pharmaceutical, biotech, and medical device client portfolio. 

What You'll Do: 

• Lead or support cross-functional project execution from initiation through closure, ensuring scope, schedule, and budget alignment with client goals 

• Develop and manage project plans, timelines, risk logs, and resource tracking tools 

• Coordinate with stakeholders across functions (Quality, Engineering, Manufacturing, IT, Facilities, etc.) to resolve technical and logistical challenges 

• Manage client communications and status updates; escalate issues and drive decision-making 

• Oversee or support project deliverables such as C&Q activities, tech transfer, system implementation, CAPEX/facilities, or product development 

• Ensure all work complies with applicable cGMP, FDA, and safety standards 

• Maintain documentation to support audit/inspection readiness and regulatory compliance 

Requirements

• 5–10 years of project management experience in pharmaceutical, biotech, or medical device environments.
• Experience with IVDR (invitro diagnostics) is a plus
• Experience with SAAD (software as a device) is a plus.

• Strong organizational, communication, and leadership skills 

• Hands-on experience managing cross-functional teams and/or capital, validation, or product development projects 

• Understanding of regulated industry standards (e.g., cGMP, GAMP, 21 CFR Part 11, validation lifecycle) 

• Proficiency with project management tools (e.g., Microsoft Project, Smartsheet, Excel) 

• Bachelor’s degree in a life sciences, engineering, or project-related field; PMP is a plus 

Hourly Range: $65-$90

Benefits

What We Offer:

· Competitive Compensation: Attractive salary and comprehensive benefits package for full-time and part-time employees, including health, dental, vision, and life insurance, a 401(k) plan with employer match, a generous paid time off policy, and additional perks. Compensation is commensurate with professional experience.

· Career Development: Opportunities for professional growth and advancement within a supportive and innovative environment.

· Work-Life Balance: Flexible work arrangements and a commitment to maintaining a healthy work-life balance

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