Highlights
Perform basic calculations and data entry Ability to assemble, disassemble, and clean process equipment Process and assemble components in accordance with documented specifications and procedures Perform mechanical, optical, and system assembly, and conduct thorough testing Perform packaging and labeling operations Perform in-process inspection of assemblies and finished products in accordance with specification criteria Perform treatment card programming Organize and clean the work areas Ability to perform validation and qualification activities (IQ/OQ/PQ/PV) 2 to 4 years of hands-on experience in medical devices, technical assembly, and both electromechanical and optomechanical environments. Perform all activities with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality management system (QMS) medical device good manufacturing practices (GMP) requirements.
Numbers & Facts
| Location | Burlington, MA |
| Industry | Staffing/Employment Agencies |
| Salary | $25 Per Hour |
| Company Size | 5,000 to 9,999 employees |
| Year Founded | 2002 |
| Website | http://www.talentburst.com/ |
Description
Title - Manufacturing Technician 2
Location - Burlington MA
Duration - 6 Months (Possibility of extension)
Vertical Description:
You will be responsible for the following:
Perform kitting operations (measure out components or raw materials)
Ability to perform activities under a microscope
Prepare components and build device assemblies
Perform packaging and labeling operations
Proficiency with hand tools, precision measurement instruments, and diagnostic equipment
Perform visual inspections
Perform documentation and data input into materials requirement planning (MRP), Batch Records (BRs), and Device History Record (DHR)
Perform all activities with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality management system (QMS) medical device good manufacturing practices (GMP) requirements.
Additional tasks as required
Requirements:
Follow, execute, and adhere to documentation in accordance with cGMP, QMS, and GDP requirements: protocols, specifications, work instructions (WIs), standard operating procedures (SOPs), batch records (BRs), device history records (DHRs), and engineering batches. Perform basic calculations and data entry Ability to assemble, disassemble, and clean process equipment Process and assemble components in accordance with documented specifications and procedures Perform mechanical, optical, and system assembly, and conduct thorough testing Perform packaging and labeling operations Perform in-process inspection of assemblies and finished products in accordance with specification criteria Perform treatment card programming Organize and clean the work areas Ability to perform validation and qualification activities (IQ/OQ/PQ/PV) 2 to 4 years of hands-on experience in medical devices, technical assembly, and both electromechanical and optomechanical environments
#TBL1
Location - Burlington MA
Duration - 6 Months (Possibility of extension)
Vertical Description:
You will be responsible for the following:
Perform kitting operations (measure out components or raw materials)
Ability to perform activities under a microscope
Prepare components and build device assemblies
Perform packaging and labeling operations
Proficiency with hand tools, precision measurement instruments, and diagnostic equipment
Perform visual inspections
Perform documentation and data input into materials requirement planning (MRP), Batch Records (BRs), and Device History Record (DHR)
Perform all activities with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality management system (QMS) medical device good manufacturing practices (GMP) requirements.
Additional tasks as required
Requirements:
Follow, execute, and adhere to documentation in accordance with cGMP, QMS, and GDP requirements: protocols, specifications, work instructions (WIs), standard operating procedures (SOPs), batch records (BRs), device history records (DHRs), and engineering batches. Perform basic calculations and data entry Ability to assemble, disassemble, and clean process equipment Process and assemble components in accordance with documented specifications and procedures Perform mechanical, optical, and system assembly, and conduct thorough testing Perform packaging and labeling operations Perform in-process inspection of assemblies and finished products in accordance with specification criteria Perform treatment card programming Organize and clean the work areas Ability to perform validation and qualification activities (IQ/OQ/PQ/PV) 2 to 4 years of hands-on experience in medical devices, technical assembly, and both electromechanical and optomechanical environments
#TBL1
About Company
For over 20 years, TalentBurst Inc. has been an award-winning provider of cutting-edge Workforce Management Solutions. With a strong commitment to staying ahead in the tech landscape, we pioneer innovative approaches to talent acquisition. Our expertise spans Life Sciences, and Healthcare Staffing, Banking, Financial, IT, and Engineering, as well as Global Employer of Record (EOR), Agent of Record (AOR), State, Local Government and Education (SLED), and IC validation/compliance services. Additionally, our division, TalentProcure, leads the industry with offerings such as High Hazard Payroll, Managed Services, and Vendor on Premise (VOP) solutions.
Due to our prioritization of excellent standards, we are Joint Commission Certified and are a certified Minority Business Enterprise (MBE) in the USA and Canada. Supporting over 130 Fortune 500 companies globally, we excel in navigating the landscape of talent acquisition. In a world of constant change, we embrace developing people-centric solutions that address the unique demands of our clients. Stay connected by visiting our website and following us on social media!