Medical Device Manufacturing Operators
Pay $29-$32
6 month+ assignment
Onsite in Campbell, CA
EDUCATION/EXPERIENCE:
• A minimum of 4 years related experience in the medical device industry; or equivalent combination of education and work experience.
• Must be certified on all processes of work area, including certified as expert on all critical processes.
• Training, skill, or experience from a trade is preferred.
• Highly skilled in product manufacturing, testing, and data collection.
• Proficient with GMP, GDP procedures and requirements as they relate to production lines.
• Strong ability to be reliable, work independently or in team setting and take initiative.
• Strong ability to coach and train others on manufacturing processes and procedures.
• High skill on operating manufacturing equipment (i.e. hot boxes, adhesives, soldering, bonding, fuse joining).
• Proficient with testing: tensile, simulated use testing, or tests related to assigned projects.
• Expert hand dexterity and ability to work with small components.
• Strong written and verbal communication skills.
• Strong computer skills, including knowledge of Microsoft office products.
• Strong interpersonal skills, effective interaction with Operations and other departments
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following:
• Operate with high skill, manufacturing and packaging equipment following Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP).
• Uses high level of expertise to work with in-house and contract manufacturers and ensure products are manufactured adhering to product plans, quality, and regulatory requirements.
• Collaborate with manufacturing and engineering personnel to understand product requirements, identify and implement process improvements.
• Perform complex troubleshooting and maintain workspace and equipment clean.
• Adhere to strict safety regulations of the company; maintain a safe, clean and organized work area, and ensure that others are doing the same.
• Perform manufacturing processes using Manufacturing Process Instructions (MPI’s), while assisting in the development of new processes or test procedures through feedback.
• Record and review accuracy of data on lot history records (LHR’s) in collaboration with manufacturing, quality, and R&D.
• Meet regular attendance and punctuality expectations and adhere to all company policies.
• Learn and adhere to safety requirements of manufacturing processes, equipment, handling of chemicals and materials, and apply high skills during complex operations.
• Accurately use computerized operating systems to run and monitor manufacturing equipment.
• May oversee the set up and operation of a variety of equipment to produce materials and assemblies.
• Monitor and record critical process parameters and ensure that proper documentation and GDP guidelines are followed by others.
• Contribute to manufacturing team meetings to ensure communication between members.
• Help build engineering prototypes and products used in preclinical/clinical evaluations.
• Must be a Certified Trainer and teach/train others on manufacturing processes.
• Actively promote and support the Quality Management System, Quality Objectives, and Quality Policy.
• Assure that you and functional subordinates (if applicable) are trained on all applicable procedures and processes according to Good Manufacturing Practices, applicable FDA, and Regulatory requirements.
Benefits (employee contribution):
All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
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