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The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; high, precarious places; outside weather conditions; and may be expected to work with electronic equipment (always being aware of one's environment and taking proper precautions is required). All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia.

YEAR

Curia Global Inc

Quality Assurance Disposition Specialist

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mîrus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. The ideal candidate will have experience in New Product Introduction (NPI), Change Control, Factory Acceptance Testing (FAT), Validation, and Process Performance Qualification (PPQ) within a regulated environment.

Mirus Consulting Group

Specialist QA - 35845

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HOUR

Demonstrate 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.

For over 20 years, TalentBurst Inc. has been an award-winning provider of cutting-edge Workforce Management Solutions. With a strong commitment to staying ahead in the tech landscape, we pioneer innovative approaches to talent acquisition. Our expertise spans Life Sciences, and Healthcare Staffing, Banking, Financial, IT, and Engineering, as well as Global Employer of Record (EOR), Agent of Record (AOR), State, Local Government and Education (SLED), and IC validation/compliance services. Additionally, our division, TalentProcure, leads the industry with offerings such as High Hazard Payroll, Managed Services, and Vendor on Premise (VOP) solutions.
Due to our prioritization of excellent standards, we are Joint Commission Certified and are a certified Minority Business Enterprise (MBE) in the USA and Canada. Supporting over 130 Fortune 500 companies globally, we excel in navigating the landscape of talent acquisition. In a world of constant change, we embrace developing people-centric solutions that address the unique demands of our clients. Stay connected by visiting our website and following us on social media!

TalentBurst, Inc.

Equipment Validation Analyst / QA Validation Specialist 3

jobdiva

About QuVa: Quva Pharma is a national, industry-leading, FDA registered 503B outsourcing services company that provides hospitals with essential medications in ready-to-administer injectable formats that are critical for effective patient care. Works in accordance with area Supervision to provide quality assurance oversight where the business is responsible for adhering to current Good Manufacturing Practices (cGMPs).

QuVa Pharma Inc

Sterility Assurance Specialist 1st shift

Ensure any Corrective / Preventative Actions and Effectiveness Checks associated with the manufacture of safe, pure, and effective sterile pharmaceuticals are investigated, written and documented in accordance with company SOPs, policies and cGMPs and within assigned timelines. ​The QA Senior Specialist - CAPA is responsible for ensuring that Corrective and Preventive Actions (CAPAs) and associated effectiveness checks are executed in compliance with company SOPs, internal policies, and applicable cGMP requirements.

American Regent, Inc, a Daiichi Sankyo Group Company, develops, manufactures, and supplies high quality sterile injectables for healthcare providers, clinics and hospitals across the United States and Canada. We have locations in New York, Ohio, and Pennsylvania and sales territories nationwide.
American Regent continues to position its business for sustainable growth, with significant investments in the modernization and expansion of our U.S. manufacturing sites. These enhancements are expected to strengthen our business and represents our commitment to the ongoing success of our company and its employees. Supporting patient health is our guiding principle and our promise is to provide the healthcare marketplace with a steady supply and broad portfolio of brand and generic specialty injectables.

American Regent

QA Sr. Specialist - CAPA

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When you join Guerbet, you: Are choosing a global leader with recognized expertise in diagnostic and interventional imaging, Are joining our 2820 collaborators who are committed every day to offering innovative solutions to improve quality of patient's life all over the world, Are joining a company where we value diversity of talents coming from various horizon. The QA Systems Specialist collaborates with cross-functional teams, including Manufacturing, Quality Control, Supply Chain, Engineering, and Regulatory Affairs, to maintain product quality, compliance, and operational excellence.

GUERBET

QA Systems Specialist

We work with many partners (citizens, communities, and businesses, all levels of government, environmental groups and educators) to prevent pollution, conserve resources, and to help ensure polluting does not have disproportionate impact on any groups of people. Two (2) years of advanced professional-level experience conducting environmental protection or pollution control activities with duties involving collection and/or validation of outdoor environmental data, laboratory data, and demonstrated experience working with Quality Assurance.

State of Minnesota

Quality Assurance Coordinator - Environmental Specialist 4

Dispose of non-saleable products as directed, including destructive audit samples, tested products, line trial samples, and excess product samples. UNICON is a workforce solutions provider with over 35 years of experience supporting organizations across a variety of industries.

UNICON International, Inc.

QA Lab Specialist

Perform approvals, as assigned, of master batch records, executed batch records, change control records, investigations, discrepancy risk assessments, complaint investigations, annual product reviews, supplier qualification records, and extension requests. Allow, endorse, or approve predefined activities (e.g., change records), assessments (e.g., trending reports), documents (e.g., protocols), and minor procedural updates (e.g., SOP revisions) in alignment with Boehringer Ingelheim governance.

Boehringer Ingelheim International GmbH

Specialist, Quality Assurance, Fremont CA ONSITE

Identify, document, and communicate quality issues or deficiencies to Quality and Laboratory Management, including stopping quality review activities when significant compliance concerns are identified. Aptar Pharma offers a competitive total rewards package including base salary or base hourly rate determined by many factors including the role, experience, knowledge, skill set and location.

AptarGroup Inc

Quality Specialist I

FULL_TIME

This position serves as a key connection between Quality, Operations, Engineering, Customer Service, and other functional teams to help ensure quality requirements are understood, documented, followed, and continuously improved. We provide the building industry with high quality, innovative garage doors at competitive prices while maintaining a reputation of quality, reliability and integrity.

