First Shift Sr. Quality Associate I/II: Position Summary: This role is responsible for the implementation, maintenance, and continuous improvement of the Laboratory Information Management System ...
First Shift Sr. Quality Associate I/II: Position Summary: This role is responsible for the implementation, maintenance, and continuous improvement of the Laboratory Information Management System ...
Schedule: First Shift Sr. Quality Associate I/II, QC: Position Summary: This role is responsible for the implementation, maintenance, and continuous improvement of the Laboratory Information ...
Schedule: First Shift Sr. Quality Associate I/II, QC: Position Summary: This role is responsible for the implementation, maintenance, and continuous improvement of the Laboratory Information ...
Quality Associate
Union City, CA · On-site
$108K/yr
BillionToOne is looking for a Quality Associate to join our Prenatal/UNITY team and support our ... , (2) generous equity options offering, (3) corporate bonus program, on top of (4) industry leading ...
Quality Associate
Union City, CA · On-site
$108K/yr
BillionToOne is looking for a Quality Associate to join our Prenatal/UNITY team and support our ... , (2) generous equity options offering, (3) corporate bonus program, on top of (4) industry leading ...
Quality Associate/Analyst
Rancho Santa Margarita, CA · On-site
$21/hr
For Associate level ... High school diploma or equivalent with two years of related quality experience, or Bachelor ...
Quality Associate/Analyst
Rancho Santa Margarita, CA · On-site
$21/hr
For Associate level ... High school diploma or equivalent with two years of related quality experience, or Bachelor ...
For Associate level ... High school diploma or equivalent with two years of related quality experience, or Bachelor ...
For Associate level ... High school diploma or equivalent with two years of related quality experience, or Bachelor ...
For Associate level ... High school diploma or equivalent with two years of related quality experience, or Bachelor ...
For Associate level ... High school diploma or equivalent with two years of related quality experience, or Bachelor ...
We are seeking a Quality Assurance Associate II to join our team. This role is critical in scaling clinical production activities, ensuring compliance with cGMP and regulatory standards. The position ...
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We are seeking a Quality Assurance Associate II to join our team. This role is critical in scaling clinical production activities, ensuring compliance with cGMP and regulatory standards. The position ...
Quality Assurance Associate II
San Diego, CA · On-site
$70K - $82K/yr
We are seeking a Quality Assurance Associate II to join our team. This role is critical in scaling clinical production activities, ensuring compliance with cGMP and regulatory standards. The position ...
Quality Assurance Associate II
San Diego, CA · On-site
$70K - $82K/yr
We are seeking a Quality Assurance Associate II to join our team. This role is critical in scaling clinical production activities, ensuring compliance with cGMP and regulatory standards. The position ...
Quality Assurance Associate II
San Diego, CA · On-site
$70K - $82K/yr
We are seeking a Quality Assurance Associate II to join our team. This role is critical in scaling clinical production activities, ensuring compliance with cGMP and regulatory standards. The position ...
Quality Assurance Associate II
San Diego, CA · On-site
$70K - $82K/yr
We are seeking a Quality Assurance Associate II to join our team. This role is critical in scaling clinical production activities, ensuring compliance with cGMP and regulatory standards. The position ...
Quality Control Associate II
$66K - $110K/yr
We are seeking an experienced QC Associate II to support direct material (raw material) testing. This role requires technical proficiency in chemical assays and compendial testing, balancing hands-on ...
Quality Control Associate II
$66K - $110K/yr
We are seeking an experienced QC Associate II to support direct material (raw material) testing. This role requires technical proficiency in chemical assays and compendial testing, balancing hands-on ...
Quality Control Associate II
Oceanside, CA · On-site
$66K - $110K/yr
We are seeking an experienced QC Associate II to support direct material (raw material) testing. This role requires technical proficiency in chemical assays and compendial testing, balancing hands-on ...
Quality Control Associate II
Oceanside, CA · On-site
$66K - $110K/yr
We are seeking an experienced QC Associate II to support direct material (raw material) testing. This role requires technical proficiency in chemical assays and compendial testing, balancing hands-on ...
QC Chemistry Associate II
San Diego, CA · On-site
The QC Chemistry Associate II is responsible for conducting moderate to complex routine analysis of raw materials, proteins, peptides and small molecules under general supervision. The position may ...
QC Chemistry Associate II
San Diego, CA · On-site
The QC Chemistry Associate II is responsible for conducting moderate to complex routine analysis of raw materials, proteins, peptides and small molecules under general supervision. The position may ...
QC Associate II - 3rd Shift
$30 - $32/hr
Your Role: QC Associate II, 3rd Shift (10 PM - 6:30 AM Sunday night - Friday morning) The Quality Control Associate II will execute critical functions to support the manufacturing of sterile drug ...
QC Associate II - 3rd Shift
$30 - $32/hr
Your Role: QC Associate II, 3rd Shift (10 PM - 6:30 AM Sunday night - Friday morning) The Quality Control Associate II will execute critical functions to support the manufacturing of sterile drug ...
