Senior Manager, Quality Management

Senior Manager, Quality Management About Servier

Servier in the U.S. is a Boston-based, commercial-stage biopharmaceutical company launched by Servier Group in 2018. As a privately held organization, Servier is uniquely positioned to advance cutting-edge science, tackle underserved therapeutic areas and make patients the focus of every strategic decision.

The Sr. Manager, Quality Management, reporting to the Director, US Regulatory Affairs and Quality Management, will support the US operational compliance with quality standards. Additionally, the role is responsible for quality document (QD) management, conducting gap assessments, proposing process changes, and leads the development of standard operating procedures (SOPs) and associated training.

• Collaborate cross functionally to ensure compliance with quality documents, including standard operating procedures (SOP) and department working practices for the US, as identified with Medical Leadership
• Review and approve local deviations, investigations, CAPAs, and change records, including providing quality management guidance
• Oversee Servier’s audit program, including audit preparation, coordination, execution, participation in the review of audit reports, and follow up to any findings
• Monitor new and updated Global SOPs for applicability to US quality documents
• Manage the US training matrix for quality documents
• Maintain and evaluate quality metrics, including time-based metrics around Change Controls, Deviations, CAPA, and complaint management.
• Responsible for maintaining local quality infrastructure in the US to ensure compliance with FDA regulations

• Bachelor’s degree required, preferably in a scientific, healthcare, or business-related field
• 5+ years of professional experience in developing and maintaining quality systems and creation of standard operating procedures
• Demonstrated understanding of GxP and ability to practically apply them internally
• Independent decision making with a high degree of initiative
• Detail-oriented with strong organizational and time management skills
• Knowledgeable in pharmaceutical drug development and manufacturing, process validation, analytical operations, compliance, and documentation
• Excellent communication and interpersonal skills, with a team-oriented mindset and ability to manage multiple tasks

• Up to 10% Travel
• Boston based preferred, but remote considered for the right candidate

Servier is committed to modeling diversity, equity, and inclusion within the industry. We are dedicated to fostering an environment that maintains equitable treatment for all and we welcome applicants who are passionate, committed, and innovative individuals. We encourage candidates to apply to our open roles as we are always willing to consider experiences and skills beyond what is listed in the job description.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

The salary range for this role is $141,000 - $161,000. An employee’s pay position within the salary range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, and business or organizational needs. We may ultimately pay more or less than the posted range, and the range may be modified in the future.

Employees in this position are also eligible for Short-Term and Long-Term incentive programs.

Servier also offers a competitive and comprehensive benefits package that includes benefits such as medical, dental, vision, flexible time off (Servier provides unlimited sick time and flex time, and does not accrue time off), 401(k), life and disability insurance, recognition programs among other great benefits (all benefits are subject to eligibility requirements). For more information on our benefits, please visit this link .