NewWastewater Specialist HP HoodWastewater SpecialistConcord, NHRegulate the flow of wastewater through the plant by controlling pumps, valves, blowers and other equipment; reads meters, gauges, and other recording devices and keeps a daily log of plant operations. Schedule / perform service and care for mechanical equipment according to preventive maintenance scheduling; Perform all PM's in a timely manner according to the PM schedule.
NewComputer Systems Validation Specialist III LonzaComputer Systems Validation Specialist IIIPortsmouth, NHThe Computer Systems Validation (CSV) Specialist III leads teams in assessing new and changing computer systems to ensure compliance with company policies and industry guidance. This role acts as the QA CSV representative for small and large-scale projects while providing technical guidance and mentorship to junior team members.
1201 RN Trainer Sevita1201 RN TrainerConcord, NHIn accordance with New Hampshire's He-M 1201 regulations, the Nurse Trainer provides healthcare oversight, develops and delivers medication administration training to non-licensed staff, and ensures the provision of quality health services in community-based residential settings. In a variety of locations and community-based settings, we offer a range of programs, including vocational and therapy programs, day treatments, and specialized services for infants, children, adolescents, Military Service Members and Veterans.
NewSenior IT Validation Engineer LonzaSenior IT Validation EngineerPortsmouth, NHThe Computer Systems Validation (CSV) Specialist III leads teams in assessing new and changing computer systems to ensure compliance with company policies and industry guidance. This role acts as the QA CSV representative for small and large-scale projects while providing technical guidance and mentorship to junior team members.
QA Specialist V - QA Inspection Audit Management LonzaQA Specialist V - QA Inspection Audit ManagementPortsmouth, New HampshireThis individual will lead and support internal audits, customer audits, and regulatory inspections, partnering closely with cross-functional teams and senior leadership to drive inspection readiness and continuous improvement. What we are looking for: Bachelor’s degree in Life Sciences, Biology, Chemistry, Pharmaceutical Sciences, or related field (advanced degree preferred).
Sr. QA Specialist - Supplier Quality PCI Pharma ServicesSr. QA Specialist - Supplier QualityBedford, 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. 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.
QA Specialist IV-Quality Risk Management LonzaQA Specialist IV-Quality Risk ManagementPortsmouth, New HampshireThis individual serves as a subject matter expert in QRM principles and tools, partnering cross-functionally to embed risk-based decision-making into quality systems and operational processes. What you will do: The QA Specialist IV – Quality Risk Management (QRM) plays a critical role in ensuring compliance with cGMP regulations by advancing and maintaining an effective, site-wide risk management program.
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 II- Validation PCI Pharma ServicesQa Specialist II- ValidationBedford, NHThe 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. ESSENTIAL DUTIES AND RESPONSIBILITIES: 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 III-Operations Lonza Group LtdQA Specialist III-OperationsPortsmouth, NHWhat you will do: The QA Specialist III operates with a high degree of autonomy while partnering closely with GMP operators and manufacturing teams to provide real-time, on-the-floor Quality Assurance support for operational areas involved in GMP activities. As an experienced member of the QA team, the QA Specialist III handles complex and time-sensitive assignments, supports inspection readiness, and may provide guidance or coaching to less experienced staff.
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.
NewQA Specialist II - Operations PCI Pharma ServicesQA Specialist II - OperationsBedford, 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 - Ops PCI Pharma ServicesQa Specialist Ii - OpsBedford, 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.
QA Specialist I - Compliance PCI Pharma ServicesQA Specialist I - ComplianceBedford, NHRequired: Associates degree plus 5 years of relevant experience or HS diploma and 10 years relevant experience Minimum of 5 years of experience in office coordination, administrative support, or documentation management, preferably in a regulated industry such as pharmaceuticals or biotechnology. 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.
QA Specialist IV-QRM Lonza Group LtdQA Specialist IV-QRMPortsmouth, NHThis individual serves as a subject matter expert in QRM principles and tools, partnering cross-functionally to embed risk-based decision-making into quality systems and operational processes. What you will do: The QA Specialist IV - Quality Risk Management (QRM) plays a critical role in ensuring compliance with cGMP regulations by advancing and maintaining an effective, site-wide risk management program.
QA Specialist III-Operations LonzaQA Specialist III-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.
Quality Assurance Loan Specialist I Bar Harbor BanksharesQuality Assurance Loan Specialist INHThis role requires prolonged periods of sitting and looking at a computer screen; repetitive motion of wrists and fingers; talking and hearing; the ability to lift/move 50 pounds. Provide back up to other Quality Assurance Specialists and records as needed Comprehend and adhere to federal banking regulations in accordance with Bar Harbor Bank & Trust's policies and procedures.
