Senior Quality Specialist - QMS & Doc Control

Humacyte; Durham (NC); On-site; USD 110,000 - 170,000; Full time

Benefits offered by this job

Stock Options

401k Plan with match

Medical, Vision and Dental

Job summary

Humacyte Inc. is seeking a Senior Quality Specialist focused on QMS and GMP Document Control. You will administer controlled documentation, maintain data integrity, and support regulatory readiness.

The role requires deep knowledge of cGMP, master control practices, and cross-functional collaboration across QA, Manufacturing, Regulatory, and IT. Responsibilities include revising SOPs, managing records, and driving continuous improvement of the Quality Management System.

Qualifications

• Bachelor’s degree in a related field preferred; HS diploma required.
• 5–7 years in Quality within biotech/pharma/medical devices required.
• 6–8 years in GMP QMS environments with strong document control.

Responsibilities

• Serve as SME for GMP Document Control and Records Management.
• Oversee lifecycle of controlled documentation and archival activities.
• Identify gaps and drive standardization and continuous improvement.
• Develop, revise, and approve SOPs, forms, and records.
• Collaborate with QA, Manufacturing, QC, Regulatory, and IT.
• Monitor QMS performance metrics and support audits.

Skills

GMP Documentation

Regulatory Compliance

Quality Systems

Data Integrity

cGMP knowledge

Education

Bachelor’s Degree

High School Diploma

Tools

MasterControl

eQMS

Job description

Senior Quality Specialist - QMS & Doc Control

Quality Assurance & Systems Full Time North Carolina, Durham, NC, US

3 days ago Requisition ID: 1256

DEPARTMENT: Quality

COMPANY: Humacyte Inc (Nasdaq: HUMA) is developing a disruptive biotechnology platform to deliver universally implantable bioengineered human tissues, advanced tissue constructs, and organ systems designed to improve the lives of patients and transform the practice of medicine. The Company develops and manufactures acellular tissues to treat a wide range of diseases, injuries, and chronic conditions. Humacyte’s initial opportunity, a portfolio of Acellular Tissue Engineered Vessel (ATEVs), is currently approved for use in vascular trauma repair and is in late-stage clinical trials targeting multiple other applications including AV access for hemodialysis and peripheral arterial disease. Preclinical development is also underway in coronary artery bypass grafts, pediatric heart surgery, treatment of type 1 diabetes, and multiple novel cell and tissue applications. Humacyte’s 6mm ATEV for AV access in hemodialysis was the first product candidate to receive the FDA’s Regenerative Medicine Advanced Therapy (RMAT) designation and has also received FDA Fast Track designation. Humacyte’s 6mm ATEV for urgent arterial repair following extremity vascular trauma also received the RMAT designation. For more information, visit www.Humacyte.com .

JOB SUMMARY:

The Senior Quality Specialist – Quality Management Systems (QMS) serves as a senior-level subject matter expert responsible for the administration, oversight, continuous improvement, and regulatory compliance of Humacyte’s Quality Management Systems, with primary emphasis on GMP Document Control, Training, Records Management, and electronic Quality Management Systems (eQMS).

This position provides technical expertise and independent oversight of controlled documentation processes, including document creation, revision, approval, issuance, reconciliation, archival, and retention. The Senior Quality Specialist ensures that GMP documentation and associated records are maintained in accordance with applicable regulatory requirements, company policies, established procedures, and data integrity principles.

The individual will serve as a key Quality Systems representative, providing guidance to cross-functional stakeholders, supporting internal and external regulatory inspections, identifying and mitigating compliance risks, and driving process improvements to strengthen QMS effectiveness and operational efficiency.

ESSENTIAL FUNCTIONS:

• Serve as a subject matter expert for GMP Document Control, Records Management, and associated Quality Management System processes.
• Provide independent oversight and administration of regulated documentation throughout the document lifecycle, ensuring compliance with applicable cGMP, cGDocP, data integrity, and internal procedural requirements.
• Assess existing QMS processes to identify compliance gaps, operational inefficiencies, and opportunities for standardization and continuous improvement.
• Develop, revise, review, and approve controlled Quality Systems documentation, including SOPs, Work Instructions, forms, templates, and associated records, within established authorization levels.
• Collaborate with Quality Assurance, Manufacturing, Quality Control, Validation, MSAT, Regulatory Affairs, and other departments to ensure effective implementation and maintenance of Quality Systems.
• Support the development, monitoring, and reporting of Quality Systems performance metrics.

