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Director R&D Quality Compliance Risk Mgt
Director R&D Quality Compliance Risk MgtBioSpace, Inc. • Boston, MA, United States
Director R&D Quality Compliance Risk Mgt

Director R&D Quality Compliance Risk Mgt

BioSpace, Inc. • Boston, MA, United States
1 day ago
Job type
  • Full-time
Job description

Director R&D Quality Compliance Risk Management

Join to apply for the Director R&D Quality Compliance Risk Management role at BioSpace.

Job Description

The Director of R&D Quality Compliance & Risk Management provides centralized leadership and expertise across R&D Quality functions to drive data‑driven proactive compliance and risk management. This role oversees R&D Quality execution of processes for ensuring compliance with global regulations, documentation / communication / mitigation of risks, and reporting / trending of metrics. The Director of R&D Quality Compliance & Risk Management contributes to organizational success through strong individual leadership, collaboration, and fostering a culture of compliance and continuous improvement.

Responsibilities

Partner cross‑functionally to enable transparency & evaluation of R&D Quality risks and issues, collaborating with functional leads to address challenges and constraints. Provide enterprise‑wide assessments and risk‑based rationale to facilitate decision‑making, demonstrate sound judgment, and support the development and execution of effective and comprehensive action plans to address risks.

Lead the implementation & management of an aligned Quality Risk Management program in R&D Quality. Provide assessment, insight and recommendations on risks across the R&D enterprise to senior R&D Quality management.

Serve as a key collaborator to R&D Quality personnel on compliance issues, preparation for audits / inspections, regulatory risk assessments, and process improvement opportunities.

Develop and oversee appropriate R&D Quality metrics reporting on the state of compliance across the R&D enterprise. Identify and drive continuous quality process improvements and risk mitigations through assessment of audit & inspection findings, quality event outcomes, and identification of trends.

Partner with Global Quality Compliance and Systems as R&D Quality business process owner for the regulatory intelligence process. Ensure robust implementation and execution of the process within R&D Quality to maintain compliance with complex and evolving global regulations.

Collaborate with R&D Quality leads to coordinate the information flow and consolidation of functional Quality Councils into an enterprise‑wide view, extract critical data / issues / risks, and develop an executive‑level assessment for review and dissemination by the Senior Director of R&D Quality Compliance, Systems, and Data.

Support the development and implementation of multi‑year organizational strategy for the R&D Quality Compliance, Systems, and Data organization.

Undertake additional duties as assigned in order to contribute to the overall success of the organization.

Qualifications

Minimum requirements :

Bachelor’s Degree in Chemistry, Biology, Engineering or related field

10+ years of increasing responsibility and experience in the biopharma / biotech industry

8+ years of Quality / Compliance experience

Preferred Requirements

Advanced degree in Chemistry, Biology, Engineering or related field

Prior people‑management experience

Desired Skills & Competencies

In‑depth knowledge of global regulations governing biopharmaceutical research & development as well as the role of Quality Management Systems, with the ability to effectively translate and articulate strategies to ensure compliance.

Knowledge and understanding of the use of data visualization and analytics to monitor performance, drive improvements, and enable data‑driven decision making.

Proven leadership, collaboration, and influencing skills, coupled with a demonstrated ability to solve problems and drive impactful change.

Proficiency in working with diverse individuals across all organizational levels.

Exceptional interpersonal, verbal, and written communication skills, enabling successful interaction with stakeholders across the enterprise.

Adaptability and flexibility to thrive in dynamic environments, along with the ability to manage and deliver multiple projects on time.

Strong attention to detail and organizational expertise, with a capacity to work independently across global settings, navigate organizational complexities, and influence without authority.

Compensation & Benefits Summary

U.S. Base Salary Range : $174,500.00 – $274,230.00

U.S. based employees may be eligible for short‑term and / or long‑term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short‑term and long‑term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well‑being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.

EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

Location

Boston, MA

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Director Quality Risk • Boston, MA, United States

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