1 - 20 of 608 Jobs

Automation Controls Engineer (with GMP experience)

Bytecubit Technologies

Gaithersburg, Maryland, USA

Contract

Job Title: Automation Controls Engineer (with GMP experience) (This is NOT an Automation Testing job) Location: Gaithersburg, MD Duration: 6+ months Pay Rate: $55/hr - $70/hr (depending on experience) Job Description: Seeking an experienced Automation Engineer with Project Management abilities with strong GMP manufacturing exposure. This role is focused on driving project ownership and execution with minimal oversight. Looking for a proactive, hands-on leader who can step into ongoing automation

GMP/Pharma Manufacturing Operator (2nd Shift)(ONSITE)

NetSource, Inc.

Raritan, New Jersey, USA

Contract

Please note that this is a 1-year contract. This role will be 2nd Shift 3pm 11:30PM / M F Requirements: GMP document experience. High School Diploma required; Bachelor s Degree preferred 3+ years of experience in medical device or pharmaceutical manufacturing Experience using SAP is preferred Proficient with using MS Office (Word, Excel, Outlook) Strong mechanical problem-solving ability and technical aptitude Ability to work independently with limited supervision and work as part of a team Able

Maintenance Mechanic/ GMP Asset Mechanic

Sunrise Systems, Inc.

Tampa, Florida, USA

Contract

Job Title: Maintenance Mechanic/ GMP Asset Mechanic Location: 4910 Savarese Circle, Tampa, FL 33634 Duration: 12 Months (Possible Extension or Conversion) Position Type: Hourly contract Position (W2 only) Description: The GMP Asset Mechanic is responsible to ensure that GMP production assets are evaluated prior to purchase, qualified and documented as needed, maintained and commissioned prior to use, and properly decommissioned and stored for future use. This individual reviews: equipment and

Calibration Instrumentation with GMP

CSI (Consultant Specialists Inc.)

Hillsboro, Oregon, USA

Contract

W2 ONLY Responsible for the maintenance and calibration of instrumentation and control system equipment within the Hillsboro Oregon facility to include utilities, Filling, Packaging, Inspection, Warehouse, Distribution Center, Tank Management, and QC laboratory instruments. Majority of maintenance and calibration will be working within QC area escorting vendors to perform maintenance and calibration activities. Provide instrument issue resolution, emergency troubleshooting and repairs of all t

Global Quality Lead, GMP, GDP Audit and Inspection - Pipeline Launch

Sanofi

Framingham, Massachusetts, USA

Full-time

Job DescriptionJob Title: Global Quality Lead, GMP, GDP Audit and Inspection - Pipeline Launch Location: Framingham, MA or Morristown, NJ About the Job We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Foster best-in-class performance by leve

Senior IT Project Manager - GMP Manufacturing

Regeneron Pharmaceutical

Troy, New York, USA

Full-time

The Senior IT Project Manager is tasked with the oversight and successful delivery of complex and strategic IT projects within the Applications and Infrastructure domains for IOPS. This role requires a strategic thinker with excellent project management skills to ensure that projects are delivered on time, within scope, and budget, while maintaining high-quality standards. As a Senior IOPS IT Project Manager, a typical day might include the following: Lead project management and business analysi

Direct Client - Quality Assurance Specialist (food or beverage manufacturing QA)

ChaTeck Incorporated

Seattle, Washington, USA

Contract, Third Party

Role: Direct Client - Quality Assurance Associate (food or beverage manufacturing QA) Location: Seattle, WA (Hybrid Tuesday, Thursday, the third day is flexible based) Duration: 12+ Months Job description "Implementing and auditing the manufacturing quality strategy, food safety, process and program quality and regulatory compliance to ensure the continuous supply of safe, wholesome and premium quality products to customers Tops Skills Needed Top Candidate Skills & How Applied Years of Ex

Quality Inspector

Stellar IT Solutions

Madison, Wisconsin, USA

Full-time, Part-time, Contract, Third Party

Job Title: Quality Inspector Medical Device Manufacturing Location: Madison, WI Job Type: Contract or Full-Time (as applicable) Job Description: We are seeking a Quality Inspector to support daily device manufacturing operations in a medical device environment. This role ensures all processes, materials, and documentation comply with current Good Manufacturing Practices (cGMP), internal quality systems, and regulatory standards, including FDA QSR and ISO 13485. Key Responsibilities: Perform in

Medical Device Assembler

Talent Groups

Compton, California, USA

Contract

Shift: 7:00 AM 3:30 PM Seeking a detail-oriented Assembler I to perform manual assembly of fiber and filtration products in a cleanroom environment.Responsibilities include assembling components, packaging, operating small tools, and following GMP and SOP guidelines.Ideal for candidates with 0 1 year of manufacturing experience; medical device background a plus.

