587 Results for

Quality Assurance Jobs in Durham, NC

Jobs

Clayton, NC

$17–$25 / hour
Contractor

p tabindex="0">Quality Assurance Inspectors work with manufacturing operations during the production process by approving the raw materials and associated documentation for incoming plasma shipments from donor collection centers and the in-process production batches (Production Units - PUs) at the Plasma Logistics Center (PLC). Quality Assurance Inspectors identify and document deviations of both materials and the manufacturing process and ensure these deviations are corrected to ensure a better finished product for prospective customers.

2 days ago

Raleigh, NC

p>The Director, Clinical Quality Assurance is primarily responsible for establishing and leading the Clinical QA function and providing independent oversight of Good Clinical Practices (GCP) activities to ensure compliance with FDA, EMA, ICH, and other applicable global and national regulatory requirements across Cellectis’ clinical programs. Knowledge and understanding of regulations regarding cell/gene therapies including but not limited to ICH guideline, GCP, and GMP as defined by the US Food and Drug Administration and European Medicines Agency.

2 days ago

Durham, NC

$98,000–$120,000

p> Determining compensation for this role (and others) at Vaco by Highspring depends upon a wide array of factors including but not limited to:

the individual’s skill sets, experience and training;
licensure and certification requirements;
office location and other geographic considerations;
other business and organizational needs.
Canadian residents may access our policies in English here and in French here.

7 days ago

Raleigh, NC

As a member of the site Quality Leadership Team, the Director partners cross-functionally with Manufacturing m QA, MSAT, AS&T, and Regulatory to support clinical and commercial manufacturing while advancing quality culture and operational excellence.

The Director, Quality Control provides strategic and operational leadership for all Quality Control (QC) activities supporting drug substance (DS) and dug product (DP) manufacturing at the site.

2 days ago

Raleigh, NC

p>• Work closely with other development managers and business analysts to gather requirements, participate in release-planning, contribute to roadmap, and help orchestrate multiple parallel delivery pipelines . In this role you will work together with other team members on design and implementation of essential computational, scalable, and resilient RESTful APIs to both our internal and external partners.

2 days ago

Chapel Hill, NC

$35.87–$51.57 / hour

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In addition to outpatient practice, there may be opportunities to provide coverage in our onsite short stay unit, where clinicians support patients in the immediate postoperative phase and assist with safe, efficient transitions home and into outpatient rehabilitation following orthopedic surgery. As clinicians gain experience, there are clear pathways for advancement through our clinical ladder, including opportunities to progress to higher clinical roles once experience, skills, contributions, and professional leadership align with role expectations.

2 days ago

Holly Springs, NC

$94,000–$174,600 / year

You will partner directly with the QC department to provide day-to-day quality compliance support, serving as a trusted gatekeeper for data integrity, support investigations and manage change controls related to laboratory systems, test methods, and digital applications, ensuring modifications do not compromise the validated state of our operations.

This position is a unique opportunity to embed quality into the site's operational design, support a continuous improvement culture, and drive operational excellence in accordance with Good Manufacturing Practices, establishing Holly Springs as a center of excellence for aseptic drug product manufacturing.

18 days ago

Research Triangle Park, NC

$40–$40 / hour

li>Providing deliverables and resolving issues; Draft SOPs/controlled documents as well as perform quality unit review and approval of Quality Management Systems requests/ records related to Learning Management, Non-Conformance Management, CAPA management, and metric/KPI reporting. Job Description:

The QA Contractor, GMP Quality Assurance, reporting to the Manager, GMP Quality Assurance, or designee, will be responsible for assisting in the management of Quality Management System (QMS) and will strongly support culture of Quality.

13 days ago

Clayton, NC

Demonstrated expertise in Regulations & quality systems in one or more of the following: product disposition, DV/CAPA, Change Control, Audits, Supplier Management, Project Management, Validation, laboratory method and equipment validation, warehouse/logistics, and IT preferred. Our Product Supply Aseptic Manufacturing (PS AM) facility in Clayton, NC is a 457,000 square foot aseptic "fill and finish" site that is responsible for producing innovative, injectable diabetes and obesity treatments.

