GMP Engineering Technician — Life Sciences

PCI Pharma Services; Rockford (IL); On-site; USD 57,000 - 64,000; Full time

Benefits offered by this job

Paid time off

Health insurance (dental & vision)

Flexible spending account

401(k)

Job summary

PCI Pharma Services is seeking an Engineering Technician in Rockford, IL for the 1st shift. The role focuses on developing technical documents, evaluating equipment, and supporting new production projects. Strong analytical skills and pharma/medical device experience are preferred.

Training across departments will be provided. The position requires a Bachelor's degree or 3–5 years related experience, with adherence to cGMP and GCP policies.

Qualifications

• Bachelor's degree in a related field or 3-5 years of related experience.
• Statistical and mathematical analysis skills.
• Intermediate computer skills and ability to perform more complex tasks.
• Full professional proficiency in English for professional needs.
• Strong reasoning and problem-solving abilities.
• Pharmaceutical or medical device experience.

Responsibilities

• Develop and implement technical documents for the department.
• Research and evaluate machines, processes, and requirements to develop quotes and documentation.
• Support new/modified production projects and implement NPI steps.
• Plan and direct on-site and off-site testing for new machines and equipment.
• Collaborate with cost estimation, production, and maintenance to optimize layouts.
• Provide training to various departments as necessary.
• Operate measurement tools such as rulers and calipers.

Skills

Statistical and advanced mathematical

Intermediate computer skills

Full professional proficiency

High reasoning

Excellent communication

Pharmaceutical or medical device

Education

Bachelor's degree in a related field

3-5 years related experience

Tools

Blue Print Reading

SolidWorks

Job description

PCI Pharma Services is seeking an Engineering Technician in Rockford, IL for the 1st shift. The role focuses on developing technical documents, evaluating equipment, and supporting new production projects. Strong analytical skills and pharma/medical device experience are preferred.

Training across departments will be provided. The position requires a Bachelor's degree or 3–5 years related experience, with adherence to cGMP and GCP policies.