1 - 20 of 495 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

QA Associate-GMP

Zachary Piper Solutions, LLC

Lansing, Michigan, USA

Full-time

Piper Companies is looking for a QA Specialist to join a clinical pharmaceuticals company located in Lansing, MI. Responsibilities of the QA Specialist include: Complete communication with both internal and external vendors Create new SOPS and improve existing ones Deal with quality records through initiation, tracking, and closure (Ex: Deviations, Change Controls, CAPAs, Out of Specification records) Complete reviews of manufacturing batch records Qualifications for the QA Specialist include

QA Consultant - GMP

Zachary Piper Solutions, LLC

Summit, New Jersey, USA

Full-time

Piper Companies is looking for a QA Consultant to support CAPA, Investigation and Remediation activities for a global consumer products company. Responsibilities for the QA Specialist include: Reviewing/Approving change controls per SOPs Owning investigations, Gaining approvals (related to product specifications and labeling) BOM approvals in SAP Support internal and external health authority audits Support Document Control and Management duties as needed Systems utilized SAP,ETQ for invest

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

Quality Assurance Specialist

GDH

Houston, Texas, USA

Full-time

Job Description: Our client is seeking a detail-oriented and motivated Quality Assurance (QA) Specialist to join their team in a GMP-regulated environment. The QA Specialist will play a vital role in ensuring that all products meet the highest standards of quality, safety, and regulatory compliance in accordance with Good Manufacturing Practices (GMP). The ideal candidate will have a strong background in quality assurance, a deep understanding of GMP guidelines, and the ability to collaborate e

Material Handler / Laboratory Technician

Pyramid Consulting, Inc.

Millsboro, Delaware, USA

Contract

Immediate need for a talented Material Handler / Laboratory Technician. This is a 06+ months contract opportunity with long-term potential and is located in Millsboro, DE(Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID: 25-77625 Pay Range: $18.50 - $19.46/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: A Lab

Packaging Engineer

Stanley David and Associates

Fort Washington, Pennsylvania, USA

Full-time

Must Have Technical/Functional Skills A minimum of 8-10 years of industry experience is required with at least 3 years of Package Development experience. Specific experience within the Consumer, OTC, or Pharmaceutical industry is must. GMP experience is must. Experience in a highly regulated environment is preferred. Demonstrated technical knowledge related to package materials, equipment, testing and package development is required. Roles & Responsibilities o Plan and execute package enginee

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

ChaTeck Incorporated

Seattle, Washington, USA

Third Party, Contract

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.

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

Sr. Inventory Coordinator

Talent Software Services, Inc

Cambridge, Massachusetts, USA

Contract

Sr. Inventory CoordinatorJob Summary: Talent Software Services is in search of a Sr. Inventory Coordinator for a contract position in Cambridge, MA. The opportunity will be a year with a strong chance for a long-term extension.Position Summary: In this role, you will report to the Onsite Manager and will work closely with the Lab and Production Services professionals to serve our customers by performing customized, mission-based lab work and research protocols that help return time back to scien

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

Cleaning Validation Engineer

Zachary Piper Solutions, LLC

Holly Springs, North Carolina, USA

Full-time

Piper Companies is seeking a Cleaning Validation Engineer located on-site in Holly Springs, NC. The Cleaning Validation Engineer will be responsible for developing and implementing cleaning validation protocols and conducting reports. Responsibilities of the Cleaning Validation Engineer include: Develop a cleaning validation program and execute protocols and reports for new facilities and equipment. Identify potential contamination sources through risk assessments and establish necessary clea

Virology Deviation Management Specialist

Zachary Piper Solutions, LLC

West Point, Pennsylvania, USA

Full-time

Piper Companies is looking for a Virology Deviation Management Specialist for a leading pharmaceutical manufacturer in West Point, PA. Responsibilities: Conduct microbiological testing within investigations to prove root causeRecommend corrective and preventive actions (CAPAs)Conduct deviation OOS investigations related to testing within pharmaceutical manufacturing Qualifications: 2+ years of experience within GMP/FDA regulated environmentFamiliarity with virology Strong background in pharm

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.