Associate Quality Control (QC) – Chemistry (Thousand Oaks)

Job Description: Job Title:

Associate Quality Control (QC) – Chemistry Location:

Holly Springs, NC (Onsite) Duration:

12 Months (possibilities of extension or conversion to FTE)

Role Summary We are seeking a highly motivated and experienced

Associate in Quality Control (QC) Chemistry

to support the startup and operational readiness of a Quality Control laboratory. Working with minimal supervision, this role will lead and contribute to system qualifications, method transfers, and routine laboratory operations within a

GMP-regulated environment .

Key Responsibilities Perform laboratory testing of manufactured materials Support QC laboratory startup and ongoing operations Collaborate cross-functionally to implement work order and preventative maintenance systems for laboratory equipment Review and contribute to validation documentation for onboarding laboratory equipment and computerized systems Draft, revise, and review technical and quality documentation including SOPs, test methods, technical assessments, validation reports, trend reports, and safety evaluations Assist with procurement of laboratory consumables and critical reagents Coordinate and execute training and method transfer activities for analytical instruments including

H/UPLC, TOC, Conductivity, Osmolality , and other chemistry-based platforms Support audit readiness activities and participate in audits and quality initiatives Participate in cross-functional projects with site or global impact Provide operational support during weekends and public holidays when required

Top 3 Must-Have Skill Sets Chemistry background GMP experience Empower experience

Basic Qualifications High School/GED with 2 years of work experience

OR Associate degree with 6 months of work experience

OR Bachelor’s degree

Preferred Qualifications Bachelor’s degree or higher in Chemistry, Compendial Testing, or a related scientific discipline Minimum of

4 years of relevant laboratory experience

in a GMP pharmaceutical or biopharmaceutical manufacturing environment Strong background in analytical testing Proficiency with analytical laboratory techniques and instrumentation Experience with

method validation, verification, and transfer Familiarity with laboratory systems such as

LIMS and LMES/CIMS Understanding of industry regulations, data integrity, and compliance standards Strong technical writing, documentation, and communication skills Excellent interpersonal skills with the ability to collaborate across teams and adapt to varying communication styles

Additional Information Fully onsite role (Holly Springs, NC) Overtime and schedule flexibility required as business needs dictate Possible extension based on performance and business need

Red Flags (Will Not Be Considered) No chemistry background No GMP experience Unable to work overtime or flexible schedules