Senior Quality Assurance Associate
Listed on 2026-05-23
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Quality Assurance - QA/QC
QA Specialist / Manager, Quality Control / Manager, Quality Technician/ Inspector, Regulatory Compliance Specialist
Job Description Summary
STEMCELL Technologies is seeking a Senior Quality Assurance Associate for our team!
As the Senior Quality Assurance Associate, you will uphold quality standards and regulatory compliance by performing key quality activities, approving product outputs, maintaining quality documentation, and recommending continuous improvement initiatives. You will play a vital role in ensuring that all products meet specified quality requirements and regulatory standards, contributing significantly to the organization’s commitment to quality and compliance.
Please note that this role requires a flexible schedule that includes occasional early mornings, late evenings, and weekends depending on business needs.
Job Description Duties and Responsibilities- Provide comprehensive quality oversight of GMP clean rooms, manufacturing processes and products to ensure continuous compliance with regulatory standards.
- Perform line clearance between batching campaigns and supporting activities, and providing real‑time guidance to promptly resolve quality and compliance issues.
- Execute and oversee key quality management system activities, including supporting change controls, maintaining robust documentation, and leading in the identification, investigation, and resolution of non‑conformances.
- Perform technical reviews of standard operating procedures, work instructions, and validation documents to guarantee accuracy, completeness and alignment with regulatory requirements.
- Support site audit readiness by continuously monitoring manufacturing compliance while identifying and implementing process improvements to aid compliance and operational efficiency.
- Bachelor’s degree in a relevant field with less than 2 years of quality assurance and/or regulatory and process improvement experience in the biotech industry or equivalent.
- Knowledge of regulatory requirements and industry standards, including ISO 13485, CE medical and IVD device directives, and cGMP, with the ability to interpret and apply technical documents, procedures, and regulations.
- Strong critical thinking, analytical, and problem‑solving skills.
- Ability to coordinate and execute quality assurance responsibilities, manage multiple priorities in a fast‑paced environment, and demonstrate strong project and time‑management skills.
- Excellent communication, technical report writing, presentation, and interpersonal skills, with a self‑motivated approach, independent work ethic, and willingness to learn and take on new responsibilities.
This is an opportunity to work with highly motivated colleagues in a science‑oriented, creative, and dynamic environment. We offer a competitive salary, excellent benefits, and meaningful career development opportunities.
As an equal opportunity employer, STEMCELL is dedicated to ensuring that every employee feels safe, valued, and respected for who they are. We know that scientific progress and innovation occur when diverse, creative minds come together and we are committed to nurturing a culture of inclusivity and belonging. Selection decisions are solely based on job‑related factors.
The annual salary for this job ranges from:
$71,200.00 – $96,400.00
STEMCELL determines an individual’s pay within this range based on factors including experience, education, job‑related skills, and equity within the team or organization. In addition to base salary, STEMCELL offers a comprehensive total rewards package including health benefits, retirement savings, and more.
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