QC Chemistry Associate II
San Diego, CA · On-site
The QC Chemistry Associate II is responsible for conducting moderate to complex routine analysis of raw materials, proteins, peptides and small molecules under general supervision. The position may ...
QC Chemistry Associate II
San Diego, CA · On-site
The QC Chemistry Associate II is responsible for conducting moderate to complex routine analysis of raw materials, proteins, peptides and small molecules under general supervision. The position may ...
The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
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The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
Quality Control Associate II, Controls
San Diego, CA · On-site
$75K - $87K/yr
The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
Quality Control Associate II, Controls
San Diego, CA · On-site
$75K - $87K/yr
The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
Quality Control Associate II, Controls
San Diego, CA · On-site
$75K - $87K/yr
The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
Quality Control Associate II, Controls
San Diego, CA · On-site
$75K - $87K/yr
The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
Senior Operational Quality Associate, Hybrid
Glendale, CA · On-site
$40K - $67K/yr
. The Senior Operational Quality Associate plays a critical role on the SOP Reconciliation team ... In this role, you will report to the Manager, Fulfillment and work a hybrid/remote work schedule (2 ...
Senior Operational Quality Associate, Hybrid
Glendale, CA · On-site
$40K - $67K/yr
. The Senior Operational Quality Associate plays a critical role on the SOP Reconciliation team ... In this role, you will report to the Manager, Fulfillment and work a hybrid/remote work schedule (2 ...
Senior Operational Quality Associate, Hybrid
Glendale, CA · On-site
$40K - $67K/yr
. The Senior Operational Quality Associate plays a critical role on the SOP Reconciliation team ... In this role, you will report to the Manager, Fulfillment and work a hybrid/remote work schedule (2 ...
Senior Operational Quality Associate, Hybrid
Glendale, CA · On-site
$40K - $67K/yr
. The Senior Operational Quality Associate plays a critical role on the SOP Reconciliation team ... In this role, you will report to the Manager, Fulfillment and work a hybrid/remote work schedule (2 ...
QC Associate II
Fremont, CA · On-site
$28 - $33/hr
Experience following safety, quality, and compliance procedures in regulated environments. Responsibilities: * Execute routine and non-routine testing of bulk drug substances and intermediates.
Quick apply
QC Associate II
Fremont, CA · On-site
$28 - $33/hr
Experience following safety, quality, and compliance procedures in regulated environments. Responsibilities: * Execute routine and non-routine testing of bulk drug substances and intermediates.
Quality Associate Two information

Grifols rating
6.5
Based on 268 frontline employees who took The Breakroom Quiz
67th of 71 rated pharmaceutical
Job description
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
Schedule: First Shift
Sr. Quality Associate I/II:
Position Summary:
This role is responsible for the implementation, maintenance, and continuous improvement of the Laboratory Information Management System (LIMS) used within the Grifols Therapeutics Quality Control (QC) department, referred to internally as the Laboratory Electronic System (LES). The LES supports the transition toward a fully paperless laboratory by electronically capturing all elements of the QC testing process across multiple highcomplexity assays.
Key Responsibilities:
- Lead the design, configuration, and ongoing management of the LES, including defining required data elements and establishing appropriate input parameters.
- Oversee validation activities associated with system updates, enhancements, and change implementations.
- Serve as a member of the QC computer validation team, ensuring compliance with regulatory and internal validation standards.
- Support additional computerized systems within the QC environment, including software validation oversight and custom field configuration.
- Act as a technical resource for troubleshooting and resolving issues related to electronic laboratory systems.
- Manage and document change controls related to software and system modifications.
Qualifications:
- Experience with electronic laboratory systems and computerized system validation.
- Working knowledge of QC laboratory test methods and workflows.
- Demonstrated experience with change control processes and software/computer validation activities.
- Strong analytical, documentation, and problemsolving skills.
Education and Experience Requirements by Level:
Quality Associate III, QC - BA/BS - preferably in a STEM (science, technology, engineering, or mathematics) curriculum and 3 yrs of relevant experience or an equivalent combination of education and experience. Experience managing, projects, teams, etc. is recommended
Sr. Quality Associate I, QC - BA/BS - preferably in a STEM (science, technology, engineering, or mathematics) curriculum and 5 yrs of relevant experience or an equivalent combination of education and experience. Experience managing, projects, teams, etc. is recommended
Sr. Quality Associate II, QC - BA/BS - preferably in a STEM (science, technology, engineering, or mathematics) curriculum and 6 yrs of relevant experience or an equivalent combination of education and experience. Experience managing, projects, teams, etc. is recommended.
Equivalency: Depending on the area of assignment, directly related experience-or a combination of related education, experience, and competencies-may be considered in place of the stated requirements. For example, if a job level requires a Bachelor's degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience.
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location: NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton
Learn more about Grifols
About Grifols
Sourced by ZipRecruiter
Industry
Pharmaceutical product wholesalers
Company size
10,000+ Employees
Headquarters location
Los Angeles, CA, US
Year founded
2013