Sr. Cost Accountant

Medical Device R&D Build Assembler

Pay $28-32 6 month+ assignment. Onsite in Campbell, CA. Must have UV cure adhesive bonding experience and prior experience with medical devices built in a clean room. Experience supporting Engineering/R&D. Robotics/med device experience with cleanroom device assembly of fluidic, catheter adhesive bonding, and mechatronic assemblies.

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): Health insurance, Health savings account, Dental insurance, Vision insurance, Flexible spending accounts, Life insurance, Retirement plan.