Job Posting for Manufacturing Coordinator at Zortech Solutions
Job Title: Manufacturing Coordinator
Location: Norfolk, VA, 23508
Duration: 3 Months
Schedule: 3, 10 hour days and 2 shorter days
Tuesday, Wednesday and Thursday - 3 10 hour days
Monday and Friday - Shorter Days
Job Summary
This position is responsible for the production of quality medical devices. This position supports Production and Logistics by performing and documenting daily manufacturing operations that involves operation of various process equipment and other tasks in support of the production schedule. This person will comply with safety requirements, current Good Manufacturing Practices and Standard Operating Procedures and coordinate the cleaning, assembly and preparation of equipment and final products according to written instructions. The manufacturing specialist will further support P&L by maintaining raw material stock, cleanroom readiness and final product inventory.
Principal Duties And Responsibilities
With oversight from supervisor and mentorship by senior peers:
Responsible for performing the daily manufacturing steps required to produce Embody's medical devices.
Maintain the integrity of ISO class 7 & 8 Cleanrooms by performing proper gowning, entry and cleaning procedures.
Perform in-process quality checks on sub-assemblies and finished products.
Responsible for inspection, labeling, packaging and shipping of final products.
Perform daily equipment checks and preventive maintenance per established procedures.
Utilize small hand tools, calibrated instruments, measurement equipment, and test fixtures.
Perform cleaning of equipment, labware and manufacturing areas in accordance with SOPs
Responsible for maintaining raw material inventory and performing incoming inspections.
Assist in ongoing process improvement and subsequent validation activities.
Participate in line and production planning meetings as needed.
Work with engineers, technicians and management to resolve line issues and suggest improvements.
Maintain accurate records and documentation related to quality, work in progress, test results and special projects.
May interact with external customer contacts including participating in tours for visitors including VIPs
and may be questioned and/or observed during audits.
Adhere to general safety rules, manufacturing procedures, company policies and procedures, ISO and FDA regulations.
This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act.
Expected Areas Of Competence (i.e., Knowledge, Skills And Abilities)
Experience working with laboratory chemicals and equipment including pipettes, balances, sealers and vacuum ovens.
Ability to follow SOP's, work instructions, and maintain daily records in a timely and reliable fashion
Must be a highly organized individual who works independently with minimum supervision in a fast-paced environment.
Must have a high level of hand-eye coordination
Excellent communication skills both written and verbal
Comfortable working under an ISO 13485 or 9001 Quality Management System
Education/Experience Requirements
High school diploma or equivalent
Minimum (2) years working in a manufacturing environment, preferably within the medical device or tissue banking industry
Minimum (2) years working with an electronic manufacturing and inventory system such as Fishbowl or SAP
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