Job description
BioIVT is a leading global provider of research models and value-added research services for drug discovery and development. We specialize in control and disease-state biospecimens, including human and animal tissues, cell products, blood and other biofluids. Our unmatched portfolio of clinical specimens directly supports precision medicine research, aiming to improve patient outcomes by coupling comprehensive clinical data with donor samples. As the premier supplier of hepatic products, including hepatocytes and subcellular fractions, BioIVT enables scientists to better understand the pharmacokinetics and drug metabolism of newly discovered compounds and their effects on disease processes. By combining our technical expertise, exceptional customer service and unparalleled access to biological specimens, BioIVT serves the research community as a trusted partner in elevating science
Position Summary:
The Quality Engineer plays a critical role in promoting, supporting, and fostering a culture of quality throughout the organization. This position is responsible for ensuring that products, processes, and quality systems meet applicable regulatory requirements, industry standards, and customer expectations. The Quality Engineer supports the development, implementation, and maintenance of quality management systems (QMS) and compliance programs while driving continuous improvement initiatives across multiple business functions.
A significant portion of this role involves the creation, review, approval, and maintenance of Standard Operating Procedures (SOPs), training materials, and quality documentation. The Quality Engineer will also facilitate training programs to ensure employees understand and comply with applicable regulations, internal policies, and quality system requirements in a practical, fit-for-purpose manner that supports business objectives.
Location Requirement:Candidates must reside within the Eastern Time Zone (EST/EDT). While we consider applicants from most states, we are unable to hire in AK, HI, NM, ND, SD, RI, or VT.
Regulatory and Compliance Requirements
The Quality Engineer is responsible for ensuring compliance with applicable Environmental Health and Safety (EHS) policies and regulatory requirements, including but not limited to:
Good Documentation Practices (GDP)
Good Laboratory Practices (GLP)
Current Good Manufacturing Practices (cGMP)
FDA regulations and guidance
Standard Operating Procedures (SOPs)
State Departments of Health requirements
Clinical Laboratory Improvement Amendments (CLIA)
College of American Pathologists (CAP) standards
United States Pharmacopeia (USP) requirementsGood Clinical Practice (GCP)
Human Research Protection (HRP) regulations and standards
Global data privacy regulations
ISO 9001 standards (2015;13485)
USDA regulations
Human Tissue Authority (HTA) licensing requirements, where applicable
DEA and state-controlled substance regulations, where applicable
Other applicable federal, state, and international regulations
Essential Duties and Responsibilities
The responsibilities listed below are representative of the role and are not intended to be all-inclusive.
Quality Systems and Compliance
Develop, implement, and maintain compliant GxP Quality Management Systems (QMS) for assigned BioIVT sites.
Establish and monitor quality programs to evaluate product quality, process performance, and regulatory compliance.
Support site readiness for internal, customer, and regulatory inspections.
Audit Management
Support and participate in internal audit programs through risk-based facility and process audits.
Prepare audit reports, communicate findings to management, and ensure appropriate documentation and follow-up activities.
Coordinate corrective actions and verify effective closure of audit observations.
Support supplier and vendor qualification audits, including routine and for-cause assessments.
Quality Investigations and CAPA
Lead or support root cause investigations related to deviations, nonconformances, complaints, and quality events.
Collaborate cross-functionally to resolve quality issues and drive systemic improvements.
Facilitate the development, implementation, and effectiveness verification of Corrective and Preventive Actions (CAPA).
Validation and Product Release Support
Coordinate, review, and approve validation protocols, reports, and supporting documentation.
Provide quality oversight for qualification and validation activities.
Support product release decisions by evaluating specifications, quality data, and risk assessments.
Quality Metrics and Continuous Improvement
Collect, compile, analyze, and trend quality and operational data to identify improvement opportunities.
Monitor key quality performance indicators and provide recommendations to enhance product quality and process consistency.
Prepare and present quality metrics and performance reports for Quality Assurance and Regulatory Affairs leadership.
Participate in continuous improvement initiatives focused on quality system effectiveness and operational excellence.
Cross-Functional Collaboration
Partner with Production, Operations, Laboratory, Regulatory Affairs, and other functional teams to address quality concerns and improve processes.
Participate in routine cross-functional meetings to review quality performance and resolve issues.
