304 Results for

Quality Control Specialist Jobs in Durham, NC

Jobs

Clayton, NC

Join a growing furniture manufacturing team as a Production CAD Specialist in Clayton, NC, where you’ll play a key role in transforming innovative furniture designs into high-quality finished products.

Today

Chapel Hill, NC

$31.04–$44.62 / hour

The Specialist works in collaboration with the laboratory supervisor and laboratory directors to address analytical problems and maintain scientific oversight of routine patient testing.

The Microbiology Laboratory is currently recruiting a Medical Laboratory Specialist for the Central Processing, Bacteriology, and Special Microbiology areas of the laboratory.

1 day ago

Holly Springs, NC

$98,000–$182,000 / year

li>

You possess a working understanding of database management/relational tables, preferably with experience working with Labware (LIMS), Binova (LES), SAP, Mettler Toledo LabX, Waters Empower Chromatography Data System or similar cGMP QC systems. This plant meets today's demand for CVRM (Cardiovascular, Renal, and Metabolism) medicines and is scalable to grow with the portfolio, which focuses on next-generation metabolic medicines specifically targeting the global obesity epidemic and Type 2 diabetes.

30+ days ago

Fuquay-Varina, NC

li>Collaboration with Cross-Functional Teams: work closely with all members of the project team - Project Managers, Engineers, Superintendents, etc., and have ultimate responsibility for the day-to-day distribution and management of documents pertaining to the jobsite.

Revision Control: Maintain strict revision control processes, ensuring only current revisions of documents are in use, with obsolete versions properly archived.

30+ days ago

Holly Springs, NC

You’ll lead critical instrumentation initiatives that keep our QC operations accurate, compliant, and inspection-ready: Lead the execution of qualification, maintenance, continuous improvement, and decommissioning of QC analytical instruments, applying deep expertise in instrumentation, validation, and regulatory compliance. 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.

11 days ago

Durham, NC

$41.06–$76.25 / hour

p>Key Responsibilities:

Execute routine and non-routine analysis for cGMP release and characterization testing using techniques including but not limited to chromatography (HPLC, UPLC), AUC, SEC, compendial assays (pH, Conductivity, Osmolality), electrophoresis (CE, Western Blot) and assist with data review.
Essential Requirements:
- Bachelors degree in scientific disciplines such as Biochemistry, Biology, Microbiology or related field with 5 years' experience in GMP environment or 4 years' at GTx.

30+ days ago

Holly Springs, NC

p>You'll lead critical instrumentation initiatives that keep our QC operations accurate, compliant, and inspection-ready:

Lead the execution of qualification, maintenance, continuous improvement, and decommissioning of QC analytical instruments, applying deep expertise in instrumentation, validation, and regulatory compliance. 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.

11 days ago

Holly Springs, NC

Prior hands-on experience with analytical instrumentation associated with the following technologies: UPLC/HPLC, capillary electrophoresis/imaged capillary isoelectric focusing, gel electrophoresis/Western blot, plate readers, qPCR, spectrophotometry, and mass spectrometry. 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.

30+ days ago

Holly Springs, NC

$33–$50 / hour

li>Author, revise, and review documents and reports, including SOPs, test methods, safety assessments, trend reports, qualification/validation summary reports, and technical reports. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.

6 days ago

Holly Springs, NC

30+ days ago

Holly Springs, NC

$45–$55 / hour

Operating within the QC Systems group and reporting to the Manager of Digital Laboratory Systems, this role partners closely with QC subject matter experts to analyze workflows, identify inefficiencies, and build scalable digital solutions that enhance data accessibility, reporting, and operational efficiency. Doctorate degree and 2 years of experience, or Master's degree and 6 years of experience, or Bachelor's degree and 8 years of experience, or Associate degree and 10 years of experience, or high school diploma / GED and 12 years of experience.

22 days ago

Durham, NC

strong>Position Type: Hourly Contract Position (W2 only)

The Quality Inspector conducts inspections of products (parts, assemblies, raw materials, tooling, instruments, etc.) to validate compliance to design data requirements which include drawings, specifications, and contract requirements at predetermined steps in the manufacturing process using basic inspection methods and tools. Our client, a leading Medical Device Manufacturing Company is looking for Quality Control - Inspector 2 and This is for an initial duration of 12 MonthsContract – Durham, NC.

30+ days ago

p>The QA Specialist II, Quality Operations is responsible for quality operation activities related to clinical and commercial drug products in adherence with current Good Manufacturing Practices (cGMP) and corporate policies and procedures at the RTP campus.

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 activities.

4 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.

