NewSeasonal Repair Specialist SafeliteSeasonal Repair SpecialistKingston, NHLearn to repair vehicle glass (in the classroom and hands on) with a focus on the Safelite Way of Fitting under the guidance of experienced technicians and Safelite leaders. • Manage work orders, customer documentation and customer communication through the Safelite handheld Mobile Resource Management (MRM) technology.
Child Life Specialist - FT Days - Pediatrics and PICU - Jefferson Lehigh Valley Health NetworkChild Life Specialist - FT Days - Pediatrics and PICU - JeffersonJefferson, NHFinally, Lehigh Valley Hospital - Cedar Crest, Lehigh Valley Hospital - Muhlenberg, Lehigh Valley Hospital- Hazleton, and Lehigh Valley Hospital - Pocono each received an 'A' grade on the Hospital Safety Grade from The Leapfrog Group in 2020, the highest grade in patient safety. We're a Magnet(tm) Hospital, having been honored five times with the American Nurses Credentialing Center's prestigious distinction for nursing excellence and quality patient outcomes in our Lehigh Valley region.
Child Life Specialist - FT Days - Pediatrics and PICU - Lancaster Lehigh Valley Health NetworkChild Life Specialist - FT Days - Pediatrics and PICU - LancasterLancaster, NHFinally, Lehigh Valley Hospital - Cedar Crest, Lehigh Valley Hospital - Muhlenberg, Lehigh Valley Hospital- Hazleton, and Lehigh Valley Hospital - Pocono each received an 'A' grade on the Hospital Safety Grade from The Leapfrog Group in 2020, the highest grade in patient safety. We're a Magnet(tm) Hospital, having been honored five times with the American Nurses Credentialing Center's prestigious distinction for nursing excellence and quality patient outcomes in our Lehigh Valley region.
Child Life Specialist - FT Days - Pediatrics and PICU - Bristol Lehigh Valley Health NetworkChild Life Specialist - FT Days - Pediatrics and PICU - BristolBristol, NHFinally, Lehigh Valley Hospital - Cedar Crest, Lehigh Valley Hospital - Muhlenberg, Lehigh Valley Hospital- Hazleton, and Lehigh Valley Hospital - Pocono each received an 'A' grade on the Hospital Safety Grade from The Leapfrog Group in 2020, the highest grade in patient safety. We're a Magnet(tm) Hospital, having been honored five times with the American Nurses Credentialing Center's prestigious distinction for nursing excellence and quality patient outcomes in our Lehigh Valley region.
Child Life Specialist - FT Days - Pediatrics and PICU - Strafford Lehigh Valley Health NetworkChild Life Specialist - FT Days - Pediatrics and PICU - StraffordStrafford, NHFinally, Lehigh Valley Hospital - Cedar Crest, Lehigh Valley Hospital - Muhlenberg, Lehigh Valley Hospital- Hazleton, and Lehigh Valley Hospital - Pocono each received an 'A' grade on the Hospital Safety Grade from The Leapfrog Group in 2020, the highest grade in patient safety. We're a Magnet(tm) Hospital, having been honored five times with the American Nurses Credentialing Center's prestigious distinction for nursing excellence and quality patient outcomes in our Lehigh Valley region.
NewQuality Specialist - Designated Supplier Quality Representative (DSQR) Smiths Group PlcQuality Specialist - Designated Supplier Quality Representative (DSQR)Laconia, NHMust be able to use various precision equipment as prescribed in Inspection Levels I and II, perform all forms of mechanical inspection, and provide technical assistance to subordinate inspectors, QEs, and MEs when required. While performing the duties of this job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; talk and hear.
Sr. QA Specialist - Supplier Quality PCI Pharma ServicesSr. QA Specialist - Supplier QualityBedford, NHWe envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture. This position is part of PCI's Quality Compliance team responsible for the quality aspects of supplier quality management for suppliers that provide raw materials, components, contract test labs and services for GMP operations.
Analytical Quality Specialist Katalyst Healthcares & Life SciencesAnalytical Quality SpecialistPortsmouth, NHThe QC Technical Transfer Specialist supports laboratory operations by conducting analytical testing, coordinating method transfer activities, reviewing quality data, and maintaining compliance documentation within a GMP-regulated pharmaceutical or biotechnology environment. 3 5 years of experience in a Quality Control, Analytical Laboratory, or Quality Systems role within the pharmaceutical, biotechnology, or life sciences industry.
