GMP QA Associate II - Pharma Compliance & CI

Seranbio; Bend (OR); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Paid time off

Health plans

Retirement contributions

Employee Assistance Program

Pet insurance

Job summary

Serán BioScience in Bend, Oregon, is looking for a Quality Assurance Associate to support regulatory compliance in drug manufacturing. The role involves tasks like auditing, risk management, and quality systems oversight. Candidates should have a Bachelor’s degree and a minimum of 3 years in quality assurance or related experience.

Serán offers benefits including over four weeks of paid time off, retirement contributions, and health plan options to meet diverse needs. Join us to contribute to high-quality pharmaceutical products!

Qualifications

• Minimum of 3 years of quality assurance experience.
• Ability to lift up to 15 pounds and wear PPE.
• Collaborative and cross-functional teamwork experience.

Responsibilities

• Participates in internal and third-party audits.
• Supports client audits and regulatory inspections.
• Assists in the oversight of the company’s quality systems.

Skills

Knowledge of GMP and FDA regulations for drug manufacturing

Excellent verbal and written communication skills

Time management skills

Organizational skills and attention to detail

Analytical and problem-solving skills

Education

Bachelor’s Degree in a scientific discipline

Tools

Veeva

Job description

Serán BioScience in Bend, Oregon, is looking for a Quality Assurance Associate to support regulatory compliance in drug manufacturing. The role involves tasks like auditing, risk management, and quality systems oversight. Candidates should have a Bachelor’s degree and a minimum of 3 years in quality assurance or related experience.

Serán offers benefits including over four weeks of paid time off, retirement contributions, and health plan options to meet diverse needs. Join us to contribute to high-quality pharmaceutical products!