25 days ago

Clayton, NC

25 days ago

Clayton, NC

28 days ago

RTP, NC

$38.07–$38.07 / hour

Providing deliverables and resolving issues; Draft SOPs/controlled documents as well as perform quality unit review and approval of Quality Management Systems requests/ records related to Learning Management, Non-Conformance Management, CAPA management, and metric/KPI reporting. The QA Contractor, GMP Quality Assurance, reporting to the Manager, GMP Quality Assurance, or designee, will be responsible for assisting in the management of AskBio’s Quality Management System (QMS) and will strongly support AskBio’s Culture of Quality.

13 days ago

Research Triangle Park, NC

Minimum Requirements + Bachelor’s Degree in a scientific or related technical discipline + 2+ years of relevant pharmaceutical industry experience in a cGMP regulated environment + Ability to work independently and as part of a multi-functional team, being able to manage and prioritize workloads, stressful situations, and deadlines and work extended hours to support business needs + Able to work extended hours to support business needs, as applicable + Ability to effectively communicate with internal customers at various levels in the organization; written and oral + Ability to handle confidential company data, projects, information, etc. + Ability to interpret data in relation to a vast number of company procedures as well as current GMP requirements + Experience in review of batch records, production records, process control records + Proficient in Microsoft Excel, Word, and Adobe Acrobat Preferred Requirements + 2+ years of experience in combination products + Knowledge of Enterprise Resource Planning System (ERP), TrackWise Digital, Systems Application and Products (SAP S4HANA), and MasterControl Job Location United Therapeutics requires this candidate to be on-site at our RTP, North Carolina location 100% of the time.

5 days ago

Research Triangle Park, NC

Escalate unresolved issues or concerns to Quality Management and affected area management + Participate in client meetings and projects as it relates to manufacturing, product scheduling, batch records, supply chain, etc. to support product pipelines + Support regulatory authority (FDA, MHRA, EMA, QP, etc.) inspections and internal audits, including documentation audit team, pre-audit facility inspections, etc Minimum Requirements + Bachelor’s Degree in a scientific or related technical discipline + 5+ years of relevant pharmaceutical industry experience in a cGMP regulated environment + Ability to work independently and part of a multi-functional team, being able to manage and prioritize workloads, stressful situations, and deadlines and work extended hours to support business needs + Able to work extended hours to support business needs, as applicable + Experience in review of batch records, production records, process control records + Ability to interpret data in relation to a vast number of company procedures as well as current GMP requirements + Ability to effectively communicate (written and oral) with internal and external customers at various levels in the organization + Ability to handle confidential company data, projects, information, etc. + Review GMP documentation, including logbooks, pest control, waterlogs, calibration and maintenance reports, temperature monitoring, batch records, protocols, etc., as it relates to Combination products for accuracy, completeness, and compliance with UT policies and procedures + Perform quality assurance functions, including inspection of production equipment for cleanliness, gowning, area line clearances, in-process packaging checks, AQL inspections and floor audits, in support of manufacturing and packaging operations + Review and disposition manufacturing, packaging and Combination Products batch records and raw materials and components for clinical and commercial processes + Review of quality control final product and stability data + Process rejected lots of raw materials, components and Combination products identified for destruction.

5 days ago

Research Triangle Park, NC

Bachelor’s degree in a scientific field and 4+ years of experience in GMP based Quality Assurance, particularly in support/oversight of a company QMS, or 10+ years of GMP based Quality Assurance experience using a company QMS.

11 days ago

Durham, NC

$113,000–$156,000 / year

Provides QA oversight of analytical and microbial laboratory activities including but not limited to method qualification, method transfers, method validations, creation and revision of test methods, specifications, stability studies, laboratory investigations and laboratory deviations. The Principal QA Specialist provides exemplary service to both internal and external customers by ensuring patient safety and regulatory compliance while supporting product lifecycle activities for timely delivery of products to clients for patients.

30+ days ago

Morrisville, NC

$35.87–$51.57 / hour

Promotes the improvement of patient care and clinical excellence in clinical information systems via effective collaboration with healthcare providers, business and quality analysts, and leaders of clinical programs and quality initiatives. In this role, the objectives would include improving clinical care as well as clinical documentation and reporting for treatment, prevention, and drug administration regimens, record keeping practices, workflow procedures, medical decision-making practices, and pay-for-performance programs.

