Quality Control Associate I / II
$25 - $33 per hourPharmaron
Overview Position: Quality Control Associate I / II Location: Carlsbad, CA (on-site) Hourly Range: $25.00 - $33.00 (DOE) About Pharmaron Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services. We\'re proud of the impact we make and just last year, we supported over 780 discovery projects , 1,000+ CMC programmes , and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADCs, biologics, and gene therapies and we work with more than 3,000 global customers . To learn more, visit Job Overview The Quality Control Associate I / II plays a critical role in ensuring the integrity, accuracy, and regulatory compliance of preclinical study data. This individual will serve as a key quality partner across scientific and operational teams, reviewing study documentation, identifying discrepancies, and ensuring adherence to GLP standards, protocols, and internal quality systems. This role offers strong exposure to preclinical research, regulatory frameworks, and cross-functional collaboration, with opportunities to grow into advanced QC, QA, or compliance-focused roles. Responsibilities Perform detailed reviews of study data, reports, and documentation to ensure accuracy, completeness, and GLP compliance Verify adherence to study protocols, SOPs, and regulatory requirements Identify, document, and follow up on deviations, ensuring timely resolution Support and maintain documentation within electronic quality management systems (eQCM) Ensure all records meet internal and regulatory standards for audit readiness Contribute to continuous improvement of document control and quality processes Partner with scientific and operational teams to resolve data discrepancies and improve data quality Coordinate training activities to ensure alignment with SOPs and quality expectations Work across departments to streamline workflows and enhance efficiency Support QC verification for study-related sample shipments Manage multiple priorities in a fast-paced, deadline-driven environment Contribute to departmental and quality improvement initiatives Other duties as determined by management What We Are Looking For B.S. in Life Sciences or related field 3–6+ years of experience in Quality Control, Quality Assurance, or regulated laboratory environments Strong knowledge of GLP regulations, SOPs, and documentation practices Experience reviewing scientific data, study reports, or regulated documentation Proficiency in Microsoft Office (Word, Excel, Outlook) Experience in CRO, biotech, or pharmaceutical environments Familiarity with electronic quality systems (eQCM or similar) Exposure to preclinical or in vivo studies (preferred) Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China, Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China. Collaborative Culture You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators. Benefits Insurance including Medical, Dental & Vision with significant employer contributions Employer-funded Health Reimbursement Account Healthcare & Dependent Care Flexible Spending Accounts 100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance 401k plan with generous employer match Access to an Employee Assistance Program How to Apply Ready to seize this incredible opportunity? Apply online today to join Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. About Pharmaron: Pharmaron (Stock Code: 300759.SZ/3759.HK) is a premier R&D service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and CGT products. With over 19,000 employees, and operations in China, the U.S., and the U.K., Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan and China. Pharmaron is proud to be an Equal Employment Opportunity and Affirmative Action employer. #J-18808-Ljbffr
$66.2k - $110k
...The Position We are seeking an experienced QC Associate II to support direct material (raw material) testing. This role requires technical... ...in general chemical testing assays. GMP Compliance & Quality Systems: Extensive experience working in a GMP environment with...SuggestedWork at officeLocal areaRelocation package- ...Pharmaron Beijing Co. Ltd. is looking for a Quality Control Associate I / II in Carlsbad, CA. This role focuses on ensuring the integrity and compliance of preclinical study data. Responsibilities include reviewing documentation, identifying discrepancies, and supporting...Suggested
- ...Pharmaron in Carlsbad, CA is seeking a Quality Control Associate I / II to ensure the integrity and compliance of preclinical study data. The role demands 3-6 years of experience in quality environments and strong knowledge of GLP regulations. Your responsibilities include...Suggested
$35 - $52 per hour
...Overview The QA Specialist II is responsible for supporting day-to-day Quality Assurance operations within a GMP... ...position focuses on GMP documentation control, quality system oversight, and... ..., and approve quality events and associated documentation. Support internal...SuggestedContract workWork at office- ...the world. Job Title : QA Specialist - II Location: Oceanside, CA... ...highly motivated individual to join us as a Quality Assurance Specialist II. In this role... ...Provide Quality oversight/approval of Quality Control activities (Method transfer, Certificate...SuggestedNight shift
- ...Job Summary: Quality Assurance Specialist II will provide hands-on support for production and quality... ...oversight and approval of Quality Control activities, including method... ...experience, OR Master's degree, OR Associate degree with 4+ years of experience,...Work at office
- VARITE is looking for a qualified QA Specialist - II in Oceanside, CA. Job Title: Quality Assurance Specialist II Location: Oceanside, CA Contract Duration... ...) Provide Quality Oversight/approval of Quality Control activities (Method transfer, Certificate of Analysis, and...Contract workNight shift
$32.11 - $42.11 per hour
Quality Assurance Specialist II - Onsite Location: Oceanside, CA. Contract: July 6 2026 - July 5 2027 (12‑month onsite). We are seeking a highly... ...and closure of discrepancies, Deviations, CAPAs and Change Controls Ensure timely assessment and closure of Laboratory...Hourly payContract workMonday to FridayNight shift$40 - $45.32 per hour
Net2Source (N2S) is seeking a Quality Assurance Specialist II in Oceanside, CA. This role includes executing a variety of Quality activities to ensure... ...-related activities, provide oversight for Quality Control, and ensure compliance with GMP guidelines. The position...$32.11 - $42.11 per hour
AGW is looking for a dedicated Quality Assurance Specialist II in Oceanside, CA, to execute various quality activities ensuring compliance with regulatory... ..., is required. Strong communication skills and a background in quality control will be advantageous. #J-18808-Ljbffr AGWHourly pay- ...Job Description Job Title: QC Analyst II Location: Oceanside, CA 92056 Duration: 12 months contract with possible extension Description: Conduct quality control testing on products and materials Analyze test results and report deviations Ensure compliance...Contract work
- A biopharma company in California is seeking a highly motivated Quality Assurance Specialist II to ensure compliance with quality objectives in a fast-paced environment. The role involves performing QA-related production activities, providing oversight for QC tasks, ensuring...
