As the Quality Associate II (Quality Control), you will be responsible for the maintenance, archiving, and retrieval of all controlled documents and records required by applicable regulatory ...
As the Quality Associate II (Quality Control), you will be responsible for the maintenance, archiving, and retrieval of all controlled documents and records required by applicable regulatory ...
Quality Associate II
Waukesha, WI · On-site
As the Quality Associate II (Quality Control), you will be responsible for the maintenance, archiving, and retrieval of all controlled documents and records required by applicable regulatory ...
Quality Associate II
Waukesha, WI · On-site
As the Quality Associate II (Quality Control), you will be responsible for the maintenance, archiving, and retrieval of all controlled documents and records required by applicable regulatory ...
As the Quality Associate II (Quality Control), you will be responsible for the maintenance, archiving, and retrieval of all controlled documents and records required by applicable regulatory ...
As the Quality Associate II (Quality Control), you will be responsible for the maintenance, archiving, and retrieval of all controlled documents and records required by applicable regulatory ...
As the Quality Associate II (Quality Control), you will be responsible for the maintenance, archiving, and retrieval of all controlled documents and records required by applicable regulatory ...
As the Quality Associate II (Quality Control), you will be responsible for the maintenance, archiving, and retrieval of all controlled documents and records required by applicable regulatory ...
Quality Associate II
Waukesha, WI · On-site
As the Quality Associate II (Quality Control), you will be responsible for the maintenance, archiving, and retrieval of all controlled documents and records required by applicable regulatory ...
Quality Associate II
Waukesha, WI · On-site
As the Quality Associate II (Quality Control), you will be responsible for the maintenance, archiving, and retrieval of all controlled documents and records required by applicable regulatory ...
Shift: Day - Monday through Friday 8:00am-5:00pm Sr. Quality Associate II/ Principle Quality Associate: The successful candidate must have a strong knowledge of cGMPs, the ability to perform ...
Shift: Day - Monday through Friday 8:00am-5:00pm Sr. Quality Associate II/ Principle Quality Associate: The successful candidate must have a strong knowledge of cGMPs, the ability to perform ...
Shift: Day - Monday through Friday 8:00am-5:00pm Sr. Quality Associate II/ Principle Quality Associate: The successful candidate must have a strong knowledge of cGMPs, the ability to perform ...
Shift: Day - Monday through Friday 8:00am-5:00pm Sr. Quality Associate II/ Principle Quality Associate: The successful candidate must have a strong knowledge of cGMPs, the ability to perform ...
Quality Associate II
Kansas City, MO · On-site
Associate II, Quality Assurance Position Summary * 100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture ...
Quality Associate II
Kansas City, MO · On-site
Associate II, Quality Assurance Position Summary * 100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture ...
Day Shift The Quality Associate II/III provides routine technical support for various tasks, assignments, and projects in the QA Fractionation business unit. This includes pre-pooling release of ...
Day Shift The Quality Associate II/III provides routine technical support for various tasks, assignments, and projects in the QA Fractionation business unit. This includes pre-pooling release of ...
Quality Associate II/III
Clayton, NC · On-site
Day Shift The Quality Associate II/III provides routine technical support for various tasks, assignments, and projects in the QA Fractionation business unit. This includes pre-pooling release of ...
Quality Associate II/III
Clayton, NC · On-site
Day Shift The Quality Associate II/III provides routine technical support for various tasks, assignments, and projects in the QA Fractionation business unit. This includes pre-pooling release of ...
Shift: Day - Monday through Friday 8:00am-5:00pm Sr. Quality Associate II/ Principle Quality Associate: The successful candidate must have a strong knowledge of cGMPs, the ability to perform ...
Shift: Day - Monday through Friday 8:00am-5:00pm Sr. Quality Associate II/ Principle Quality Associate: The successful candidate must have a strong knowledge of cGMPs, the ability to perform ...
