Director, GxP Quality Governance and Partnerships

Ladders; United States; Remote; USD 201.000 - 251.000; Vollzeit

Benefits dieser Stelle

Robust equity awards

Strong benefits package

Significant learning and developmentOp

Zusammenfassung

Ladders is seeking a Director for GxP Quality Governance and Partnerships to join a leader in the Pharmaceuticals & Biotech space. The role focuses on building and managing Quality Agreements with external partners and internal stakeholders while ensuring clear accountability and risk-based decision making across clinical and commercial operations.

The position supports new product launches and geographic expansion through effective quality arrangements, with a remote work option and a

Qualifikationen

• Bachelor's degree in life sciences or a related field.
• 12+ years of experience in the biotechnology, pharmaceutical, or medical device industry.
• Proven track record in developing and managing Quality Agreements.
• Experience with GxP service providers and contract negotiations.
• Strong collaboration skills with cross-functional teams.

Aufgaben

• Lead the development and execution of Quality Agreements for clinical and commercial operations
• Manage agreements with external partners and internal entities
• Establish clear Quality responsibilities and oversight expectations
• Collaborate with stakeholders to align Quality Agreements with business needs
• Resolve complex agreement-related issues and make risk-based decisions
• Develop a risk-based Quality Agreement lifecycle management framework
• Support new product launches and geographic expansions with appropriate Quality arrangements

Kenntnisse

Quality governance

Contract negotiations

Cross-functional collaboration

GxP awareness

Risk-based decisions

Ausbildung

Bachelor's degree in life sciences

Jobbeschreibung

For our client, we are seeking a Director, GxP Quality Governance and Partnerships to join the team of a leader in the Pharmaceuticals & Biotech space.

This leader will own the governance and partnership framework that supports compliant clinical and commercial operations across the product lifecycle. The role will focus on building and managing Quality Agreements with external partners and internal stakeholders, ensuring clear accountability, oversight expectations, and risk-based decision-making. This position will also play a key role in supporting new product launches and geographic expansion through effective quality arrangements.

Location: Remote

Compensation: $201,000 – $251,000 annually

Responsibilities

• Lead the development and execution of Quality Agreements for clinical and commercial operations
• Manage agreements with external partners and internal entities
• Establish clear Quality responsibilities and oversight expectations
• Collaborate with stakeholders to align Quality Agreements with business needs
• Resolve complex agreement-related issues and make risk-based decisions
• Develop a risk-based Quality Agreement lifecycle management framework
• Support new product launches and geographic expansions with appropriate Quality arrangements

Qualifications

• Bachelor's degree in life sciences or a related field
• 12+ years of experience in the biotechnology, pharmaceutical, or medical device industry
• Proven track record in developing and managing Quality Agreements
• Experience with GxP service providers and contract negotiations
• Strong collaboration skills with cross-functional teams

Benefits

• Robust equity awards
• Strong benefits package
• Significant learning and development opportunities

Our client is an equal opportunity employer. We encourage you to apply even if you don’t meet every qualification—your background could be exactly what this team needs.