CONTRACTOR

FEED

UNKNOWN

You will collaborate with cross-functional teams, including design engineers, production personnel, and quality assurance, to optimize manufacturing operations and drive continuous improvement initiatives. As a Manufacturing Engineer, your primary responsibility will be to develop and improve manufacturing processes and systems to ensure the efficient and cost-effective production of defense and aerospace products.

We are a national technical recruiting firm.   At GCR, you'll discover a team of experienced and technically knowledgeable recruiters all working for you. We specialize in contract, contract to hire, and permanent staffing solutions across a variety of industries including, Information Technology, Commercial, Automotive, Medical Device, Pharmaceutical, and Manufacturing. We have well established relationships with companies from startup to large enterprise organizations.

GCR Professional Services

Manufacturing Engineer III (NH)

Youll own how we test AI-led products in the UK - agentic workflows, LLM-based features, non-deterministic behaviour that doesnt fit a traditional pass/fail script. Every day, prior authorizations delay prescriptions, pharmacists lose hours to paperwork instead of patients, and prescriptions slip through the cracks between health systems.

Foundation Health Global Inc

QA Lead

ADAPTED_NOW

This role is ideal for someone with quality assurance experience who is ready to take on leadership responsibilities and help support production and training initiatives. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

HOUR

When we talk about us, we’re really talking about our people—the best staffing and recruiting experts on the planet. They connect over 88,000 people to great jobs across the country every single day. That makes us one of America’s biggest employers. Our people are also the go-to workforce management partners for a lot of Fortune 500 companies. And thousands of American workers, in almost every industry and profession, rely on them for career advice. When you’re ready to find out what we can do for you, stop by one of our more than 900 career centers in the U.S., or visit adeccousa.com today.

Adecco

Quality Assurance

Adecco USA

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. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

PCI Pharma Services

QA Specialist I - Supplier Quality

Summary of Objective: 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. 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 - Supplier Quality

PCI Services

ea_via_bold

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. 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.

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. 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.

Sr. QA Specialist - Supplier Quality

Assists in the maintenance of processes which support improvement and safety, enable the collection, storage, and analysis of improvement and safety data, and enable compliance with external regulatory agency requirements; Identifies trends and significant safety issues and communicates them to the Director of Quality & Patient Safety; Assists with coordination of the Weekly Occurrence Review meeting and Regulatory activities, providing education, establishing and measuring outcomes for effectiveness; Uses clinical and operational knowledge in formal and informal consultation with individual staff, providers, clinicians, and managers, to address clinical quality and safety concerns. Assists departments/units with performance improvement activities related to Patient Safety: In conjunction with the Director of Quality & Patient Safety and in collaboration with other department members, participates in and/or facilitates clinical adverse event evaluation and root cause analysis; Monitors, interprets and recommends action based upon identified risks related to Patient Safety; Provides oversight for sustainable process changes and recommends replication when appropriate; Communicates concerns, progress and results of interventions regarding patient safety to the Director and other appropriate personnel.

Dartmouth-Hitchcock Medical Center

Quality Improvement & Safety Registered Nurse Quality Assurance and Safety

OTHER

Assists in the maintenance of processes which support improvement and safety, enable the collection, storage, and analysis of improvement and safety data, and enable compliance with external regulatory agency requirements; Identifies trends and significant safety issues and communicates them to the Director of Quality & Patient Safety; Assists with coordination of the Weekly Occurrence Review meeting and Regulatory activities, providing education, establishing and measuring outcomes for effectiveness; Uses clinical and operational knowledge in formal and informal consultation with individual staff, providers, clinicians, and managers, to address clinical quality and safety concerns. In conjunction with the Director of Quality & Patient Safety and in collaboration with other department members, participates in and/or facilitates clinical adverse event evaluation and root cause analysis; Monitors, interprets and recommends action based upon identified risks related to Patient Safety; Provides oversight for sustainable process changes and recommends replication when appropriate; Communicates concerns, progress and results of interventions regarding patient safety to the Director and other appropriate personnel.

Dartmouth-Hitchcock Health

Quality Improvement & Safety Registered Nurse - Quality Assurance and Safety

[AW]-iCims

Review and approve non-DMS documents (QA Monthly Preventative Maintenance, Engineering Preventative Maintenance documents, CMMS Forms, Instrumental Data Sheets, Functional Equivalent Memos, DMS Withdrawal Forms, Periodic Review Audit Trail and Misc. Follow associated documentation revision and review procedures and issues / concerns escalated to senior QA Specialist or management for mentoring through process while working with internal customers to gain information required to resolving those issues/concerns.

Katalyst Healthcares & Life Sciences

QA Documentation Specialist 2

jobdiva

The 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.

Karwell Technologies

QA Compliance Specialist 2

The 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

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.

Lonza

Quality Assurance Manager, Operations

What 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.

Lonza Group Ltd

Reporting to the Mobile Team Lead, the Quality Assurance Analyst's key responsibilities will include: Create, maintain, and execute test plans, test cases, and test scripts for new features, bug fixes, integrations, customer scenarios, and release validation, including functional, exploratory, regression, and developer work item testing. Document, investigate, reproduce, track, and validate software defects, enhancement requests, and customer-reported issues in collaboration with developers, product owners, support staff, and other stakeholders.

YEAR

Harris Computer Systems

Quality Assurance Analyst

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. 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.

Quality Assurance Lead Jobs in New Hampshire

Manufacturing Engineer III (NH) GCR Professional Services

QA Lead Foundation Health Global Inc

Quality Assurance Adecco

QA Specialist I - Supplier Quality PCI Pharma Services

QA Specialist II - Supplier Quality PCI Pharma Services

QA Specialist II - Supplier Quality PCI Services

QA Specialist I - Supplier Quality PCI Services

Sr. QA Specialist - Supplier Quality PCI Pharma Services

Sr. QA Specialist - Supplier Quality PCI Services

Quality Improvement & Safety Registered Nurse Quality Assurance and Safety Dartmouth-Hitchcock Medical Center

Quality Improvement & Safety Registered Nurse - Quality Assurance and Safety Dartmouth-Hitchcock Health

QA Documentation Specialist 2 Katalyst Healthcares & Life Sciences

QA Compliance Specialist 2 Karwell Technologies

QA Compliance Specialist 2 Katalyst Healthcares & Life Sciences

QA Specialist II - Doc Control PCI Services

QA Specialist II - Doc Control PCI Pharma Services

Quality Assurance Manager, Operations Lonza

Quality Assurance Manager, Operations Lonza Group Ltd

Quality Assurance Analyst Harris Computer Systems

Qa Specialist Ii - Ops PCI Pharma Services

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