NewQA 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.
NewQA Compliance Specialist 2 eTeam Inc.QA Compliance Specialist 2Portsmouth, NHSelf-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. Monitor compliance metrics and prepare management reports through trending and visual KPI management.
QA Validation Specialist 3 eTeam Inc.QA 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 states.
NewQA Compliance Specialist 2 Tailored ManagementQA Compliance Specialist 2Portsmouth, NH$72.99–$86.26 / hourThis role leads structured gap assessments of local procedures against Group procedures, identifies compliance gaps, coordinates remediation activities, and ensures timely implementation of required changes. Driving Results: Proactively identify gaps, address issues, and implement improvements to streamline workflows.
QA Validation Specialist Tailored ManagementQA Validation SpecialistPortsmouth, NH$94.54 / hourDemonstrate 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 assigned Quality Systems activities within Document Management System (DMS), TrackWise Quality System (Change Control, Deviation, CAPA).
NewQA 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.
NewQA 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.
Equipment Validation Specialist, Level III LonzaEquipment Validation Specialist, Level IIIPortsmouth, New HampshireDemonstrate 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.
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.
NewQA 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 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 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 MindlanceQA 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.
Engineering Specialist, Quality Fresenius Kabi AGEngineering Specialist, QualityNorth Andover, MA$160,000–$170,000 / yearStrengthen and maintain the QMS structure for design and software quality by defining workflows, templates, and governance for document control, change control, design reviews, DHF/DMR readiness, and inspection preparedness. • Position is eligible to participate in a bonus plan with a target of 15% of the base salary (include only if applicable to the grade level) • Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.
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.
Principal Specialist, Scheduling RTX CorpPrincipal Specialist, SchedulingMAProvide production floor support including replacement part management, shop floor material staging, Work in Progress (WIP) movement through shared resource areas, completion of units in shop floor and MRP system, delivery to next step (inventory or shipment), and meeting MRP schedule. The successful candidate has experience with Material Requirements Planning (MRP) systems in a manufacturing environment and utilizes data-driven decision making to enable effective material and workforce forecasting.
Laboratory 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).
Laboratory 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).
ROCHESTER: Manufacturing Training Associate Elevated ResourcesROCHESTER: Manufacturing Training AssociateNewburyport, MassachusettsThe Manufacturing Training Associate will support the Quality Department for controlling, indexing, filing, report generation, recordkeeping, quality system applications and database maintenance and manage various documentation, while also ensuring their accuracy, quality and integrity. Maintains various databases with accurate information of REI capability to supply government part numbers.
New1463 Senior QA Compliance Specialist Harvest Technical Services1463 Senior QA Compliance SpecialistPortsmouth, New HampshireThe role leads structured gap assessments, identifies and drives remediation activities, coordinates implementation of required changes, and partners with Global Quality and cross‑functional stakeholders to sustain compliance and continuous improvement. The base pay actually offered will take into account internal equity, and may also vary depending on candidate's geographic region, job-related knowledge, skills, and experience amongst other factors.