Manager, Quality Assurance

Summit Therapeutics, Inc.; Princeton (NJ); On-site; USD 139,000 - 163,000; Full time

Job summary

Summit Therapeutics Inc. in New Jersey is seeking a Manager of QA to oversee the Product Complaint program and audit readiness. You will lead investigations, ensure regulatory compliance, and author/update SOPs and QTAs for both clinical and commercial materials.

The role requires 5+ years of experience, strong GMP knowledge, and excellence in communication. Office-based role with emphasis on rapid corrective actions and continuous improvement.

Qualifications

• Bachelor’s degree in chemistry, biochemistry, biotechnology, or other related life science discipline.
• Minimum of 5+ years of relevant experience.
• Experience managing product complaints.
• Strong knowledge of FDA, EMA, MHRA, ICH, PIC/S and international GMP/GDP regulations.
• Experience serving as an auditor in internal and external audits.
• Experience reviewing and approving QTAs.
• Experience working with CMOs.
• Excellent oral and written communication skills.

Responsibilities

• Serve as liaison for our product complaint call center and manage clinical product complaints.
• Ensure complaints are investigated and resolved per internal requirements and regulatory expectations.
• Support product complaint reconciliation with call center and Pharmacovigilance.
• Improve internal product complaint program in line with laws and regulations.
• Serve as Auditor for internal and external audits.
• Ensure audit responses and CAPAs are identified and resolved timely.

Skills

Quality management

Auditing

Regulatory compliance

Process improvement

Project management

Education

Bachelor’s degree in chemistry/biochemistry/biotechnology or related life science

Tools

eQMS

QTAs

Job description

About Summit

Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit’s core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.

About Summit

Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit’s core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.

Summit’s Team Is Inspired To Touch And Help Change Lives Through Summit’s Clinical Studies In The Field Of Oncology. Summit Has Multiple Global Phase 3 Clinical Studies, Including

Non-small Cell Lung Cancer (NSCLC)

• HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.
• HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
• HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC.

Colorectal Cancer (CRC)

• HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.

Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China’s National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.

Overview Of Role

The Manager of QA reports to the Director of QA and will provide quality oversight for the Product Complaint program. This will include investigation resolution for complaints associated with clinical and commercial material. The Manager will also be responsible for ensuring Summit departments and systems are inspection ready by way of conducting internal and external audits, supporting inspection readiness activities, and authoring and updating internal procedures and Quality Technical Agreements (QTA).

Role And Responsibilities

• Serve as the liaison for our commercial product complaint call center and also manage clinical product complaints.
• Ensure product complaints are investigated and resolved, in accordance with internal requirements and regulatory expectations.
• Support product compliant reconciliation with the call center and Pharmacovigilance.
• Continuously improve the internal product complaint program in accordance with applicable laws and regulations.
• Serve as Auditor for internal audits and external audits.
• Ensure internal and external audit responses and appropriate CAPAs are identified and managed through to resolution in a timely manner and deliverables are met.
• Continuously improve internal and external audit programs to remain current with applicable laws and regulations.
• Provide support for the initial review, periodic review, and revision of Summit QTAs.
• Write, revise, review and/or approve SOPs and other controlled documents.
• Ensure issues are identified and managed through resolution in a timely manner, management is notified, and deliverables are met.
• Participate in developing, reporting, reviewing and trending of quality and performance metrics, including in support of Annual Product Reviews (APRs).
• Support GMP inspection readiness activities.
• All other duties as assigned.

Experience, Education And Specialized Knowledge And Skills

• Bachelor’s degree in chemistry, biochemistry, biotechnology, or other related life science discipline.
• Minimum of 5+ years of relevant experience.
• Experience managing product complaints.
• Strong knowledge of FDA, EMA, MHRA, ICH, PIC/S and international GMP/ GDP regulations governing clinical and commercial biologics.
• Experience serving as an auditor in both internal and external audits.
• Experience reviewing and approving QTAs.
• Demonstrated ability working within an eQMS to manage and close quality records in accordance with established timelines.
• Experience working with CMOs.
• Excellent communication skills both oral and written.
• Ability to work in a fast paced environment and efficiently manage projects and timelines.
• Experience working individually and within a team while balancing priorities.
• Attention to detail, accuracy, and thoroughness expected in all aspects of work.
• Self-motivated with a strong sense of work ethic.

This is the pay for this position

Pay Transparency

$139,000 - $163,000 USD

Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.

Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining diverse environment. We do not discriminate in recruitment, hiring, training or promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.