Accounts Receivable Specialist CFSAccounts Receivable SpecialistSeabrook, NH$60,000–$75,000 / yearThis is an excellent opportunity for an experienced AR professional seeking a collaborative team environment, leadership visibility, and the chance to contribute to meaningful process improvements. Responsibilities : • Manage accounts receivable functions including invoicing, cash applications, collections, and account reconciliations.
Software and Warranty Operations Specialist PC Connection IncSoftware and Warranty Operations SpecialistMerrimack, NHAssist purchasing activities to learn and gain an understanding of the customer vendor contracts/agreements and program rules for an assigned business segment, including (but not limited to): price lists from vendors/distributors, SKUs, how best cost is negotiated, audits purchase orders for compliance to vendor program specifications and internal controls, ensures internal controls are followed, research and updates ETA's to set appropriate customer expectations, obtains vendor/distribution authorizations for customer returns and generates reports to support the daily purchasing operations. Articulate with the ability to express oneself clearly and professionally in written and oral communication.•Discreet with demonstrated ability to work in a confidential executive environment using good judgment while acting as an ambassador for the company.•Routine problem solver in situations where most problems have occurred before and solutions are familiar.
Software and Warranty Operations Specialist ConnectionSoftware and Warranty Operations SpecialistMerrimack, New HampshireFull timeHandles purchasing activities based on the customer vendor contracts/agreements and program rules for an assigned business segment, including (but not limited to): obtains price lists from vendors/distributors and negotiates best cost, audits purchase orders for compliance to vendor program specifications and internal controls, ensures internal controls are followed, researches and updates ETA’s to set appropriate customer expectations, and obtains vendor/distribution authorizations for customer returns. Working under minimal supervision of the Supervisor, Licensing and Warranty Operations, referring only exceptional problems and issues for management review or approval, the Software and Warranty Operations Specialist monitors the lifecycle operations of the company’s Software License, Cloud, Activations and Warranty business and associated services while individually overseeing an assigned multi-million-dollar segment.
QA Specialist II - Doc Control PCI 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 - Doc Control PCI Pharma ServicesQA Specialist II - Doc ControlBedford, New HampshireThe 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 - 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.
Qa Specialist Ii - Ops PCI 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 - 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 II - Operations PCI 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, 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 Lonza, Inc.QA Specialist II - 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. What we are looking for: Associate or bachelor's degree in a scientific or engineering discipline (e.g., Chemistry, Biology, Biochemistry, Chemical Engineering, or related field) preferred; equivalent relevant experience may be considered.
QA Specialist II - Operations Lonza Group LtdQA Specialist II - 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. What we are looking for: Associate or bachelor's degree in a scientific or engineering discipline (e.g., Chemistry, Biology, Biochemistry, Chemical Engineering, or related field) preferred; equivalent relevant experience may be considered.
QA Specialist II-Operations LonzaQA Specialist II-OperationsPortsmouth, New HampshireApply data integrity principles in all aspects of work and support continuous improvement initiatives, audits, inspections, deviations, and quality-related activities as assigned. The QA Specialist II operates with increasing independence, supports more complex quality initiatives, and serves as a visible Quality presence on the manufacturing floor.
QA Specialist II-Operations Lonza Group LtdQA Specialist II-OperationsPortsmouth, NHApply data integrity principles in all aspects of work and support continuous improvement initiatives, audits, inspections, deviations, and quality-related activities as assigned. The QA Specialist II operates with increasing independence, supports more complex quality initiatives, and serves as a visible Quality presence on the manufacturing floor.
QA Specialist Ii-Operations Lonza, Inc.QA Specialist Ii-OperationsPortsmouth, NHApply data integrity principles in all aspects of work and support continuous improvement initiatives, audits, inspections, deviations, and quality-related activities as assigned. The QA Specialist II operates with increasing independence, supports more complex quality initiatives, and serves as a visible Quality presence on the manufacturing floor.
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.
Quality Specialist 3 (7226) SubCom LLCQuality Specialist 3 (7226)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 (7226) Subcom, LLCQuality Specialist 3 (7226)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.
