1 - 20 of 64 Jobs

OQ Compliance

ElevaIT Solutions

Binghamton, New York, USA

Contract

Domain: Energy Title: OQ Compliance Duration: Through 01/2025 W2 Location: Onsite either Rochester NY or Binghamton NY Hours: Ideally 7:30-4:00PM EST Rate: 37.48 per hour W2 Track and report OQ compliance: Coordinate, track and report the schedule of employees to complete OQ tests Schedule Prometrics for requalification of Written Exams Coordinate OQ training schedule with HR Training and Gas Operations Track and report the verification that contractors are qualified to company Plan Maintains OQ

ECQ Engineer

Zachary Piper Solutions, LLC

Hopewell Township, New Jersey, USA

Full-time

Piper Companies is looking for an ECQ Engineer for a Pharmaceutical manufacturer in the Titusville, NJ. Responsibilities for the ECQ Engineer include: Experience Pharmaceutical Laboratory Operations Must be familiar and have experience with laboratory instrument selection, installation (IQ/OQ) and qualification (PQ) Experience supporting laboratory investigations Hands-on experience with laboratory GMP instruments Commissioning & Decommissioning of Lab Equipment Qualifications for the ECQ

Equipment Engineer

Zachary Piper Solutions, LLC

Baltimore, Maryland, USA

Full-time

Piper Companies is currently seeking a Senior Manufacturing Engineer. The Manufacturing Engineer will support contract medical device and component manufacturing. This position will be on-site. Responsibilities of the Manufacturing Engineer: Responsible for ownership of manufacturing activities related to both production for external clients and establishment of internal processes Supports design reviews, qualifying accuracy and integrity of produced parts--able to 'print read' Estimates m

ECQ Engineer

Zachary Piper Solutions, LLC

Hopewell Township, New Jersey, USA

Full-time

Piper Companies is currently seeking a ECQ Engineer for an opportunity in Titusville, New Jersey (NJ), to join a global pharmaceutical company. Responsibilities of the ECQ Engineer 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 Commission new laboratory equipment and decommissio

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

Analytical Validation Engineer

Zachary Piper Solutions, LLC

Raritan, 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 Raritan, 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, including

Validation Specialist in Summit, NJ (Local Only)

Synkriom

Summit, New Jersey, USA

Full-time

Role : Specialist, MSEO Manufacturing Systems ValidationLocation : Summit, NJ (Local only )ONSITE - HYBRID - REMOTE: 50% OnsiteLOCATION: 556 Morris Avenue, Summit, NJ 07901 JOB DETAILS: Minimum 50% onsite required every week(Candidate is supposed to align the onsite days with manager and be available onsite when manager requests) Bachelor's degree required in Life Science or Engineering Duration: 6 months(Possibility of extension for the right candidate) The Specialist works cross-functionall

Validation - Specialist, MSEO Manufacturing Systems Validation

Sunrise Systems, Inc.

Summit, New Jersey, USA

Contract

Job Description: Minimum 50% onsite required every week (Candidate is supposed to align the onsite days with manager and be available onsite when manager requests) The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing. This role is primarily an individual contributor but will routinely support project and production works. The Specialist will partner

Staff Manufacturing Engineer

Jobot

Santa Clara, California, USA

Full-time

Staff Manufacturing Engineer needed for Medical company which is focused on developing and commercializing products intended to transform the treatment of vascular disease This Jobot Job is hosted by: Joseph Calabrese Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $130,000 - $155,000 per year A bit about us: We are a well-established medical device company which is focused on developing and commercializing products intended to transform th

Instrument Validation Specialist - Contractor

EY

West Point, Pennsylvania, USA

Contract

Contract Description We currently have a contract opportunity for an Instrument Validation Specialist - Contractor to assist our client with the validation of their laboratory equipment through a hybrid work schedule. Develop, review, and execute validation protocols for laboratory instruments, including qualification activities such as IQ (Installation Qualification), OQ(Operational Qualification), and PQ (Performance Qualification) within the manufacturing division of the client. Monitor and a

Validation Engineer

Jobot

Henderson, Minnesota, USA

Full-time

Come be apart of our great culture! This Jobot Job is hosted by: Kevin Saxby Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $90,000 - $118,000 per year A bit about us: A leading global manufacturer, marketer and distributor of animal health products and veterinary pharmaceuticals Why join us? We have a caring, family culture which ensures employees feel supported in their personal and professional lives. We work through challenges togeth

Process Engineer II

KARL STORZ Endoscopy - America

Charlton, Massachusetts, USA

Full-time

Role Overview The purpose of this position is to provide hands-on engineering support to the operations to produce high quality medical devices. This position will lead continuous improvement activities, implement and document manufacturing processes, devise engineering solutions to manufacturing problems and to help introduce new products and processes. Key Responsibilities Work with Global Research & Development (GRD), Project Engineering, Operations, Quality, Maintenance and other core functi

Process Engineer II

KARL STORZ Endoscopy - America

Charlton, Massachusetts, USA

Full-time

Role Overview The purpose of this position is to provide hands-on engineering support to the operations to produce high quality medical devices. This position will lead continuous improvement activities, implement and document manufacturing processes, devise engineering solutions to manufacturing problems and to help introduce new products and processes. Key Responsibilities Work with Global Research & Development (GRD), Project Engineering, Operations, Quality, Maintenance and other core functi

Engineer II, Validation

Thermo Fisher Scientific

Florence, South Carolina, USA

Full-time

Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protectin

Validation Engineer

Jobot

Ansonia, Connecticut, USA

Full-time

Validation Engineer - (Responsive) This Jobot Job is hosted by: David Six Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $80,000 - $90,000 per year A bit about us: Are you a dynamic, detail-oriented engineer with a passion for problem-solving and a desire to make a significant impact in the manufacturing industry? We are seeking a Permanent Validation Engineer to join our client's team. You will be responsible for validating and qualifying

Associate Metrologist

Thermo Fisher Scientific

Middleton, Wisconsin, USA

Full-time

Job Description At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing

Manufacturing Quality Engineer II - Abiomed

Johnson & Johnson

Danvers, Massachusetts, USA

Full-time

Description At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for huma

Engineer III, Validation

Thermo Fisher Scientific

Plainville, Massachusetts, USA

Full-time

Job Description Position summary Validation engineers lead, inspect, calibrate, test and modify the instrumentation, equipment, mechanics and procedures used in manufacturing. A critical aspect of their job is documenting this process so there is evidence that systems are operating safely and efficiently. How will you make an impact? As part of our team, what you do contributes directly to our mission; enabling our customers to make the world healthier, cleaner and safer. Key Responsibiliti

Sr Measurement Process Development Engineer

Johnson & Johnson

Danvers, Massachusetts, USA

Full-time

Description Johnson & Johnson is recruiting a Sr Measurement Process Development (Metrology) Engineer, to be located at New Brunswick, NJ. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across

Engineer II, Internal Instrument Service

Thermo Fisher Scientific

Austin, Texas, USA

Full-time

Job Description Job Description When you are part of the team at Thermo Fisher Scientific, you'll do important work. And you'll have the opportunity for continual growth and learning in a culture that empowers your development. With annual revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make meaningful contributions to the world. Location/Division Specific Information Work Location: Austin, TX (on-site