Quality Complaints Senior Associate

Randstad Life Sciences US; Thousand Oaks (CA); On-site; USD 80,000 - 100,000; Full time

Job summary

Randstad Life Sciences US is seeking a Quality Complaints Senior Associate for an exciting opportunity in Thousand Oaks, CA. The role involves managing product complaints and requires a Bachelor's degree and experience in Quality Assurance. Join a leading innovator in the biotech industry and contribute to advancing biologic medicine.

Benefits

Medical, dental, and vision benefits

401K

Short-term disability

Life insurance

AD&D insurance

Qualifications

• Bachelor's Degree in Life Sciences or related field or equivalent experience.
• Two (2)+ years of Quality Assurance (QA) experience in a GMP pharmaceutical or medical device industry.
• Knowledge of documentation and operations as per company guidelines.

Responsibilities

• Receive, clean, and evaluate product complaint return samples.
• Interface with various company sites and manage complaint sample inventory.
• Author technical assessment reports.

Skills

SOP

Quality Assurance

GMP

Sample Testing

Manufacturing Operations

Education

Bachelor's Degree in Life Sciences

Job description

Join to apply for the Quality Complaints Senior Associate role at Randstad Life Sciences US

Job Summary

Immediate opportunity for a Quality Complaints Senior Associate to work with a leading innovator in biologic medicine, recognized for advancing the use of living cells in drug development and shaping the future of the biotech industry. This role is based in Thousand Oaks, CA.

Schedule/Shift

1st shift, Mon.-Fri. 8-4:30 (30 minute lunch)

Responsibilities

• Receive, clean, and evaluate product complaint return samples
• Interface with various company sites and business partners
• Manage complaint return sample inventory
• Author technical assessment reports

Work Environment

• Role may involve periods of prolonged sitting and standing.
• Role may involve lifting boxes and storage containers of up to 50lbs.
• Role may involve transporting samples to different buildings across campus.

Location

Newbury Park, California

Job Details

• Type: Contract
• Salary: $28.00 - 32.86 per hour
• Work hours: 9 to 5
• Education: Bachelor’s Degree

Qualifications

Required

• Bachelor's Degree in Life Sciences or related field or the equivalent combination of education and/or experience.
• Two (2)+ years of related Quality Assurance (QA) or manufacturing experience in a GMP pharmaceutical or medical device industry.
• Evaluate documentation and operation according to company guidelines.

Preferred

• Documentation practices (GDP experience) and complaints experience are both a plus.

Skills

SOP, Quality Assurance, GMP, Sample Testing, Manufacturing Operations

Additional Information

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

We welcome people of all abilities and are committed to accessible hiring processes. For accommodations, contact [e-mail].

Pay will be based on various factors including education, experience, location, and certifications. Benefits include medical, dental, vision, AD&D, life insurance, short-term disability, and 401K.

This posting is open for thirty (30) days.

Qualified applicants with criminal histories will be considered in accordance with applicable laws.

Additional Details

• Seniority level: Not Applicable
• Employment type: Contract
• Job function: Quality Assurance
• Industries: Pharmaceutical Manufacturing