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Downstream Process Automation Engineer

Zachary Piper Solutions, LLC

Holly Springs, North Carolina, USA

Full-time

Piper Companies is seeking a Downstream Process Automation Engineer to join a growing leader in the pharmaceutical/biotechnology space for an onsite position in Holly Springs, North Carolina (NC). The Downstream Process Automation Engineer will oversee DeltaV DCS automation systems in a cGMP pharmaceutical environment, managing system integration, documentation review, and cross-functional coordination while ensuring compliance with FDA regulations and validation requirements. Responsibilities

Validation Specialist

Zachary Piper Solutions, LLC

Clayton, North Carolina, USA

Full-time

The Validation Specialist join a leading global pharmaceutical company that is rapidly expanding its international presence, with plans to double in both size and production in the coming years. The Validation Specialist will be responsible for executing and reviewing revalidations, ensuring compliance with regulatory standards, and collaborating with cross-functional teams to support validation protocols and investigations. This role is essential in maintaining the accuracy of validation proces

Facilities Technician III

Sunrise Systems, Inc.

Portsmouth, New Hampshire, USA

Contract

Job Title: Facilities Suite & Elastomer Maintenance Mechanic Location: Portsmouth, NH 03801 Duration: 12 Months with possibility of extension Position Type: Hourly contract Position (W2 only) Job Description Summary The Facilities Suite & Elastomer Maintenance Mechanic Level provides support to the Engineering Services group by operating and performing daily checks on Direct and Indirect Maintenance equipment/systems and assists higher level mechanics with repairs in compliance with company

Senior Validation Engineer

Zachary Piper Solutions, LLC

Copiague, New York, USA

Full-time

Piper Companies is seeking a Senior Validation Engineer to join a leading pharmaceutical manufacturing company located in Long Island, NY. The Senior Validation Engineer will ensure compliance by developing and executing testing protocols for equipment, processes, and utilities in a pharmaceutical cGMP environment. Responsibilities of the Senior Validation Engineer include: Manage end to end, hands on, validation for products, processes, equipment and packaging Supports all qualification tasks

Manufacturing Tech 1, Service - Night Shift (B/D)

bioMerieux

Durham, North Carolina, USA

Full-time

Benefits at bioMerieux: Low-cost medical, dental, and vision benefits starting day one. 11 paid holidays 160 hours of paid time off Annual bonus 9.5% 401k company contribution with no vesting period Tuition reimbursement up to $10,000 per calendar year Onsite cafeteria with daily food stipend Position Summary & Responsibilities: Normal working hours: 7:00pm - 7:30am working a 2-2-3 rotation schedule. The anticipated hiring range for this role is $19.25 - 20.00/hr with shift differential and an

Computer System Validation (CSV) Engineer

Jobot

Scottsdale, Arizona, USA

Full-time

Computer System Validation (CSV) Engineer with strong knowledge of FDA and cGMP regulations and documentation practices and 21 CFR Part 11. needed! (**Full relocation provided**) This Jobot Job is hosted by: Ryan Sullivan Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $130,000 - $145,000 per year A bit about us: We are a fast-growing, Medical Device Manufacturer in Scottsdale, AZ, passionate about improving the lives of patients suffering

QC Analyst I/II (Microbiology)

Zachary Piper Solutions, LLC

Rockville, Maryland, USA

Full-time

Piper Health & Sciences is seeking a QC Analyst I/II, Microbiology to support a biotechnology research company in the Rockville, MD area. This position is 1 st shift hours, Monday - Friday. Responsibilities for the QC Analyst I/II include: Perform Environmental Monitoring of Grade C/D Cleanrooms and aseptic filling isolators, including sampling of viable surfaces, viable air and non-viable particulates in a Phase /Commercial GMP Manufacturing facility. Conducts routine sampling and testing of Cl

Manufacturing Engineer

Stryker

Chandler, Arizona, USA

Full-time

Work Flexibility: Onsite What you will do- Support and improve existing processes using Statistical, Lean, Good Manufacturing Practice (GMP) and Six Sigma methodologies Foster an environment of continuous improvement and provide support to customers in all functional areas Reduce Reject Rates(scrap)and optimize manufacturing processes Identify and implement safety improvements on production lines Lead the development and execution of technical protocols and, generation of reports Develop and i

Engineering - Bio Process Associate - 3rd Shift , Devens MA - Immediate position

Futran Solutions

Massachusetts, USA

Contract

Job Description: Bio Process Associate 3rd shift role--so shift diff included on Rate Onsite in Devens--Local Candidates Only Operates control systems and processes in Biotechnology Pilot Plants as assigned. Prepares process buffers and reagents. Cleans equipment and maintain area in clean and orderly fashion. Recognizes and reports safety, maintenance and operational variances to area management. Communicates status of operations to area management in a timely manner. Follows detailed SOP

Microbiologist 2nd Shift

Civica Rx

Petersburg, Virginia, USA

Full-time

About Civica: Over the past two decades, shortages of generic, injectable medications critical to the lifesaving work of hospitals in the United States have become commonplace and have reached an all time high. Over 300 essential medications are reported to be in shortage, according to industry and FDA reports. "Race to the bottom" pricing of mostly sterile injectable medications, manufacturing challenges and predatory pricing are both the causes and results. Who suffers most? Patients. Civic

Quality Control Chemist I

Sunrise Systems, Inc.

