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Quality Control Associate I Jobs (NOW HIRING)

Integrated Resources INC

NC · On-site

The Quality Control Raw Materials Associate I is responsible for contributing to key functional, tactical, strategic and operational aspects of the Quality Control Raw Materials group at the Client ...

Lonza

Quality Control Associate I

Vacaville, CA · On-site

$63K - $106K/yr

Join Lonza in Vacaville, CA as a Quality Control(QC) Associate I. You will be a team member of the Quality Control department to support production of in-process, drug substance, drug product, raw ...

TekWissen LLC

QC Laboratory Associate

Vacaville, CA · On-site

$20 - $25/hr

Job Title: QC Associate I / QC Laboratory Associate Location: Vacaville, CA - 95688 Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Summary With limited supervision, the QC ...

Collabera

QC Associate I

San Diego, CA · On-site

Qualifications Education: BS/MS in Biology/Molecular Biology, biochemistry, chemistry or related discipline 2 to 5 years of industry experience with Functional analysis QC of molecular-biology-based ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

With limited supervision, QC Associate I, is responsible for the performance of direct materials testing in accordance with cGMP regulations. * These duties include execution of laboratory testing ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

With limited supervision, QC Associate I, is responsible for the performance of direct materials testing in accordance with cGMP regulations. * These duties include execution of laboratory testing ...

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How much do quality control associate i jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for quality control associate i in the United States is $25.46, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $31.01 per hour, depending on experience, location, and employer.

What is a quality control associate I?

A Quality Control Associate I is an entry-level professional responsible for ensuring that products and processes meet established quality standards in industries such as pharmaceuticals, biotechnology, and manufacturing. They perform routine inspections, tests, and analyses of materials, in-process samples, and finished goods to verify compliance with regulatory and company requirements. Additionally, they document findings, maintain laboratory equipment, and help identify areas for process improvements. This role is essential for maintaining product safety, efficacy, and consistency.

What are the key skills and qualifications needed to thrive as a quality control associate I?

To thrive as a Quality Control Associate I, you need a solid understanding of laboratory techniques, quality assurance protocols, and often a bachelor's degree in a science-related field. Familiarity with laboratory information management systems (LIMS), analytical instruments, and compliance standards such as GMP or ISO is typically required. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for ensuring accuracy and collaborating with cross-functional teams. These skills and qualifications ensure product quality, regulatory compliance, and the overall integrity of testing processes.

What are some common challenges faced by a quality control associate I, and how can they be effectively managed?

Quality Control Associate I professionals often encounter challenges such as maintaining strict adherence to standard operating procedures, handling repetitive tasks with consistent accuracy, and managing tight deadlines for sample analysis. Effective time management and attention to detail are key to overcoming these hurdles. Collaborating with more experienced team members and actively seeking feedback can also help new associates navigate complex testing protocols and ensure high-quality results.

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Quality Control Associate I jobs near you

Quality Control Associate I

Durham, NC • On-site

Integrated Resources INC
Recruiting and Staffing Services • 51 - 200 employees
Learn more about Integrated Resources INCexternal

Contractor

Re-posted 11 days ago

Key responsibilities

  • Perform QC raw material sampling and testing activities.

  • Support transfer qualification, validation activities, and maintain compliant cGMP documentation.

  • Provide technical support and communicate effectively with Quality management while adhering to GMP and GLP requirements.

Job description

Company Description

A Few Words About Us - Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.


This position is with my direct client 

Job Description

Position Details: 

Client Direct Client

Location Research Triangle Park, NC

Job Title Quality Control Associate I

Duration 1 Year+

Must have skill-set [Job Description] Job Summary:

The Quality Control Associate I is responsible for supporting key functional, tactical, and operational aspects of the Quality Control Chemistry group .


Responsibilities:

This includes performing QC Raw Material sampling and testing as well as all activities associated with this sampling and testing.

The Associate I responsibilities include, but are not limited to sampling, training, testing support for raw materials, support for transfer qualification and validation activities as appropriate, robust and compliant cGMP documentation practices, and providing sound technical support as a subject matter expert in one or more key functional areas. 

Process all associated documentation and computer system entries. 

Has a fundamental understanding of the Quality Systems and apply it in their daily support functions. 

Additional responsibilities include adherence to all GLP/GMP requirements, a basic understanding of FDA/EMEA regulations, effective interactions/communication with Quality management, personal development, and support of investigations impacting the QC Chemistry department. 

The Associate I may also support the Supervisor/Manager for activities related to interviewing and training of employees, compliance with GMP, and identifying and implementing corrective actions on the floor. 

The Associate I should be able to work effectively within the group, within Quality and across site. 

This requires solid written and verbal communication skills. 

The Associate I should actively seek to understand their personal leadership approach and communication style. 

Weekend and overtime work may be required.


Additional Information/Requirements: 

The Quality Control Associate I will possess technical knowledge regarding Quality Control Chemistry release and stability methodology. The position requires but is not limited to the following: 

Bachelor's degree in Chemistry or equivalent discipline with 1 - 2 years, OR Associate degree or High School Diploma with appropriate equivalent experience (Typically 3 + years) 

Knowledge and limited use/application of basic scientific theory and principles. 

Able to apply basic understanding of scientific data/literature to conduct experiments 

Knowledge of commonly used laboratory instrumentation (HPLC, GC, UV-vis, Dissolution, and FT-IR) and software 

Knowledge of cGMP/cGLP requirements and laboratory safety

Computer literacy 

Lifts and carries laboratory solvents/supplies up to 10-20 pounds

Remains standing/on feet for extended durations throughout day

Exposure to chemicals, dust, fumes, odor, and hazardous lab waste

Weekend and overtime work may be required


Feel free to forward my email to your friends/colleagues who might be available




Additional Information


Thanks!!!

Warm Regards,

Amrit Singh

Clinical Recruiter

Integrated Resources, Inc

IT REHAB CLINICAL NURSING

Tel: (732) 429 1634  

Fax: (732) 549 5549

http://www.irionline.com

Inc. 5000 - 2007, 2008, 2009, 2010, 2011, 2012,2013 & 2014 (8th Year)

Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70


Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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