28 days ago

Chapel Hill, NC

$35.87–$51.57 / hour

p>About the Role:

Lead trauma process improvement and patient safety initiatives for a Level I Adult & Pediatric Trauma Center, utilizing data-driven quality improvement strategies to enhance patient outcomes and reduce preventable trauma-related morbidity and mortality.
Promotes the improvement of patient care and clinical excellence in clinical information systems via effective collaboration with healthcare providers, business and quality analysts, and leaders of clinical programs and quality initiatives.

30+ days ago

Cary, NC

$35.87–$51.57 / hour

li>

Promotes the improvement of patient care and clinical excellence in clinical information systems via effective collaboration with healthcare providers, business and quality analysts, and leaders of clinical programs and quality initiatives. Assists OBGYN dept with meeting our Women's Health Improvement Collaborative goals for screening/treatment of depression, Social Drivers of Health, 5Ps, cervical cancer & breast cancer screenings.

20 days ago

Raleigh, North Carolina

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The QA Specialist, External Manufacturing Quality Operations (EMQO) supports Quality Assurance activities at the Eisai Raleigh facility by assisting with routine operational quality tasks under direction and supervision. For additional information on Company employee benefits programs, visit https://careers.eisai.com/us/en/compensation-and-benefits.

6 days ago

Raleigh, NC

$66,200–$86,800 / year

For additional information on Company employee benefits programs, visit https://careers.eisai.com/us/en/compensation-and-benefits. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States.

5 days ago

Research Triangle Park, North Carolina

Examples of activities within the scope of oversight and auditing include but are not limited to: preclinical animal studies, sample analysis from clinical and preclinical studies, qualification and/or validation of methods, equipment/software validation, laboratory processes, etc. Must be able to effectively collaborate cross-functionally with peers, scientific and technical staff; and be comfortable working in a matrixed team.

23 days ago

20 TW Alexander Dr, Research Triangle Park,, NC

$30–$32 / hour

Quality Assurance Specialist - Bachelor's degree, in a health care or relevant scientific field and 3+ years of relevant industry experience.

30+ days ago

Raleigh, NC

Qualifications & Education: Bachelor's Degree in Computer Science or Information Technology or equivalent professional experience • 5+ years of relevant technical QA experience or similar role • Retail, Fuel Pharmacy, Restaurant, or POS experience is a big plus Technical Skills: • Office Skills (Word, Excel, PPT) o Basic SQL / Databases o Basic Linux o XML o Ability to work with various QA/Testing tools and technologies (i.e. Jira, Testlink, SOAP UI, Postman) o Scripting (Python) experience is advantage • Problem analysis • Retail Process Knowledge (Retail Experience) a big plus o POS / Backoffice o Store processes o ERP Competencies: Analytical - Synthesizes complex or diverse information; Collects and researches data; Uses intuition and experience to complement data; designs work flows and procedures. Written Communication - Writes clearly and informatively; Edits work for spelling and grammar; Varies writing style to meet needs; Presents numerical data effectively; Able to read and interpret written information.

30+ days ago

Mebane, NC

$27.10–$27.50 / hour
Temporary

p>ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2022 ManpowerGroup was named one of the World's Most Ethical Companies for the 13th year - all confirming our position as the brand of choice for in-demand talent.

7 days ago

Mebane, NC
$27.10–$27.50 / hour
Temporary
p>ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2022 ManpowerGroup was named one of the World's Most Ethical Companies for the 13th year - all confirming our position as the brand of choice for in-demand talent.

