QA Specialist I, cGMP Biotech Operations

Abeona Therapeutics; Cleveland (OH); On-site; USD 60,500 - 71,500; Full time

Benefits offered by this job

Medical insurance

Dental and vision coverage

401(k) match plan

Lifestyle spending account

Job summary

A biopharmaceutical company in Cleveland is seeking a Specialist I in Quality Assurance to ensure compliance with cGMP guidelines and support manufacturing operations. The ideal candidate will hold a Bachelor's degree and have at least one year of experience in a regulated manufacturing environment. Responsibilities include documentation review and quality control processes. Competitive annual salary ranges from $60,500 to $71,500, with a comprehensive benefits package.

Qualifications

• 1 year of experience in quality or manufacturing in a cGMP regulated environment.
• Knowledge of cGMPs and relevant ISO standards.
• Experience in aseptic manufacturing processes.

Responsibilities

• Perform routine quality assurance activities for cell and gene therapies.
• Ensure compliance with regulatory and cGMP guidelines.
• Review and reconcile batch-related documentation.

Skills

Organizational skills

Attention to detail

Communication skills

Interpersonal skills

Education

Bachelor's degree in related field

Tools

MS Word

Excel

Power Point

Job description

A biopharmaceutical company in Cleveland is seeking a Specialist I in Quality Assurance to ensure compliance with cGMP guidelines and support manufacturing operations. The ideal candidate will hold a Bachelor's degree and have at least one year of experience in a regulated manufacturing environment. Responsibilities include documentation review and quality control processes. Competitive annual salary ranges from $60,500 to $71,500, with a comprehensive benefits package.