GMP QA Associate II/III — Evening Shift (2pm–1am)

Serán BioScience; Bend (OR); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Over four weeks of paid time off annually

Employer contributions to a retirement account

Various health plans

Employee Assistance Program

Pet insurance

Job summary

A pharmaceutical company in Bend, Oregon, is seeking a Quality Assurance Associate to support regulatory compliance for manufacturing oral solid dosage drug products. Key responsibilities include reviewing production records and ensuring GMP regulations are followed. Candidates should have a bachelor's degree in a scientific discipline, with 3-6 years of GMP experience in QC or QA roles. This role offers various benefits, including paid time off and health plans.

Qualifications

• 3 years of GMP experience within a QC or QA role for Associate II
• 6 years of GMP experience for Associate III
• Pharmaceutical Manufacturing experience required, Oral Solid Dosage preferred

Responsibilities

• Documents authorships, reviews, and approves of SOPs and production records
• Initiates and oversees investigations and CAPA actions
• Supports internal and client audits

Skills

Knowledge of GMP and FDA regulations

Analytical and problem-solving skills

Organizational skills

Effective communication

Proficiency in Microsoft Office Suite

Education

Bachelor's degree in a scientific discipline

Job description

A pharmaceutical company in Bend, Oregon, is seeking a Quality Assurance Associate to support regulatory compliance for manufacturing oral solid dosage drug products. Key responsibilities include reviewing production records and ensuring GMP regulations are followed. Candidates should have a bachelor's degree in a scientific discipline, with 3-6 years of GMP experience in QC or QA roles. This role offers various benefits, including paid time off and health plans.