7 days ago

Research Triangle Park, NC
$34–$34 / hour
li>Examples of activities within the scope of oversight and auditing include but are not limited to: preclinical animal studies, sample analysis from clinical and preclinical studies, qualification and/or validation of methods, equipment/software validation, laboratory processes, etc. Akarsh YathirajSenior Recruiter
C. (415) 322-5419
D. (415) 322-5419
A. 611
22 days ago
Durham, NC
Remote
$120,000–$155,000 / year
As a global leader in smallpox and mpox vaccines, our growing portfolio includes market-leading vaccines against rabies, tick-borne encephalitis, cholera, typhoid, and Ebola. The ideal candidate will have deep expertise in aseptic GMP manufacturing environments, strong knowledge of sterile operations, and hands-on experience managing quality oversight of external manufacturing partners.
30+ days ago
Henderson, North Carolina
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Quality Assurance Specialist. • Address and discuss issues and proposed solutions with all department management teams and Regulatory/Compliance Manager.
30+ days ago
Durham, North Carolina
Provides QA oversight of analytical and microbial laboratory activities including but not limited to method qualification, method transfers, method validations, creation and revision of test methods, specifications, stability studies, laboratory investigations and laboratory deviations. The Principal QA Specialist provides exemplary service to both internal and external customers by ensuring patient safety and regulatory compliance while supporting product lifecycle activities for timely delivery of products to clients for patients.
30+ days ago
Durham, NC
p>Demonstrated solid Body of Knowledge of Quality systems and functions supporting drug or related FDA governed manufacturing obtained from professional Quality roles Includes a balance of, from such areas as Supplier Quality Assurance, Compliance, Audits/Inspections, Shop Floor Support, Batch / Material release, Quality document control, review and approval, Validation, QC, Deviations, Prior direct regulatory agency, and audit management /r support experience a plus.
Ability to work effectively with others and communicate in customer-facing forums to progress issues and obtain positive results Able to navigate conflict to achieve deliverables and drive to targeted outcomes Ability to work professionally and facilitate positive interdepartmental interactions with a diverse group of people Voluntarily communicates needs and suggestions clearly and effectively Listens and is attentive to others' ideas and contributions.
30+ days ago
Durham, NC
$55,000–$86,900 / year
This includes performance of compliance review of records (master batch records, executed batch records, and internal support records such as logbooks), aid in deviation determination/generation, general Quality guidance. In addition to supporting Manufacturing, MQA Specialists are responsible for the execution of core activities, including but not limited to:
Executed Batch record review and approval.
30+ days ago
Morrisville, North Carolina
p style="margin:0px">At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record. Job Summary:
The Senior Quality Assurance Specialist is accountable for driving results in a fast-paced environment by effectively performing activities as directed to ensure quality and compliance with applicable regulatory requirements and internal procedures.
15 days ago
Morrisville, North Carolina
p style="margin:0px">At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record. Job Summary:
The Senior Quality Assurance Specialist is accountable for driving results in a fast-paced environment by effectively performing activities as directed to ensure quality and compliance with applicable regulatory requirements and internal procedures.
23 days ago
Morrisville, North Carolina
p style="margin:0px">At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record. Job Summary:
The Senior Quality Assurance Specialist is accountable for driving results in a fast-paced environment by effectively performing activities as directed to ensure quality and compliance with applicable regulatory requirements and internal procedures.
30+ days ago
Durham, NC
p>Job Responsibilities:
Works directly with Manufacturing, QA and other departments responsible for GMP activities to resolve production related deviations and other compliance issues in a timely manner.
Minimum Requirements:
Minimum BS in scientific field with 14+ years' experience or MS and 11+ years' experience in a QA cGMP regulated environment within Biopharmaceuticals or equivalent.
30+ days ago
New
Raleigh, NC
When you join Guerbet, you :
Are choosing a global leader with recognized expertise in diagnostic and interventional imaging,
Are joining our 2820 collaborators who are committed every day to offering innovative solutions to improve quality of patient's life all over the world,
Are joining a company where we value diversity of talents coming from various horizon.
Primary QA event response personnel that will respond to exceptions within the operations/packaging areas, having functions of initial exception impact assessment, product containment, bracketing, initial scope identification, and direction of immediate actions to take prior to resuming processing.
5 days ago
Research Triangle Park, NC
$33
Examples of activities within the scope of oversight and auditing include but are not limited to: preclinical animal studies, sample analysis from clinical (GCLP guidelines) and preclinical studies (GLP regulations), qualification and/or validation of methods, laboratory processes, etc. Education/ Qualifications:
Quality Assurance Specialist - Bachelor’s degree, in health care or relevant scientific field and 3+ years of relevant industry experience.
21 days ago
Durham, NC
The company maintains a portfolio of clinical programs across a range of neuromuscular, central nervous system, cardiovascular, and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure, limb-girdle muscular dystrophy, multiple system atrophy, Parkinsons disease, and Pompe disease. This key individual performs vendor assessments and occasional audits (virtual and on-site) alongside subject matter experts, ensuring vendor qualification activities support compliance with applicable GLCP, GLP, GCP, and GMP guidelines and relevant national/international/local regulations.
