Chemist (QC Associate)

Job Title: MCS Associate Quality Control Location: Thousand Oaks CA – 100% onsite Duration: 12 Months with possible extension Terms: Contract W2 Schedule: Monday–Friday, 8:00 AM–5:00 PM Description: Note: Candidate must be someone near the office or can travel to the office without any problem. Contract Duration: 1 year (possible extension up to 3 years) Location: Thousand Oaks, CA (100% on-site) Schedule: Monday–Friday, 8:00 AM–5:00 PM The ideal candidate for this role is: • A recent graduate (or early-career professional) with a Bachelor’s in Biology, Chemistry, Biochemistry, or related field, OR a candidate with hands-on QC GMP experience who may not hold a degree. • Highly trainable and eager to learn analytical testing techniques in a regulated QC lab. • Brings strong reliability, time management, and a collaborative attitude to the team. • Comfortable with basic computer skills and documentation systems. • Familiarity with GMP principles is a plus, but not a strict requirement. Job Summary Under general supervision, this position performs routine laboratory testing and related activities in support of Quality Control operations. The role requires adherence to current Good Manufacturing Practices (cGMP), safety guidelines, and regulatory requirements while supporting analytical testing, documentation, and laboratory operations. Key Responsibilities • Perform routine laboratory procedures and analytical testing in a regulated QC environment • Document, calculate, compile, interpret, and enter laboratory data accurately and in a timely manner • Operate, maintain, and troubleshoot laboratory instruments and specialized equipment as required. • Maintain laboratory reagents and maintain an inspection ready area • Maintain complete and compliant laboratory documentation, including logbooks, worksheets, and electronic records • Follow all applicable safety guidelines, cGMPs, and CFR requirements • Maintain training records and comply with written procedures and laboratory systems • Support controlled document updates and change implementation activities • Identify and escalate compliance, safety, or data integrity issues as appropriate • May recommend and implement improvements related to routine job functions Ideal Candidate Profile • The ideal candidate is a motivated, reliable individual who is eager to grow in a regulated Quality Control laboratory environment. This role is well-suited for: • Recent graduates or early-career professionals with a Bachelor’s degree in Biology, Chemistry, Biochemistry, or a related scientific field • Candidates with hands-on QC GMP laboratory experience, even if a degree is not held • Individuals who are highly trainable and enthusiastic about learning analytical testing techniques • Team-oriented professionals with strong time management, reliability, and organizational skills • Candidates comfortable working with basic computer systems and laboratory documentation • Familiarity with GMP principles is preferred but not required Preferred Qualifications • Ability to follow regulatory requirements, written procedures, and safety guidelines • Ability to review and evaluate data and documentation in accordance with company and regulatory standards • Strong organizational skills with the ability to manage multiple priorities and meet deadlines • Excellent attention to detail • Strong written and verbal communication skills • Flexibility and adaptability in a fast-paced, regulated environment • Understanding of when and how to appropriately escalate issues • Ability to identify, recommend, and implement improvements related to routine job functions • Commitment to continuous learning and compliance with cGMP and safety requirements Top 3 Must Have Skill Sets: cGMP Compliance & Documentation Laboratory Execution & Analytical Skills Reliability, Organization & Time Management Day to Day Responsibilities: • Perform routine laboratory testing in accordance with approved SOPs and schedules • Prepare samples, reagents, and materials required for testing • Accurately document laboratory activities and enter data into approved systems • Operate and maintain laboratory instruments as trained • Maintain a clean, organized, and inspection-ready lab environment • Follow all cGMP, safety, and data integrity requirements and escalate issues as needed