Shift: Day - Monday through Friday 8:00am-5:00pm Sr. Quality Associate II/ Principle Quality Associate: The successful candidate must have a strong knowledge of cGMPs, the ability to perform ...
Shift: Day - Monday through Friday 8:00am-5:00pm Sr. Quality Associate II/ Principle Quality Associate: The successful candidate must have a strong knowledge of cGMPs, the ability to perform ...
Associate II, Quality Assurance Position Summary * 100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture ...
Associate II, Quality Assurance Position Summary * 100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture ...
Quality Associate II
Summerville, SC · On-site
Quality Associate II Department: Quality Assurance Employment Type: Full Time Location: Summerville, SC Description At Thorne, we work to deliver high-quality, science-backed solutions to empower ...
Quality Associate II
Summerville, SC · On-site
Quality Associate II Department: Quality Assurance Employment Type: Full Time Location: Summerville, SC Description At Thorne, we work to deliver high-quality, science-backed solutions to empower ...
Quality Associate - II - Hybrid Location: Deerfield, IL Duration: 12 Months Essential Duties and Responsibilities: * Provide post market surveillance support by owning and resolving issues within ...
Quick apply
Quality Associate - II - Hybrid Location: Deerfield, IL Duration: 12 Months Essential Duties and Responsibilities: * Provide post market surveillance support by owning and resolving issues within ...
Quality Associate I Quality Associate II PHYSICAL DEMANDS - Being able to meet the Physical Demands of the job is an essential duty of the job. Employees at Thorne Research perform the ...
Quality Associate I Quality Associate II PHYSICAL DEMANDS - Being able to meet the Physical Demands of the job is an essential duty of the job. Employees at Thorne Research perform the ...
Quality Associate II
Round Lake, IL · On-site
$88K - $121K/yr
Schedules and coordinates Management Review and Quality Data Review meetings, including publishing of summaries of the data presented, conclusions, and meeting minutes. Prepares and publishes annual ...
Quality Associate II
Round Lake, IL · On-site
$88K - $121K/yr
Schedules and coordinates Management Review and Quality Data Review meetings, including publishing of summaries of the data presented, conclusions, and meeting minutes. Prepares and publishes annual ...
Quality Associate II - QMS
Boerne, TX · On-site
The Quality Associate II - Quality Management System (QMS) supports the development, maintenance, and continuous improvement of the QMS in alignment with ISO 13485, ISO 9001, FDA QMSR, MDSAP and ...
Quality Associate II - QMS
Boerne, TX · On-site
The Quality Associate II - Quality Management System (QMS) supports the development, maintenance, and continuous improvement of the QMS in alignment with ISO 13485, ISO 9001, FDA QMSR, MDSAP and ...
Quality Associate II - QMS
$28 - $37/hr
The Quality Associate II - Quality Management System (QMS) supports the development, maintenance, and continuous improvement of the QMS in alignment with ISO 13485, ISO 9001, FDA QMSR, MDSAP and ...
Quality Associate II - QMS
$28 - $37/hr
The Quality Associate II - Quality Management System (QMS) supports the development, maintenance, and continuous improvement of the QMS in alignment with ISO 13485, ISO 9001, FDA QMSR, MDSAP and ...
Quality Associate II - QMS
Boerne, TX · On-site
$28 - $37/hr
The Quality Associate II - Quality Management System (QMS) supports the development, maintenance, and continuous improvement of the QMS in alignment with ISO 13485, ISO 9001, FDA QMSR, MDSAP and ...
Quick apply
Quality Associate II - QMS
Boerne, TX · On-site
$28 - $37/hr
The Quality Associate II - Quality Management System (QMS) supports the development, maintenance, and continuous improvement of the QMS in alignment with ISO 13485, ISO 9001, FDA QMSR, MDSAP and ...
Quality Associate Ii information
See salary details
$11.06 - $14.66
8% of jobs
$14.66 - $18.27
16% of jobs
$18.39 is the 25th percentile. Wages below this are outliers.
$18.27 - $21.88
24% of jobs
The median wage is $22.26 / hr.
