Supervisory Engineer

Posted 8 Hours Ago
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Fort Worth, TX, USA
In-Office
Mid level
Biotech • Consulting • Pharmaceutical • Manufacturing
The Role
Supervises daily engineering and operational activities in a GMP-regulated environment. Coordinates Engineering, Operations, Maintenance, Quality, contractors, and site personnel; provides technical guidance; supports equipment, utilities, facilities, and operational troubleshooting; ensures safety, GMP compliance, and accurate documentation; participates in deviations, investigations, CAPAs, and change controls; manages priorities, escalations, resources, and continuous improvement initiatives.
Summary Generated by Built In

Pinnaql is a trusted consulting partner to regulated life sciences companies, providing deep technical, validation, and quality expertise across every stage of the product lifecycle. We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity, accelerate project timelines, and maintain a strong state of compliance and audit readiness.

We are seeking a talented, dedicated individual committed to work under the highest ethical standards for the following position:

  • Supervisory Engineer

Description:

We are seeking an experienced Supervisory Engineer to provide day-to-day leadership and operational support within a GMP-regulated environment. This individual will be responsible for coordinating daily engineering and operational activities, providing guidance to site personnel, supporting GMP compliance, and helping ensure work is executed safely, efficiently, and in accordance with established procedures. The ideal candidate is a hands-on engineer with strong supervisory, organizational, and communication skills who is comfortable working closely with Operations, Engineering, Maintenance, Quality, and other site functions. Strong written and verbal English communication skills are required.

Key Responsibilities:

  • Provide day-to-day supervision and coordination of engineering and operational activities.
  • Support daily site operations and ensure priorities, issues, and required actions are effectively managed.
  • Provide direction and technical guidance to employees, contractors, and other personnel as required.
  • Coordinate activities across Engineering, Operations, Maintenance, Quality, and other functional groups.
  • Ensure activities are performed in accordance with GMP requirements, site procedures, safety standards, and applicable quality requirements.
  • Monitor daily activities, identify operational or technical issues, and facilitate timely resolution.
  • Support troubleshooting of equipment, utilities, facilities, and operational issues.
  • Participate in daily operational meetings and communicate priorities, progress, risks, and escalations to site leadership.
  • Support deviations, investigations, CAPAs, change controls, and other GMP documentation as required.
  • Ensure appropriate documentation of engineering and operational activities.
  • Coordinate resources and priorities to minimize disruptions and support operational schedules.
  • Promote a strong culture of safety, quality, accountability, and continuous improvement.

Qualifications:

  • Qualifications Bachelor’s degree in Engineering or a related technical discipline.
  • Experience working in a GMP-regulated operational environment.
  • Demonstrated experience supervising, coordinating, or leading day-to-day technical or operational activities.
  • Strong understanding of GMP principles and controlled operating procedures.
  • Strong leadership, organizational, problem-solving, and decision-making skills.
  • Ability to manage multiple priorities in a fast-paced operational environment.
  • Strong interpersonal skills and ability to work effectively with cross-functional teams.
  • Fluent English, both written and verbal, is required.
  • Ability to work independently while maintaining close communication with site leadership.
  • Previous supervisory or team-lead experience in an engineering or operations environment.
  • Experience with equipment troubleshooting, maintenance coordination, facilities, utilities, or operational support.
  • Familiarity with deviations, CAPAs, change controls, investigations, and GMP documentation.
  • Experience supporting continuous improvement initiatives within a regulated environment.

At Pinnaql, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Pinnaql is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

#LI-LN1

#LI-ONSITE

Skills Required

  • Bachelor's degree in Engineering or a related technical discipline
  • Experience working in a GMP-regulated operational environment
  • Experience supervising, coordinating, or leading day-to-day technical or operational activities
  • Strong understanding of GMP principles and controlled operating procedures
  • Strong leadership, organizational, problem-solving, and decision-making skills
  • Ability to manage multiple priorities in a fast-paced operational environment
  • Strong interpersonal skills and ability to work effectively with cross-functional teams
  • Fluent written and verbal English communication skills
  • Ability to work independently while maintaining close communication with site leadership
  • Previous supervisory or team-lead experience in an engineering or operations environment
  • Experience with equipment troubleshooting, maintenance coordination, facilities, utilities, or operational support
  • Familiarity with deviations, CAPAs, change controls, investigations, and GMP documentation
  • Experience supporting continuous improvement initiatives within a regulated environment
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The Company
154 Employees
Year Founded: 2019

What We Do

Pinnaql, Inc. is a professional services consulting firm providing quality, regulatory, and operational excellence solutions to biopharmaceutical, medical device, and CDMO companies worldwide. The company specializes in laboratory validation, engineering, and compliance, helping regulated life sciences organizations navigate manufacturing challenges, reduce execution risks, and accelerate the transition from lab innovation to commercial market readiness.

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