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Manufacturing Engineer II; 3rd Shift

Job in Windsor, Weld County, Colorado, 80550, USA
Listing for: Tolmar
Full Time position
Listed on 2026-07-01
Job specializations:
  • Pharmaceutical
    Quality Engineering, Validation Engineer
Job Description & How to Apply Below
Position: Manufacturing Engineer II (3rd Shift)

Manufacturing Engineer II

Job Category:
Production

Location:

Windsor, CO 80550, USA

Description

Available

Shifts:

A

Shift: Sunday
- Wednesday, 5:00 am - 5:30 pm, every other Wednesday off

B

Shift: Sunday
- Wednesday, 5:00 pm - 5:30 am, every other Wednesday off

C

Shift: Wednesday
- Saturday, 5:00 am - 5:30 pm, every other Wednesday off

D

Shift: Wednesday
- Saturday, 5:00 pm - 5:30 am, every other Wednesday off

Purpose and Scope:

This role provides critical on-floor technical leadership for aseptic manufacturing operations, ensuring robust, compliant, and efficient processes. The engineer serves as a primary technical resource during sterile operations, monitoring critical process parameters, identifying and mitigating risks in real time, and driving a culture of right-first-time performance. The position also leads technical investigations, authors high-quality reports, and partners with Manufacturing, Quality, Engineering, and MS&T to implement sustainable process and quality improvements.

Essential Duties & Responsibilities:

On-Floor Technical Support:

  • Serve as the primary technical engineering resource on the manufacturing floor during aseptic bulking, cleaning, milling, and filling activities.
  • Actively monitor and verify critical operational steps, environmental controls, and in-process parameters to ensure compliance with cGMP and aseptic best practices.
  • Provide real-time decision support for process deviations, equipment malfunctions, and unexpected process conditions.
  • Support manufacturing execution by ensuring processes consistently run within defined control limits and established batch record requirements.

Technical Investigations & Documentation:

  • Lead or support complex root cause investigations, deviations, CAPAs, and change controls; write clear, technically sound, inspection-ready reports.
  • Use appropriate and approved tools to gather data and drive scientifically justified conclusions.
  • Develop, revise, and optimize SOPs, Wis, batch records, and control documentation to strengthen process robustness and clarity.

Process Monitoring, Validation & Improvement:

  • Conduct and support on-floor studies and process verifications.
  • Support cleaning validation, process validation, and ongoing process capability monitoring.
  • Partner with Quality, Validation, and Engineering to ensure process changes and enhancements are technically justified and compliant.
  • Lead and contribute to continuous improvement initiatives that improve yield, reduce variability, strengthen aseptic behaviors, and enhance equipment reliability.
  • Assist in evaluating and implementing new technologies, process automation, analytics, and equipment enhancements to support commercial operation.

Training & Cross-Functional Support:

  • Provide hands-on training, technical coaching, and aseptic technique reinforcement for operators and supervisors.
  • Support onboarding of new operators and engineers with a focus on sterile technique, process understanding, and technical problem-solving.
  • Act as a subject matter resource for internal audits, regulatory inspections, and cross-functional technical discussions.

Other Duties:

  • Participate in hazardous waste, chemical handling, and spill response training; ensure compliance with all safety requirements.
  • Perform additional responsibilities as assigned.

Knowledge, Skills & Abilities:

  • Strong knowledge of aseptic processing, sterile technique requirements, and pharmaceutical manufacturing systems.
  • Demonstrated ability to monitor and troubleshoot aseptic operations and process performance issues.
  • Strong analytical and problem-solving skills, including use of statistical tools and experimental design.
  • Excellent technical writing skills; able to produce clear, concise, and scientifically sound investigations and reports.
  • Effective communicator with the ability to collaborate across manufacturing, quality, engineering, and development teams.
  • High attention to detail, strong sense of personal accountability, and ability to excel in a fast-paced environment with shifting priorities.
  • Ability to work independently with minimal oversight and make sound technical decisions in real time.
  • Ability to analyze complex development problems and provide…
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