
Industrial Process Optimizer
hace 19 horas
About Us
EQVAL Group, Inc. is a leading provider of services to the manufacturing industry, specializing in Medical Devices, Pharmaceuticals, and Biotechnologies. Our team of professionals works closely with customers to deliver high-quality services.
The Role
We are seeking a highly motivated Manufacturing Engineer to join our team. The successful candidate will have experience in Medical Device or Pharmaceutical industries and will be responsible for executing validation (IQ, OQ, PQ) and optimizing manufacturing processes.
Key Responsibilities
Lead and execute validation activities for equipment and process changes, including IQ, OQ, PQ, and associated documentation.
Design and optimize manufacturing processes, ensuring efficient production layouts, material handling, and tool fabrication.
Troubleshoot and improve production equipment and processes to enhance operational efficiency and product quality.
Collaborate with cross-functional teams to support investigations (NCRs, Complaints) and implement corrective actions.
Requirements
Bachelor's degree in an Engineering field.
Proven experience in developing and executing validation documentation, including Validation Plans, URS, FRS, IQ, OQ, PQ, and related reports.
Strong knowledge and experience in cGMP for Medical Device manufacturing environments.
Familiarity with statistical analysis (GR&R) and data management, including tools like Minitab.
1-3 years of experience in areas such as investigations (NCRs, Complaints, CAPA), Lean Manufacturing, and Six Sigma tools.
What We Offer
Competitive salary and benefits package.
Opportunities for professional growth and development.
Collaborative and dynamic work environment.
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