4 days ago

Cary, NC

Oversee QA/QC site-related activities: oversee testing, inspection, and acceptance of work; inspect and accept materials and equipment; identify deficiencies and non-conformances and track them through resolution and acceptance; prepare and submit quality control reports; review quality control documentation for specialty items and shop and field operations for subcontracted trades. Develop, plan, manage, and administer the implementation of project-specific Construction Quality Control and Quality Assurance (QA/QC) Plans with CM team, contractors, and clients (multiple Quality Control (QC) specialists, Commissioning, and/or jurisdictional inspection and testing personnel/agencies).

30+ 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.

24 days ago

Clayton, NC

24 days ago

Clayton, NC

27 days ago

Holly Springs, North Carolina

$41,600–$62,400

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering.

26 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.

17 days ago

Cary, North Carolina

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Extensive knowledge with Oracle based testing and programming payroll processes;

Considerable knowledge of the Department of Public Instruction (DPI) licensure and salary system;

Considerable knowledge of the Budget Utilization Development (BUD) system;

Considerable knowledge of Microsoft Office specifically Excel, Word Power Point; Google Apps;

Working knowledge of database systems with the ability to analyze and organize data;

Strong analytical and problem solving skills, attention to detail with a high level of accuracy;

Effective time management skills with the ability to meet deadlines;

Ability to communicate clearly and concisely both in oral and written form using a variety of communication techniques and tools to ensure the appropriate flow of information, collaborative efforts, and feedback;

Ability to exercise independent initiative to perform both original and recurring assignments, and exercise judgment in the absence of clear directives;

Ability to understand, interpret, and apply specific rules and regulations governing the processing of fiscal documents, maintenance of financial records, and the preparation of reports;

Ability to communicate and maintain working relationships with school system employees, vendors, and other outside agencies.

Bachelor’s degree in accounting, finance, business administration, or directly related field;
Two years of experience in payroll, bookkeeping, accounting, or related field;
Other combinations of applicable education, training, and experience which provide the knowledge, skills, and abilities necessary to perform effectively in the position may be considered.

30+ days ago

Cary, NC

p>The Company DPS Group, Inc. is proudly part of the Arcadis Group of Companies and is a global EPCM firm offering full-service solutions within the Life Sciences (pharmaceutical, biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and solar) industries. DPS is dedicated to delivering successful projects with a client-first mentality and personal touch across a range of market sectors: Project and Program Management, Procurement, Design, Construction Management, Health and Safety Management, Commissioning, Qualification, and Start-up.

4 days ago

Clayton, NC

$128,470–$192,710 / year

As a recognized technical authority, this position collaborates across engineering, manufacturing, validation, commercial, and customer-facing teams to deliver production-ready, high-quality control solutions. The Advanced Technology team within Building Construction Products (BCP) is seeking a Control Systems Engineering Specialist (KD14) to lead machine feature development across multiple BCP platforms.

30+ days ago

Raleigh, NC

$70,000–$85,000 / year

Job Summary The Senior ICS Fuel Inventory Control Specialist is a key assurance role responsible for overseeing fuel inventory accounting processes across Swissports Maintenance & Operations (M&O) and Intoplane fueling locations. The position plays a critical role in identifying and investigating fuel inventory variances, strengthening internal controls, and ensuring that all stations complete billing within 48 hours of month-end.

30+ days ago

Raleigh, NC

li>Strong analytical and problem-solving mindset with high attention to detail, with the ability to explain complex system topics to non-technical stakeholders, and comfortable working independently in a fast-paced, high-growth environment.

Prepare and validate relevant SAP CO and PS structures to support Controlling requirements, and validate master and hierarchical objects including Cost Centers, Profit Centers, Internal Orders, and WBS / Project structures.

30+ days ago

Research Triangle Park, NC

$33–$33 / hour

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

(415) 322-5419

611

30+ days ago

Raleigh, North Carolina

We execute the entire spectrum of electrical infrastructure projects—including the construction of transmission lines and substations, the modernization of distribution systems, and the development of both Oil & Gas facilities and Renewable Energy initiatives.

As a Project Controls Specialist, you will work with Operations to ensure efficient and effective budgeting, scheduling, and project coordination processes.

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.

6 days ago

New
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.