QA Specialist III-Operations Lonza Group LtdQA Specialist III-OperationsPortsmouth, NHThe ideal candidate will bring strong technical writing and review experience, a solid understanding of quality systems, and the ability to work independently while collaborating effectively across the organization. Independently review and approve GMP documentation, including SOPs, work instructions, forms, and electronic batch records within the document management system.
QA Specialist IV-Operations LonzaQA Specialist IV-OperationsPortsmouth, New HampshireThe ideal candidate will bring strong technical writing and review experience, a solid understanding of quality systems, and the ability to work independently while collaborating effectively across the organization. Independently review and approve GMP documentation, including SOPs, work instructions, forms, and electronic batch records within the document management system.
QA Specialist I - Supplier Quality PCI Pharma ServicesQA Specialist I - Supplier QualityBedford, NHThis position is part of PCI's Quality Compliance team responsible for the quality aspects of supplier quality management for suppliers that provide raw materials, components, contract test labs and services for GMP operations. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
QA Specialist II - Doc Control PCI Pharma ServicesQA Specialist II - Doc ControlBedford, NHThe Document Control QA Specialist II will evaluate document needs and participate in the processing of Documents and Records, maintain databases and Quality Management System tools and supports personnel and functional areas as needed. Issues and reconciles batch records, testing data capture sheets, lab books, equipment log books, room log books, and Quality System event documents.
QA Specialist I - Compliance PCI Pharma ServicesQA Specialist I - ComplianceBedford, New HampshireWe envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture. Reporting to the Director of Quality Systems & Compliance, the QA Specialist – Compliance is responsible for providing essential administrative support to the Compliance team and managing various client and internal audit documentation.
Qa Specialist II- Validation PCI Pharma ServicesQa Specialist II- ValidationBedford, New HampshireThe QA Specialist II – Validation is a member of the Quality Assurance department and partners with other members of the QA, Operations, QC and Validation organization to work and perform an array of defined QA validation activities in support of cGMP pharmaceutical/medical device contract manufacturing across multiple PCI facilities. Review and approve Validation plans, User Requirement Specifications (URS), Validation protocols and summary reports, associated with the commissioning and validation of equipment and utilities, cleaning validation, process validation and method validations without supervision.
Qa Specialist Ii - Ops PCI Pharma ServicesQa Specialist Ii - OpsBedford, NHQUALIFICATIONS: Required: Bachelors Degree in a relevant scientific discipline preferred with a minimum of 5-7 years of pharmaceutical or biotech industry experience with 3+ years of experience in a QA Operations role supporting late stage clinical and/or commercial production. ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform review of batch documentation for release of internal and external clinical products/commercial products, while ensuring compliance with cGMPs, site SOPs, and regulatory requirements.
Quality Specialist 3 (6947) SubCom LLCQuality Specialist 3 (6947)Newington, NHWhether you're a seasoned applicant seeking a new and exciting challenge, or you're new to the workforce and looking for a flexible, rewarding, and fast-paced position with an innovative and stable organization (since 1953), SubCom has opportunities to advance your career. Position Overview: A Quality Specialist III will be assigned to the following areas: Optical Products and Systems (OPS), or Optical Sub Assemblies (OSA).
QA Specialist II-Records Lonza Group LtdQA Specialist II-RecordsPortsmouth, NHThe specialist leverages advanced problem-solving skills to manage complex requests, improve systems, and ensure the integrity, accuracy, and timely availability of records. What will you do: The QA Specialist II - Records serves as a subject matter expert (SME) in records center operations, with a strong understanding of good documentation and records management practices.
QA SPECIALIST II - OPS PCI Pharma ServicesQA SPECIALIST II - OPSBedford, NHQUALIFICATIONS: Required: Bachelor's Degree in a relevant scientific discipline preferred with a minimum of 5-7 years of pharmaceutical or biotech industry experience with 3+ years of experience in a QA Operations role supporting late stage clinical and/or commercial production. ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform review of batch documentation for release of internal and external clinical products/commercial products, while ensuring compliance with cGMPs, site SOPs, and regulatory requirements.
