Medical Device Packaging Engineer

Required Qualifications: Bachelor's degree in computer science, Information Systems, or related field; advanced degree preferred. 5+ years of experience in data architecture, data engineering, or a related role. Proficiency in cloud platforms such as AWS and Azure, with hands-on experience deploying and managing data solutions in these environments. Strong...

Job Title - Data Architect with Medical DevicesLocation – Raritan, NJ (Onsite)Duration: - Long Term Job Description: -As a Data Architect, you will play a crucial role in designing and implementing scalable, high-performance data solutions to support our business objectives. You will be responsible for defining the overall data architecture, including data...

Job Title - Data Architect with Medical DevicesLocation – Raritan, NJ (Onsite)Duration: - Long Term Job Description: -As a Data Architect, you will play a crucial role in designing and implementing scalable, high-performance data solutions to support our business objectives. You will be responsible for defining the overall data architecture, including data...

Experience in Life science domain specially in Medical Devices area In-depth understanding of medical devices product pricing process, discounts, contracting processes, etc. Analytical skill to analyze product pricing components from existing contracts, static reports, dashboards, etc. and evaluate insights Ability to collaborate with sales, finance,...

Job Title: Senior Regulatory Affairs Specialist Employment Type: Full Time or 1 year Contract with potential extension Location: Raritan, NJ (Selected candidate should be able to work 3 days every week at Raritan, NJ office). We are looking for Candidates with Proven experience in regulatory affairs in Class III medical devices and PMA submissions in this...

Job Title: Senior Regulatory Affairs SpecialistEmployment Type: Full Time or 1 year Contract with potential extensionLocation: Raritan, NJ (Selected candidate should be able to work 3 days every week at Raritan, NJ office).We are looking for Candidates with Proven experience in regulatory affairs in Class III medical devices and PMA submissions in this...

Senior Quality Engineer, Medical DevicesOur client has engaged GForce to identify a Senior Quality Engineer with in-depth understanding of medical device quality system requirements, with specific experience in applying the following: Medical Device product risk management, Medical devices process validation, and Medical Device Design...

Senior Quality Engineer, Medical DevicesOur client has engaged GForce to identify a Senior Quality Engineer with in-depth understanding of medical device quality system requirements, with specific experience in applying the following: Medical Device product risk management, Medical devices process validation, and Medical Device Design...

Senior Quality Engineer, Medical DevicesOur client has engaged GForce to identify a Senior Quality Engineer with in-depth understanding of medical device quality system requirements, with specific experience in applying the following: Medical Device product risk management, Medical devices process validation, and Medical Device Design...

Senior Quality Engineer, Medical Devices Our client has engaged GForce to identify a Senior Quality Engineer with in-depth understanding of medical device quality system requirements, with specific experience in applying the following: Medical Device product risk management, Medical devices process validation, and Medical Device Design Control. ...

Ethicon, a member of Johnson & Johnson's Family of Companies, is currently recruiting for a Principal Engineer in the New Product Development group within Wound Closure and Healing-Biosurgery R&D. The position is located in Raritan, New Jersey. The Ethicon business offers a broad range of products, platforms and technologies including sutures, topical...

Description: Documentation of development studies (analysis, author protocols and reports with limited supervision) Perform studies supporting New Product Development activities Coordinate and submit testing of samples Support lab experiments Hands on preparation of samples for development studies through process Coordinate testing of samples Manage...

Seeking 1 New Product Development Engineer Onsite in Raritan NY Description: NPD Contract Engineer: Will be a technical writing heavy engineering role. • Documentation of development studies (analysis, author protocols and reports with limited supervision) • Perform studies supporting New Product Development activities • Coordinate and submit testing...

**_Validation & Engineering Group, Inc. _**(V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated...

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual...

Job DescriptionEthicon Inc, is recruiting for a Wound Closure & Healing (WC&H) or Biosurgery Global Technical Operations Engineering Co-Op, located in Raritan, NJ.Ethicon, Inc. is a member of the Johnson & Johnson Family of Companies. At Ethicon Inc, we support products across the WC&H and Biosurgery platforms, as well as across the Endo-Mechanical, Energy,...

Senior Specialist - Package Implementation Job Req Id: 1272044 About Us: Job Title: Senior Specialist - Package Implementation Work Location: Raritan, NJ Job Description: Evaluate requirements and transform into abstract business models, as well as into logical and technical views. Provide in-depth technical expertise and configure the Blue Yonder WMS...

Description: • Support the Site Instrument Officer during execution to the site calibration procedure. • Coordinate the activities associated with the non-conformance process by supporting engineers and gauge owners. • Responsible for conducting multiple reviews for conformance. • Perform database queries regarding usage of gauges or measurement...

At Labcorp we have a passion in helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career stepLabCorp seeking a Service Representative/Courier to join our...

Description: * Support the Site Instrument Officer during execution to the site calibration procedure * Coordinate the activities associated with the non-conformance process by supporting engineers and gauge owners * Responsible for conducting multiple reviews for conformance * Perform database queries regarding usage of gauges or measurement devices that...