Process Engineer - Pharmaceutical Manufacturing

YOH Services LLC

Noblesville (IN)

Sur place

USD 80 000 - 110 000

Plein temps

Il y a 4 jours
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Avantages offerts par ce poste

Medical, Prescription, Dental & Vision
Health Savings Account (HSA)
Life & Disability Insurance
401K Retirement Plan
EAP
Direct Deposit & weekly pay
Referral Bonus Programs

Résumé du poste

Yoh Life Sciences is seeking a Process Engineer to support a pharmaceutical manufacturing operation in Noblesville, Indiana. This direct-hire, full-time role onsite offers a salary range of $80,000 to $110,000 per year and requires strong hands-on engineering skills in a regulated environment.

The successful candidate will lead process improvements, troubleshoot equipment, develop KPIs, and collaborate cross-functionally with Quality and Validation to ensure cGMP compliance.

Qualifications

  • Bachelor's degree in Engineering required; Mechanical preferred; other engineering disciplines considered.
  • 5+ years in a cGMP manufacturing environment.
  • Experience improving manufacturing processes and equipment performance.

Responsabilités

  • Lead process improvement initiatives focusing on equipment reliability, efficiency, throughput, and performance.
  • Troubleshoot equipment and recurring process issues; identify root causes; implement corrective actions.
  • Develop, monitor and improve process performance indicators (KPIs).
  • Lead root cause investigations and develop CAPAs.
  • Prepare technical documentation, including engineering protocols, reports, and process improvements.
  • Collaborate with Manufacturing, Quality, and Validation to ensure cGMP compliance.
  • Support equipment qualification, process validation, change control, and continuous improvement.
  • Assist with developing and maintaining manufacturing procedures, batch records, and training materials.
  • Coordinate engineering projects; track milestones; assess costs and resources.

Connaissances

Process improvement
Root cause analysis
Equipment reliability
KPIs
Cross-functional collaboration
Documentation

Formation

Bachelor's degree in Engineering

Description du poste

Process Engineer - Pharmaceutical Manufacturing

Location: Noblesville, IN 46060

Employment Type: Direct Hire | Full-Time

Salary: $80,000-$110,000 annually

Schedule: Monday-Friday | Onsite

Yoh Life Sciences is seeking an experienced Process Engineer to support a pharmaceutical manufacturing operation in Noblesville, Indiana.

This position is ideal for a hands‑on engineer who enjoys solving complex manufacturing challenges, improving equipment reliability, optimizing production processes, and driving measurable operational improvements in a regulated environment.

What You'll Do
  • Lead manufacturing process improvement initiatives focused on equipment reliability, efficiency, throughput, and operational performance.
  • Troubleshoot manufacturing equipment and recurring process issues, identify root causes, and implement sustainable corrective actions.
  • Develop, monitor, and improve process performance indicators (KPIs) to support manufacturing objectives.
  • Lead root cause investigations, author deviations, and develop corrective and preventive actions (CAPAs).
  • Prepare technical documentation, including engineering protocols, reports, and process improvement documentation.
  • Collaborate with Manufacturing, Quality, and Validation teams to ensure compliance with cGMP requirements.
  • Support equipment qualification, process validation, change control, and continuous improvement activities.
  • Assist with the development and maintenance of manufacturing procedures, batch records, and training materials.
  • Coordinate engineering projects, track milestones, and provide input on project costs and resource requirements.
What We're Looking For
  • Bachelor's degree in Engineering required. Mechanical Engineering preferred; Chemical, Biochemical, Biotechnology, or related engineering disciplines considered.
  • 5+ years of relevant engineering experience in a cGMP manufacturing environment.
  • Demonstrated experience improving manufacturing processes, equipment performance, and operational reliability.
  • Hands‑on experience troubleshooting production equipment and resolving manufacturing issues.
  • Experience leading formal root cause analysis and implementing corrective and preventive actions.
  • Working knowledge of cGMP, validation, quality systems, and document control.
  • Experience developing or utilizing process KPIs to measure and improve manufacturing performance.
  • Strong technical documentation, project management, and cross‑functional collaboration skills.
Preferred Qualifications
  • Experience with automated visual inspection systems or pharmaceutical packaging equipment.
  • Background supporting automated manufacturing lines, equipment optimization, or reliability improvement initiatives.
  • Experience in pharmaceutical manufacturing, medical devices, or other highly regulated production environments.
Why Consider This Opportunity?
  • Direct‑hire opportunity with an established pharmaceutical manufacturing organization.
  • Opportunity to lead meaningful equipment and process improvements.
  • Collaborative, cross‑functional engineering environment.
  • Work on manufacturing operations where quality, reliability, and continuous improvement are essential.

Estimated Min Rate: $80000.00

Estimated Max Rate: $110000.00

What's In It for You?
  • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
  • Health Savings Account (HSA) (for employees working 20+ hours per week)
  • Life & Disability Insurance (for employees working 20+ hours per week)
  • MetLife Voluntary Benefits
  • Employee Assistance Program (EAP)
  • 401K Retirement Savings Plan
  • Direct Deposit & weekly epayroll
  • Referral Bonus ProgramsCertification and training opportunities

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Visit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.

For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh's hiring clients' preferences. To learn more about Yoh's privacy practices, please see our Candidate Privacy Notice: https://www.yoh.com/privacy-notice

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