Overview
MCS Associate Quality Control Jobs in Thousand Oaks, CA at Aditi Consulting
Title: MCS Associate Quality Control
Company: Aditi Consulting
Location: Thousand Oaks, CA
Payrate: $22.00 – $25.90/hr.
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. Lab performs compendial based testing (e.g. pH, Protein Concentration, Water Testing, Endotoxin, Appearance, Color, Clarity).
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.
Qualifications:
- 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 with 2 years of experience.
- 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.
- Strong fundamental laboratory skills with a demonstrated ability to accurately follow established laboratory procedures.
Desired Skills:
- 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.
Pay Transparency: The typical base pay for this role across the U.S. is: $22.00 – $25.90/hr. Non-exempt positions are eligible for overtime at a rate of 1.5 times the base hourly rate for all hours worked in excess of 40 in a work week, or as required by state or local law. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, health savings accounts with qualified medical plan enrollment, 10 paid days off, 3 days paid bereavement leave, 401(k) plan participation with employer match, life and disability insurance, commuter benefits, dependent care flexible spending account, accident insurance, critical illness insurance, hospital indemnity insurance, accommodations and reimbursement for work travel, and discretionary performance or recognition bonus. Sick leave and mobile phone reimbursement provided based on state or local law.
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