6 days ago

20 TW Alexander Dr, Research Triangle Park,, NC
$30–$32 / hour
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. Education/ Qualifications:
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
li>Perform all daily inspection and test of the scope and character necessary to achieve the quality of electrical construction required in the drawings and specifications for all works under the contract performed ON or OFF site.
Requires familiarity in the use of computers and software packages needed to support the documentation, analysis and retention of quality records.
30+ 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

New
Raleigh, NC
After making a conditional offer and running a background check, if Eaton is concerned about conviction that is directly related to the job, you will be given the chance to explain the circumstances surrounding the conviction, provide mitigating evidence, or challenge the accuracy of the background report.
In this function you will:
Assist in quality audits, workmanship defect reduction efforts, corrective and preventive action identification, analysis and reporting, inspection of returned units, special inspections.
3 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.
22 days ago

Durham, NC
p>OXB collaborates with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. In this role, you will be responsible for overseeing all Facilities operations within an FDA-approved clinical cGMP manufacturing facility, playing a key part in advancing our mission and making a real difference.
30+ days ago

Durham, NC
$140,000–$185,000 / year
Beams suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.
The role will provide Quality oversight of routine manufacturing, testing, and related operations to ensure that systems and processes are maintained in compliance with Good Manufacturing Practices (GMP), and ultimately to Good Distribution Practices (GDP) as the programs move to the commercial phase.
30+ days ago

Morrisville, NC
As a Quality Specialist III, you will maintain regulatory compliance and drive continuous improvement of quality systems to support our mission of enabling customers to make the world healthier, cleaner, and safer.
The Document Control Specialist is responsible for managing and optimizing document control processes within the MasterControl Quality Management System (QMS).
30+ 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

Raleigh, NC
This role is responsible for selling products and services to a wide range of highly complex or major accounts and customers and/or a specific supplier, accountable for increasing sales/client ratio and expanding customer base.
Demonstrate expertise knowledge of principles and methods for showing, promoting, and selling products or services that are considered specialized, fine wine, vintage, luxury, and/or specific to a designated supplier's portfolio of brands.
30+ days ago

Chapel Hill, NC
$31.04–$44.62 / hour
p>Summary:
Provides technical expertise in specific laboratory discipline or program specialty, monitor and direct the workload and provides consultative and diagnostic results to clinicians. If, however, you are presently an employee of another North Carolina agency and currently participate in TSERS or the ORP, you will be eligible to continue participating in those plans at UNC Health.
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

Raleigh, NC
Remote
$22–$25 / hour
p>Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base compensation may vary based upon, but not limited to, relevant experience and skill set, base compensation of internal peers, business sector, and geographic location. With climate change posing an imminent threat, Eurofins and its many companies recognize their duty to proactively reduce or offset the environmental impact of essential operations while also helping our clients do the same-serving as a true ESG Enabler.
14 days ago

Cary, NC
$39.24–$58.87 / hour
li>Environmental Noise Assessments - Supports siting, permitting, and licensing studies for new and modified facilities by reviewing applicable local, state, and federal noise regulations and land use compatibility criteria; identifying sensitive receptors; conducting ambient noise surveys; developing and applying environmental noise models; evaluating construction and operational noise impacts; recommending mitigation; and preparing technical reports and supporting documentation for agency and public review.
Acoustical Design and Compliance - Performs acoustical design studies to support engineering, procurement, and construction activities; develops equipment sound level specifications and mitigation requirements; prepares test protocols and performs or supports noise emissions performance testing to demonstrate compliance with regulatory and contractual requirements; and may support licensing proceedings, client presentations, and expert testimony as needed.
21 days ago

Raleigh, NC
Responsibilities include: preparing and providing technical quality control for environmental documents and permit applications developing and executing dispersion modeling approaches and protocols preparing emissions inventories, health risk evaluations (as applicable), and compliance analyses mentoring staff and coordinating and reviewing technical work across project phases developing task scopes, budgets, and schedules, and supporting proposal and marketing efforts when requested helping project managers to integrate air quality strategy into broader project planning and environmental compliance frameworks, including beginning to advise project teams and clients on regulatory interpretation and risk considerations and serving as a technical resource where appropriate in client and agency interactions. A senior-level environmental planner at Anchor QEA can expect: Strategic, impact-focused role, shaping project approaches and outcomes Highly supportive environment as part of multi-disciplinary, collaborative teams Opportunities for client and agency interaction, helping to guide key decision makers Contribution to business development strategies emphasizing valued relationships Strong emphasis on professional development for technical and leadership growth Culture of flexibility and accountability with an emphasis on work-life balance.
24 days ago

Durham, North Carolina
Data Analytics and Digital, gmp knowledge, HSE Knowledge, Inventory Management, Logistics and Transportation Management, Master Data, Operational Excellence, Order Management, Resilience and Risk Management, Sap Erp, supply chain management, Supply Planning, Warehouse Management
As a Warehouse Inventory Control and Logistics Specialist, you will play a pivotal role in ensuring seamless inventory management, data-driven decision-making, and regulatory compliance across warehouse and logistics activities.

