Quality Control Associate I / II, Carlsbad
Quality Control Associate I / II, Carlsbad
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Carlsbad 92002, USA
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Posted: less than a week ago
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Description
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, ADC's, 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.
Key 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:
As part of our commitment to your well-being, we offer a comprehensive benefits package:
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? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
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. Join us in our mission to make a difference in the world of life sciences.
#LI-JF1
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, ADC's, 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.
Key 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:
As part of our commitment to your well-being, we offer a comprehensive benefits package:
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? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
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. Join us in our mission to make a difference in the world of life sciences.
#LI-JF1
Highlights
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Company namePharmaron
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Job positionQuality Control Associate I / II
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