Manufacturing Engineer - PD - North Puerto Rico Region

Reposted 2 Months Ago
Be an Early Applicant
Dorado, PRI
In-Office
Entry level
Food • Professional Services • Business Intelligence • Pharmaceutical
The Role
Supports process development in manufacturing by optimizing equipment, troubleshooting issues, ensuring product quality, and participating in continuous improvement projects.
Summary Generated by Built In

Engineer, Manufacturing Provides support to the Process Development team to efficiently facilitate operations within the production area, optimizing processes, and ensuring production goals are met. Monitors performance of equipment, machines and tools and

corrects equipment problems or process parameters that produce non-conforming products, low yields or product quality issues.

 Key Responsibilities:

·       Support manufacturing basic daily activities and/or continuous improvement projects such as equipment troubleshooting, root cause analysis and non-conforming product evaluation.

·       Completes technical activities leading to new or improved products or process, for current programs, next generation programs and to meet strategic goals and objectives of the company. Prepares reports, publishes, and makes presentations to communicate findings.

·       Analyzes and solves problems from basic engineering principles, theories and concepts through to a wide range of problems which require novel and new innovative approaches.

·       Cultivates internal and external networks of resources to complete tasks. Participate in project teams to complete goals and objectives for the projects.

·       Interacts cross functionally and with internal and external customers.

·       Support process and/or equipment validation activities (IQ, OQ, PQ); process performance qualification activities and develop Master validation plans for new processes or products.

·       Work with the Process Development team to efficiently qualify new processes; assist with statistical sampling plans, and other development procedures.

·       Generate manufacturing instructions for new processes being developed.

 


Requirements

Quality System Requirement:

In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all other documented quality processes

and procedures.

·       Assured that appropriate resources (personnel, tools, etc.) are maintained to assure Quality System compliance and adherence to the SITE Quality Policy.
·       Establishes and promotes a work environment that supports the Quality Policy and Quality System.


Skills Required

  • Support manufacturing daily activities and continuous improvement projects
  • Complete technical activities for product or process improvements
  • Analyze and solve engineering problems
  • Assist with process validation activities
  • Generate manufacturing instructions for new processes
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The Company
11 Employees

What We Do

ISPV Inc. is a Life Science company that leads Productivity & Validation projects for the Pharmaceutical and Food industries.

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