QA Specialist II - Operations PCI Pharma ServicesQA Specialist II - OperationsBedford, New HampshireBachelor’s Degree in a relevant scientific discipline preferred with a minimum of 5-7 years of pharmaceutical or biotech industry experience with 3+ years of experience in a QA Operations role supporting late stage clinical and/or commercial production. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.
Quality Specialist 3 (6323) SubCom LLCQuality Specialist 3 (6323)NHResponsibilities and Duties: *Performs characterization tests on fiber optic cables, including OTDR, Chromatic Dispersion, Polarization Mode Dispersion, Electrical Tests (High Voltage, IR and DCR). Whether you're a seasoned applicant seeking a new and exciting challenge, or you're new to the workforce and looking for a flexible, rewarding, and fast-paced position with an innovative and stable organization (since 1953), SubCom has opportunities to advance your career.
Quality Specialist 2 (6448) SubCom LLCQuality Specialist 2 (6448)NHPerforms characterization tests on fiber optic cables, including OTDR, Chromatic Dispersion, Polarization Mode Dispersion, Electrical Tests (High Voltage, IR and DCR). Advanced skills to include: an understanding and certification in high voltage safety requirements and test techniques, electro-optical fault location and diagnosis and System level testing.
QA Specialist II-Lot review Lonza Group LtdQA Specialist II-Lot reviewPortsmouth, NHWhat you will do: The QA Specialist II - Lot Review is responsible for supporting the accurate and timely review of manufacturing batch records and associated documentation to ensure compliance with GMP and regulatory requirements. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
QA Specialist II-Lot review LonzaQA Specialist II-Lot reviewPortsmouth, New HampshireWhat you will do : The QA Specialist II – Lot Review is responsible for supporting the accurate and timely review of manufacturing batch records and associated documentation to ensure compliance with GMP and regulatory requirements. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow.
Quality System Specialist Loftware IncQuality System SpecialistPortsmouth, NHWith over 500 industry experts and 1,000 global partners, Loftware maintains a global presence with offices in the US, UK, Germany, Slovenia, China, and Singapore making us a trusted partner for companies in automotive, chemicals, clinical trials, consumer products, electronics, food & beverage, manufacturing, medical device, pharmaceuticals, retail/apparel, and more. About us We make the Supply Chain work At Loftware, our end-to-end cloud-based labeling platform helps businesses of all sizes manage labeling across their operations and supply chain and our solutions are used to print over 51 billion labels every year.
Quality Control Specialist Lonza Group LtdQuality Control SpecialistPortsmouth, NHYou will perform laboratory testing on in-process materials, raw materials, environmental monitoring samples, stability studies, and finished products while analyzing data and supporting investigations. You will also contribute to continuous improvement initiatives, support quality systems, and help ensure products meet regulatory and quality requirements.
Quality Control Specialist LonzaQuality Control SpecialistPortsmouth, New HampshireYou will perform laboratory testing on in-process materials, raw materials, environmental monitoring samples, stability studies, and finished products while analyzing data and supporting investigations. You will also contribute to continuous improvement initiatives, support quality systems, and help ensure products meet regulatory and quality requirements.
QA Validation Specialist 3 Katalyst Healthcares & Life SciencesQA Validation Specialist 3Portsmouth, NHDemonstrate a general understanding of biopharmaceutical manufacturing equipment and validation procedures for Installation Verification (IV/IQ), Clean-In-Place (CIP), Steam-In-Place (SIP), Autoclaves, Clean Utilities Shipping Validation, Temperature Mapping Controlled Storage Rooms and Equipment. Perform Equipment Validation activities to include Validation Maintenance Quality Systems review and requalification to ensure GMP equipment is continuously maintained in a validated state.
QA Operations Specialist II - LSA (Dayshift) LonzaQA Operations Specialist II - LSA (Dayshift)Portsmouth, New HampshireWe are seeking an experienced QA Operations Specialist III to provide real-time quality oversight and on-the-floor support for GMP manufacturing operations. The ideal candidate brings strong technical expertise, sound judgment, and the ability to operate independently while mentoring others.
QA Operations Specialist IV - LSA (Nightshift) LonzaQA Operations Specialist IV - LSA (Nightshift)Portsmouth, New HampshireParticipate in Deviation lifecycle, including but not limited to, determination, review of minor deviations and approval of minor deviations. We are seeking an experienced QA Operations Specialist IV to provide real-time quality oversight and on-the-floor support for GMP manufacturing operations.
