good manufacturing practice jobs

Piscataway, New Jersey

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Today

Summary: Support patch management, antivirus updates, and Windows/server maintenance for lab PCs and software systems in coordination with IT infrastructure teams. Demonstrated experience in tracking changes, coordinating document reviews and maintaining GxP-compliant SOPs and providing end-user training for regulated IT systems. Perform regular system health checks, monitor logs, and escalate issues to infrastructure or vendor support teams as needed. Support systems connectivity and softwa

Full-time

Process Engineer Level I-II (Downstream)

Lebanon, New Hampshire

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Today

About the Department Site New Hampshire, located in West Lebanon, is where Novo Nordisk's life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications. What we offer you: Leading pay and annual performance bonus for all positions36 Paid days off including vacation, sick days & company holidaysHealth Insurance, Dental Insurance, Vision InsuranceGuarant

Full-time

Validation Engineer II

Vacaville, California

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Today

Job Description: A great opportunity for a Validation Engineer II to support QC laboratory equipment qualification activities within a world-class biopharmaceutical environment. This role ensures full compliance with cGMP, corporate quality standards, and regulatory expectations, all while contributing directly to patient safety and operational excellence. Responsibilities: Perform equipment qualification per EQ policies and procedures. Partner with QC lab staff to define qualification requirem

Full-time

Senior CQV Engineer

Thousand Oaks, California

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Today

Job Summary : The Senior CQV Engineer will play a critical role in the successful startup and qualification of a new early-phase clinical biomanufacturing facility, encompassing cleanrooms, utilities, and a wide range of systems and equipment. This position is responsible for planning, executing, and documenting commissioning, qualification, and validation (CQV) activities to ensure all systems meet stringent regulatory and client-specific requirements Roles & Responsibilities: uthoring, editin

Full-time

Automation Engineer II

Ogden, Utah

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Today

PURPOSE AND SCOPE: Supports engineering and operations in the design, installation, and troubleshooting of various control systems. Performs current state analysis, documents gaps against desired future states, defines new or improved processes, and works with management to determine feasibility of solution opportunities. Documents and communicates project plans and process workflows as required. PRINCIPAL DUTIES AND RESPONSIBILITIES: Supports engineering and operations in the design, installat

Full-time

Process Validation Engineer

Warsaw, Indiana

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Today

Job Summary: The Process Validation Engineer supports medical device manufacturing by developing, executing, and maintaining validated manufacturing and test processes. The role ensures compliance with FDA QSR (21 CFR 820), ISO 13485, and cGMP requirements while collaborating cross-functionally to improve process capability, quality, and efficiency across a variety of manufacturing operations. Roles & Responsibilities: Develop and execute process validation strategies, including process characte

Full-time

Senior Validation Engineer

Thousand Oaks, California

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Today

Job Description: This position is responsible for planning, executing, and documenting commissioning, qualification, and validation (CQV) activities to ensure all systems meet stringent regulatory and client-specific requirements. The Senior Validation Engineer will act as a subject matter expert, collaborating closely with cross-functional teams, including Manufacturing, Facilities, Quality Control and Quality Assurance to deliver robust validation strategies that enable compliant and efficient

Full-time

Validation Engineer III

Plainsboro Township, New Jersey

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Today

Job Description: Qualified candidates must be experienced in one or more of the following areas of validation: Equipment Qualification. Process Qualification. Responsibilities: Responsibilities associated with this position are directly associated with the introduction and launching of new equipment or products and processes into a manufacturing facility. The candidate must utilize problem solving techniques to resolve issues and conflicts to meet the high level goals set forth by the organizati

Full-time

Manager, IT Quality Engineering (LIMS) - El Segundo, CA or Frederick, MD

El Segundo, California

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Today

We're here for one reason and one reason only - to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great l

Full-time

USD 123,930.00 - 160,380.00 per year

CSV Engineer

Costa Mesa, California

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Today

Roles & Responsibilities: Bachelor's degree in engineering, Computer Science, Life Sciences, or related field. 2-10+ years of experience in computerized systems validation within pharmaceutical, biotechnology, or life sciences industries. Direct experience with GxP equipment, IT systems, or manufacturing automation systems. FDA and cGMP regulations and documentation practices. GAMP 5 guidance. 21 CFR Part 11 and Annex 11. Computer system validation methodologies. Familiarity with risk-based

Full-time

Manufacturing Lead Investigator

Round Lake Beach, Illinois

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Today

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's and . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: The Lead Investigator will initiate and execute deviations in support of Manufacturing. Responsibilities include defining problem statements,

Full-time

USD 70,000.00 - 110,000.00 per year

Engineer III, QA

Allentown, Pennsylvania

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Today

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a g

Full-time

Electrical Engineer - Mission Critical (Healthcare & Pharmaceutical Projects)

Philadelphia, Pennsylvania

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Today

Sr Electrical Engineer (Mission Critical) Hybrid + Fully Remote This Jobot Job is hosted by: Tony Barhoum Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $115,000 - $135,000 per year A bit about us: A leading multidisciplinary engineering and design firm in Philadelphia is seeking an experienced Electrical Engineer to join its mission critical team. This role focuses on delivering high-reliability electrical systems for healthcare and pharm

Full-time

USD 115,000.00 - 135,000.00 per year

Electrical Engineer - Mission Critical (Healthcare & Pharmaceutical Projects)

Philadelphia, Pennsylvania

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Today

Full-time

USD 115,000.00 - 135,000.00 per year

Drug Product MSAT Engineer- Fill Finish

Rensselaer, New York

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Today

Regeneron is currently looking for a DP (Drug Product) MSAT (Manufacturing Science and Technology) Engineer to join our Process Science Drug Product Engineering department. This role focuses on lifecycle management & fill finish operations. They will support equipment selection, CMO selection strategy, management of equipment qualification and process validation activities, and will be hands-on solving issues following technology transfer and cGMP start-up. The MSAT team establishes best practic

Full-time

USD 62,355.00 - 128,700.00 per year

Fractionation Production Specialist

Social Circle, Georgia

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Today

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's and . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: The role is responsible for overseeing Fractionation processes by utilizing resources in production while strictly adhering to cGMP, environm

Full-time

USD 86,500.00 - 135,960.00 per year

Lead Validation Engineer

Massachusetts

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Today

Job Summary: We are seeking an experienced and highly skilled Lead Validation Engineer to support validation, quality, engineering, and manufacturing programs within a cGMP-regulated biopharmaceutical environment. The ideal candidate brings deep expertise in cleaning validation, equipment qualification, CQV, tech transfer support, and quality systems, along with the ability to lead cross-functional teams through complex validation and deviation resolution activities. This role is responsible for

Full-time

Engineer - FUME & CSQ PRD Quality Assurance

Indianapolis, Indiana

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Today

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined

Full-time

USD 65,250.00 per year

Business Transformation Consultant

Rolling Meadows, Illinois

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30+d ago

Role Overview: The Senior Business Transformation Consultant is a key member of Clients Business Transformation & Strategy service line. The role reports to the Senior-Executive of Business Transformation Management. This role supports the successful delivery of business-led transformation engagements, providing strategic insights, capability analysis, and structured roadmaps that drive measurable business outcomes. This consultant serves as a trusted advisor to business stakeholders, helping t

Contract

Depends on Experience

Associate Director-MQ IT LP2

Lebanon, Indiana

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Today

Full-time

USD 132,000.00 - 193,600.00 per year

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good manufacturing practice jobs