QA Specialist IV-QRM Lonza Group LtdQA Specialist IV-QRMPortsmouth, NHWorking closely with Manufacturing, Quality Control, Engineering, and Technical Operations teams, you will play a key role in identifying, evaluating, and mitigating quality and operational risks that support the delivery of life-changing therapies. In this highly visible role, you will lead cross-functional risk assessments, maintain the site's Quality Risk Management framework, and partner with teams across the business to drive continuous improvement and regulatory compliance.
QA Specialist Ii-Lot Review Lonza, Inc.QA 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. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow.
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 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.
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 Iv-Operations Lonza, Inc.QA Specialist Iv-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 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 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.
QA Specialist Ii-Records Lonza, Inc.QA 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-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 V-Quality Risk Management LonzaQA Specialist V-Quality Risk ManagementPortsmouth, New HampshireWorking closely with Manufacturing, Quality Control, Engineering, and Technical Operations teams, you will play a key role in identifying, evaluating, and mitigating quality and operational risks that support the delivery of life-changing therapies. In this highly visible role, you will lead cross-functional risk assessments, maintain the site's Quality Risk Management framework, and partner with teams across the business to drive continuous improvement and regulatory compliance.
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 I - Compliance PCI ServicesQA Specialist I - ComplianceBedford, 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. 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.
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.
NewSenior Computer Systems Validation Specialist TekWissen LLCSenior Computer Systems Validation SpecialistPortsmouth, NH$45–$55Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps its customers deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, bioscience, biopharmaceuticals, custom manufacturing, biotechnology, life science ingredients, nutrition, microbial control, agriculture, materials science, personal care, and cell and gene therapy.
QA Compliance Specialist 2 Karwell TechnologiesQA Compliance Specialist 2Portsmouth, NHThe role leads structured gap assessments of local procedures against Group procedures, identifies compliance gaps, coordinates remediation activities, and ensures timely implementation of required changes. Self-starter, solid written and verbal communication, good attention to detail, works effectively individually and with teams, positive attitude, customer focused, Practices safety awareness at all times.
Software Developer II Idexx Laboratories IncSoftware Developer IINH$90,000–$100,000 / yearAn innovation leader in every industry we serve, we follow our Purpose and Guiding Principles to help pet owners worldwide keep their companion animals healthy and happy, to ensure safe drinking water for billions, and to help farmers protect livestock and poultry from diseases. IDEXX values a diverse workforce and workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply.
QA Specialist V - QA Inspection Audit Management Lonza Group LtdQA Specialist V - QA Inspection Audit ManagementPortsmouth, NHThis 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).
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).
Lead Engineer, Software Celestica IncLead Engineer, SoftwareNHRemoteToday, Celestica delivers innovative supply chain solutions globally to customers in strategic two operating and reporting segments: Advanced Technology Solutions (ATS) and Connectivity and Cloud Solutions (CC): ATS: This segment serves customers in complex, regulated and high-reliability markets such as Industrial & Smart Energy, Aerospace & Defense, Semiconductor Capital Equipment, and HealthTech. The following competencies may also be required and performed with help or under supervision: Coaching/Mentoring; Communication/Negotiation/Presentation; Creative Problem Solving; Customer Interaction/Stakeholder Management; Quality & Lean; Working Effectively with Others; D/PFMEA; 8D/Corrective Action; Equipment Safety; Design of Experiments (DOE).
Lead Automation Script Specialist Celestica IncLead Automation Script SpecialistMerrimack, NHRemote$101,000–$150,000 / yearToday, Celestica delivers innovative supply chain solutions globally to customers in strategic two operating and reporting segments: Advanced Technology Solutions (ATS) and Connectivity and Cloud Solutions (CC): ATS: This segment serves customers in complex, regulated and high-reliability markets such as Industrial & Smart Energy, Aerospace & Defense, Semiconductor Capital Equipment, and HealthTech. Network Protocol Proficiency: Understanding of L2/L3 protocols (STP, BGP, OSPF, VLANs, VXLAN), port features (LLDP, MLAG, and ACLs), network services (SNMP, DHCP, DNS), and network security (SSL, DoS).
QA Compliance Specialist 2 Sunrise Systems IncQA Compliance Specialist 2Portsmouth, NHThe role leads structured gap assessments of local procedures against Group procedures, identifies compliance gaps, coordinates remediation activities, and ensures timely implementation of required changes. Self-starter, solid written and verbal communication, good attention to detail, works effectively individually and with teams, positive attitude, customer-focused.