QA Operations Specialist IV - LSA (Nightshift) Lonza Group LtdQA Operations Specialist IV - LSA (Nightshift)Portsmouth, NHParticipate in Deviation lifecycle, including but not limited to, determination, review of minor deviations and approval of minor deviations. What will you do: We are seeking an experienced QA Operations Specialist IV to provide real-time quality oversight and on-the-floor support for GMP manufacturing operations.
QA Operations Specialist III - LSA Lonza Group LtdQA Operations Specialist III - LSAPortsmouth, NHWhat will you do: We are seeking an experienced QA Operations Specialist III to provide real-time quality oversight and on-the-floor support for GMP manufacturing operations. The ideal candidate brings strong technical expertise, sound judgment, and the ability to operate independently while mentoring others.
QA Operations Specialist II - LSA (Dayshift) Lonza Group LtdQA Operations Specialist II - LSA (Dayshift)Portsmouth, NHWhat will you do: We are seeking an experienced QA Operations Specialist III to provide real-time quality oversight and on-the-floor support for GMP manufacturing operations. The ideal candidate brings strong technical expertise, sound judgment, and the ability to operate independently while mentoring others.
QA Operations Specialist III - LSA (Nightshift) LonzaQA Operations Specialist III - LSA (Nightshift)Portsmouth, New HampshireWe are seeking an experienced QA Operations Specialist III to provide real-time quality oversight and on-the-floor support for GMP manufacturing operations. The ideal candidate brings strong technical expertise, sound judgment, and the ability to operate independently while mentoring others.
QA Operations Specialist III - LSA (Dayshift) LonzaQA Operations Specialist III - LSA (Dayshift)Portsmouth, New HampshireWe are seeking an experienced QA Operations Specialist III to provide real-time quality oversight and on-the-floor support for GMP manufacturing operations. The ideal candidate brings strong technical expertise, sound judgment, and the ability to operate independently while mentoring others.
QA Validation Specialist 3 HireTalentQA Validation Specialist 3Portsmouth, NHDemonstrate a general understanding of biopharmaceutical manufacturing equipment and validation procedures for Installation Verification (IV/IQ), Clean-In-Place (CIP), Steam-In-Place (SIP), Autoclaves, Clean Utilities, Shipping Validation, Temperature Mapping Controlled Storage Rooms and Equipment. Perform Equipment Validation activities to include Validation Maintenance Quality Systems review and requalification to ensure GMP equipment is continuously maintained in a validated state.
QA Validation Specialist 3 Karwell TechnologiesQA Validation Specialist 3Portsmouth, NHDemonstrate a general understanding of biopharmaceutical manufacturing equipment and validation procedures for Installation Verification (IV/IQ), Clean-In-Place (CIP), Steam-In-Place (SIP), Autoclaves, Clean Utilities Shipping Validation, Temperature Mapping Controlled Storage Rooms and Equipment. Perform Equipment Validation activities to include Validation Maintenance Quality Systems review and requalification to ensure GMP equipment is continuously maintained in a validated state.
Clinical Quality Specialist Home Health & Hospice CareClinical Quality SpecialistMerrimack, New HampshireThe Quality Clinical Specialist serves as the subject matter expert for clinical documentation, Epic workflows, regulatory compliance, and staff education across Homecare, Hospice, and Hospice House programs. This role partners with clinical, quality, education, and IT teams to optimize documentation processes, support Epic system enhancements, ensure compliance with Medicare requirements, and provide ongoing training and support to staff.
LSA QA Sr. Compliance Specialist Lonza Group LtdLSA QA Sr. Compliance SpecialistPortsmouth, NHThe successful candidate will partner cross-functionally with Manufacturing, QC, Validation, Engineering, and site leadership to ensure compliance with regulatory requirements and continuous improvement of quality processes. QA Compliance Specialist serves as a key member of the Quality Assurance organization and acts as a subject matter expert for Quality Systems and GMP Compliance.
LSA QA Sr. Compliance Specialist LonzaLSA QA Sr. Compliance SpecialistPortsmouth, New HampshireThe successful candidate will partner cross-functionally with Manufacturing, QC, Validation, Engineering, and site leadership to ensure compliance with regulatory requirements and continuous improvement of quality processes. QA Compliance Specialist serves as a key member of the Quality Assurance organization and acts as a subject matter expert for Quality Systems and GMP Compliance.
