QA Inspector I (2nd Shift- 1p-9:30p (Monday - Friday)

Gilead Sciences; La Verne (CA); On-site; USD 55,000 - 73,000; Full time

Job summary

A leading company in the biopharmaceutical industry is seeking an entry-level QA Inspector I for the 2nd shift. The role involves inspecting in-process and finished products, ensuring compliance with GMP standards, and maintaining accurate documentation. Ideal candidates will have a high school diploma and relevant experience, with strong communication skills and the ability to follow instructions independently.

Benefits

Medical insurance

Dental insurance

Vision insurance

Life insurance

Qualifications

• At least 2 years of relevant experience.
• Prior experience in a cGMP environment preferred.
• Familiarity with SOPs and Master Batch Records.

Responsibilities

• Assist in QA inspection of incoming materials and products.
• Perform routine inspections for conformance to specifications.
• Document and maintain inspection records accurately.

Skills

Good communication skills

Proficiency in Microsoft Office

Ability to follow instructions

Education

High School Diploma

Job description

QA Inspector I (2nd Shift- 1p-9:30p (Monday - Friday))

Join to apply for the QA Inspector I (2nd Shift- 1p-9:30p (Monday - Friday)) role at Gilead Sciences.

Job Overview

Gilead Sciences is dedicated to discovering, developing, and delivering therapies that improve the lives of patients with life-threatening illnesses worldwide. We are seeking an entry-level QA Inspector responsible for inspecting in-process and finished products, as well as incoming, intermediate, and outgoing materials, ensuring conformance to specifications and compliance with GMP standards.

Key Responsibilities

• Assist in QA inspection of incoming materials, in-process, clinical, and commercial products following SOPs and detailed instructions.
• Perform routine inspections for proper identification and conformance to specifications.
• Support sampling, identification, and quarantine of materials per GMP requirements.
• Document and maintain inspection records accurately.
• Support collection, retention, and storage of product samples.
• Manage controlled documents such as SOPs and test methods.
• Utilize Computerized Management Systems (CMS) effectively.
• Follow directions with moderate supervision and report deviations to QA management.

Shift Details

• 2nd shift, 1:00 PM - 9:30 PM, Monday to Friday

Basic Qualifications

• High School Diploma with at least 2 years of relevant experience.
• Prior experience in a cGMP environment preferred.
• Familiarity with SOPs and Master Batch Records.
• Good communication skills and proficiency in Microsoft Office.
• Ability to follow instructions and work independently.
• Ability to pass annual vision and eye exams for inspection.

Compensation and Benefits

Salary range: $55,930 - $72,380, with potential bonuses and incentives. Benefits include medical, dental, vision, life insurance, and more. For details, visit Gilead Benefits.

Equal Opportunity Employment

Gilead is committed to diversity and inclusion. We provide equal employment opportunities and reasonable accommodations for applicants with disabilities. For assistance, contact [e-mail].

Additional Information

Applicants should apply via the internal portal in Workday if currently employed by Gilead.