Hormann Northwest Door LLC

Quality Specialist

Ensure any Corrective/Preventative Actions and Effectiveness Checks associated with the manufacture of safe, pure, and effective sterile pharmaceuticals are investigated, written and documented in accordance with company SOPs, policies and cGMPs and within assigned timelines. The QA Senior Specialist - CAPA is responsible for ensuring that Corrective and Preventive Actions (CAPAs) and associated effectiveness checks are executed in compliance with company SOPs, internal policies, and applicable cGMP requirements.

American Regent Laboratories

QA Sr. Specialist - Capa

The work scope includes on-the-floor Quality oversight of manufacturing activities including observing formulation and aseptic processes, performing AQL visual inspection of finished drug product vials, GMP documentation and Batch Record review, line clear and product changeover activities, disposition of incoming raw materials, review and approval of facility work orders, and other various QA functions as needed. ESSENTIAL DUTIES AND RESPONSIBILITIES: The QA Operations Specialist I - Floor Support is responsible for providing QA support of Manufacturing and Visual Inspection activities for clinical and commercial drug product in a GMP facility.

PCI Pharma Services

QA Operations Specialist I - Floor Support - C shift (Sunday-Wednesday 330pm-2am)

The work scope includes on-the-floor Quality oversight of manufacturing activities including observing formulation and aseptic processes, performing AQL visual inspection of finished drug product vials, GMP documentation and Batch Record review, line clear and product changeover activities, disposition of incoming raw materials, review and approval of facility work orders, and other various QA functions as needed. The QA Operations Specialist I – Floor Support is responsible for providing QA support of Manufacturing and Visual Inspection activities for clinical and commercial drug product in a GMP facility.

QA Operations Specialist I - Floor Support - C shift (Sunday-Wednesday 3:30pm-2am)

The work scope includes on-the-floor Quality oversight of manufacturing activities including observing formulation and aseptic processes, performing AQL visual inspection of finished drug product vials, GMP documentation and Batch Record review, line clear and product changeover activities, disposition of incoming raw materials, review and approval of facility work orders, and other various QA functions as needed. ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform QA on-the-floor activities supporting client projects, including room release, auditing critical processes, reviewing GMP documentation in real time.

PCI Services

QA Operations Specialist I - Floor Support - C Shift (Sunday-Wednesday 3:30Pm-2Am)

Degree in a related field with applicable experience: Doctorate, Master's + 2 years of experience, Bachelor's + 4 years of experience, Associate's + 8 years of experience, High School Diploma/GED + 10 years of experience. We are seeking a Specialist QA with GMP manufacturing experience in Quality Assurance, including review and approval of change controls, validations, FATs, NPI and PPQs.

QRC Group

Specialist QA

OTHER

Job Responsibilities Generate, execute, review, and approve qualification and validation protocols, summary reports, and associated documentation in accordance with regulatory requirements, SOPs, specifications, and acceptance criteria. Required Qualifications Bachelor's degree in Life Sciences or a related field; equivalent proven experience may be considered in place of formal education.

Intellectt INC

QA Validation Specialist

Ceipal

Base Pay Range Per Hour: $28.00 – 35.00 / hour Individual compensation will vary based on factors such as qualifications, skill level, competencies, work location and shift, and will increase over time based on meeting performance and business needs. As a QA Document Specialist II, you will play a pivotal role at Penumbra providing timely and accurate support of quality processes related to Document Services to ensure compliance with Penumbra procedures and regulatory requirements.

Penumbra

QA Document Specialist I - Temp

Following a $45 million expansion announced in 2025, the Madison site has significantly increased capacity, added new equipment, and created approximately 200 highly skilled biohealth jobs, further strengthening its role within Catalent's global biologics network and Wisconsin's growing life sciences ecosystem. Located at 726 Heartland Trail in Madison, the approximately 102,700‑square‑foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single‑use systems to enable rapid scale‑up and customization.

Catalent Pharma Solutions, Inc.

Specialist III - Quality Assurance, Systems

Production record review and Product disposition for drug substance, drug product, device assembly and finished goods. Skills: Knowledge of relevant government regulations and agency rules for labeling (CFR & EudraLex Volume 4, Annex 13).

Qa Specialist Jobs in the United States

Quality Assurance Disposition Specialist Curia Global Inc

Specialist QA - 35845 Mirus Consulting Group

Equipment Validation Analyst / QA Validation Specialist 3 TalentBurst, Inc.

Sterility Assurance Specialist 1st shift QuVa Pharma Inc

QA Sr. Specialist - CAPA American Regent

QA Systems Specialist GUERBET

Quality Assurance Coordinator - Environmental Specialist 4 State of Minnesota

QA Lab Specialist UNICON International, Inc.

Specialist, Quality Assurance, Fremont CA ONSITE Boehringer Ingelheim International GmbH

Quality Specialist I AptarGroup Inc

Quality Specialist Hormann Northwest Door LLC

QA Sr. Specialist - Capa American Regent Laboratories

QA Operations Specialist I - Floor Support - C shift (Sunday-Wednesday 330pm-2am) PCI Pharma Services

QA Operations Specialist I - Floor Support - C shift (Sunday-Wednesday 3:30pm-2am) PCI Pharma Services

QA Operations Specialist I - Floor Support - C Shift (Sunday-Wednesday 3:30Pm-2Am) PCI Services

Specialist QA QRC Group

QA Validation Specialist Intellectt INC

QA Document Specialist I - Temp Penumbra

Specialist III - Quality Assurance, Systems Catalent Pharma Solutions, Inc.

QA Sr. Specialist GMP Integrated Resources, Inc

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