gmp Jobs

61 - 80 of 547 Jobs

Document Control AssociateJob Title - Document Control Associate

Aditi ConsultingCompany Name - Aditi Consulting

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Manassas, Virginia, USA

Contract

Payrate: $30.00 - $32.00/hr. Summary: The creation and maintenance of the Quality System documentation. Communicate any deviations to management. Assist the Quality Assurance team with special projects as required. Comply with SQF, Food Safety Plan (HACCP), Food Quality Plan (FQP) standards. Job Duties: Create, revise, and maintain all documentation related to the Quality System using technical writing best practices, ensuring proper formatting, numbering, and document control. Issue batch recor

Analytical Validation EngineerJob Title - Analytical Validation Engineer

Zachary Piper Solutions, LLCCompany Name - Zachary Piper Solutions, LLC

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Hopewell Township, New Jersey, USA

Full-time

Piper Companies is seeking an Analytical Validation Engineer to join a major pharmaceutical manufacturing company located in Titusville, NJ. This role is 100% onsite. The Analytical Validation Engineer will ensure the accuracy and reliability of processes, equipment, and systems in pharmaceutical manufacturing by conducting thorough validation, commissioning, and decommissioning activities to maintain compliance and operational excellence. Responsibilities of the Analytical Validation Engin

CMMS Data SpecialistJob Title - CMMS Data Specialist

Cushman & WakefieldCompany Name - Cushman & Wakefield

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Boston, Massachusetts, USA

Full-time

Job Title CMMS Data Specialist Job Description Summary The role involves managing asset-related data within the Computerized Maintenance Management System (CMMS) to support operational readiness at all Vertex sites, including labs and facilities. Key responsibilities include submitting electronic change requests for asset maintenance, calibration, and spare parts, as well as tracking the progress and activation of CMMS attributes. The position requires ensuring accurate asset information input,

Manufacturing Engineer-Medical DeviceJob Title - Manufacturing Engineer-Medical Device

Trelleborg GroupCompany Name - Trelleborg Group

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Paso Robles, California, USA

Full-time

Join Our Team at Trelleborg Medical Solutions! Imagine working for one of the world's leading contract medical device manufacturers, nestled just 30 miles from California's stunning Central Coast. At Trelleborg Medical Solutions, we are not just a premier manufacturer of life-saving medical components; we are a forward-thinking company committed to excellence and innovation. Our journey in lean manufacturing has been ongoing for years, and we are on the path to becoming a showcase of excellence

Controls EngineerJob Title - Controls Engineer

Plastipak HoldingsCompany Name - Plastipak Holdings

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Woodbridge Township, New Jersey, USA

Full-time

As the Controls Engineer you are responsible for maintaining, servicing, and troubleshooting manufacturing site equipment. Applying your electrical and mechanical knowledge, you will implement preventative maintenance programs and reduce equipment downtime. You will play a fundamental role in upholding Plastipak's standard of excellence and exceeding customer expectations. You Will: Maintain machinery and equipment, including vision systems, production equipment, palletizers, and plant support

Scientific - Assistant ScientistJob Title - Scientific - Assistant Scientist

Futran SolutionsCompany Name - Futran Solutions

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Seattle, Washington, USA

Full-time

Job Description: Job Title: Assistant Scientist Location: Seattle, WA*Onsite Schedule: M-F normal business hours Top Skills: Associate Degree in Biology, Chemical Engineering, Bioengineering or relevant scientific discipline with 0-2 years of industry bioprocess experience. Mammalian cell culture and cell banking experience Experience with cell therapy process development or manufacturing Job scope or job description: The Global Manufacturing Sciences team plays a key role in supporting activ

QA Associate 1Job Title - QA Associate 1

Manpower EngineeringCompany Name - Manpower Engineering

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Winchester, Kentucky, USA

Full-time

Our client, a global pharmaceutical manufacturing leader, is seeking a QA Associate 1 to join their team. As a QA Associate 1, you will be part of the Quality Assurance Department supporting Manufacturing and Production Teams. The ideal candidate will have attention to detail, strong problem-solving skills, and effective communication skills, which will align successfully in the organization. Job Title: QA Associate 1 Location: Winchester, KY (On-site) Pay Range: $24.00/hr (Day Shift) or $27.60/

