Quality Control Associate I
Integrated Resources Inc.
Job Description Client: Direct Client Location: Research Triangle Park, NC Job Title: Quality Control Associate I Duration: 1 Year+ Summary: The Quality Control Associate I supports key functional, tactical, and operational aspects of the Quality Control Chemistry group. Responsibilities: Perform QC Raw Material sampling and testing, including all associated activities. Support sampling, training, testing of raw materials, transfer qualification, validation activities, and maintain compliant cGMP documentation. Provide technical support as a subject matter expert in key functional areas. Process documentation and computer system entries. Apply understanding of Quality Systems in daily functions. Adhere to GLP/GMP requirements and understand FDA/EMEA regulations. Interact effectively with Quality management, support investigations, and participate in employee training and compliance activities. Work effectively within the team and across the site, demonstrating strong communication skills. Support activities such as interviewing, training, and corrective actions. Work weekends and overtime as required. Requirements: Bachelor’s degree in Chemistry or related field with 1-2 years of experience, or Associate degree/High School Diploma with equivalent experience (typically 3+ years). Knowledge of scientific principles and data analysis. Experience with laboratory instrumentation (HPLC, GC, UV-vis, Dissolution, FT-IR). Understanding of cGMP/cGLP requirements and laboratory safety. Ability to lift 10-20 pounds and stand for extended periods. Exposure to chemicals, dust, fumes, and hazardous waste. Weekend and overtime work may be required. Additional Information: Feel free to share this opportunity with colleagues. Thanks! Warm Regards, Amrit Singh Clinical Recruiter Integrated Resources, Inc Tel: View phone number on click.appcast.io This job posting is active and available. #J-18808-Ljbffr Integrated Resources Inc.
$26 - $29 per hour
...Details: Provides direct support on quality and compliance to internal departments... ...Responsibilities: Performs quality control tests/inspections as needed. Collect... ...Minimum Job Requirements: ~2 year associates degree required, ~ Minimum of 2 years'...SuggestedFor subcontractorWork at office- ...Quality Control Analyst I Position Summary The QC Analyst I, reporting to the Manager of Quality Control, will be responsible for serving as a performing routine GMP testing on analytical methods in the Quality Control laboratories. Job Responsibilities ~ Perform...Suggested
- ...questions and most serious unmet medical needs. We work to restore quality of life to those with debilitating conditions for which there... ...The QA Specialist will perform quality inspections, in-process controls, and finished product testing in accordance with established...SuggestedLocal areaShift work
$63k - $86.9k
KBI Biopharma, Inc. is hiring a Senior QC Analyst to perform crucial laboratory testing during 2nd shift hours. Candidates must hold a relevant degree and have 4-8 years of experience in the biopharmaceutical industry, particularly in protein analytics. Responsibilities...SuggestedAfternoon shift- ...proud to partner with some of the most admired Fortune 500 brands in the world. The QC Analyst I, reporting to the Manager of Quality Control, will be responsible for serving as a performing routine GMP testing on analytical methods in the Quality Control laboratories....Suggested
- ...Summary: The Operational Area Senior Quality Specialist will provide QA support of manufacturing operations, analytical laboratory operations and materials management for the external manufacturing programs at VCGT. This role will review batch data, including batch...Work at office
$27 - $29.85 per hour
...Quality Assurance Associate II Location: RTP NC Duration: 06 Months Pay rate: $27.00/hr - $29.85/hr The Quality Assurance Associate II (Contractor) is responsible for contributing to the oversight of key strategic, and operational aspects within Quality Assurance...For contractors- ...regulated environment preferably with 1 or more years of auditing experience, or Equivalent combination of education and regulatory, quality, compliance and/or industry experience. Skills and Abilities Excellent written and verbal communication and...Contract workTemporary workFor subcontractorWork at office
$58.7k - $88k
QC Lead Analyst Position Summary The Quality Control (QC) Biochemistry Lead Analyst provides front-line leadership for the QC Biochemistry team performing routine testing of raw materials, intermediates, finished goods, and stability samples. The role oversees and may execute...Temporary workShift work- ...environmental monitoring, GMP documentation, investigations, and quality systems. Key Responsibilities Perform environmental... ...related assays. Support product release testing and quality control activities. Investigate laboratory deviations, out-of-specification...Full time
$85.1k - $106.4k
...highly motivated, and experienced individual for the position of Quality Assurance Specialist II reporting to the Senior Manager Quality... ...Operations team, and support the Quality Systems, Quality Control and Quality Compliance functions. The ideal candidate is dedicated...Full timeWorldwideFlexible hoursShift work$89.6k - $166.4k
