PTC Therapeutics is a global commercial biopharmaceutical company. For over 25 years our team has been deeply committed to a unified purpose: Extending life’s moments for children and adults living with a rare disease.
At PTC, we cultivate an inclusive culture where everyone feels valued, respected, and empowered. We welcome candidates from all backgrounds to join our team, fostering a strong sense of belonging.
Visit our website to learn more about our company and culture!
Site: www.ptcbio.com
This involves engaging and collaborating with cross functional internal teams to evaluate CMC processes, procedures, and activities for adherence to relevant industry standards, regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.
She/He may manage direct reports.Job Description:
Responsibilities for the role include:
The incumbent works cross-functionally with internal departments and external resources on GxP QA related issues.
The Senior Manager, Quality Assurance – GxP supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs), as appropriate.
- Contributes to and executes PTC’s GxP risk-based audit strategy to achieve compliance with applicable current regulatory requirements.
- Performs internal and external audits as assigned to ensure compliance with GMP and GDP regulations (may include internal processes, Contract Manufacturing Organizations (CMOs), laboratories distributors, and other vendors).
- Communicates audit results to stakeholders and writes audit report.
- Assesses audit responses and ensures closure of corrective and preventative actions (CAPAs).
- Leads backroom activities during regulatory authority inspections and assists with GxP inspection readiness activities.
- Supports Quality Management System (QMS) including, but not be limited to, the following activities:
- QA review/approval of deviations, CAPAs and change controls.
- Drafts, reviews, and approves SOPs.
- May manage, coach, and mentor direct reports.
- Performs other tasks and assignments as needed and specified by management
Requirements for the role include:
- Bachelor’s degree in a scientific discipline and a minimum of 6 years of relevant experience in Quality Assurance, Regulatory Affairs, Manufacturing, or a related role in a pharmaceutical, biotechnology or related environment.
- Demonstrated ability to work as a team player: listens, promote exchanges, communicates, adapts and advises.
- Detailed knowledge and understanding of GMP regulations.
- Demonstrated experience leading and/or conducting audits.
- Demonstrated experience executing risk-based audit plans.
- Demonstrated ability to develop and foster positive, collaborative relationships with internal staff as well as with external, third-party vendors.
- Demonstrated leadership ability and experience managing, coaching, and mentoring direct reports.
- Experience supporting regulatory agency inspections.
- Proficiency with Microsoft Office.
- Excellent verbal and written communication skills.
- Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.
- Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects.
- Knowledge and experience in Good Clinical Practice (GCP), Good Laboratory Practice (GLP) and/or Good Pharmacovigilance Practice (GVP).
- Registered GxP Quality Assurance Certifications.
Travel requirements 50%
EEO Statement:
PTC Therapeutics is an equal opportunity employer. We welcome applications from all individuals, regardless of race, color, national origin, gender, age, physical characteristics, social origin, disability, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, disability, veteran status or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.
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Skills Required
- Bachelor's degree in a scientific discipline and a minimum of 6 years of relevant experience in Quality Assurance, Regulatory Affairs, Manufacturing, or related role in pharmaceutical/biotech
- Detailed knowledge and understanding of GMP regulations
- Demonstrated experience leading and/or conducting audits
- Demonstrated experience executing risk-based audit plans
- Experience assessing audit responses and ensuring closure of CAPAs
- Experience supporting regulatory agency inspections and inspection readiness
- QA review/approval experience for deviations, CAPAs and change controls
- Experience drafting, reviewing, and approving SOPs
- Demonstrated leadership ability and experience managing, coaching, and mentoring direct reports
- Demonstrated ability to develop collaborative relationships with internal staff and external vendors
- Proficiency with Microsoft Office
- Excellent verbal and written communication skills
- Knowledge and experience in GCP, GLP and/or GVP
- Registered GxP Quality Assurance Certifications
- Ability to work independently and collaboratively in a fast-paced, matrixed environment and manage multiple priorities
What We Do
PTC is a patient-centered biopharmaceutical company focused on discovering, developing & commercializing medicine for patients with rare and serious disease
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