$35 - $45 per hour
Overview QA Specialist II / III - Batch Record Review Location: Carlsbad, CA Schedule... ...manufacturing organization supporting critical Quality Assurance operations within a GMP-... ...Proficiency with Microsoft Office applications Associate degree candidates with equivalent GMP...Contract workWork at officeImmediate startMonday to FridayFlexible hours- ...Quality Control Testing Position The Opportunity Conduct quality control testing on products and materials Analyze test results and report deviations Ensure compliance with GMP and regulatory standards Document quality control procedures and findings...
$52.6k - $84k
...The Position We are seeking a QC Associate to support direct material (raw material) testing. As a Quality Control Associate I, you will be responsible for compendial method testing, direct material (raw material), reagent preparation, and sample management for biopharmaceutical...Work at officeLocal areaRelocation package$52.6k - $84k
...Genentech is seeking a QC Associate in Oceanside, California, responsible for the quality control of biopharmaceutical products through direct material testing and compliance with GMP regulations. You will execute routine compendial testing and maintain laboratory equipment...- ...Quality Control Inspector Location: San Marcos, CA Pay: DOE Shift: 1st Shift (Overtime as needed) Position Summary We are seeking a detail-oriented Quality Control Inspector to join a growing manufacturing team in San Marcos. This...Shift workDay shift
$24 - $29 per hour
...Quality And Maintenance Associate Join Our Team at Pierre Landscape as a Quality and Maintenance Associate! Ready to launch your career with... ...company. Key Responsibilities: Conduct daily quality control inspections on maintenance and construction jobs to...Hourly payWork at office- Advanced Clinical is seeking a Quality Assurance Specialist II to join their team in Oceanside, CA. This role is vital in ensuring product quality and compliance with GMP standards in a fast-paced biopharmaceutical environment. You will engage in essential QA activities...
- Katalyst CRO is actively seeking a Quality Assurance Specialist II based in Oceanside, California. This role encompasses hands-on support for production quality, including batch record reviews and regulatory compliance in a biopharmaceutical environment. The successful...
- ACL Digital is seeking a highly motivated Quality Assurance Specialist II in Oceanside, CA. This role includes executing quality activities to ensure... ...with regulatory requirements, overseeing quality control, and providing on-the-floor QA support. The ideal candidate...Night shift
$32 - $34 per hour
...reagents and consumables. Argonaut provides quality and regulatory expertise to assure the... ...Overview The Quality Assurance Associate plays a key role in supporting product quality... ...standards for electronic document control (21 CFR Part 11). This role also supports...Hourly payContract workTemporary workLocal areaMonday to FridayFlexible hoursWeekend work- ...Sr. Quality Assurance Specialist Location: CA-Vista, US Contract Type: Regular Full-Time Area: MANUFACTURING Would you like to... ...Direct experience in Quality Assurance, Quality Operations, Quality Control or Quality Engineering function is required. Knowledge |...Full timeContract work
$94k - $130k
.... The primary responsibility of the Sr. Quality Assurance (QA) Specialist is to work with... ...Assurance, Quality Operations, Quality Control or Quality Engineering function is required... ...could include 8 years of experience, an Associate’s degree with 6 years of experience, or...$94k - $130k
...The primary responsibility of the Sr. Quality Assurance (QA) Specialist is to work... ...Assurance, Quality Operations, Quality Control or Quality Engineering function is required... ...could include 8 years of experience, an Associate's degree with 6 years of experience, or...Full time- ...responsible for data collection, analysis, and reporting, ensuring compliance with cGMP, GLP, and GDP standards to maintain product quality and safety. Key Responsibilities Conduct microbiological and chemical testing per established SOPs. Collect, analyze, and report...Long term contract
- We are seeking a highly motivated Quality Assurance Specialist II to join our team and help ensure compliance with quality objectives and regulatory... ...Ensure timely closure of deviations, CAPAs, change controls, laboratory investigations, and batch/material holds Conduct...
- ...specifications and report and investigate anomalous data. Ensure the quality and safety of manufactured products. Job Responsibilities... ...all responsibilities, skills, efforts, or working conditions associated with a job. While this description is intended to be an...Permanent employmentContract workImmediate start
$25.53 per hour
...equipment. Review and evaluate data for conformance to specifications and report and investigate anomalous data. Ensure the quality and safety of manufactured products. Job Responsibilities Proficient in cGMP practices in all aspects of laboratory...Hourly payLocal areaImmediate start- ...Quality Assurance Specialist Trammell Crow Residential (TCR) is a national multifamily real estate developer. Over 40 years, TCR has built over 275,000 premier multifamily residences, delivering amenity-rich communities in economically thriving locations nationwide....Local area
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