Software and Warranty Operations Associate PC Connection IncSoftware and Warranty Operations AssociateMerrimack, NHAssist purchasing activities to learn and gain an understanding of the customer vendor contracts/agreements and program rules for an assigned business segment, including (but not limited to): price lists from vendors/distributors, SKUs, how best cost is negotiated, audits purchase orders for compliance to vendor program specifications and internal controls, ensures internal controls are followed, research and updates ETA's to set appropriate customer expectations, obtains vendor/distribution authorizations for customer returns and generates reports to support the daily purchasing operations. Articulate with the ability to express oneself clearly and professionally in written and oral communication.•Discreet with demonstrated ability to work in a confidential executive environment using good judgment while acting as an ambassador for the company.•Routine problem solver in situations where most problems have occurred before and solutions are familiar.
QA Compliance Specialist 2 Katalyst Healthcares & Life SciencesQA Compliance Specialist 2Portsmouth, NHThe role leads structured gap assessments of local procedures against Group procedures, identifies compliance gaps, coordinates remediation activities, and ensures timely implementation of required changes. Self-starter, solid written and verbal communication, good attention to detail, works effectively individually and with teams, positive attitude, customer focused, Practices safety awareness at all times.
Print Production Specialist RicohPrint Production SpecialistManchester, New HampshireDo you thrive in a fast-paced production environment and have a passion for delivering high-quality print work? If you're a detail-oriented print professional who takes pride in producing flawless work, we'd love to hear from you!
QA Compliance Specialist 2 HireTalentQA Compliance Specialist 2Portsmouth, NHThe role leads structured gap assessments of local procedures against Group procedures, identifies compliance gaps, coordinates remediation activities, and ensures timely implementation of required changes. Self-starter, solid written and verbal communication, good attention to detail, works effectively individually and with teams, positive attitude, customer focused,Practices safety awareness at all times.
QA Specialist I - Supplier Quality PCI 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. 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 - Supplier Quality PCI Pharma ServicesQA Specialist I - Supplier QualityBedford, New HampshireThis 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. 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.
Senior Staff Engineer, Software Celestica IncSenior Staff Engineer, SoftwareSan Jose, NHToday, Celestica delivers innovative supply chain solutions globally to customers in strategic two operating and reporting segments: Advanced Technology Solutions (ATS) and Connectivity and Cloud Solutions (CC): ATS: This segment serves customers in complex, regulated and high-reliability markets such as Industrial & Smart Energy, Aerospace & Defense, Semiconductor Capital Equipment, and HealthTech. AI/ML Practice: Practical experience deploying local LLMs, building Retrieval-Augmented Generation (RAG) systems, and utilizing agentic developer tools (e.g., Windsurf, Claude Code, Ollama, LlamaIndex, Docker).
QC Specialist 2 LancesoftQC Specialist 2Portsmouth, NH$30Works entire assigned shift, including arriving on time Has experience with or currently uses the following software: SoftmaxPro, Empower, SoloVPE Has experience with software validations including but not limited to: writing GMP procedures and validation documents and executing test scripts. The Quality Control Technical Transfer Analyst 3 will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities.
Electro-Mechanical Engineer - Process Specialist ESAB USAElectro-Mechanical Engineer - Process SpecialistUSA, NH$105,702–$122,878 / yearDrive the technical design and development of sophisticated automated cutting and marking systems, incorporating plasma and Oxy-Fuel torches, advanced consumables, plasma cutting and marking gas control, cutting machine integration, inverter power supply integration, plasma process development, LASER, WaterJet, Printing Systems, and Drilling technologies. With a primary focus on innovating multiple cutting and marking processes, you will be a key contributor to the full system architecture - integrating system electronics, precise process controls, consumable design, and machine intelligence.
Research Hydrographer / Ocean Mapping Specialist University System Of New HampshireResearch Hydrographer / Ocean Mapping SpecialistDurham, NHThe Center for Coastal and Ocean Mapping (CCOM) at the University of New Hampshire invites applications for an hourly Research Hydrographer / Ocean Mapping Specialist to support applied technical development in hydrographic data acquisition, marine geospatial systems, and next-generation navigation products. The University actively promotes a dynamic learning environment in which qualified individuals of differing perspectives, life experiences, and cultural backgrounds pursue academic goals with mutual respect and shared inquiry.