Quality Assurance Specialist

Kriya Therapeutics, Inc.; Milwaukee (WI); On-site; USD 100,000 - 130,000; Full time

Benefits offered by this job

Time Off & Work-Life Balance

Health & Wellness

Equity & 401(k)

Job summary

Kriya Therapeutics, Inc. is seeking a Quality Assurance professional to support manufacturing, supply chain, and clinical operations. You will review batch records and label material documentation, ensuring cGMP compliance and regulatory alignment.

The role includes QA input for site start-up activities, risk assessments, and electronic batch record implementation, expanding to on-the-floor support as operations scale.

Qualifications

• Bachelor's degree in a scientific, engineering, or related discipline with 2+ years of cGMP QA experience in biologics or pharmaceutical manufacturing.
• Familiarity with clinical labeling, batch record review, deviations, CAPAs, and change control.
• Experience with regulatory requirements for drug substance/drug product labeling.

Responsibilities

• Provides timely Quality review and approval of clinical labels and batch records.
• Contributes to Shiloh Glenn start-up projects and Electronic Batch Record implementation.
• Reviews deviations, change controls, and CAPAs to ensure cGMP compliance.
• Authors and approves SOPs and controlled documents for clinical labeling and QA systems.
• Supports risk assessments and qualification of new materials during onboarding.
• Provides on-the-floor QA support for manufacturing operations during steady-state transitions.

Skills

cGMP QA experience

Regulatory knowledge

Documentation

Cross-functional

Education

Bachelor's degree in science/engineering

Tools

Electronic Batch Record (EBR) systems

Job description

Description

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

Department

Quality Assurance

Location

Research Triangle Park, NC

Description

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.”

Role Overview

This role provides support to Manufacturing, Supply Chain, and Clinical operations by providing reviews of batch production records and documents, raw material and consumable inspection and release, as well as review and approval for clinical labels and clinical material labeling batch records, ensuring labeling operations meet cGMP and applicable regulatory requirements prior to release. The role also provides Quality input to Shiloh Glenn site start-up activities, including risk assessments, the frozen Drug Substance/Drug Product project, new material onboarding, and Electronic Batch Record implementation, helping establish a compliant quality infrastructure as the site comes online. As Shiloh Glenn transitions to steady-state operations, this role expands to include on-the-floor Quality support for Manufacturing Operations.

Key Responsibilities

• Provides timely Quality review and approval of clinical labels and executed clinical material labeling batch records.
• Provides Quality input to Shiloh Glenn start-up projects, including the frozen Drug Substance/Drug Product project and Electronic Batch Record implementation.
• Reviews and approves deviations, change controls, and CAPAs, ensuring investigations and corrective actions meet cGMP and Kriya quality standards.
• Authors and approves SOPs and other controlled documents supporting clinical labeling and Shiloh Glenn Quality systems.
• Participates in risk assessments and change control activities to support qualification of new materials during onboarding.
• Provides on-the-floor Quality support for Manufacturing Operations, reviews executed batch records, and dispositions raw materials as Shiloh Glenn transitions to steady-state manufacturing (longer-term scope).

Experience & Skills and Work Environment

Experience & Skills

• Bachelor's degree in a scientific, engineering, or related discipline with 2+ years of cGMP Quality Assurance experience in biologics or pharmaceutical manufacturing, including direct experience with clinical labeling, batch record review, deviations, CAPAs, and change control.
• Working knowledge of cGMP and applicable global regulatory requirements for clinical drug substance/drug product manufacturing and labeling is preferred.
• Demonstrated experience authoring and reviewing SOPs and other controlled documents.
• Experience supporting site start-up activities, material onboarding, or risk assessments preferred.
• Experience with electronic batch record (EBR) systems preferred.
• Experience with quality oversite of Fill Finish operations and Visual Inspection reviews is preferred but not required.
• Strong attention to detail and ability to work cross-functionally with Manufacturing, Supply Chain, and Regulatory teams.
• Ability to manage daily work activities of this role with minimal supervision.
• An equivalent combination of education and experience will be considered.

Work Environment

• Primarily desk-based, generally in an office or home office setting.
• May involve extended periods of sitting and computer use.
• Some lifting of equipment or materials may be required.
• Work may involve exposure to chemicals or biological materials; proper handling and disposal procedures must be followed.
• Must be able to don grade C and D level cleanroom gowning and work in a cleanroom environment.
• Must be willing to work outside of normal business hours, as necessary, to support the manufacturing process.

Life at Kriya

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.

Rewards & Benefits

• Time Off & Work-Life Balance: Flexible Time Off Paid Parental & Medical Leave Paid Company Holidays
• Health & Wellness: Fertility & Family Building Benefits Medical, Dental, and Vision Insurance Employee Assistance Program (EAP) Life Insurance Short- and Long-Term Disability Coverage
• Financial Security:Equity 401(k) with Company Match Identity Theft Protection
• 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.