Quality Specialist, Incoming Quality NovartisQuality Specialist, Incoming QualityDurham, North CarolinaIf, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1 (877)395-2339 and let us know the nature of your request and your contact information. As a Quality Specialist, Incoming Quality Assurance, you will play a critical role in safeguarding product integrity from the very first point of entry, ensuring that incoming materials meet the highest quality and compliance expectations.
NewQuality Engineer / Quality Systems Specialist Stark Pharma SolutionsQuality Engineer / Quality Systems SpecialistDurham, NCContract Quality Engineer / Quality Systems SpecialistLocation: Durham, NCDuration: Long TermWe are seeking an experienced Quality Engineer / Quality Systems Specialist to support a fast‑paced FDA‑regulated medical device manufacturing environment. This role will focus on driving CAPAs, Non‑Conformances, investigations, and Quality System improvements while helping reduce quality backlog and ensuring compliance with regulatory requirements.
QA Specialist II, Quality Operations (Combination Products) United TherapeuticsQA Specialist II, Quality Operations (Combination Products)Research Triangle Park, NCMinimum 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.
Senior QA Specialist, Quality Operations (Combination Products) United TherapeuticsSenior QA Specialist, Quality Operations (Combination Products)Research Triangle Park, NCEscalate 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.
QA Specialist – Medical Device Manufacturing | 2nd Shift | $27+/hr | Manpower EngineeringQA Specialist – Medical Device Manufacturing | 2nd Shift | $27+/hr |Mebane, NC$27.10–$27.50 / hourTemporaryp> 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.
KBI: US - Principal QA Specialist KBI BiopharmaKBI: US - Principal QA SpecialistDurham, North CarolinaProvides 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.
KBI: US - Principal QA Specialist KBI Biopharma IncKBI: US - Principal QA SpecialistDurham, NC$113,000–$156,000 / yearProvides 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.
Advanced Practice Provider (NP/PA) - Clinical Quality Specialist I Avance CareAdvanced Practice Provider (NP/PA) - Clinical Quality Specialist IDurham, North CarolinaFull timeAvance Care is seeking an experienced Advanced Practice Provider (Nurse Practitioner or Physician Assistant) for an exciting opportunity to grow your career in a role that offers both meaningful patient connection and broader organizational impact. If you’re looking for a role where you can care for patients, influence meaningful change, and grow as a clinical leader, we invite you to join Avance Care and be part of the future of high-quality, data-driven healthcare.
QA Specialist (GMP) – 3rd Shift | $27.50/hr | 3 Month Contract | Onsite Manpower EngineeringQA Specialist (GMP) – 3rd Shift | $27.50/hr | 3 Month Contract | OnsiteMebane, NC$27.10–$27.50 / hourTemporaryp> 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.
Sr. Quality Specialist - cGMP Manufacturing - 12-Hr Night Shift 2-2-3 Alcami CorporationSr. Quality Specialist - cGMP Manufacturing - 12-Hr Night Shift 2-2-3Morrisville, North CarolinaFull timeAt 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.
Quality Assurance Area Specialist III (QA for Utilities) Novo Nordisk ASQuality Assurance Area Specialist III (QA for Utilities)Clayton, NCDemonstrated 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.
NewQuality Specialist Becton Dickinson and CoQuality SpecialistNC$95,900–$153,400 / yearBuild and maintain strong cross-functional relationships, enabling collaboration across all levels while leading or supporting end-to-end QMS activities and initiatives. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance.
Quality Systems Improvement Specialist Guerbet SAQuality Systems Improvement SpecialistRaleigh, NCWhen 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. Working cross-functionally with Quality, Operations, and other stakeholders, the Specialist ensures quality systems are robust, compliant, and effectively embedded across the organization.
Quality Specialist III Precision BiosciencesQuality Specialist IIIDurham, NCRequired: 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.
Supplier Quality Specialist Guerbet SASupplier Quality SpecialistRaleigh, NCWhen 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. Provide ongoing quality oversight of suppliers supporting GMP manufacturing, including raw materials, consumables, external laboratories, and transportation providers.
QA Specialist (Hybrid) Eisai IncQA Specialist (Hybrid)Raleigh, NC$66,200–$86,800 / yearE-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. 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.
QA Specialist (Hybrid) EisaiQA Specialist (Hybrid)Raleigh, North CarolinaE-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. 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.
Manufacturing QA Specialist Guerbet SAManufacturing QA SpecialistRaleigh, NCWhen 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.
Manufacturing QA Specialist - 2nd shift Guerbet SAManufacturing QA Specialist - 2nd shiftRaleigh, NCWhen 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.
Senior QA Specialist Deviations and CAPAs KBI BiopharmaSenior QA Specialist Deviations and CAPAsDurham, North CarolinaJob 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.
Quality Specialist III Precision Biosciences IncQuality Specialist IIIDurham, NCRequired: 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.
