1 - 20 of 168 Jobs

Manufacturing Execution Systems (MES) Engineer

Tekaccel, Inc

Remote

Contract, Third Party

About the Role: We are seeking a skilled MES Engineer to join our team, where you ll work closely with the Global IT organization and site stakeholders to understand and address critical business needs in Pharmaceutical/Biotech manufacturing environments. You ll play a key role in designing, implementing, validating, and supporting cutting-edge MES (Manufacturing Execution System) solutions, ensuring systems remain compliant and deliver meaningful value to operations. Key Responsibilities: Colla

Sr QC Instrument Validation Engineer

Bytecubit Technologies

Phoenix, Arizona, USA

Contract

Job Title: Sr QC Instrument Validation Engineer Location: Phoenix, AZ Duration: 6 months Consultant Rate: $45/hr-$70/hr (depending on experience) Job Description: Need a validation engineer for a Project that involves the completion of various qualifications of Quality Control (QC) chemistry instruments. Consultant will be responsible for writing and performing Installation Qualification (IQ), Operational Qualification (OQ), and potential Performance Qualification (PQ) and summary reports to sup

Senior Engineer, R&D

Stryker

Salt Lake City, Utah, USA

Full-time

Work Flexibility: Onsite Job Description: Stryker is looking for an Senior Engineer, R&D to join the R&D Ops team supporting all new and existing equipment in our R&D labs for Stryker's Neurovascular Division. This role is on-site, in Salt Lake City, Utah with the expectation to come into the office 5 days a week. What You Will Do Join a driven, growing team in a fast-paced environment where engineering excellence matters. In this role you will support equipment in our R&D labs from procureme

IT Co-ordinator

Teceze Ltd

St. Peters, Missouri, USA

Contract

PhaseIndicative list of activities Project Prep a) Capture AS-IS floor plans, power and LAN cabling diagrams WI-FI survey reports and WAN utilization reports from site contacts and global network teams b) Capture AS-IS hardware inventory covering peripherals like RF scanners, Label Printers, RF Handheld devices, Sample & PM Stock Label Printers, Report printers, Multifunction Printers, Desktop PCs, Tablet PCs c) Capture AS-IS network hardware inventory covering network switches, Wi-Fi access po

Process Engineering Manager

Thermo Fisher Scientific

Fair Lawn, New Jersey, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Various outside weather conditions, Warehouse Job Description Job Overview: At Thermo Fisher Scientific Inc., we offer an exceptional opportunity for a bold Process Engineering Manager to lead our divisional LCD Process improvement program. You will play

Manufacturing Engineer

Trelleborg Group

Delano, Minnesota, USA

Full-time

Trelleborg Medical Solutions is seeking a Manufacturing Engineer to join their team. Responsible for the design and development of optimal engineering solutions for cost-effective lean manufacturing processes. Perform validation activities as necessary in a clean-room manufacturing environment. Recommends improvements to production processes, methods and controls. Supports and may manage manufacturing launch for new or revised products. Salary range Depending on Qualifications and Experience: $

Pharmaceutical Equipment Commissioning & Qualification Engineer

Zachary Piper Solutions, LLC

Hopewell Township, New Jersey, USA

Full-time

Piper Companies is currently seeking a Pharmaceutical Equipment Commissioning & Qualification Engineer for an opportunity in Titusville, New Jersey or Raritan, New Jersey , to join a global pharmaceutical company. Responsibilities: Maintain, calibrate, qualify and validate equipment used in the production, testing and packaging of pharmaceutical products Develop, execute, and document equipment qualification protocols and test plans in accordance with cGMP regulations and industry standards C

CQV Engineer

Zachary Piper Solutions, LLC

Pittsburgh, Pennsylvania, USA

Full-time

Piper Companies is currently seeking a highly skilled and motivated CQV Engineer to join our team in Pittsburgh, PA, supporting a greenfield biologics manufacturing facility. This role is ideal for professionals with a strong background in Commissioning, Qualification, and Validation (CQV) within the biopharmaceutical industry, particularly those with hands-on experience in greenfield site start-ups. Responsibilities for the CQV Engineer: Lead and execute CQV activities for facility, utility, a

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 deviation management supporting a Virology quality control team Conduct technical writing of deviation investigation results and initiate CAPAs Fully support all aspects of assigned projects and run the business activities, including but not limited to: participate in decision making, leading laboratory investigations, issue ident

