Quality Complaints Senior Associate Location:

Thousand Oaks, CA Onsite Flexibility:

Onsite Contract Details Position Type:

Contract Contract Duration:

12 months

Pay Rate:

$30.00 $32.00 / Hour (USD) Shift /

Schedule:

9:00 AM 5:30 PM (30-minute lunch)

Work Authorization:

Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. Job Summary This is an urgent, 100% onsite Quality Complaints Senior Associate role based in Thousand Oaks, CA. The position is lab-based with no opportunity for remote work. The role involves receiving, evaluating, and managing product complaint return samples while authoring technical assessment reports and interfacing with various sites and business partners. Key Responsibilities Receive, clean, and evaluate product complaint return samples, including taking photos, X-rays, and performing written inspections. Interface with various sites and business partners. Manage complaint return sample inventory. Author technical assessment reports. Receive, open, and verify returned samples from patients and healthcare providers. Photograph and perform X-ray evaluations of the returned samples. Document a written inspection of the returned unit to submit in the GMP BioConnect System. File completed samples in storage. Maintain inventory through filing, creating transfer documentation, performing destruction and reconciliation cycles. Clean and prepare Biomailers for the mail center to ship to patients/HCP. Transfer units to the warehouse for shipment to other sites. Required Skills Attention to detail Organizational skills strong organizational skills with the ability to manage multiple projects or assignments Communication skills written and verbal communication and collaboration skills Evaluate documentation and operation according to company guidelines Be self-motivated, attentive to detail, and able to prioritize and meet deadlines Basic statistical and mathematical skills, including the ability to trend data Basic project management skills; independently understand, follow, and implement instructions Strong word processing, database, and spreadsheet application skills Preferred Skills Documentation practices (GDP experience) GMP knowledge Previous lab experience Complaints experience Education Requirements Bachelor's Degree in Life Sciences or related field, or the equivalent combination of education and/or experience Basic Qualifications (minimum): High school diploma/GED + 4 years of work experience, OR Associate's degree + 2 years of work experience, OR Bachelor's degree + 6 months of work experience, OR Master's Degree Required Experience Typically 2+ years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry Nice-to-Have Experience GDP (Good Documentation Practices) experience GMP experience Previous lab experience Complaints experience Work Environment / Physical Requirements Role may involve periods of prolonged sitting and standing. Role may involve lifting boxes and storage containers of up to 50 lbs. Role may involve transporting samples to different buildings across campus. Benefits Medical, Vision, and Dental Insurance Plans 401k Retirement Fund Important Notes Local candidates only. No relocations.

Interview process:

1 thirty-minute phone interview with hiring manager and one phone panel interview with three lab staff. Shortlisting will begin Wednesday, 09/09 please submit candidates promptly. About GTT GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking, financial services, technology, life sciences, biotech, utilities, and retail sectors throughout the U.S. and Canada.

Job Number:

26-13240

Industry:

Manufacturing & Operations #LI-Onsite #gttic #gttmf