Support engineering projects related to process improvement, equipment qualification, and technology transfer.
Assist in troubleshooting and resolving technical issues in production or quality systems.
Collaborate with cross-functional teams to ensure compliance with regulatory standards (FDA, ISO, GMP).
Prepare and maintain technical documentation, protocols, and reports.
Contribute to continuous improvement initiatives to enhance efficiency and product quality.

\nQualifications:\n\n

Bachelor’s degree in Engineering (Mechanical, Chemical, Electrical, Biomedical, or related field).
2–4 years of experience in an engineering role within a regulated industry (pharmaceutical, biotech, or medical device preferred).
Familiarity with Good Manufacturing Practices (GMP) and regulatory compliance requirements.
Bilingual (English/Spanish)

\nThis 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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