GMP Document Control & Training

• Oversee the issuance, distribution, reconciliation, archival, retrieval, and retention of controlled documentation in accordance with approved procedures.
• Ensure documentation processes support traceability, accuracy, completeness, contemporaneous recording, and appropriate record retention.
• Lead or support periodic assessments of training and document control processes to identify documentation discrepancies, compliance risks, and opportunities for improvement.
• Evaluate and resolve complex documentation discrepancies, including missing, incomplete, improperly issued, or unreconciled controlled documents.
• Partner with applicable departments to implement sustainable corrective actions addressing recurring documentation and records management deficiencies.
• Serve as a key Quality Systems resource for administration, maintenance, and continuous improvement of electronic document management and eQMS platforms, including MasterControl or equivalent systems.
• Support implementation, configuration, testing, and enhancement of electronic Quality Systems workflows in collaboration with system owners, IT, Validation, and business process stakeholders.
• Participate in user acceptance testing, change control assessments, procedural updates, and training activities associated with QMS system enhancements.
• Identify opportunities to streamline document lifecycle management, improve electronic workflow efficiency, and reduce manual administrative activities.
• Support the preparation of audit responses, investigation documentation, and CAPA commitments related to assigned Quality Systems processes.
• Promote a proactive culture of regulatory compliance, inspection readiness, and continuous improvement.

EXPERIENCE & QUALIFICATIONS:

• High School or GED required, Bachelor’s Degree, preferred
• 5-7 years of experience in Quality within the biotechnology, pharmaceutical, or medical device field, required
• Minimum of 6–8 years of progressive experience in pharmaceutical, biotechnology, biologics, or medical device manufacturing environments, with substantial experience supporting GMP Quality Management Systems.
• Minimum of 5 years of direct experience in GMP Document Control, Quality Systems administration, regulated documentation management, or related Quality Assurance functions.
• Demonstrated experience independently managing complex document control activities and regulated records management processes.
• Experience with electronic Quality Management Systems, preferably MasterControl or a comparable platform.
• Experience supporting internal audits, regulatory inspections, Quality Events, investigations, change controls, and CAPA activities.
• Strong understanding of regulations CFR and FDA Guidance for Industry
• Strong understanding of applicable FDA regulations, including 21 CFR Parts 210, 211, and 11, and relevant ICH guidance.
• Comprehensive understanding of controlled document lifecycle management, GMP records retention, document issuance, reconciliation, and archival requirements.
• Understanding of cGMP compliance in the biotech/bioprocessing manufacturing environment
• Effectively communicates high level concepts to Quality and scientific leadership
• Strong oral and written communication skills
• Clearly communicates with co-workers and supervision and communicates in a timely manner
• Strong understanding of root cause analysis; change control requirements; Deviation/CAPA and other fundamental elements of Quality Systems
• Advanced working knowledge of current Good Manufacturing Practices (cGMP), current Good Documentation Practices (cGDocP), and data integrity principles.

COMPENSATION & BENEFITS HIGHLIGHTS:

• Stock Options
• 401k Plan with 4% Match and no Vesting Schedule
• Medical, Vision and Dental Plans
• Company Paid Long Term/Short Term Disability
• Company Paid Life Insurance
• 23 Days Paid Time Off (PTO)
• 10 Company Designated Holidays + 2 Floating Holidays
• Paid Parental Leave Policies

** Please note, Humacyte does not provide U.S. employment sponsorship and does not accept unsolicited resumes from 3 rd party firms and/or agency recruiters. **

The statements in this position profile are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. The manager may assign additional responsibilities and assignments from time to time. Humacyte is an equal opportunity employer and is committed to providing equal employment opportunities without regard to age, race, religion, sex, sexual orientation, gender identity, national origin, Veterans status, disability and/or other protected class characteristics. Additionally, Humacyte is committed to achieving its business objectives in compliance with all federal, state and local law.