...Specialist II is a highly skilled laboratory professional who will support the start-up and growth of Novartis' Small Molecules Quality Control laboratory in Morrisville, North Carolina. This role serves as a technical subject matter expert for complex analytical...Work experience placement- ...Job Title: Quality Control Analyst I Job ID: 25-06076 Location: Morrisville, NC Duration: 10 month's Contract on W2 Duties: Perform environmental monitoring of the cleanrooms, biosafety cabinets (BSC), isolators, and other support areas....Contract work
- ...our employees to embark on the opportunity to help improve the quality of life for millions of people around the world. In NC, we... ...environments with hearing protections. Qualifications Associate’s degree in life sciences or related field from an accredited...Local areaShift workAfternoon shift
- ...our employees to embark on the opportunity to help improve the quality of life for millions of people around the world.In NC, we operate... ...in the pharmaceutical industry requiredMay consider an Associate’s Degree in Chemistry, Engineering or a relevant field of study...Local area
- Quality Control Analyst The purpose of the Analyst I, Quality Control (Non-Clinical) is to perform analytical testing to support the release of Non-Clinical grade rAAV vector lots manufactured in various departments (including, Pre-Clinical Manufacturing, Process Development...Work experience placement
- ...on the opportunity to help improve the quality of life for millions of people around the... ...NNPILP sitesPerform deviation & change control activitiesSupport other NNPILP sites when... ...accredited university requiredMay consider an Associate’s Degree from an accredited university...Local area
- ...our employees to embark on the opportunity to help improve the quality of life for millions of people around the world.In NC, we operate... ...combination of education and experienceMay consider an Associate’s degree in chemistry or relevant field of study from an accredited...Local area
- ...Quality Assurance Specialist This position is responsible for providing QA oversight and auditing activities related to clinical... ...assure study, project, and process compliance with protocols, controlled documents, and applicable regulations and guidelines through audits...Flexible hours
- Kriya Job Post Kriya is a biopharmaceutical company whose mission is to develop life-changing gene therapies for diseases affecting millions of patients around the world. We leverage our proprietary computational engine, in-house manufacturing infrastructure, and integrated...
- Almac Group is currently seeking a Quality Assurance Associate for our Durham, NC location. The Quality Assurance Associate is primarily concerned with the review of packaging and labeling batch records and the release of clinical supplies. The Quality Assurance Associate...Temporary workWorldwide
$28 - $31 per hour
...knowledge of cGMP in a Biomanufacturing field. 1+ years' experience would be amazing. RTP Onsite Duration: 6 Months The Quality Assurance Associate II (Contractor) is responsible for contributing to the oversight of key strategic, and operational aspects within Quality...Contract workFor contractorsRemote workNight shift- ...standards and expectations into appropriate quality standards and provide mentorship to... ...trending of site metrics. Support activities associated with QA release of Drug Substance, Drug... ..., development of new procedures and controls, and maintenance of established programs...
- ...Quality Auditor Date: Sep 2, 2026 Location: Morrisville, NC, US Company: Teleflex Expected Travel : Up to 50% Requisition ID :14037 About Teleflex Incorporated As a global provider of medical technologies, Teleflex is driven by our purpose to improve...Work at office
- ...Job Description Job Description Overview Clinical Quality Specialist (CQS) – Expereienced Advanced Practice Provider (NP/PA) Avance Care is seeking an experienced Advanced Practice Provider (Nurse Practitioner or Physician Assistant) for an exciting opportunity...Work at office
$43.08 - $80 per hour
Summary Quality is not just a checkpoint here—it is the promise we make to patients. As a Manufacturing Quality Assurance Specialist at Novartis, you will be a hands-on partner to manufacturing teams, ensuring every stage of production meets the highest standards...Hourly payRelocation packageMonday to FridayShift workDay shift- ...Quality AuditorTeleflex is seeking a Quality Auditor to join our Strategic Compliance department. The successful candidate must possess the ability to analyze and assess quality management systems to ensure compliance and conformance to the intent of the applicable regulations...Work at office
- ...About the job Quality Assurance Specialist Quality Assurance Specialist needs 3 years of experience... ...areas. Archive finalized Master Specifications and associated release documentation in the document control room, maintaining accurate and organized records....Work experience placementFlexible hours
- ...vendor data ecosystem? As a Sr. Vendor Data Quality Analyst at Fidelity Investments, you... ...business and technology partners to develop controls, monitor data health, identify root... ...may restrict Fidelity from hiring and/or associating with individuals with certain Criminal Histories...Full time
- Role: Quality Assurance Auditor within GLP-regulated environments, focusing on audits of studies, facilities, and compliance with FDA, EPA, and international GLP standards. Responsibilities: conduct facility and process audits review documentation prepare audit reports...Work at office
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