Provide guidance and support on quality requirements and best practices throughout the organization.
Additional Responsibilities
Perform other duties as assigned that are consistent with the employee's training, experience, and qualifications.
Travel Requirements
This is a remote position; however, travel is required to support site operations, audits, inspections, training, and other business needs.
Up to 40% travel may be required annually.
Qualifications
Education and Experience
Bachelor's degree in a scientific discipline (e.g., Biology, Chemistry, Biotechnology, Microbiology, or related field) required.
Minimum of 15 years of relevant experience in Quality Assurance, Quality Systems, Operations, Manufacturing, or related functions within the pharmaceutical, biopharmaceutical, biotechnology, medical device, or regulated life sciences industries.
Strong working knowledge of cGMP, GLP, GDP, and other applicable quality and regulatory compliance requirements.
Equivalent combinations of education and relevant experience may be considered.
Knowledge, Skills, and Abilities
Comprehensive understanding of Quality Management Systems and GxP regulations.
Strong knowledge of biological products, laboratory operations, and cell culture best practices.
Understanding of analytical test methods, product specifications, and data interpretation.
Proven experience conducting audits, investigations, risk assessments, and CAPA management.
Excellent analytical, problem-solving, and decision-making abilities.
Strong organizational skills with exceptional attention to detail and documentation accuracy.
Excellent written and verbal communication skills, including technical writing and report preparation.
Demonstrated ability to work effectively in cross-functional teams and influence stakeholders at multiple organizational levels.
Proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, and database systems.
Experience with electronic Quality Management Systems (eQMS); MasterControl experience is preferred.
Physical Demands
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.
While performing the duties of this role, the employee may be required to:
Sit, stand, walk, bend, stoop, kneel, crouch, and reach.
Use hands and fingers to operate computer equipment and laboratory tools.
Communicate effectively through speaking, hearing, and writing.
Maintain visual acuity, including close vision, color vision, depth perception, and focus adjustment.
Frequently lift and/or move objects weighing up to 10 pounds and occasionally lift and/or move objects weighing up to 30 pounds.
Work Environment
This position is classified as a combination of Administrative and Laboratory Support.
The employee will regularly work in a professional office environment and may periodically work in laboratory, manufacturing, warehouse, or other controlled environments.
Exposure may include:
Personal protective equipment (PPE) requirements
Biological materials and biohazards
Hazardous chemicals and controlled substances
Airborne particles and laboratory fumes
Flammable materials
Radiation sources (where applicable)
Mechanical equipment and moving parts
Electrical equipment
Noise levels are generally moderate but may occasionally require hearing protection. Work may be performed in a variety of indoor and outdoor environments and environmental conditions.
Disclaimer
This job description is intended to describe the general nature and level of work performed by employees assigned to this position. It is not intended to be an exhaustive list of all duties, responsibilities, or qualifications. Responsibilities may change based on business needs. Employees may be required to perform other job-related duties as assigned and must comply with all applicable company policies and federal, state, and local regulations.
Employment is at-will unless otherwise governed by applicable law or a written employment agreement.
We offer a comprehensive benefit package for eligible team members, including medical, dental, vision, short-term/long-term disability, life insurance, hospital indemnity and accident insurance. We also provide a generous retirement plan with a company match. Eligible employees enjoy competitive time-off policies and a collaborative environment that promotes growth from within. Enjoy company-sponsored events for the entire team!
Join Us!
We can’t wait to work with you! At BioIVT, we believe that diversity and inclusion are key drivers of innovation and success. We are committed to creating a workplace where everyone feels valued, respected and empowered to bring their unique perspectives to the table. We seek to build a diverse team and encourage applications from people of all backgrounds, experiences and identities.
To Learn more about our mission and team culture, click here!
BioIVT is an equal opportunity employer. We celebrate diversity and are dedicated to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.
We strongly encourage veterans and individuals with disabilities to apply and are committed to providing reasonable accommodations throughout the application and employment process.
Originally posted on Himalayas
Who can apply
Eligible countries: United States. Accepted UTC offsets: UTC-10, UTC-9, UTC-8, UTC-7, UTC-6, UTC-5, UTC+14. Review the full description for employer-specific work authorization, residency and schedule requirements.