Cleaning Validation specialist MindlanceCleaning Validation specialistPortsmouth, NH$75–$83 / hourContractorWe are seeking a QA Validation Specialist III to support equipment validation and cleaning validation activities within a GMP biopharmaceutical manufacturing environment. The ideal candidate will have hands-on experience with Kneat, equipment qualification, validation lifecycle documentation, and GMP quality systems.
Computer Systems Validation Specialist III LonzaComputer Systems Validation Specialist IIIDover, 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.
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 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.
Quality 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.
Quality Control Technician II (2nd Shift) Ascensia Diabetes CareQuality Control Technician II (2nd Shift)Portsmouth, New HampshireOur diverse perspectives are enriched by many dimensions, including race, ethnicity, gender, age, physical and mental ability, sexual orientation, religious beliefs, culture, language, and education, as well as professional and life experience. We use our innovation and specialist expertise in diabetes to develop high quality solutions and tools that make a positive, daily difference for people.
Document Control Specialist 1 (Sw) Eversource EnergyDocument Control Specialist 1 (Sw)NH$48,670–$54,080 / yearThe successful candidate will be expected to communicate effectively with project team members, have a high level of initiative and motivation to deliver quality results, have strong problem-solving skills and a demonstrated ability to work within a team environment providing value-added, innovative solutions and maintaining strong client relationships. § Interface with Adept group users such as Substation Engineering, Transmission Line Engineering, Siting and Survey Engineering to maintain file consistency and proper controls in the Adept library.
Document Control Specialist Smiths Group PlcDocument Control SpecialistLaconia, NHUtilizing user-friendly, structured tools and processes to help teammates to complete tasks in a PRO-ACTIVE, efficient, and cost-effective manner, as it pertains to internal documentation, as well as all customer and 3rd party related specifications within the STSL Quality Management System (QMS). Education and/or Experience: Two-year college or university program certificate; or one to two years related experience and/or training; or equivalent combination of education and experience.
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.
Inventory Control Specialist PICA Manufacturing SolutionsInventory Control SpecialistDerry, NHFull timeThe Inventory Control Specialist is responsible for maintaining accurate inventory records and ensuring material availability to support production schedules in a fast-paced electronic contract manufacturing environment. This position plays a critical role in inventory accuracy, cycle counting, material transactions, receiving verification, stockroom organization, and material traceability.
NewQA Specialist II - Operations LonzaQA Specialist II - OperationsPortsmouth, New HampshireWhat 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 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 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.
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 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 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 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 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 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 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.
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.
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 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.
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.
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, 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- 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.
Quality Specialist FreudenbergQuality SpecialistNorthfield, New HampshireAdvise and Support : Provide advice and support to production supervision on quality-related matters, enabling timely decisions for business continuity and protecting both our customers and FST. Collaborate for Success : Work collaboratively with operations and engineering teams to ensure appropriate customer and commercial outcomes, driving continuous improvement and market success.
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.
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 ...
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).
Medical Director of Infection Control & Infectious Disease Physician, Dover, NH Mass General BrighamMedical Director of Infection Control & Infectious Disease Physician, Dover, NHDover, NHOur Infectious Disease team provides comprehensive care for patients with HIV, tick-borne diseases, post-surgical infections, and complex medical conditions, and participates in system-wide quality initiatives. The clinical portion of this role includes providing both inpatient and outpatient infectious disease consultations, managing a broad spectrum of infectious conditions, and collaborating with colleagues across subspecialties.
Industrial Controls Engineer II Ascensia Diabetes CareIndustrial Controls Engineer IIPortsmouth, New HampshireAs a Industrial Controls Engineer , you’ll support a diverse manufacturing plant with multiple value streams, taking ownership of controls activities such as sustaining projects, change control, new equipment design and commissioning, issue resolution, and continuous improvement. Manufacturing Engineering Manager, you’ll work alongside a dynamic team of engineers while gaining hands-on experience with unique processes and developing valuable skills in a collaborative, growth-focused environment.
Quality Engineer - 1st Shift Turbocam, Inc.Quality Engineer - 1st ShiftNHOur Culture In Action: Here at TURBOCAM, we have a Commitment to Excellence in everything that we do - whether that's the delivery of flow path components and innovative manufacturing solutions, our relationships with customers around the globe, or the investment in those that make TURBOCAM such an exceptional place to work. Enjoy comprehensive benefits with company-paid dental and life insurance (with optional add-ons for yourself and dependents), short- and long-term disability, subsidized medical (or medical opt-out bonus if covered elsewhere), and voluntary vision coverage.
NewQuality Assurance/Machine Operator Express Employment ProfessionalsQuality Assurance/Machine OperatorHampton, NHCategory:Quality Control, Keywords:Quality Control / Quality Assurance Specialist, Location:Hampton, NH-03842 Fully comprehend using a ruler, measuring and math skills.
NewLaboratory Operations and Quality Manager Optima DermatologyLaboratory Operations and Quality ManagerPortsmouth, NHThe manager serves as the operational leader on the floor - coordinating staffing, workflow, and equipment - and as the lab''s quality authority, driving continuous improvement and inspection readiness. The Laboratory Operations & Quality Manager oversees the day-to-day operations of the Histology Laboratory while developing and maintaining its Quality Management System (QMS).
QC Specialist 2 HireTalentQC Specialist 2Portsmouth, NHJob Description: 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. Has experience with software validations including but not limited to: writing GMP procedures and validation documents and executing test scripts.
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).
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.
NewQC Specialist 2 NET2SOURCE INCQC Specialist 2Portsmouth, NHWorks 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. Description: 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.
Food Safety & Brand Specialist Rentokil Initial plcFood Safety & Brand SpecialistManchester, NH$19–$21 / hourBy applying to this job, you agree to receive initial texts from systems used on behalf of Rentokil North America, Inc., possibly including Workday, Loop, and HireVue. We are extremely proud of our legacy of excellence and constantly work to fulfill our mission to "protect people, enhance lives, and preserve the planet.".
Construction Specialist ESPO CorporationConstruction SpecialistLondonderry, NH$43 / hourAdditional responsibilities: • Ensures the execution of overhead/underground construction duties such as: placing hard-line cables, frame and strand poles, transfer facilities between poles, placing cable in joint trench, and safe operation of construction vehicles and cable trailers. The Construction Specialist would be responsible for tracking the progress of assigned projects, reviewing and approving contractor invoices, communicating with other vendors for proper documentation into the tracking system (P2), and adhering to timelines set forth for the project.
Regulatory Reporting & Compliance Specialist (Hybrid) American Family Insurance GroupRegulatory Reporting & Compliance Specialist (Hybrid)Keene, NH$62,000–$103,000 / yearAdditional Preferred Qualifications: Ability to translate reporting requirements into controlled, repeatable workflows using SQL/BigQuery, Excel, and work-tracking tools (e.g., Jira), with strong documentation to enhance operational efficiency and transparency. Work closely with regulators, states, boards, bureaus, vendors and stat agents related to new and existing regulations, new product, state development, legacy retirements, new data source development.
Equipment Validation Specialist, Level III Lonza Group LtdEquipment Validation Specialist, Level IIIPortsmouth, NHDemonstrate a thorough understanding of biopharmaceutical manufacturing equipment and validation procedures for Installation Qualification (IQ), Steam-In-Place (SIP), Autoclaves, Clean Utilities, Shipping Validation, Temperature Mapping Controlled Storage Rooms. This role provides Operations, Quality Assurance, clients, and regulatory bodies with scientifically sound, documented evidence that systems and processes perform reliably to maintain a compliant manufacturing environment.