30+ days ago
Research Triangle Park, NC
$18.02–$38.61 / hour
Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Troubleshoot and provide QA systems support to reconcile issues in systems, such as, inventory control systems (SAP), laboratory LIMS system (Darwin) and other systems as required (TrackWise.
30+ days ago
NC
$140,000–$210,000 / year
The annual allocation to the ESOP is fully funded by BDO through investments in company stock and grants employees the chance to grow their wealth over time as their shares vest and grow in value with the firm's success, with no employee contributions. The Lead Engineer leads the development and execution of comprehensive test plans, while mentoring junior team members and collaborating with cross-functional teams to deliver high-quality solutions.
19 days ago
Durham, North Carolina
Includes a balance of, from such areas as Supplier Quality Assurance, Compliance, Audits/Inspections, Shop Floor Support, Batch / Material release, Quality document control, review and approval, Validation, QC, Deviations, Prior direct regulatory agency, and audit management /r support experience a plus.
Minimum 5 years prior experience in the Pharmaceutical/Biotechnology industry with a thorough knowledge of Quality Systems, Quality Assurance and Quality Control including solid knowledge of global GMP Quality and Regulatory requirements.
30+ days ago
Holly Springs, NC
Provides QA oversight and supports DSM operations in accordance with governing processes and procedures• Provides QA support of DSM tasks such as o Batch Record and Solution Lot Record review, including exception-based oversight using Quality Review Management tool o Real time event triage and implementation of immediate response to identified deviations o Area changeover and return to service o Real time WO oversight per applicable procedures• Ensures department objectives are met within desired timelines and/or in accordance with identified KPIs• Contribute to the development of QA documentation, procedures, and processes for operational readiness objectives and QA support of manufacturing operations in cGMP regulated facility• Participate in streamlining or efficiency improvement initiatives with other FUJIFILM Diosynth Biotechnologies sites. Minimum Requirements: BS/BA in Life Sciences or Engineering or equivalent with 2+ years of relevant experience OR• Masters in Life Sciences or Engineering or equivalent with 0 years' relevant experience• 1-3 years' experience in a GMP environment• Experience in Validation, cGMP manufacturing operations and/or Quality oversight, in an FDA regulated facility.
27 days ago
Durham, North Carolina
This includes performance of compliance review of records (master batch records, executed batch records, and internal support records such as logbooks), aid in deviation determination/generation, general Quality guidance. In addition to supporting Manufacturing, MQA Specialists are responsible for the execution of core activities, including but not limited to:
Executed Batch record review and approval.
22 days ago
Raleigh, NC
$145,000–$217,000 / year
li>Develop engineering procedures, including document control, submissions management, creation and tracking of Requests For Information (RFIs), material samples documentation, and tracking of potential cost changes documentation, and tracking of approved change orders within budgetary requirements.
Position Description: Responsible for planning, coordinating, and developing the project-specific Quality Assurance/Quality Control (QAQC) Plan that incorporates the policies and procedures necessary to deliver the project fully compliant with the contract documents.
30+ days ago
Raleigh, NC
$120,000–$217,000 / year
li>Develop engineering procedures, including document control, submissions management, creation and tracking of Requests For Information (RFIs), material samples, documentation and tracking of potential cost changes, documentation and tracking of approved change orders within budgetary requirements.
Position Description: Responsible for planning, coordinating and developing the project-specific Quality Assurance/Quality Control (QA/QC) Plan that incorporates the policies and procedures necessary to deliver the project fully compliant with the contract documents.
30+ days ago
NC
$93,000–$191,000 / year
p>Information for applicants with a need for accommodation: https://www2.deloitte.com/us/en/pages/careers/articles/join-deloitte-assistance-for-disabled-applicants.html. Our team supports client-facing teams in how they approach the marketplace, develop service offerings, evaluate and onboard prospective clients, contract for services, deliver quality client service, and fulfill post-engagement and other recurring obligations.
26 days ago
Raleigh, NC
This role focuses on supporting product quality across the lifecycle-working closely with R&D, regulatory, and cross-functional teams to uphold Ascom's Integrated Management System while enabling efficient and compliant product development. By ensuring adherence to design controls, supporting risk management, and driving resolution of product and process nonconformities, you will help safeguard patient safety, maintain regulatory confidence, and improve operational effectiveness.
24 days ago
Durham, North Carolina
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The Senior Specialist, Quality Assurance provides Quality Assurance (QA) oversight of AskBio’s Vendor Qualification Program for GCLP, GLP, GCP (and GMP vendors, as needed). This key individual performs vendor assessments and occasional audits (virtual and on-site) alongside subject matter experts, ensuring vendor qualification activities support compliance with applicable GLCP, GLP, GCP, and GMP guidelines and relevant national/international/local regulations.
30+ days ago
Holly Springs, NC
All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).
30+ days ago
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Quality Assurance Jobs in Durham, NC