Senior Electrical Engineer

Aditi Consulting

New Albany, Ohio, USA

Contract

Payrate: $50.00 - $54.00/hr. Summary: The Engineer position reports to the Manager of Engineering under the Engineering & Maintenance team at the facility. This position requires the application of diverse and advanced engineering and scientific principles in support of commercial GMP Final Drug Product (FDP) operations in the manufacturing facility. The site of the new advanced product assembly and packaging plant, this role will apply advanced and diverse engineering principles to the design a

Engineer II, Quality

Thermo Fisher Scientific

Asheville, North Carolina, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description Join Thermo Fisher Scientific Inc. as an Engineer II, Quality in Asheville, and be part of an exceptionally dedicated team! We are a company that thrives on innovation and collaboration, and we are looking for an ambitious individual who is ready to contribute to our world-class projects. This is an outstanding opportunity to work in an environ

Quality Technician

Stellar IT Solutions

St. Louis, Missouri, USA

Full-time, Part-time, Contract, Third Party

Job Title: Quality Technician Location: St. Louis, MO Duration: Long-Term Contract Schedule: Monday to Friday, 8-hour shifts (potential for night, weekend, and holiday work) Job Summary: We are seeking a Quality Technician to provide entry-level technical support within a microbiology laboratory environment. This role involves evaluating material and product quality by performing microbiological analysis on raw materials, finished products, stability samples, water, and environmental monitor

Process Engineer

Katalyst Healthcares and Lifesciences

Remote or New York, USA

Full-time

Responsibilities: Senior Process Engineer responsible for tech transfers within the manufacturing team. Support GMP-related activities. Experience in tech transfer and project management. Strong technical skills, including report writing and problem-solving. Excellent communication skills, with the ability to clearly relay technical information. Cell Therapy (CAR-T) experience (preferred). Willingness to travel (approximately 25%). t least 5 years of relevant experience.

Process Validation Engineer

Katalyst Healthcares and Lifesciences

East Windsor, New Jersey, USA

Full-time

Responsibilities: Previous experience as a validation engineer in an aseptic pharmaceutical fill/finish environment. Prior experience executing validation protocols on a pharmaceutical fill/finish line. Specific line components include. Lyophilizers. Depyrogenation tunnels. Autocalves. Previous experience with the project management requirements of validation project in a GMP environment. Requirements: Managing validation schedule. Communication of delays and changes to timelines. Coor

Automation Controls Engineer (2ndShift)

Bytecubit Technologies

Indianapolis, Indiana, USA

Contract

Job Title: Automation Controls Engineer (2nd Shift)Location: Indianapolis, INDuration: 6 monthsPay Rate: $45/hr-$55/hr (depending on experience) Job Description: This role will be responsible for supporting the design, installation, and validation for the sterile purification and recycling isolators into commercial production. Bachelor s degree in engineering, Computer Science, Automation, or related field with 7+ years of relevant engineering experience in the Pharmaceutical or Chemical indust

Process Validation Engineer

Katalyst Healthcares and Lifesciences

Swiftwater, Pennsylvania, USA

Full-time

Roles & Responsibilities: Bachelor's degree in science or engineering (MS accepted, PhD is overqualified). Minimum 2+ years in Process Validation within the biotech/pharma industry. Writing and executing process validation documents. Strong Process Performance Qualification (PPQ) experience. Hands-on experience collecting process samples. Must have on-the-floor manufacturing experience. Familiarity with GMP best practices. Proficient in MS Office (Word, Excel, PowerPoint). Strong w

Maintenance Technician

System One

Ayer, Massachusetts, USA

Contract

Job Title: Maintenance Technician Location: Devens, Massachusetts Type: Contract Shift: Day Shift (8am-5pm) Pay Rate: $30-38/hr based on experience About the Role: We are seeking two skilled Maintenance Technicians for newly created roles on the Day Shift at our Devens, MA facility. This is an excellent opportunity to join a fast-paced environment supporting critical maintenance operations. The ideal candidates will have strong mechanical aptitude, a proactive approach to safety, and experi

Component Engineer - Validation (IQ/OQ/PQ)

Katalyst Healthcares and Lifesciences

Irvine, California, USA

Full-time

Job Description: Experienced Component Engineer with strong expertise in equipment and process validation, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). Proven ability to manage component selection, supplier coordination, and quality documentation to ensure compliance with FDA, ISO 13485, and GMP standards. Roles & Responsibilities: Component validation activities including creation and execution of IQ/OQ/PQ protocols and reports.

Principal Process Engineer

Katalyst Healthcares and Lifesciences

Wilson, North Carolina, USA

Full-time

Job Description: We are seeking a Principal Process Engineer with a strong background in GMP manufacturing and engineering. The ideal candidate will have hands-on experience in biologics, process systems, automation, and utilities with a focus on upstream and/or downstream processes. The role will be initially remote and then onsite in Wilson , NC, once the facility opens. Responsibilities: Provide technical leadership in GMP large molecule biologics manufacturing. Engineer and modify proce

Maintenance Technician

Cafe Spice

New Windsor, New York, USA

Full-time

pm//css/froala_editor.pkgd.min.css rel= stylesheet type= text/css > About Us We are a fast-paced and growing food manufacturing company committed to delivering high-quality products to our customers. With a strong focus on safety, efficiency, and continuous improvement, we take pride in our people-first culture and collaborative environment. Position Overview We are seeking an experienced Maintenance Technician to join our team in a fast-paced food manufacturing facility. If you have a strong