Temp Pharma QA Associate – GMP & Documentation

Alkermes; Wilmington (OH); On-site; USD 27,552 - 34,440; Part time

Job summary

A leading pharmaceutical company in Ohio is seeking a Temp-QA Associate for a temporary position in Quality Assurance. The role involves managing GxP documentation, supporting the documentation lifecycle, and developing quality-related procedures. Candidates should have a Bachelor's degree in a scientific field and 0-2 years of QA experience. Strong communication skills and knowledge of GMP regulations are essential. This is an entry-level role, ideal for motivated individuals.

Qualifications

• Requires 0-2 years’ experience in a Quality Assurance role in the pharmaceutical industry.
• Detail-oriented and able to work in a fast-paced environment.

Responsibilities

• Issuance of GxP documentation.
• Support documentation lifecycle activities.
• Develop Standard Operating Procedures and quality documents.

Skills

Pharmaceutical Quality Assurance

Knowledge of US and European GMP regulations

Strong written and oral communication skills

Support of quality systems

Knowledge of Drug Product GMP requirements

Education

Bachelor’s degree in a scientific discipline

Job description

A leading pharmaceutical company in Ohio is seeking a Temp-QA Associate for a temporary position in Quality Assurance. The role involves managing GxP documentation, supporting the documentation lifecycle, and developing quality-related procedures. Candidates should have a Bachelor's degree in a scientific field and 0-2 years of QA experience. Strong communication skills and knowledge of GMP regulations are essential. This is an entry-level role, ideal for motivated individuals.