Manager, Quality Assurance Audits and Supplier Qualifications

Kriya Therapeutics, Inc.; Morrisville (NC); On-site; USD 80,000 - 120,000; Full time

Job summary

An established industry player is seeking a dedicated Manager for Quality Assurance Audits and Supplier Qualifications. In this pivotal role, you will oversee the supplier quality qualification program, ensuring compliance with regulatory standards and company SOPs. Your expertise in GxP auditing will be essential as you conduct risk-based assessments of various organizations, including contract manufacturers and research entities. This position offers the chance to contribute significantly to the advancement of clinical programs, making a real impact in the biopharmaceutical field. Join a collaborative team that values quality and innovation, and take your career to the next level!

Benefits

Medical, Dental and Vision

401(k) with Company Match

Short and Long-term Disability Benefits

Company Paid Holidays

Flexible Time Off

Cyber Safety Protection

EAP

Life Insurance

Equity

Qualifications

• 5+ years of experience in Quality Assurance within the pharmaceutical industry.
• Proven experience in conducting GxP audits and managing supplier qualifications.
• Strong computer skills and ability to manage daily activities with minimal supervision.

Responsibilities

• Lead and perform audits of CMOs, CROs, and suppliers ensuring compliance.
• Write and issue audit reports, communicating findings to project teams.
• Manage Quality Assurance documentation and participate in system improvements.

Skills

Quality Assurance

GxP Auditing

Regulatory Compliance

Change Control Management

Communication Skills

Attention to Detail

Education

Bachelor’s degree in science/technical field

Master’s degree (preferred)

Tools

MS Office

Adobe Acrobat Pro

DocuSign

Dot Compliance

Job description

Manager, Quality Assurance Audits and Supplier Qualifications

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Manager, Quality Assurance Audits and Supplier Qualifications

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About Kriya

Kriya is a biopharmaceutical company whose mission is to develop life-changing gene therapies for diseases affecting millions of patients around the world.

About Kriya

Kriya is a biopharmaceutical company whose mission is to develop life-changing gene therapies for diseases affecting millions of patients around the world.

We leverage our proprietary computational engine, in-house manufacturing infrastructure, and integrated design platform to engineer technologies and therapeutics with the potential to transform the treatment of a broad universe of diseases of high unmet need, with a focus on metabolic disorders, neurology, and ophthalmology.

We are proud to have been named Triangle Business Journal’s Life Sciences 2024 “Best Private Company to Work For,” recognized by Forbes as one of “America’s Best Startup Employers of 2024,”and honored as one of BioSpace’s “2025 Best Places to Work.”

Who You Are

The Manager of Quality Assurance Audits and Supplier Qualifications is responsible for supporting the day-to-day execution of the supplier quality qualification program. This role requires strong attention to detail, effective communication skills, and adaptability to changing business needs. The primary focus of this position is to support the advancement of Kriya’s Clinical programs by providing quality assurance support. The GxP Auditor plays a crucial role in Kriya’s programs by performing external risk-based audits of contract manufacturing organizations (CMOs), contract research organizations (CROs), contract testing organizations (CTOs), vendors, clinical sites, and suppliers. They are responsible for vendor oversight and ensuring day-to-day compliance, including quality event management, escalation, and change management.

How You Contribute

• Support the planning and maintenance of the annual audit program schedule, including coordinating audits as assigned.
• Lead, perform, and report on audits addressing qualification, routine, or critical issues at CMOs, CROs, CTOs, vendors, suppliers, and clinical sites. Ensure their quality and production systems comply with regulatory, GxP, and Company SOPs.
• Write and issue audit reports in accordance with Kriya SOPs, templates, and timelines, ensuring clear communication of audit findings to the project team.
• Evaluate responses to audit findings, track deliverables, and follow up on actions to closure (e.g., CAPAs, ECs) to ensure timely completion, effectiveness, and quality.
• Assess, prepare, and process change controls for changes submitted by supplier sites for material and supplier-related changes.
• Manage the review, negotiation, and signature gathering of Quality Agreements to ensure all parties are aligned and compliant.
• Evaluate the impact of changes on systems, documentation, and product quality. Monitor the completion of change control action items and track changes to closure.
• Author, review, and revise site SOPs to ensure compliance with GMPs, regulatory requirements, and corporate standards.
• Assist in managing and maintaining Quality Assurance documentation.
• Participate in quality system improvements to enhance overall efficiency and compliance.
• Perform other duties as assigned by Quality Assurance Management, contributing to the overall success of the team.
  
  

What You Bring to the Team

Education & Experience

• Bachelor’s degree in science/technical field (e.g., biochemistry, bioengineering, clinical research, etc.), or equivalent combined education and experience; Master’s degree a plus
• Minimum of 5 years of experience in Quality Assurance within the pharmaceutical, biotechnology, or related industry.
• Proven experience in conducting GxP audits, including CMOs, CROs, CTOs, vendors, and suppliers.
• Demonstrated ability to manage supplier qualification activities and change controls.
• Experience working in small to mid-size pre-IND to commercial organization a plus
• Extensive experience in GxP auditing covering GMP, GVP, and GLP functions; GCP experience a plus
• Auditor experience required, certifications a plus
• Strong computer skills (preferably MS Office, Adobe Acrobat Pro, DocuSign and Dot Compliance)
  
  

Competencies

• Commitment to maintaining high standards of quality and ensuring compliance with regulatory requirements and company SOPs.
• Current and strong working knowledge, interpretation, and implementation of United States FDA Regulations, ICH Guidelines, and other local government regulatory requirements governing biopharmaceutical research
• Extensive knowledge and application of ALCOA+ standard, GxP, and global guidelines
• Ability to interpret and apply regulations, regulatory guidance, and identify and recommend compliance changes as appropriate
• Ability to meticulously review and analyze data, documents, and processes to ensure accuracy and compliance.
• Highly diplomatic and tactful individual with the ability to work collaboratively with internal and external stakeholders, fostering a cooperative and productive work environment.
• Well-organized and detailed oriented professional with excellent verbal and written communication skills
• Ability to manage daily work activities of this role with minimal supervision.
• Strong orientation for quality and cGMPs
• Strong collaborative skills.
• Highly self-motivated and detail oriented.
• Demonstrated level of respect for individuals
• High level of integrity and personal responsibility
  
  

Working Conditions

• Work is normally performed: at a desk
• Lifting requirements: Under 20 lbs
• Travel requirements: Frequent 25 % or more
  
  

Discover True Collaborative Teamwork

We have an ambitious set of goals, but our confidence – and our inspiration – stems from our people. From California to North Carolina, our teammates bring a spirit of Collaboration, Leadership, and Innovation to their work every day.

We’re always looking for teammates with the drive and energy to help us grow. If you want to be a part of a company with an entrepreneurial culture, a bold vision, and a meaningful purpose, join us.

What We Offer

Medical, Dental and Vision ∙ 401(k) with Company Match ∙ Short and Long-term Disability Benefits ∙ Company Paid Holidays ∙ Flexible Time Off ∙ Cyber Safety protection ∙ EAP ∙ Life Insurance ∙ Equity ∙ and more!

Kriya is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

All job requirements in the job description provided indicate the minimum level of knowledge, skills, and/or abilities deemed necessary to perform the job competently. Job descriptions are an overview of the duties, responsibilities, and requirements of the position. Employees may be required to perform other job-related assignments as requested.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

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