What are the responsibilities and job description for the Quality Assurance Associate position at ZEO ScientifiX?
About Us:
ZEO ScientifiX is a clinical-stage biotechnology company focused on developing cell-derived and extracellular vesicle-based therapeutics. We are dedicated to advancing innovative biologic therapies for patients with unmet medical needs.
Position Summary:
ZEO ScientifiX is seeking an entry-level Quality Assurance / Quality Control Associate to support clinical manufacturing and drug development activities in a GMP-regulated environment. This is a great opportunity for individuals looking to begin their careers in biotech, particularly in quality and regulatory compliance.
Key Responsibilities:
- Receive and qualify incoming materials and reagents according to GMP requirements
- Review batch records, laboratory notebooks, and QC testing results for completeness and compliance
- Assist in deviation investigations and document change control processes
- Support the organization and maintenance of the electronic document control system
- Ensure compliance with internal SOPs and applicable cGMP regulations
- Participate in internal audits and prepare documentation for regulatory inspections
- Assist with data verification and archiving of quality-related records
- Contribute to creation and revisions of SOPs, forms, and controlled documents
- Assist with risk assessment and process validation review
Qualifications:
- Associate’s or Bachelor’s degree in Biomedical Sciences, Life Sciences, or a related field
- Candidates with degrees in Data Management, Health Information Technology, Technical Writing, Supply Chain Management, or Communications who are looking to enter the biotech industry are also encouraged to apply
- Strong attention to detail and organizational skills
- Effective written and verbal communication skills
- Ability to review and interpret technical documents and records
- Self-motivated with the ability to work independently and as part of a team
- Comfortable using digital tools and electronic documentation systems
- Willingness to work in a GMP-regulated laboratory environment
Why Join Us:
- Gain hands-on experience in a regulated biotech setting
- Join a mission-driven team working on cutting-edge biologic therapies
- Grow professionally in a supportive and fast-paced environment