Validation EngineerJob Title - Validation Engineer

ACL DigitalCompany Name - ACL Digital

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California, USA

Full-time

Job Title: Validation Engineer Location: La Verne, CA Duration: 12+ Months Description: Independent engineer who have in depth knowledge about validation lifecycle management and be able to write VMP, protocols and corresponding summary reports ble to execute test protocols independently and resolve deviation and collaborate with engineering team, business process owner and QA to make changes if necessary. Able to investigate failure and write deviation and change control records. Experienc

Facilities/Utilities SMEJob Title - Facilities/Utilities SME

Zachary Piper Solutions, LLCCompany Name - Zachary Piper Solutions, LLC

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Bloomington, Indiana, USA

Full-time

Piper Companies is seeking a BioPharma Facilities/Utilities Subject Matter Expert (SME) to join an expansion project team of a new facility build for a CDMO out in Bloomington, IN. The role has an onsite expectation and slated through 2026 and potentially beyond. The SME will provide technical expertise and strategic guidance for all utility systems-both clean and plant-throughout the design, construction, and commissioning of our new GMP manufacturing facility. This role is critical to ensuring

HVAC SMEJob Title - HVAC SME

Zachary Piper Solutions, LLCCompany Name - Zachary Piper Solutions, LLC

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Bloomington, Indiana, USA

Full-time

Piper Companies is seeking a BioPharma HVAC Subject Matter Expert (SME) to join an expansion project team of a new facility build for a CDMO out in Bloomington, IN. The role has an onsite expectation and slated through 2026 and potentially beyond. The SME will lead the implementation, and qualification of complex HVAC systems for the new GMP manufacturing facility. This role requires deep technical knowledge and hands-on experience with HVAC systems designed for cleanrooms, controlled environmen

Senior Supplier Quality EngineerJob Title - Senior Supplier Quality Engineer

JobotCompany Name - Jobot

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Aurora, Colorado, USA

Full-time

Full-Time & Direct Hire Senior Supplier Quality Engineer needed for Global Health-Tech Leader! This Jobot Job is hosted by: James Thai Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $90,000 - $120,000 per year A bit about us: Based in Colorado Springs, CO, we are reimagining healthcare through breakthrough technologies and human-centered design. Our company is a global leader in health innovation, creating smart systems that improve lives

Manufacturing Technical Writer-SOPJob Title - Manufacturing Technical Writer-SOP

Advantage TechnicalCompany Name - Advantage Technical

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Norton, Massachusetts, USA

Full-time

Technical Writer-SOP Location: Norton, MA Position type: Long Term contract Pay: $40-$55/HR (depending on experience) We're looking for an experienced Manufacturing Technical Procedure Writer to join our team. In this role, you'll be responsible for drafting, revising, and maintaining SOPs, batch records, and technical documentation that meet GMP and global regulatory standards. You'll collaborate with cross-functional teams to ensure clarity, accuracy, and compliance in all documents used o

Electrical/Automation SMEJob Title - Electrical/Automation SME

Zachary Piper Solutions, LLCCompany Name - Zachary Piper Solutions, LLC

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Bloomington, Indiana, USA

Full-time

Piper Companies is seeking a BioPharma Electrical/Automation Subject Matter Expert (SME) to manage the construction and communication of a new facility build for a CDMO out in Bloomington, IN. The role has an onsite expectation and slated through 2026 and potentially beyond. The SME will provide technical leadership and subject matter expertise throughout the design, construction, commissioning, and qualification of a new pharmaceutical manufacturing facility. This role will be responsible for e