Quality Assurance Inspector People Make Us

Director, Clinical Quality Assurance Cellectis

Insurance Quality Analyst Vaco LLC

Director, Quality Control Cellectis

Senior Software Developer- Contractor Align Technology, Inc.

Physical Therapist I - Ambulatory Care Center UNC Health

Senior QA Specialist, QA for QC (CVRM) Genentech Inc

QA Contractor, GMP Quality Assurance Leadstack Inc

Quality Assurance Area Specialist III (QA for Warehouse & Logistics) Novo Nordisk AS

Quality Assurance Area Specialist III (QA for Utilities) Novo Nordisk AS

Quality Assurance Area Specialist III - QA IT / Utilities Novo Nordisk AS

QA Contractor, GMP Quality Assurance TalentBurst, Inc.

QA Specialist II, Quality Operations (Combination Products) United Therapeutics

Senior QA Specialist, Quality Operations (Combination Products) United Therapeutics

QA Contractor, GMP Quality Assurance Lancesoft

KBI: US - Principal QA Specialist KBI Biopharma Inc

Clinical Quality Assurance Specialist - Pediatrics UNC Health

Clinical Quality Assurance Specialist - Trauma Program UNC Health

Clinical Quality Assurance Specialist - UNC OB-GYN at Panther Creek UNC Health

QA Specialist (Hybrid) Eisai

QA Specialist (Hybrid) Eisai Inc

Quality Assurance Specialist - Lab IntelliPro Group

Quality Assurance Specialist II TalentBurst, Inc.

QA Analyst Computer Task Group, Inc

QA Specialist (GMP) – 3rd Shift | $27.50/hr | 3 Month Contract | Onsite Manpower Engineering

QA Specialist – Medical Device Manufacturing | 2nd Shift | $27+/hr | Manpower Engineering

Quality Assurance Specialist II Leadstack Inc

Senior QA Specialist, External Manufacturing, US Bavarian Nordic AS

Quality Assurance Associate Carolina CoPacking

KBI: US - Principal QA Specialist KBI Biopharma

Principal QA Specialist KBI Biopharma Inc

KBI: US - QA Specialist II KBI Biopharma Inc

Sr. Quality Assurance Specialist - 3rd Shift Alcami Corporation

Sr. Quality Assurance Specialist - 2nd Shift Alcami Corporation

Sr. Quality Assurance Specialist Alcami Corporation

Senior QA Specialist Deviations and CAPAs KBI Biopharma Inc

Manufacturing QA Specialist Guerbet SA

Quality Assurance Specialist Lancesoft

Sr. Quality Assurance Specialist AskBio Inc

Technician - Process Quality Assurance Floor Support (Night Shift) Eli Lilly and Co

Lead QA Engineer - Tax Product Development (SDET) BDO USA PC

Principal QA Specialist KBI Biopharma

QA Specialist, DSM (0600 1800/2 2 3) FUJIFILM Biotechnologies USA Inc

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Quality Assurance - Quality Control Manager Turner Construction Co

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QRM Support Manager - National Tax Quality Assurance (NTQA), Quality Risk Deloitte Touche Tohmatsu Ltd

QA Engineer - Patient Systems Legal, Quality & Regulatory · US Raleigh Ascom Holding AG

Sr. Quality Assurance Specialist AskBio

QA Specialist, Warehouse (Supply Chain) FUJIFILM Biotechnologies USA Inc

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