What are the responsibilities and job description for the QUALITY OPERATIONS SPECIALIST position at 20BLOC?
Located in Thousand Oaks, California, 20BLOC is a small privately held development-stage biopharmaceutical company, driven by a mission to create breakthrough protein-based drugs to save lives. Our lead product is an innovative solution to provide oxygen to tissues. Check us out at www.20bloc.com.
We are looking for a motivated and hands-on Quality Operations Specialist to join our team.
How you will add value to 20BLOC
The Quality Operations Specialist supports the Quality Assurance function by ensuring compliance with Good Manufacturing Practice (GMP) requirements. This role is responsible for review and approval of batch documentation and analytical data, management of quality events, and support of the Quality Management System (QMS). The Quality Operations Specialist works closely with Manufacturing, QC, and other cross-functional teams to ensure product quality, data integrity, and regulatory compliance.
Key Responsibilities
GMP Documentation & Review
- Review and approve manufacturing batch records for accuracy, completeness, and GMP compliance (ALCOA )
- Review analytical data, test results, and associated documentation to support batch disposition
- Support batch release activities in accordance with internal procedures and regulatory requirements
Quality Systems
- Initiate, investigate, and document deviations, including root cause analysis and CAPA development
- Manage and support change control activities, including impact assessments and approvals
- Support SOP lifecycle activities including drafting, review, revision, and implementation
- Ensure documentation practices comply with data integrity and GMP requirements
Compliance & Continuous Improvement
- Support internal audits and regulatory inspections, including preparation of documentation and responses
- Assist in tracking and trending quality events and quality metrics
- Support risk assessments and continuous improvement initiatives
- Ensure timely closure of deviations, CAPAs, and change controls
Cross-Functional Support
- Collaborate with Manufacturing, QC, and other departments to resolve quality issues
- Provide GMP guidance and support to operational teams
- Participate in training activities related to GMP and quality procedures
Education
- Bachelor’s degree in Life Sciences or a related field
Experience
- 4 years of experience in Quality Assurance within a GMP-regulated pharmaceutical environment
- Hands-on experience with batch record review and analytical data review
- Experience managing deviations, change control, and SOPs
- Familiarity with regulatory requirements (e.g., FDA, EMA, ICH guidelines)
Skills & Competencies
- Strong understanding of GMP and pharmaceutical quality systems
- High attention to detail and strong documentation skills
- Ability to investigate issues and perform root cause analysis
- Strong organizational and time management skills
- Effective written and verbal communication skills
- Ability to work independently and collaboratively in a team environment
- Proficiency with electronic QMS systems is an advantage
Please apply at jobs@20bloc.com – in subject line: Quality Operations Specialist
This is a full-time, on-site position located in Thousand Oaks, California, and requires working on-site Monday through Friday.All applicants must be authorized to work in the United States. We are not sponsoring employment visas.
Compensation: The salary range for this position is $82,000.00. to $109,00.00 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location.
20BLOC is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status, or other applicable legally protected characteristics.
We offer competitive compensation and benefits including health, dental, vision and life insurance, 401(k) and paid time off.
Salary : $10,900 - $82,000