Job Description
Needs to set on site.
Job Duties and Responsibilities:
Optimize current solution manufacturing processes to improve quality, reduce costs, improve
regulatory compliance and resolve documentation issues.
Oversee production of solutions, review documentation, work with team and facilities to
streamline processes.
Review and update production documentation, work with Quality and SMEs to align
instructions to actions.
Apply known/typical process metrics and KPIs to offer areas of improvement, characterize
process improvements.
Work with planners, buyers, and production supervisors to maximize output.
Perform root-cause investigations on systems and components to correct problems, improve
product quality and reliability.
This position will Interface with Manufacturing, R&D, Compliance, Quality, Purchasing,
Manufacturing, and Product Management groups.
Utilize Design for Manufacturability and Design for Assembly concepts to optimize
manufacturing processes, ease of service, and identify cost saving opportunities.
Qualifications:
Requires a bachelor's or master's degree in chemistry, Chemical Engineering, Pharmaceutical
Sciences, or related field
Strong knowledge of formulation science, chemical processes, and process engineering
principles
Adept at working in fast paced setting, acting with urgency
Minimum of 3 Years of experience in manufacturing within ISO 13485 environment
Familiar with Bill of Materials (BOM)
Excellent communication and interpersonal skills
Excellent problem-solving skills and attention to detail
Ability to work independently and manage multiple projects simultaneously
Ability to communicate and work well in cross-functional team environments
Knowledge and experience in Analytical Chemistry is a plus
Job Tags
Hourly pay,
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