Engineering Technician

Placement within the range will be based on qualifications, experience, internal equity, and demonstrated competencies.

• Technical degree, two-year associate degree, or equivalent industry-related experience.
• Basic computer proficiency, including Microsoft Word and Excel, with the ability to learn additional software applications.
• Professional communication and interpersonal skills.
• Ability to maintain positive working relationships with coworkers, supervisors, and vendors.
• Ability to work on-site on a regular basis.

• →Assist in the execution and reporting of engineering protocols and formal studies.
• →Support the evaluation, installation, and qualification of new instrumentation and equipment.
• →Evaluate, select, and order parts and components for engineering batches.
• →Perform hands-on setup and preparation of sterile pharmaceutical products and components.
• →Support validation activities, including equipment setup and execution of validation studies.
• →Perform Pharmaceutical Operator II duties as needed to support operations.
• →Participate in product and process development initiatives.
• →Maintain validation activities in compliance with cGMP requirements.
• →Review operational deviations, change controls, validation protocols, and formal studies, as applicable.
• →Collaborate effectively with Engineering, Operations, Quality, and other departments to support manufacturing objectives.

• Experience in pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
• Working knowledge of cGMP requirements and validation principles.
• Experience supporting manufacturing equipment, engineering projects, or validation activities.
• Familiarity with aseptic processing and sterile manufacturing operations.
• Strong mechanical aptitude and troubleshooting skills.
• Ability to work independently while contributing effectively within a cross-functional team.