mirus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the involved project management.
Job Description
Develops and reviews documentation and procedures and provides automation systems testing and validation in support of Process Development and/or Manufacturing Process Engineering.
Support process and/or equipment validation activities (IQ, OQ, PQ); process performance qualification activities and develop Master validation plans for new processes or products.
Responsible for reviewing and developing process validation protocols and reports. Support other functional areas during the validation activities.
Work with the Process Development team to efficiently qualify new processes; assist on statistical sampling plans, and other development procedures.
Design and develop in-process and receiving quality systems for new processes and components
Generate equipment documentation, such as equipment entries, evaluations, PM and calibration procedures, as required.
Define gages, tools and equipment for the test methods developed.
Generate manufacturing instructions for new processes being developed
Work cross-functionally with other departments to accomplish PD tasks.
Be able to manage process development projects from conception to implementation, ensuring project deadlines and objectives are met.
Familiarity with a variety of technologies and equipment used in the industry to carry out manufacturing processes, such as Laser Welding, Stringing, Staking, Heat Bonding, Injection Molding, Vision Systems, general experience with automated equipment (PLC/Servos/Pneumatics/ Sensors), etc.
Experience with design of experiments (DOE) to characterize and optimize processes, as well as analyze the resulting data to draw meaningful conclusions.
Ability to identify areas of improvement in processes and develop strategies to optimize the efficiency, quality and/or yield of those processes that are being developed.
Understand and evaluate the risks associated with these manufacturing processes and develop ideas/solutions to minimize these risks. Also work with PFMEA methodology for risk analysis documentation.
Ability to collaborate with other engineers, scientists, and production personnel to achieve manufacturing process development objectives and solve problems effectively.
Education
Engineering Bachelor Degree
Preferred Qualifications
Manufacturing background.
Medical Device industry experience.
Good technical writing skills.
Ability to read electrical prints and schematics.
2-8 years of related experience
Proven record of working closely and successfully with manufacturing and process development engineers
Basic understanding of medical device documentation requirements
Great attitude and strong desire to learn new skills
This Company is an equal employment opportunity employer. We adhere to a policy of making employment decisions without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age or disability. We assure you that your opportunity for employment with this Company depends solely on your qualifications.
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