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Process Engineer (Indianapolis)

Brooksource, Indianapolis, IN, United States


Process Engineer – DAP Manufacturing
Location:

Indianapolis, IN (Onsite)
Client:

Pharmaceutical Manufacturing
Employment Type:

Full-Time
Overview
Brooksource is hiring a

Process Engineer

to join the Device Assembly & Packaging manufacturing team. You’ll support process optimization, equipment reliability, troubleshooting, and documentation activities within a highly regulated GMP environment. This role offers strong growth potential with opportunities to learn from senior engineers and expand into project leadership.

Key Responsibilities
Safety & Quality Support
Follow all HSE guidelines and participate in safety activities.
Use proper PPE and promote safe work habits on the manufacturing floor.
Process & Equipment Support
Learn process equipment and become a technical resource for your assigned area.
Assist with troubleshooting equipment issues alongside senior engineers.
Maintain and update process flow documentation and equipment procedures.
Participate in data monitoring and basic performance analysis to identify improvement opportunities.
Documentation & Compliance
Support deviation investigations and help implement corrective actions.
Assist with change control documentation, work orders, and qualification activities (IQ/OQ/PQ).
Ensure documentation and practices align with GMP requirements.
Cross‑Functional Collaboration
Partner closely with Operations, Maintenance, and Quality teams.
Participate in process team meetings and contribute to discussions around downtime reduction, process efficiency, and equipment reliability.
Continuous Improvement
Help identify small improvement projects or upgrades within the process area.
Support the rollout of new procedures, training materials, or equipment enhancements.

Required Skills
0-5 years of engineering experience (process, mechanical, chemical, or related).
Strong communication and teamwork skills.
Ability to learn complex manufacturing processes and equipment.
Basic experience with data analysis tools (Excel, Power BI, etc.).
Ability to work safely and follow GMP procedures.
Preferred Skills
Experience in pharmaceutical, medical device, or other regulated manufacturing environments.
Exposure to troubleshooting, process optimization, or equipment reliability.
Experience supporting small projects or continuous improvement initiatives.

Education
Bachelor’s degree in Engineering or equivalent experience.

Additional Details
Standard 8‑hour days with some after-hours/weekend support as needed.
Occasional travel for training or project work.