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Contamination Control Engineer Jobs in Colorado (NOW HIRING)

Maintain strict adherence to SOPs, processing standards, cleanroom behavior, and contamination control practices. * Partner cross-functionally with Quality Assurance, Engineering, Supply Chain, and ...

Ability to read and interpret engineering drawings, exploded diagrams, and optical assembly procedures * Familiarity with cleanroom operations, ESD control, and contamination-sensitive environments

Master's Degree in Engineering, Science or related field. PhD is preferred. Compensation: $170,000 ... Demonstrated leadership in enforcing cleanliness, contamination control, and process discipline ...

Master's Degree in Engineering, Science or related field. PhD is preferred. Compensation: $170,000 ... Demonstrated leadership in enforcing cleanliness, contamination control, and process discipline ...

Sr. Electro-Optical Engineer

Longmont, CO · On-site

$170K - $210K/yr

Master's Degree in Engineering, Science or related field. PhD is preferred. Compensation: $170,000 ... Demonstrated leadership in enforcing cleanliness, contamination control, and process discipline ...

Master's Degree in Engineering, Science or related field. PhD is preferred. Compensation: $170,000 ... Demonstrated leadership in enforcing cleanliness, contamination control, and process discipline ...

Ability to read and interpret engineering drawings, exploded diagrams, and optical assembly procedures * Familiarity with cleanroom operations, ESD control, and contamination-sensitive environments

Maintain proper ESD and contamination control practices. Required Qualifications Education * Associate degree or Technical Diploma in: * Semiconductor Manufacturing Technology * Chemical Engineering ...

Maintain proper ESD and contamination control practices. Required Qualifications Education * Associate degree or Technical Diploma in: * Semiconductor Manufacturing Technology * Chemical Engineering ...

Maintain proper ESD and contamination control practices. Required Qualifications Education * Associate degree or Technical Diploma in: * Semiconductor Manufacturing Technology * Chemical Engineering ...

Eng Sr Prin - Optical

Boulder, CO · On-site

$132K - $226K/yr

The Engineering, Science and Analysis (ESA) Strategic Capabilities Unit comprises the technical ... contamination control design. * Proven ability to communicate effectively with technical and ...

Read and interpret engineering drawings, geometric dimensioning and tolerancing (GD&T), schematics ... Cleanliness and contamination control for close-clearance parts, including FOD prevention. * Leak ...

... contamination control standards. Required Qualifications * 5+ years of hands-on operations ... pulling an engineer off their build * Early-stage startup experience, especially as an early ...

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Showing results 1-20

Contamination Control Engineer information

See Colorado salary details

$57.8K

$101.5K

$137.7K

How much do contamination control engineer jobs pay per year?

As of Jun 29, 2026, the average yearly pay for contamination control engineer in Colorado is $101,549.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,800.00 and $113,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Contamination Control Engineer position, and why are they important?

A successful Contamination Control Engineer typically holds a degree in engineering or a related scientific field and possesses expertise in contamination control protocols, cleanroom practices, and environmental monitoring. Familiarity with relevant standards (such as ISO 14644), particulate and microbial detection systems, and certification in contamination control or cleanroom operations are often essential. Excellent attention to detail, problem-solving abilities, and strong communication skills help these engineers implement rigorous protocols and collaborate with multidisciplinary teams. These competencies are crucial to ensuring compliance with regulatory requirements, maintaining product quality, and protecting critical manufacturing or laboratory environments from contamination risks.

What is a Contamination Control Engineer job?

A Contamination Control Engineer is responsible for identifying, mitigating, and preventing contamination in controlled environments such as cleanrooms, manufacturing facilities, and laboratories. They develop and enforce protocols to control particles, microbes, and other contaminants that could impact product quality and safety. Their role often involves collaborating with cross-functional teams to ensure compliance with industry regulations and standards. Additionally, they conduct risk assessments, implement contamination control strategies, and oversee facility cleanliness to maintain optimal working conditions.

What are the typical challenges faced by Contamination Control Engineers in the workplace?

Contamination Control Engineers often encounter the challenge of identifying and mitigating sources of particulate and microbial contamination in highly regulated environments such as pharmaceutical, semiconductor, or aerospace facilities. They must stay updated with evolving industry standards and continuously optimize processes despite changes in production or facility design. Collaboration with quality assurance, production, and facilities teams is routine, requiring strong communication to implement preventive measures effectively. These challenges can be rewarding, as overcoming them is essential to ensuring product quality, regulatory compliance, and a safe working environment.

What are popular job titles related to Contamination Control Engineer jobs in Colorado? For Contamination Control Engineer jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Contamination Control Engineer jobs in Colorado look for? The top searched job categories for Contamination Control Engineer jobs in Colorado are:
Manager Production - Aseptic

Manager Production - Aseptic

Tolmar Inc.

Windsor, CO

Full-time

Posted 25 days ago


Job description

Location: Windsor, CO

Shift: Monday – Friday days with flexibility to support off shifts as required

About Tolmar

Tolmar is an innovative pharmaceutical company focused on developing and manufacturing specialty therapies for patients with unmet medical needs. Headquartered in Northern Colorado, Tolmar combines scientific rigor, operational excellence, and a collaborative culture to make a meaningful impact on patients and communities.

