Quality Systems Manager

POSITION TITLE

Quality Systems Manager

Location: This position may be performed remotely but requires flexibility and a willingness to travel to the Boston area as needed.

Position Summary

The Quality Systems Manager is responsible for supporting GxP compliance across Praxis programs. They will help design, implement, maintain, and enhance Quality Systems company-wide, including development, pre-clinical, clinical, safety, validation, registration, and commercialization efforts. This role involves serving as a key contributor on GxP compliance and fostering collaborations across various departments.

The Quality Systems Manager will contribute to the development and execution of a tailored Quality compliance strategy for Praxis and support the evolution of Quality Systems aligned with the company's path to commercialization.

The ideal candidate will thrive in a results-driven, highly accountable setting with significant potential for impact. They should possess the ability to navigate regulatory landscapes, build effective internal partnerships, and support Quality compliance excellence within the organization. The Quality Systems Manager will contribute to advancing Praxis' mission and driving continuous improvement in Quality Systems to support the company's growth and success.

Primary Responsibilities

• Design, implement, and maintain company-wide stage-appropriate Quality Systems aligned with GxP principles.

• Regularly assess and enhance GxP practices to meet evolving regulations.

• Collaborate with cross-functional teams to drive GxP excellence.

• Provide training on GxP requirements to personnel at all levels.

• Provide coaching and guidance on Quality best practices, procedures, record review, and regulatory requirements.

• Support implementation and training on new quality processes, supporting quality management initiatives.

• Conduct compliance risk assessments, trend analysis, and provide recommendations for compliant business activities.

• Support oversight of the Supplier Quality Management program, Training, and Document Control.

• Ensure only adequate/approved suppliers and vendors are utilized by the company.

• Establish, compile, track, and present Quality Metrics to support Quality Management Review.

• Provide input into decisions required for change management and CAPA programs.

• Support inspection readiness activities, including participation in internal and external audits and regulatory inspections.

• Monitor industry inspection trends, regulations, and guidelines for impact on programs and operations.

• Work with department heads to support data integrity initiatives.

• Provide feedback on trends and quality issues or non-compliances detected during GMP and GDP activities.

• Ensure that CAPAs associated with assigned programs and studies are tracked and closed out appropriately and timely.

• Write, review, or approve Standard Operating Procedures and internal investigations, as applicable.

Qualifications and Key Success Factors

• Bachelor’s degree in life sciences, engineering, or a related field (with a preference for Chemistry or Biology) or an equivalent combination of education and relevant job experience may also be considered.

• 5–7 years of relevant quality experience, including implementing and supporting GxP (Good Practice) quality systems within the pharmaceutical or biotech industry.

• Experience in Electronic Document Management Systems (EDMS) and Quality Management Systems (QMS); familiarity with Veeva is preferred.

• Experience working in quality systems and/or quality operations.

• Strong knowledge of global regulations, particularly those from the EU and US.

• Strong understanding of GxPs (Good Practices), especially GMP (Good Manufacturing Practices).

• Proficiency in Microsoft Office, particularly Excel, PowerPoint, and Word.

• Experience working in a pharmaceutical GMP environment.

• The physical and mental requirements of our roles include but are not limited to regular use of a computer, devices or other office equipment, clear communication, and occasional movement. You'll need comfort with screen work, basic hand coordination, and focus. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions.

Compensation & Benefits

At Praxis, we believe that taking care of our people (and their people) is important, so we provide a world class benefits package to help you thrive. This includes 99% of the premium paid for medical, dental and vision plans. We also provide company-paid life insurance, AD&D, disability benefits, and voluntary plans to personalize your coverage. Thinking about the future? We match dollar-for-dollar up to 6% on eligible 401(k) contributions and sweeten the deal with long-term stock incentives and ESPP. We provide a discretionary quarterly bonus, an extremely flexible wellness benefit, generous PTO, paid holidays and company-wide shutdowns. Not to mention, you'll also be joining a phenomenal crew of colleagues who are smart, engaged and inspiring. We aim high, collaborate hard, and produce results. Let’s achieve the impossible together!

Annualized Base Salary
$124,000—$144,000 USD

Company Overview

Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders characterized by neuronal imbalance. At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high impact medicines for patients and families affected by and living with complex brain disorders. Our core Values of Trust, Ownership, Curiosity and Results are foundational to every aspect of our business and are exemplified by each and every one of our team members.

Diversity, Equity & Inclusion
Guided by our core values, at Praxis Precision Medicines, Inc. we continue to DARE FOR MORE® to advance, promote, and champion diversity, equity, and inclusion by encouraging individuals to bring their authentic selves and perspectives to work each day. We are an equal opportunity employer and committed to providing opportunities to all qualified applicants without regard to race, religious creed, color, gender identity or expression, age, national origin, sexual orientation, disability, genetics, military service and veteran status, or any other characteristic protected by federal, state, or local laws.

Attention: Job Scam Alert
Praxis has recently become aware of fraudulent job recruitment postings from individuals claiming to represent Praxis. These postings seek financial information in connection with fraudulent opportunities for employment. If you suspect any fraudulent activity or misrepresentation in connection with a Praxis job opportunity, please report it to [email protected].

Praxis does not accept unsolicited submissions from recruitment agencies for open positions. We ask all recruitment agencies to refrain from contacting any Praxis employee regarding any position. All unsolicited resumes submitted by recruitment agencies to any Praxis employee in any form or method will be deemed to be the property of Praxis, and Praxis explicitly reserves the right to hire those candidate(s) without any financial obligation to the recruitment agency.