Site Quality Director (Somerset New Jersey)

About the role

Lead end-to-end GMP compliance, drive improvements, and empower a high-performing team for patient-focused growth.

Qualifications

• Education or Equivalent: BS or BA in Chemistry, Biological Sciences, or other related scientific discipline or equivalent experience.
• Experience: 15 + years of Scientific or Quality Assurance and/or Quality Control Experience
• Knowledge/Skills Requirements:
• Clear understanding of cGMPs.
• Open and clear communication with direct reports.
• Communicates clearly with internal and external clients, both verbal and written.
• Cooperates with co-workers; is a team player. Willingness to contribute to team activities.
• Demonstrates flexibility in organizing work and priorities.
• Excellent organizational skills relating to management of associates daily activities.
• Excellent problem-solving skills and decision-making skills to identify and solve work related issues.

Alignment with Ardena’s CARE values

Communicative, Accountable, Reliable, and Excellent

What Ardena Offers

• Competitive salary and tailored benefits package (adjusted per role and location)
• Flexible working arrangements and paid annual leave (where applicable, depending on role and site)
• International and collaborative work environment across European and US sites
• Access to professional development and training programs
• Meaningful work on pharmaceutical development projects that advance patient health
• A values-driven culture guided by Ardena’s CARE principles: Communicative, Accountable, Reliable, and Excellent

Pay

$200,000 - $220,000

Schedule

Hybrid