Quality Assurance Associate I/ II jobs in United States
cer-icon
Apply on Employer Site
company-logo

Capricor Therapeutics, Inc. · 2 months ago

Quality Assurance Associate I/ II

Capricor Therapeutics is a biotechnology company dedicated to advancing transformative therapies for rare diseases. They are seeking a Quality Assurance Associate I/II to assist in ensuring compliance with cGMP and regulatory standards while supporting clinical production activities.

BiotechnologyHealth CareMedicalTherapeutics
check
H1B Sponsor Likelynote

Responsibilities

Assist in batch record review and disposition for clinical product manufacturing, including label issuance, product packaging, and shipping activities
Support the issuance, tracking, and archiving of controlled documentation in compliance with GxP (GLP/GCP/GMP) regulations
Maintain and manage controlled records, including batch/test records, logs, reports, and quality management documentation
Assist in preparing materials for internal audits and ensuring documentation readiness for regulatory inspections
Help process and track training records to ensure company-wide GxP compliance
Participate in the review and release of incoming materials in accordance with company standards
Support controlled label issuance, including inventory tracking and updating lot numbers
Collaborate with senior team members to improve and implement quality management systems and training programs
Assist in preparing reports and documentation related to deviations, corrective actions, and change controls
Support the maintenance and management of documentation systems, both manual and electronic, ensuring timely and accurate record-keeping
Perform additional quality assurance tasks as assigned

Qualification

CGMP complianceGLP/GCP regulationsBatch record reviewRegulatory standards knowledgeMicrosoft Office SuiteAttention to detailOrganizational skillsWritten communicationVerbal communicationTeam collaboration

Required

Bachelor's degree in a relevant field (e.g., Biology, Biotechnology, or related discipline) or equivalent experience
0-3 years of experience in a regulated environment (e.g., cGMP, GLP, GCP)
Strong attention to detail and excellent organizational skills for managing documentation and records
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and familiarity with database systems
Strong written and verbal communication skills for effective collaboration and reporting
Ability to work independently and as part of a team in a dynamic, fast-paced environment
Comfortable gowning and working in classified areas as required

Preferred

Familiarity with regulatory standards such as 21 CFR 210 and 211, ICH, ISO9001, and FDA guidelines preferred

Company

Capricor Therapeutics, Inc.

twittertwitter
company-logo
Capricor Therapeutics is a publicly traded (NASDAQ: CAPR) biotechnology company with a mission to develop groundbreaking therapies that make a meaningful impact on patients’ lives.

H1B Sponsorship

Capricor Therapeutics, Inc. has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2021 (2)
2020 (1)

Funding

Current Stage
Public Company
Total Funding
$329.5M
Key Investors
Nippon ShinyakuNational Institutes of HealthCalifornia Institute for Regenerative Medicine
2025-12-05Post Ipo Equity· $150M
2024-10-17Post Ipo Equity· $75M
2024-09-17Post Ipo Equity· $15M

Leadership Team

leader-logo
AJ Bergmann
Chief Financial Officer
linkedin
Company data provided by crunchbase