$21.88 - $25.48
15% of jobs
$28.86 is the 75th percentile. Wages above this are outliers.
$25.48 - $29.09
13% of jobs
$29.09 - $32.69
6% of jobs
$32.69 - $36.30
9% of jobs
$36.30 - $39.90
6% of jobs
$39.90 - $43.51
1% of jobs
$43.51 - $47.12
1% of jobs
$47.12 - $50.72
0% of jobs
$11
$26
$50
How much do quality associate ii jobs pay per hour?
What is the difference between Quality Associate Ii vs Quality Control Technician?
| Aspect | Quality Associate II | Quality Control Technician |
|---|---|---|
| Required Credentials | Typically an associate degree or higher in a related field | Often an associate degree or technical certification |
| Work Environment | Office and manufacturing settings, supporting quality processes | Laboratory and production environments, performing testing and inspections |
| Employer & Industry Usage | Common in manufacturing, pharmaceuticals, and biotech | Primarily in manufacturing and production sectors |
| Search & Comparison Intent | Understanding roles, responsibilities, and career path | Focus on testing procedures and technical skills |
The main difference between a Quality Associate II and a Quality Control Technician lies in their focus and responsibilities. Quality Associate II roles often involve supporting quality systems, documentation, and process improvements, while Quality Control Technicians primarily perform testing and inspections to ensure product quality. Both roles require similar educational backgrounds but differ in daily tasks and work environments.
What are some typical challenges a Quality Associate II might face when working on cross-departmental projects?
What are Quality Associate IIs?
What are the key skills and qualifications needed to thrive as a Quality Associate II, and why are they important?

Werfen rating
8.7
Based on 27 frontline employees who took The Breakroom Quiz
Job description
Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.
Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.
OverviewWe are looking to hire a Quality Associate II (Quality Control) to join our Document Control team. As the Quality Associate II (Quality Control), you will be responsible for the maintenance, archiving, and retrieval of all controlled documents and records required by applicable regulatory requirements. If you've got the necessary skills and experience to excel in this position, we want to hear from you. Apply today!
This position is not eligible for sponsorship for work authorization by Werfen, Inc. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.
Quality Associate II (Document Control - Quality Control)
ResponsibilitiesKey Accountabilities:
As a Quality Associate II (Quality Control), you will assist in maintaining the Document Control Center and relevant Standard Operating Procedures (SOPs) for the proofing, filing, copying, scanning, archiving, retrieval, and maintenance of all controlled documents and records required by applicable regulations.
Additional responsibilities include:
- Serving as custodian for all controlled documents and records filed in the Document Control Center and archived at the on-site warehouse or off-site contracted storage facility
- Responsibility for storage, retrieval, and archiving of controlled documents and records
- Filing master copies of new or revised controlled documents in the Document Control Center and archiving obsolete documents as instructed in relevant departmental SOPs
- Performing tasks for the distribution of controlled documents (hard copy or electronic) and for the retrieval of obsolete documents from circulation
- Updating document histories and controlling obsolete documents
- Performing tasks for the maintenance of the controlled documents master lists/database to identify current revisions
- Tracking, monitoring, and reporting of training status
Quality Associate II (Document Control - Quality Control)
QualificationsMinimum Knowledge & Experience required for the position:
- Associate's degree or equivalent, or 6 months to 1 year of related experience
- Exceptional organizational skills
- Ability to proofread controlled documents with a keen eye for detail, receive direction well and work independently.
- Excellent verbal and written communication skills
- Proficient with Microsoft Excel, Word, Access, and Outlook
Quality Associate II (Document Control - Quality Control)
ClosingIf you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.
Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact NAtalentacquisition@werfen.com for assistance.
We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team.
www.werfen.com
Employment Type: FULL_TIMEAbout Werfen
Sourced by ZipRecruiter
Industry
Health care and social assistance
Company size
1,001 - 5,000 Employees
Headquarters location
L'Hospitalet de Llobregat, Barcelona, ES