Quality Systems And Training Support Specialist HEXCEL CorpQuality Systems And Training Support SpecialistAmesbury, MA$56,980–$97,680 / yearThe selected individual will be responsible for but not limited to the following obligations: Support the implementation and ongoing data management for select database systems including but not limited to the: CMMS (computerized maintenance management system) used to schedule and record equipment maintenance and repair activities. NCM (nonconforming material) and CAPA (corrective / preventative action) databases used to record occurrences of nonconforming material along with associated material dispositions, causes of the nonconformances and corrective / preventative actions taken to prevent recurrence.
Quality Systems and Training Support Specialist Hexcel CorpQuality Systems and Training Support SpecialistAmesbury, MA$56,980–$97,680 / yearThe selected individual will be responsible for but not limited to the following obligations: Support the implementation and ongoing data management for select database systems including but not limited to the: CMMS (computerized maintenance management system) used to schedule and record equipment maintenance and repair activities. NCM (nonconforming material) and CAPA (corrective / preventative action) databases used to record occurrences of nonconforming material along with associated material dispositions, causes of the nonconformances and corrective / preventative actions taken to prevent recurrence.
Quality Specialist Globus Medical Inc.Quality SpecialistMethuen, MAPosition Summary: The Quality Specialist will be responsible for achieving the highest quality level of manufacturing quality and quality system performance while ensuring compliance with all company policies and procedures and maintaining compliance with US FDA and international medical device regulations and ISO 13485 quality system requirements. Collaborate with cross‑functional partners-Product Development, Operations, Supply Chain, Regulatory and Field Service-to clarify requirements, close gaps, and drive timely approval of documentation packages.
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 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.
1076 GMP Validation Specialist - Equipment and Cleaning Harvest Technical Services1076 GMP Validation Specialist - Equipment and CleaningPortsmouth, New HampshireDemonstrate 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 Sunrise Systems IncQA 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.
Manufacturing Quality Specialist Mace Precision MachiningManufacturing Quality SpecialistExeter, NHIdentify and document non-conformances, and work collaboratively with production teams to implement corrective actions. We are seeking a dedicated and detail-oriented Manufacturing Quality Specialist to join our team in Exeter, NH.
Site Quality Lead Ascensus Specialties LLCSite Quality LeadNewburyport, MA$140,000–$170,000 / year7-10+ years of progressive experience in Quality Assurance, Quality Systems, or Quality Management within a chemical, pharmaceutical, life science, specialty materials, or regulated manufacturing environment with a focus on QMS implementation and continuous improvement. This position is accountable for quality systems, quality assurance, internal audits, external audits, corrective and preventive actions, change management, document control, investigations, training and regulatory compliance activities.
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).
Site Quality Lead Ascensus SpecialtiesSite Quality LeadNewburyport, MA$140,000–$170,000 / year7-10+ years of progressive experience in Quality Assurance, Quality Systems, or Quality Management within a chemical, pharmaceutical, life science, specialty materials, or regulated manufacturing environment with a focus on QMS implementation and continuous improvement. This position is accountable for quality systems, quality assurance, internal audits, external audits, corrective and preventive actions, change management, document control, investigations, training and regulatory compliance activities.
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 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 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.
Environmental, Health, and Safety Specialist Straumann Holding AGEnvironmental, Health, and Safety SpecialistAndover, MA$92,000–$112,000 / yearThe position independently manages assigned EHS programs and partners with all departments to ensure regulatory compliance, drive continuous improvement, reduce environmental impacts, and foster a proactive safety culture. We develop, manufacture, and supply dental implants, clear aligners, instruments, CADCAM prosthetics and biomaterials for use in esthetic dentistry, tooth replacement and restoration solutions or to prevent tooth loss.
Process Engineer HEXCEL CorpProcess EngineerAmesbury, MA$68,665–$117,700 / yearRequired Qualifications: Bachelor's of Science degree in any of the following: Plastics Engineering, Chemical Engineering, Mechanical Engineering, Chemistry, Industrial Engineering, Materials Science, Materials Engineering, or Polymer Chemistry. As a part of Hexcel, we at ARC Technologies LLC are propelling the future of flight, energy generation, transportation, and recreation through excellence in advanced material solutions that create a better world.
PC - Project Coordinator - Commercial Sales Division Alpen High Performance Products IncPC - Project Coordinator - Commercial Sales DivisionWindham, NH$80,000–$90,000 / yearThe Project Coordinator plays a central role in maintaining project visibility, tracking progress, and ensuring that scope, schedule, and documentation remain aligned throughout the lifecycle. This role is responsible for coordinating projects from contract through production, delivery, and closeout—ensuring alignment between sales, technical teams, customers, and manufacturing.
Quality Technician (With a Focus on Special Process) C/A Design IncQuality Technician (With a Focus on Special Process)Exeter, New HampshireCoordinate and maintain schedules for Temperature Uniformity Surveys (TUS), System Accuracy Tests (SAT), furnace calibrations, and other required compliance activities to minimize production interruptions. Maintain detailed and accurate records associated with special process compliance activities including TUS, SAT, calibrations, certifications, furnace documentation, and validation records.