Quality Operations Specialists Merrimack ManufacturingQuality Operations SpecialistsManchester, NHFull timeThe Quality Operations Specialist serves as a key quality representative within manufacturing operations and works closely with Production, Engineering, Supply Chain, and Quality teams to ensure timely review of production records, resolution of documentation issues, and compliant product disposition decisions. The Quality Operations Specialist is responsible for supporting manufacturing quality operations through comprehensive review of Device History Records (DHRs), product release activities, and production quality documentation.
NewTemporary Quality Assurance Specialist HealthPlanOne LLCTemporary Quality Assurance SpecialistNHFor 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).
Sr. QA Specialist - Pharmaceutical Manufacturing Novo Nordisk ASSr. QA Specialist - Pharmaceutical ManufacturingNHThe Position This position is responsible for working together with the management team to set future quality direction and supporting the implementation of our ambitious goals by bringing the best practices from other Novo Nordisk sites. Responsible for identifying and assessing training needs and delivering training materials and programs, to include training of team members on compliance related issues and other QA related topics.
Senior Clinical Quality Performance Specialist AmeriHealth CaritasSenior Clinical Quality Performance SpecialistManchester, NHRemoteManages activities related to plan accreditation, preventive health improvement, business analysis, and clinical and service quality improvement, including state withholds, Healthcare Effectiveness Data and Information Set (HEDIS), and Consumer Assessment of Healthcare Providers and Systems (CAHPS). Role Overview: The Senior Clinical Quality Performance Specialist is responsible for overseeing, designing, and implementing quality initiatives, identifying root causes, establishing and executing work plans to implement effective interventions.
QA Compliance Specialist Lonza Group LtdQA Compliance SpecialistPortsmouth, NHIn this role, you will act as a change agent-driving compliance, promoting inspection readiness, and supporting key review boards-while contributing to continuous improvement initiatives to ensure adherence to all applicable regulatory requirements. Serve as a compliance champion by promoting inspection readiness, modeling quality behaviors, and supporting cross-functional review boards (e.g., DRB, CAPA Review Board, Change Control Board).
QA Compliance Specialist LonzaQA Compliance SpecialistPortsmouth, New HampshireIn this role, you will act as a change agent—driving compliance, promoting inspection readiness, and supporting key review boards—while contributing to continuous improvement initiatives to ensure adherence to all applicable regulatory requirements. Serve as a compliance champion by promoting inspection readiness, modeling quality behaviors, and supporting cross-functional review boards (e.g., DRB, CAPA Review Board, Change Control Board).
QA Validation Specialist 3 LancesoftQA Validation Specialist 3Portsmouth, NH$80Notes from intake - Role is Equipment validation and Cleaning Validation Experience with Kneat is absolutely required. Experience with Ellab for Temp Mapping is a plus Manager is looking for candidates with Cleaning Val (CIP, COP, SIP). 95% of equipment is Single Use, so the Cleaning Val is limited mostly to Media Hold/Media ...
Quality Inspector I AlkegenQuality Inspector IRochester, New HampshireAlkegen brings together two of the world’s leading specialty materials companies to create one new, innovation-driven leader focused on battery technologies, filtration media, and specialty insulation and sealing materials. With over 60 manufacturing facilities with a global workforce of over 9,000 of the industry’s most experienced talent, including insulation and filtration experts, Alkegen is uniquely positioned to help customers impact the environment in meaningful ways.
Quality Assurance Manager, Operations Lonza Group LtdQuality Assurance Manager, OperationsPortsmouth, NHWhat you will do: We are seeking an experienced Quality Assurance Manager, Operations to lead a team supporting GMP compliance and quality oversight across site operations. This role is responsible for ensuring quality objectives are achieved, supporting cross-functional teams, and promoting a strong culture of quality and continuous improvement.
Quality Assurance Manager, Operations LonzaQuality Assurance Manager, OperationsPortsmouth, New HampshireWe are seeking an experienced Quality Assurance Manager, Operations to lead a team supporting GMP compliance and quality oversight across site operations. This role is responsible for ensuring quality objectives are achieved, supporting cross-functional teams, and promoting a strong culture of quality and continuous improvement.