Senior QA Specialist Deviations and CAPAs KBI Biopharma IncSenior QA Specialist Deviations and CAPAsDurham, NCJob 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.
NewSenior Specialist, Quality Engineer Kyowa Kirin Pharmaceutical Research IncSenior Specialist, Quality EngineerSanford, NC$116,000–$152,300 / yearManager, Quality Systems & Compliance, this role helps implement and sustain Quality Engineering processes that enable GMP operations, regulatory compliance, audit defense, and compliant risk-based decision making across manufacturing-related systems. Summary: Kyowa Kirin is a Japanese-based company with a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease.
Quality Specialist - cGMP Manufacturing - Weekend 1st Shift Alcami CorporationQuality Specialist - cGMP Manufacturing - Weekend 1st ShiftMorrisville, North CarolinaFull timeJob Summary: The Quality Specialist will provide site quality support in a fast-paced environment by effectively performing activities of substantial variety to ensure quality and compliance with applicable regulatory requirements and is proficient in all document and protocol approvals applicable to the respective processes executed at the respective lab or manufacturing facility. Activities include reviewing documents and data, supporting audits and inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed.
NewSenior GMP Supplier Quality Specialist Audits & Risk GuerbetSenior GMP Supplier Quality Specialist Audits & RiskRaleigh, NCThis role involves working closely with cross-functional teams, conducting audits, and maintaining quality documentation. The ideal candidate has a Bachelor's Degree and extensive experience in Quality Assurance within a GMP-regulated environment.
Clinical QA Systems and Documentation Specialist Grifols SAClinical QA Systems and Documentation SpecialistNCExample: 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.
Quality Training Specialist Guerbet SAQuality Training SpecialistRaleigh, NCWhen 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. This role partners with cross‑functional teams to drive training effectiveness, promote a culture of quality, and support continuous improvement through effective knowledge transfer and performance readiness.
Senior Specialist, Quality Assurance Oxford BioMedica PlcSenior Specialist, Quality AssuranceDurham, NCOXB 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.
Specialist 2, Quality Assurance Technical FUJIFILM Biotechnologies USA IncSpecialist 2, Quality Assurance TechnicalNCServing as the QA point of contact for Warehouse, Supply Chain, and QC Raw Materials, this role resolves material-related issues and escalations, conducts quality impact assessments for investigations, change controls, and supplier change notifications, and ensures compliance with applicable procedures and data integrity requirements. Situated at the cross-section of Morrisville and Research Triangle Park (RTP), North Carolina, our site is at the heart of a booming biotech hub surrounded by top universities, vibrant communities, and various outdoor opportunities.
Quality Assurance Specialist II Leadstack IncQuality Assurance Specialist IIResearch Triangle Park, NC$34 / hourExamples 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. Key Responsibilities: Assess and assure study, project, and process compliance with protocols, controlled documents, and applicable regulations and guidelines through audits of AskBio laboratories.
Part-Time Clinical Quality Specialist SonderMind IncPart-Time Clinical Quality SpecialistRaleigh, NC$40–$42 / hourThe Part-Time Clinical Quality Specialist role exists to safeguard and strengthen the clinical integrity of care delivered across the organization, with a focused lens on utilization management, payor-facing clinical audits, and clinical quality assurance. To follow the latest SonderMind news, get to know our clients, and learn about what it's like to work at SonderMind, you can follow us on Instagram, Linkedin, and Twitter.
Quality Assurance Specialist II TalentBurst, Inc.Quality Assurance Specialist II20 TW Alexander Dr, Research Triangle Park,, NC$30–$32 / hourExamples 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.
Specialist 2, Quality Assurance Technical FujifilmSpecialist 2, Quality Assurance TechnicalResearch Triangle Park, North CarolinaServing as the QA point of contact for Warehouse, Supply Chain, and QC Raw Materials, this role resolves material-related issues and escalations, conducts quality impact assessments for investigations, change controls, and supplier change notifications, and ensures compliance with applicable procedures and data integrity requirements. Situated at the cross-section of Morrisville and Research Triangle Park (RTP), North Carolina, our site is at the heart of a booming biotech hub surrounded by top universities, vibrant communities, and various outdoor opportunities.
Quality Analytics Specialist Grifols SAQuality Analytics SpecialistNCSummary: Ensures current Good Manufacturing Practices (cGMP) and FDA/Grifols Quality Systems through the participation in management, analysis and monitoring of quality data and metrics and associated quality systems. 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.
Electrical Quality Specialist Adams Electric CompanyElectrical Quality SpecialistRaleigh, NCPerform 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.
Specialist, Quality Assurance FUJIFILM Biotechnologies USA IncSpecialist, Quality AssuranceNCSituated at the cross-section of Morrisville and Research Triangle Park (RTP), North Carolina, our site is at the heart of a booming biotech hub surrounded by top universities, vibrant communities, and various outdoor opportunities. 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.