Johns Creek, Georgia, USA

Contract

Job title: Quality Control Chemist I Job ID: 25-08182 Location: Johns Creek, GA (Onsite) Duration: 24 months Contract on W2 Schedule: Two-week rotating schedule 12-hour shifts. Week 1: Monday, Thursday and Friday. Week 2: Tuesday, Wednesday, Saturday and Sunday. POSITION PURPOSE: Conduct Quality Control testing of materials and production samples as required to support contact lens production, performing assigned tasks according to approved SOP's, methods, and procedures with adherence to cG

Facilities/Utilities SME

Zachary Piper Solutions, LLC

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

Cell Culture Sr. Technician

Mitchell Martin, Inc.

Hopewell, New Jersey, USA

Full-time, Contract

Title: Cell Culture Sr. Technician.Location: Northeastern United States (Onsite)Employment Type: ContractCompensation: Pay Range:$37.73-$53.90/HrsDescription: * Enable the start-up phase of a new manufacturing facility. * Execute and support cGMP manufacturing operations. * Deliver production plans reliably and compliantly.Key Responsibilities: * Follow cGMP procedures for manufacturing execution. * Prepare and transfer media, and perform filtration. * Sample, monitor, and transfer cell cultures

Maintenance Electrician (2nd Shift)

Civica Rx

Petersburg, Virginia, USA

Full-time

About Civica: Critical shortages of essential generic injectable drugs are an ongoing crisis in U.S. healthcare and have reached an all-time high. Over 300 essential medications are currently reported to be in shortage, according to industry and FDA reports. Shortages put patients at risk and waste hospital resources. Civica is a market-based nonprofit solution created in 2018 by health systems and philanthropies for the express purpose of preventing and mitigating drug shortages. Today, near

Production Technician Filling

Sanofi EU

Swiftwater, Pennsylvania, USA

Full-time

Job title: Production Technician Filling Location: Swiftwater, PA 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. This role is for a non-exempt employee working in the Filling Department. Their Bi-weekly pay is based on prev

Regional Sales Manager - Northeast US

GEA

Columbia, Maryland, USA

Full-time

Responsibilities / Tasks The Regional Sales Manager (RSM) is responsible for driving new business and maintaining existing customer relationships for GEA's pharmaceutical technologies, including Liquid Processing, Lyophilization, Spray Drying, Continuous Manufacturing, Fluid Bed Processing, Potent Material Containment, and Tablet Presses. This role involves developing strong business relationships with key stakeholders such as pharmaceutical executives, production managers, process engineers, s

Manufacturing Specialist II - Syringe Line

Civica Rx

Petersburg, Virginia, USA

Full-time

About Civica: Over the past two decades, shortages of generic, injectable medications critical to the lifesaving work of hospitals in the United States have become commonplace and have reached an all time high. Over 300 essential medications are reported to be in shortage, according to industry and FDA reports. "Race to the bottom" pricing of mostly sterile injectable medications, manufacturing challenges and predatory pricing are both the causes and results. Who suffers most? Patients. Civic

Validation Engineer - Casa Grande, AZ - Nutrition Plant

Abbott Laboratories

Casa Grande, Arizona, USA

Full-time

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Validation Engineer - Casa Grande, AZ Nutrition Plant As the Validation Engineer, you will ensure that change control and validation activities are

QA Specialist (Nights)

CSL Seqirus

Holly Springs, North Carolina, USA

Full-time

Do you want to work with a company that tackles fascinating problems and find solutions to complex challenges? Seqirus has an exciting opportunity to join our expanding team in Holly Springs, NC. With an advanced manufacturing facility and expertise in influenza science we are one of the world leaders in the production of the influenza vaccine. We operate as one integrated global company, drawing together expert staff from different countries to collaborate. Together, we're working on the front

Manufacturing Tech 2, Line 4 - Night Shift (D)

bioMerieux

Durham, North Carolina, USA

Full-time

Benefits at bioMerieux: Low-cost medical, dental, and vision benefits starting day one. 11 paid holidays 160 hours of paid time off Annual bonus 9.5% 401k company contribution with no vesting period Tuition reimbursement up to $10,000 per calendar year Onsite cafeteria with daily food stipend Position Summary & Responsibilities: Normal working hours: 7:00pm - 7:30am working a 2-2-3 rotation schedule. The Process Technician position is responsible for the operation of high-speed equipment used in