NewQA Specialist II-Records LonzaQA Specialist II-RecordsPortsmouth, New HampshireThe specialist leverages advanced problem-solving skills to manage complex requests, improve systems, and ensure the integrity, accuracy, and timely availability of records. 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.
NewQA 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.
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 QA Specialist - Operations Lonza Group LtdSenior QA Specialist - OperationsPortsmouth, NHThe ideal candidate will bring strong technical writing skills, GMP knowledge, and the ability to work independently while contributing to team success and continuous improvement initiatives. This role is responsible for ensuring the accuracy, completeness, and compliance of production documentation while supporting cross-functional teams to meet quality and operational objectives.
Senior QA Specialist - Operations LonzaSenior QA Specialist - OperationsPortsmouth, New HampshireThe ideal candidate will bring strong technical writing skills, GMP knowledge, and the ability to work independently while contributing to team success and continuous improvement initiatives. This role is responsible for ensuring the accuracy, completeness, and compliance of production documentation while supporting cross-functional teams to meet quality and operational objectives.
Qa Specialist I - Ops PCI Pharma ServicesQa Specialist I - OpsBedford, NHThe work scope includes on-the-floor Quality oversight of manufacturing activities including observing formulation and fill processes, GMP documentation and Batch Record review, line clearance, disposition of incoming raw materials, review and approval of facility work orders, and other various QA functions as needed. The QA Operations Specialist I Floor Support is responsible for providing QA support of Manufacturing and Visual Inspection activities for clinical and commercial medical device products in a GMP facility.
NewQA 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.
NewQA 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 Specialist II - Raw Materials PCI Pharma ServicesQA Specialist II - Raw MaterialsBedford, NHThe QA Specialist II - Raw Materials assists with the initiation and review of raw material quality systems, material specifications creation and revisions, and ensures adherence to site procedures and material specification receipt, testing, and release requirements. Minimum 3 years' experience in related GMP industry working in Quality Assurance, Quality Control, or groups which support receipt, inspection, or release of materials in a pharmaceutical or biotechnology facility preferred.
QA Documentation Specialist I Lenmar Consulting, Inc.QA Documentation Specialist IPortsmouth, NHSupport PQS integration by working with the Quality Document control group to complete workflows, document gating and coordinate elements of the document change process to ensure minimal disruption to site operations. M-F 5x onsite 1st shift (8am - 5pm) We are seeking a highly motivated and experienced Quality Systems Support Specialist to join our team.
Specialist, QA Test Automation Cogeco IncSpecialist, QA Test AutomationRochester, NH$85,600–$128,400 / yearSmart Pipelines: Collaborate with DevOps specialists to inject AI evaluation metrics directly into modern CI/CD pipelines, ensuring automated gates handle fluid AI responses. Exposure to Golden Datasets: creating, maintenance, and/or scaling of high-quality golden datasets used as the source of truth for benchmarking model changes.
NewQA 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.
NewQA 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.
NewQA 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 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.
NewQA 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.
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.
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).
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.
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 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.
NewAnalytical 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.
Quality Specialist 3 (6754) SubCom LLCQuality Specialist 3 (6754)Newington, NHPosition Overview: A Quality Specialist III (Repeater Tester) in the Production Testing department is responsible for performing a variety of detailed electro-optical tests on repeaters and repeater sub-assemblies in support of Repeater Manufacturing. 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 3 (6442) SubCom LLCQuality Specialist 3 (6442)Newington, NHPosition Overview: A Quality Specialist III (Repeater Tester) in the Production Testing department is responsible for performing a variety of detailed electro-optical tests on repeaters and repeater sub-assemblies in support of Repeater Manufacturing. 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.
Quality Specialist - Medicare D Quality CVS Health CorpQuality Specialist - Medicare D QualityWork At Home, NH$18.50–$42.35 / hourOur teams reflect the customers, patients, members and communities we serve and we are committed to fostering a workplace where every colleague feels valued and that they belong. Quality Specialist- Medicare D Quality role administers the quality management system to manage the review of clinical processes, documentation, and patient records.
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.
NewSenior 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.
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.
Nondestructive Testing Quality Specialist (Manufacturing) Westinghouse Electric - USANondestructive Testing Quality Specialist (Manufacturing)Newington, NHAs production ramps, you carry out engineering-defined in-process and final inspections, applying ultrasonic, dye penetrant, radiographic, visual, and magnetic particle methods where needed. Ability to interpret engineering drawings and technical documentation, including welding and welding symbols; comfort with shop drawings and sketches.
Quality Specialist 3 (6662) SubCom LLCQuality Specialist 3 (6662)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).