Quality Control/Quality Assurance, Lab GMP, GDP Documentation (Pharma/Biotech)

Aequor; Thousand Oaks (CA); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading company in the pharmaceutical industry seeks a Quality Complaints Senior Associate for a 12+ month contract role in Thousand Oaks, CA. The position involves evaluating product complaints and ensuring compliance with GMP standards. Ideal candidates will have a Bachelor's degree in life sciences and relevant QA experience, along with strong organizational and communication skills.

Qualifications

• Typically 2+ years of related QA or manufacturing experience in GMP pharmaceutical or medical device industry.
• Ability to evaluate documentation according to company guidelines.
• Self-motivated, detail-oriented, able to prioritize and meet deadlines.

Responsibilities

• Receive, clean, and evaluate product complaint return samples.
• Interface with various Amgen sites and business partners.
• Author technical assessment reports.

Skills

Attention to Detail

Organizational Skills

GMP/GDP experience

Education

Bachelor’s Degree in Life Sciences

Tools

Word processing

Databases

Spreadsheets

Job description

Quality Control/Quality Assurance, Lab GMP, GDP Documentation (Pharma/Biotech)

Direct message the job poster from Aequor

Job Title: Quality Complaints Senior Associate

Location: Thousand Oaks, CA

Duration: 12+ Months (Possible Extension)

Terms: Contract W2

Description:

100% onsite role at Thousand Oaks, CA - 8-4:30 (30 minute lunch)

**Local Candidates only. No relocations**

Preferred Qualifications:

• Experience with documentation practices, GMP, and previous lab work

Hiring Manager Notes:

• Looking for self-motivated individuals interested in gaining expertise in a fast-paced environment
• Experience with GDP and complaints handling is a plus
• Bachelor’s degree in life sciences required

Responsibilities:

1. Receive, clean, and evaluate product complaint return samples
2. Interface with various Amgen sites and business partners
3. Author technical assessment reports

Requirements:

• Bachelor's Degree in Life Sciences or related field, or equivalent experience
• Typically 2+ years of related QA or manufacturing experience in GMP pharmaceutical or medical device industry
• Ability to evaluate documentation according to company guidelines
• Self-motivated, detail-oriented, able to prioritize and meet deadlines
• Basic statistical skills, project management skills
• Good communication and collaboration skills
• Proficiency in word processing, databases, spreadsheets
• Strong organizational skills to manage multiple projects
• Physical requirements: prolonged sitting/standing, lifting up to 50 lbs, transporting samples across campus

Basic Qualifications:

• High school/GED + 4 years’ experience, or Associate + 2 years, or Bachelor + 6 months, or Master’s Degree

Top Skills:

• Attention to Detail
• Organizational Skills
• GMP/GDP experience is a plus

Additional Details:

• Seniority level: Associate
• Employment type: Contract
• Job function: Quality Assurance
• Industries: Pharmaceutical, Chemical Manufacturing