Process Engineer IJob Title - Process Engineer I

Merck KgaACompany Name - Merck KgaA

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St. Louis, Missouri, USA

Full-time

Work Location: St. Louis, Missouri Shift: Department: LS-SC-POKMA1 Cherokee STL Technical Operations 2 Recruiter: Ashley Hennessy This information is for internals only. Please do not share outside of the organization. Your Role: The Process Engineer is responsible for developing the manufacturing process train for custom bioconjugation products in GMP manufacturing and bringing in new manufacturing equipment. This role works cross-functionally with Manufacturing, Process and Analytical Devel

Associate Process Engineer - APIJob Title - Associate Process Engineer - API

Novo Nordisk IncCompany Name - Novo Nordisk Inc

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Clayton, North Carolina, USA

Full-time

About the Department At Novo Nordisk, we are helping to improve the quality of life for millions of people worldwide. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable an

Laboratory AssistantJob Title - Laboratory Assistant

Zachary Piper Solutions, LLCCompany Name - Zachary Piper Solutions, LLC

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Baltimore, Maryland, USA

Full-time

Piper Health & Sciences is actively recruiting for several entry-level Laboratory Assistant roles to gain hands-on experience with ELISA testing, cell cultures, and other immunoassays. This is an ideal role for recent science graduates who are looking to get their first job in the industry with an incredible biotechnology research organization in the Baltimore, MD area! Responsibilities for the Laboratory Technician include: Quality Control (QC) testing to support the organization's products Pe

Lead HVAC & Maintenance Facilities Automation and Controls EngineerJob Title - Lead HVAC & Maintenance Facilities Automation and Controls Engineer

US AMR-Jones Lang LaSalle Americas, Inc.Company Name - US AMR-Jones Lang LaSalle Americas, Inc.

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Cambridge, Massachusetts, USA

Full-time

What this job involves: JLL is seeking an experienced HVAC professional with advanced expertise in Building Automation Systems (BAS), particularly Siemens Controls, for a cutting-edge role at a biotech company. This position is ideal for those looking to elevate their HVAC career by diving deep into the world of intelligent building systems. As our BAS Specialist, you'll be at the forefront of smart building technology, working with both new and legacy Siemens Controls. You'll collaborate close

Sr. Level Technical IT/OTJob Title - Sr. Level Technical IT/OT

Oxford Global ResourcesCompany Name - Oxford Global Resources

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East Hanover, New Jersey, USA

Contract

They will be looking for a Senior Technical IT/OT person working on lab systems, integrating into their system, going applications, working with domain controller, integrator level. They are looking for an IT/OT Technical person to help support the lab environment in East Hanover. This position is onsite and will be through the end of the year. highly technical person, work is done in laboratory so Life Science experience preferred but not a necessity. Manager is looking for a highly technical p

QA Clinical Supplies SpecialistJob Title - QA Clinical Supplies Specialist

Zachary Piper Solutions, LLCCompany Name - Zachary Piper Solutions, LLC

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Lansdale, Pennsylvania, USA

Full-time

Piper Companies is seeking a QA Clinical Supplies Specialist to join a major pharmaceutical manufacturing company located in Lansdale, PA. This is a Hybrid role. The QA Clinical Supplies Specialist will ensure the quality, compliance and integrity of clinical trial supplies. Responsibilities of the QA Clinical Supplies Specialist include: Ensure clinical supply materials meet company policies and regulatory standards. Lead projects aimed at improving process performance, including yiel

R&D Technician - OnsiteJob Title - R&D Technician - Onsite

VIVA USA INCCompany Name - VIVA USA INC

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Valhalla, New York, USA

Contract

Title: R&D Technician - Onsite Mandatory skills: Excel, Word, MS Outlook, setting up benchtop, pilot plant experiments, managing product inventories, product entries, purchase orders, pilot plant trials, product packing, shipping, labeling, GLP, GMP, data entry, documentation, manufacturing sites, ingredient purchasing, Citrus lab, preparation, testing, evaluation of beverage batches, prepare beverage, beverage concentrates, product development, brand maintenance, pilot plant productions, sampl