14 days ago

Durham, NC
p>Required:
Bachelors degree in Biology, Biochemistry, Chemistry, Microbiology, or a related life sciences discipline and 5+ years of relevant experience in a GMP-regulated environment, including background in quality assurance, research, or biopharmaceutical/gene therapy manufacturing, or equivalent combination of education and experience.
The Quality Specialist III is responsible for providing dedicated quality assurance support for Chemistry, Manufacturing, and Controls (CMC) operations at Precision BioSciences, including batch release review, deviation assessment, and CDMO oversight.
11 days ago

Durham, NC
Required: Bachelor’s degree in Biology, Biochemistry, Chemistry, Microbiology, or a related life sciences discipline and 5+ years of relevant experience in a GMP-regulated environment, including background in quality assurance, research, or biopharmaceutical/gene therapy manufacturing, or equivalent combination of education and experience. The Quality Specialist III is responsible for providing dedicated quality assurance support for Chemistry, Manufacturing, and Controls (CMC) operations at Precision BioSciences, including batch release review, deviation assessment, and CDMO oversight.
10 days ago

Durham, NC
Full time
strong>Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley.. This role serves as a key escalation point for automation and controls issues, supports continuous operation of syringe filling and inspection equipment, and contributes to system enhancements, troubleshooting, validation, and compliance activities.
30+ days ago

Research Triangle Park, NC
The role plays a critical part in ensuring sustained compliance with current Good Manufacturing Practices (cGMP), FDA regulations, and Grifols Quality Systems by proactively analyzing, interpreting, and monitoring quality data, key metrics, and associated systems. Ability to successfully interface with all levels of management and customers or suppliers in various functions to ensure well documented, factually supported analyses of issues related to supplier, test lab, warehouse logistics and plasma platform quality.
30+ days ago

NC
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.
19 days ago

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Quality Control Specialist Jobs in Durham, NC

Production CAD Specialist Davron LLC

Medical Lab Specialist - Microbiology Laboratory UNC Health

Principal Quality Control Specialist, Master Data Genentech Inc

Quality Document Control Specialist InServ

Senior Specialist 1, Quality Control Instrumentation Fujifilm

Specialist, Quality Control - Physical Chemistry Novartis AG

Senior Specialist 1, Quality Control Instrumentation FUJIFILM Biotechnologies USA Inc

Specialist, Quality Control Instrumentation Fujifilm

Specialist Quality Control Actalent Inc

Specialist, Quality Control Instrumentation FUJIFILM Biotechnologies USA Inc

Quality Control Senior Specialist Actalent Inc

Quality Control - Inspector 2 Sunrise Systems Inc

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

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

Quality Control Manager Integrated Project Services 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

Quality Control Analyst RD Partners

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

Administrator - Salary Quality Control Wake County Public School System

Document Controls Specialist DPS Group

Control Systems Engineering Specialist Caterpillar Inc

HQA Senior ICS Fuel Inventory Control Specialist Swissport International AG

Controlling Specialist - SAP Expert Siemens Energy AG

Quality Assurance Specialist II Leadstack Inc

Project Controls Specialist - Michels Power, Inc. Michels Corporation

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 TalentBurst, Inc.

Electrical Quality Specialist Adams Electric Company

KBI: US - Principal QA Specialist KBI Biopharma Inc

Quality Specialist - 1st Shift - RPO Eaton Corporation Plc

Quality Assurance Specialist - Lab IntelliPro Group

Senior Specialist, Quality Assurance Oxford BioMedica Plc

Sr. Specialist I, Product Quality Assurance Beam Therapeutics Inc

Document Control Specialist Thermo Fisher Scientific Inc

Senior QA Specialist, External Manufacturing, US Bavarian Nordic AS

Control States Sales Specialist Republic National Distributing Co

Medical Lab Specialist - Quality Management UNC Health

KBI: US - Principal QA Specialist KBI Biopharma

Quality Administrative Specialist, Eurofins Built Environment Testing, Remote Eurofins Scientific SE

Associate Acoustics & Noise Control Specialist Black & Veatch Holding Co

Senior Air Quality Specialist Anchor QEA LLC

Warehouse Inventory Control & Logistics Specialist Novartis

Quality Specialist III Precision Biosciences Inc

Quality Specialist III Precision Biosciences

Automation Engineer / Automation & Controls Specialist Mentor Technical Group

Quality Risk Specialist Grifols SA

Clinical QA Systems and Documentation Specialist Grifols SA

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