Quality Assurance Area Specialist III Novo Nordisk ASQuality Assurance Area Specialist IIIClayton, NCDemonstrated 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.
QA Area Specialist III - Finished Production (Validation Focus) Novo Nordisk ASQA Area Specialist III - Finished Production (Validation Focus)Clayton, NCDemonstrated 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. Quality oversight, review & approval of validation activities and documents associated with projects, new systems, changes to existing systems & maintaining validated state of equipment, processes, and systems.
Quality Assurance Area Specialist III - Finished Production Novo Nordisk ASQuality Assurance Area Specialist III - Finished ProductionClayton, NCDemonstrated 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. Quality oversight, review & approval of validation activities and documents associated with projects, new systems, changes to existing systems & maintaining validated state of equipment, processes, and systems.
QA Specialist II KBI BiopharmaQA Specialist IIDurham, North CarolinaIf any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.
Medical Lab Specialist - Quality Management UNC HealthMedical Lab Specialist - Quality ManagementChapel Hill, NC$31.04–$44.62 / hourSummary: 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.
QA Manufacturing Specialist II (Nights) KBI BiopharmaQA Manufacturing Specialist II (Nights)Durham, North CarolinaThis position will be responsible for on the floor review of executed records (batch record section review, solution records, equipment records, and logbooks) supporting all aspects of cGMP operations. MQA Specialist II: BS/BA in scientific field and 5 years experience or MS/MA degree and 3 years’ experience in a QA GMP regulated environment within Biopharmaceuticals or equivalent is required.
QA Area Specialist I - SDF (2nd shift) Novo Nordisk ASQA Area Specialist I - SDF (2nd shift)Durham, NCOur Emerging Technologies -Solid Dosage Forms US facility in Durham, NC is a 194,000 square foot tableting and packaging facility that supports the production of our innovative oral treatments for patients with type 2 diabetes. Knowledge of Quality and one or more of the following: Aseptic Production, Business Support, QC, Production Support, Warehousing/Transport, API, and/or Finished Production processes preferred.
Quality Document Control Specialist InServQuality Document Control SpecialistFuquay-Varina, NCCollaboration 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.
Senior QA Technical Specialist FUJIFILM Biotechnologies USA IncSenior QA Technical SpecialistNCThe Senior QA Technical Specialist acts independently and provides QA subject matter knowledge in the GMP domain to systems and projects with focus on key quality activities and deliverables in accordance with company policies/SOPs and regulatory requirements. Situated at the cross-section of Morrisville and Research Triangle Park (RTP), North Carolina, our site is at the heart of a booming biotech hub surrounded by top universities, vibrant communities, and various outdoor opportunities.
Senior Compliance Specialist, Supplier Quality Catalent IncSenior Compliance Specialist, Supplier QualityMorrisville, NCCatalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. The Senior Compliance Specialist, Supplier Quality is responsible for leading and executing the supplier quality management program, ensuring that all external suppliers and service providers meet regulatory and company requirements.
Senior Compliance Specialist, Supplier Quality CatalentSenior Compliance Specialist, Supplier QualityMorrisville, North CarolinaThe Senior Compliance Specialist, Supplier Quality is responsible for leading and executing the supplier quality management program, ensuring that all external suppliers and service providers meet regulatory and company requirements. The site offers comprehensive nasal development capabilities, including analytical support, device selection, spray characterization, and both clinical and commercial scale for unit‑dose, bi‑dose, and multidose nasal products.
QA Manufacturing Specialist II KBI Biopharma IncQA Manufacturing Specialist IIDurham, NCThis position will be responsible for on the floor review of executed records (batch record section review, solution records, equipment records, and logbooks) supporting all aspects of cGMP operations. MQA Specialist II: BS/BA in scientific field and 5 years experience or MS/MA degree and 3 years' experience in a QA GMP regulated environment within Biopharmaceuticals or equivalent is required.
NewTemporary Quality Assurance Specialist HealthPlanOne LLCTemporary Quality Assurance SpecialistNCFor Hybrid Roles: Must be able to commute to an office setting as required, which may include walking short distances and navigating an office environment. Physical Requirements: Must be able to remain in a stationary position (e.g., sitting or standing) for extended periods of time, typically in a cubicle environment (constant noise, fluorescent overhead lighting).
Quality Auditing Specialist (Durham, NC, US, 27712) Corning IncQuality Auditing Specialist (Durham, NC, US, 27712)Durham, NC$80,011–$110,016 / yearOur health and well-being benefits include medical, dental, vision, paid parental leave, family building support, fitness, company-paid life insurance, disability, disease management programs, paid time off, and an Employee Assistance Program (EAP) to support you and your family. This role is responsible for completing audit related activities such as acting as an internal auditor, managing auditor qualification records, and reviewing supplier assessments.