Process engineer iii - united states, san diego
adecco is currently assisting an american supplier of scientific instrumentation, reagents and consumables, and software services in recruiting for a process engineer iii in san diego, ca! this is a 9-month assignement with a pay rate of $44-55.00/hr. doe
the process engineer iii/manager will support the technical operations team in the in vitro medical diagnostics device manufacturing setting. the ideal candidate will lead a team of engineers working on process improvement projects with the goal of increasing product yield, and will design experiments to support investigations of non-conformances, process improvement, product transfers and problem-solving. the candidate will lead efforts to improve manufacturing workflows, evaluate critical attributes of key manufacturing processes, perform root cause analysis of failure modes, define specifications as well as developing implementation strategies. additional duties include defining project scope, estimating budget and timelines, presentations in multi-functional setting.
key responsibilities:
• assess existing manufacturing processes and workflows
• design and complete process engineering experiments (including doe) related to process and efficiency improvement
• develop process specifications for raw materials and manufacturing processes
• lead 1-2 process engineers
• develop relevant data tracking and trending structures to monitor processes and discover other areas for improvement
• apply process simulation software to test and find the most appropriate production strategies
• solve technical issues through a structured rccm process
• perform statistical analyses on collected datasets and employ statistics in experimental design
• design and conduct controlled experiments to address yield and quality issues and drive implementation of solutions in a production environment
• write and review manufacturing documents, standard operating procedures, technical reports, work instructions
• collaborate multi-functionally with r&d, manufacturing and quality to develop processes for new products and improve processes of existing products
• support the transfer technology, processes, products from development into a regulated manufacturing environment
• generate, analyze, and maintain critical data in a highly organized manner
• present technical data in multi-functional meetings
• prepare estimates and budgets
• additional duties as assigned
minimum requirements/qualifications:
• b.s with 8+ years or m.s. with 8+ years of experience in chemical, industrial, electrical or mechanical engineering or related study
• preferred majors: chemical engineering, electrical engineering, software engineering, mechanical engineering, biomedical
engineering or other related major
• hands-on experience in quality and business process engineering
• experience in large scale manufacturing and design
• material properties, microfluidics, lyophilization process, ultrasonic welding
• experience in statistical software and databases (e.g., jmp)
• experience in project management, spc, technical process safety aspects, engineering design or modelling software preferred
• ability to present complex data using effective communication methods and styles, including good technical report writing skills
• experience in lateral flow technology is preferred
• experience working in a regulated environment (fda/gmp/iso) is preferred
• experience in the ivd medical device and/or biotechnology industry is preferred
• excellent analytical, statistical, and mathematical skills
• strong written and oral communication skills
• excellent time management and project management skills
• experience in leading a team
• outstanding attention to detail and organizational skills.
• excellent interpersonal skills with the ability to interact with all levels of the organization both orally and in writing; consistent track record of working multi-functionally
• knowledge of process engineering software systems
• understands good laboratory practices and good manufacturing practices
• ability to multitask and complete projects in a fast-paced environment
• must be self-motivated, meticulous, organized, have ability to collaborate well with a team, a critical thinker, and a problem solver
why work for adecco?
*this client requires proof of covid-19 at time of hire.
important: this job is posted by adecco’s medical and science division, not your local adecco branch office.
click on apply now for instant consideration for this role!
equal opportunity employer/veterans/disabled
the company will consider qualified applicants with arrest and conviction records
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