Senior Manager, Quality Assurance- Vendor Management

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

Responsibilities:

• Leads minor projects, supports major projects, and facilitates major project discussion/milestone tracking, involved in the strategic development and participates in the tactical execution of the Vendor Management QA functions. This involves the development, implementation and continuous improvement of the Vendor Management QA functions that ensure GxP compliance. Vendor Quality Management QA related functions include, but are not limited to the following:
• New/Revised/Discontinued vendor requests
• Vendor qualification program
• Vendor questionnaires
• Vendor risk assessments
• Vendor approval
• Approved vendor list (AVL)
• Vendor periodic review/requalification
• Vendor risk management
• Vendor metrics
• Vendor health evaluations
• Vendor relationship management including vendor issue escalation/resolution working cross-functionally with departments within PTC.
• Quality Technical Agreement system.

• Ensures the Vendor Quality Management supports and enables compliance with regulatory requirements.
• Performs process improvements utilizing recognized quality tools to deliver programs and processes that deliver optimal quality throughout the company processes.
• Ensures Vendor Quality Management documentation is compliant and readily available for inspection, regulatory submission or other requirement(s).
• Performs assessment/approval of new or changes to vendors in Ariba to determine if they are GxP vendors requiring vendor qualification. Assure subsequent vendor requests are received in Veeva.
• Create or revise SAP Source Lists after review of request consistent with the current Approved Vendor List (AVL).
• Works with Global QA colleagues to support change management activities, deviations and/or compliant investigations, batch recall activities etc., as required.
• Supports Global QA with GMP/GDP audits of CMOs, contract testing labs and distributors, as required.
• Reviews and approves Quality documentation.
• Reviews and approves functional area procedures as necessary.
• Supports improvement of PTC quality systems and GMP practices. Identify and make recommendations for improvements to process within the overall Continuous Improvement Process of the Company.
• Participates in regulatory inspections and support formulation of audit responses, as required.
• Completes all duties as per relevant procedures; ensure compliance to GxP at all times.
• Supports other internal Quality departments to ensure departmental success.
• Supports Vendor Management relevant activity for other departments (Finance, Procurement, etc.) including source list management and vendor approval in the system.
• Performs other tasks and assignments as needed and specified by management.

Qualifications:

• Bachelor's degree in a scientific discipline and a minimum of 7 years progressively responsible relevant experience in pharmaceutical GxP Quality Assurance (QA)/ Quality Control (QC)/ Compliance role with previous management experience.
• Demonstrated proficiency in application of QA principles, concepts, industry practices and standards including Vendor Management QA related activities.
• Excellent working knowledge of regulations and sources of regulatory information.
• Detailed knowledge and understanding of GMP, GDP and/or Good Clinical Practices (GCP) regulations.
• Excellent understanding of production and laboratory systems to effect judgement decisions consistent with business needs.
• Demonstrated understanding of international quality systems regulations to adopt best in class systems/processes.
• 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.
• Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.
• Excellent planning, organization and time management skills include the ability to support and prioritize multiple projects.

Expected Base Salary Range:

$139,700- $175,800. The base salary offered will be contingent on assessment of candidate education level, background, and experience relative to the requirements of the position they are being considered for, as well as review of internal equity.

In addition to base salary, PTC employees are also eligible for short- and long-term incentives.All eligible employees may also enroll in PTC's medical, dental, vision, and retirement savings plans.

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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