Why Tolmar

At Tolmar, leaders are empowered to make decisions, improve processes, and grow their careers. Our culture is rooted in putting people first, accountability, continuous improvement, and ethical leadership. We foster an environment where transparency, respect, and ownership drive meaningful results.

Why This Role Matters

The Manager Production plays a critical leadership role in ensuring the safe, compliant, and efficient manufacture of sterile pharmaceutical products. This position directly impacts patient safety, regulatory compliance, and business performance by leading aseptic operations that consistently meet quality, cost, and delivery expectations.

What You’ll Do

  • Lead, manage, and develop production teams, including direct supervision of supervisors, to achieve high performance and departmental objectives.
  • Oversee daily manufacturing operations (in both an aseptic and Grade C environments), ensuring full compliance with cGMP, FDA, EMA, and other global regulatory requirements.
  • Maintain strict adherence to SOPs, processing standards, cleanroom behavior, and contamination control practices.
  • Partner cross-functionally with Quality Assurance, Engineering, Supply Chain, and Planning to ensure efficient, compliant production execution.
  • Establish, monitor, and improve KPIs related to OEE, process efficiency, changeover times, cost performance, and quality.
  • Drive continuous improvement initiatives, lean manufacturing practices, and support engineering with automation opportunities to enhance operational excellence.
  • Ensure audit and inspection readiness, lead responses and serve as the manufacturing SME during internal audits, regulatory inspections, deviations, and compliance findings.
  • Coordinate investigations, deviation management, and CAPA implementation for non-conforming events.
  • Review and approve batch records, change controls, deviations, work instructions/SOPs, inventory actions, and purchase requisitions impacting operations.
  • Manage production scheduling priorities, capacity planning, and resource allocation in alignment with business needs.
  • Provide technical support and troubleshooting expertise for the manufacturing processes.
  • Actively conduct and participate in Tier Board and manufacturing department meetings.
  • Foster an environment of open communication, safety, accountability, and respect across manufacturing teams.
  • Perform performance evaluations, support hiring decisions, and ensure consistent leadership practices across the organization.
  • Demonstrate integrity, reliability, and proactive leadership while modeling Tolmar’s core values.

What Sets This Role Apart

  • Opportunity to lead complex operations with high visibility and impact on patient outcomes.
  • Strategic influence on process improvement, compliance readiness, and operational performance.
  • Hands-on leadership in a collaborative manufacturing environment that values continuous improvement and people development.
  • Direct contribution to regulatory excellence and long-term manufacturing capability.

What You Bring

  • Strong working knowledge of cGMP regulations related to pharmaceutical manufacturing.
  • Proven leadership capability with experience managing supervisors and frontline manufacturing teams.
  • Strong analytical, problem-solving, and decision-making skills within time-sensitive environments.
  • Excellent written and verbal communication skills, including technical writing and document review.
  • Deep expertise in aseptic processing, sterile filling operations, cleanroom environments, and contamination control strategies.
  • Proficiency in Microsoft Office (Excel, Word, Outlook).
  • High attention to detail, strong documentation practices, and commitment to data integrity.
  • Ability to lead change, support management decisions, and communicate proactively and positively.

Core Values

This position is expected to operate within the framework of Tolmar’s Core Values:

  • Center on People: We commit to support the well-being of our patients. We are committed to treating our employees and those we serve as valued partners. By placing people at the heart of our actions, we actively engage, invigorate, acquire knowledge, and grow together.
  • Are Proactive & Agile: We embody a culture of engagement and action. With a hands-on approach, we fearlessly adapt to change. We anticipate, respond swiftly and efficiently to ignite a spirit that propels us towards extraordinary outcomes.
  • Act Ethically: We are committed to consistently conducting our business in an ethical, compliant, and socially aware manner, in line with our purpose of positively impacting lives. We actively cultivate diversity, equity, inclusion & sustainability in our workplace.
  • Constantly Improve: We are committed to a collaborative & proactive effort to improve our products, systems, processes, and services by reducing waste, increasing efficiency & improving quality.
  • Are Accountable: We think, act, and communicate with honesty, transparency, and clarity in alignment with our core values. We don't compromise our values for near term gain. We take accountability & ownership of our work, actions, successes, and setbacks. We strive to deliver our best as we shape the future.

Education & Experience

  • Bachelor’s degree in scientific discipline or related field or equivalent experience strongly preferred.
  • Five or more years of experience in pharmaceutical manufacturing, with at least three years in production leadership roles
  • Experience in Aseptic / Sterile production strongly preferred.

Additional Requirements

  • Shift work in a manufacturing and warehouse environment.
  • May require weekend and evening work

Compensation and Benefits

  • Annual pay range $125,000 - $130,000
  • Bonus eligible
  • Benefits information: https://www.tolmar.com/careers/employee-benefits

Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidates qualifications and experience.

Tolmar is an Equal Opportunity Employer. We do not discriminate on the basis age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law. It is our intention that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors.


Tolmar logo

About Tolmar

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Fort Collins, CO, US

Year founded

2006