Analytical Validation Engineer

Zachary Piper Solutions, LLC

Hopewell Township, New Jersey, USA

Full-time

Piper Companies is looking for an Analytical Validation Engineer to support commissioning and decommissioning activities for a major pharmaceutical company in the Titusville, NJ area. Responsibilities for the Analytical Validation Engineer include: Experience in Pharmaceutical Laboratory Operations Must be familiar and have experience with laboratory instrument selection, installation (IQ/OQ) and qualification (PQ) Experience supporting laboratory investigations from beginning to end, includ

Senior CQV Engineer (Biopharma)

Zachary Piper Solutions, LLC

Raleigh, North Carolina, USA

Full-time

Piper Companies is actively seeking a Senior CQV (Commissioning, Qualification, and Validation) Engineer to join our team. The ideal candidate will have 7-10 years of CQV experience with large-scale process equipment, including upstream, downstream, and CIP (Clean-In-Place) systems. This role is critical to ensuring the successful commissioning and validation of our biopharmaceutical manufacturing processes. This is a Monday - Friday, traditional hours role located on-site in the greater Raleigh

Senior Process Engineer

Jobot

Rochester, New Hampshire, USA

Full-time

Our client is an industry leading manufacturer and supplier of material used in aerospace and mass automotive manufacturing! This Jobot Job is hosted by: Matt Tassoni Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $90,000 - $125,000 per year A bit about us: Our client is an industry leading manufacturer and supplier of material used in aerospace and mass automotive manufacturing! Why join us? Medical Dental Vision 401k PTO and more Job

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

Junior Manufacturing Engineer

Sanmina-SCI

San Jose, California, USA

Full-time

Sanmina Corporation (NASDAQ: SANM) is a leading integrated manufacturing solutions provider serving the fastest-growing segments of the global Electronics Manufacturing Services (EMS) market. Recognized as a technology leader, Sanmina Corporation provides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, c

Senior Manufacturing Engineer - Capital Equipment & Packaging Systems

Jobot

Coppell, Texas, USA

Full-time

Hands-On Role, Path to Engineering Director This Jobot Job is hosted by: Tracy Hann Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $100,000 - $135,000 per year A bit about us: We are a privately held manufacturer in the health and wellness industry, producing a broad portfolio of nutritional supplements, ready-to-drink beverages, and personal care items. With decades of experience and operations across the southern U.S., we manage the full

Senior IT BRM

Abbott Laboratories

Columbus, Ohio, 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. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. Yo

Sr. Manufacturing Engineer

Sanmina-SCI

San Jose, California, USA

Full-time

Sanmina Corporation (NASDAQ: SANM) is a leading integrated manufacturing solutions provider serving the fastest-growing segments of the global Electronics Manufacturing Services (EMS) market. Recognized as a technology leader, Sanmina Corporation provides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, c

Quality/Validation Engineer

TEKsystems c/o Allegis Group

Scarborough, Maine, USA

Full-time

Description We are seeking a highly motivated and detail-oriented Validation/Quality Engineer to support our manufacturing operations. This role is critical in ensuring compliance with FDA regulations (21 CFR Part 820) and ISO 13485 standards. The ideal candidate will lead validation activities, maintain robust quality systems, and drive continuous improvement initiatives across manufacturing processes. Key Responsibilities: Validation & Qualification: Develop and execute validation protocols (I

Senior CQV Engineer

Zachary Piper Solutions, LLC

Raleigh, North Carolina, USA

Full-time

Piper Companies is actively seeking a Senior CQV (Commissioning, Qualification, and Validation) Engineer to join our team. The ideal candidate will have 7-10 years of CQV experience with large-scale process equipment, including upstream, downstream, and CIP (Clean-In-Place) systems. This role is critical to ensuring the successful commissioning and validation of our biopharmaceutical manufacturing processes. This is a Monday - Friday, traditional hours role located in the greater Raleigh, NC are

Manufacturing Engineer

Pentair

Backus, Minnesota, USA

Full-time

Job Description: At Pentair, you will work alongside passionate problem-solvers who are committed to the future of our planet. We put our purpose into practice, helping people sustainably move, improve, and enjoy water, life's most essential resource. From our residential and commercial water solutions to industrial water management and everything in between, our 9,750 global employees serve customers in more than 150 countries, working to help improve lives and the environment around the world