Top 248 Validation engineer Jobs in Indianapolis In

Process Engineer
Yoh, A Day & Zimmermann Company —Noblesville, IN
- $95,000 - $110,000 a year
- Monday to Friday
- 5 years
- Engineering
- Analysis skills
- Health savings account
- Disability insurance
Quick Apply
Sr. Equipment Engineer
BMS —Indianapolis, IN
- $107,904 - $130,754 a year
- Email
- 5 years
- Bachelor of Science
- Engineering
- Paid holidays
- Disability insurance
Systems Engineer
PA Solutions —Indianapolis, IN
- Customer service
- English
- Mid-level
7d
Senior Platform Controls Software Engineer
Allison Transmission —Indianapolis, IN
- Full-time
- Computer science
- Computer Science
- Software troubleshooting
- Wellness program
- Paid parental leave
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Validation Engineer, Sterility & CQV
BMS —Indianapolis, IN
- $96,148 - $116,508 a year
- Email
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Paid holidays
- Disability insurance
4d
Lead Validation Engineer
BMS —Indianapolis, IN
- $124,449 - $150,803 a year
- Email
- 5 years
- Bachelor of Science
- Mentoring
- Paid holidays
- Disability insurance
Validation Engineer
Yoh, A Day & Zimmermann Company —Noblesville, IN
- $80,000 - $86,000 a year
- Mid-level
- Fair chance
- Training & development
- Health savings account
- Disability insurance
Quick Apply
2d
Application Support Engineer
PA Solutions —Indianapolis, IN
- Computer Science
- Engineering
- Mid-level
7d
Senior Validation Engineer
Beacon Hill Staffing Group —Indianapolis, IN
- Full-time
- 5 years
- Engineering
- Analysis skills
- Dental insurance
- Vision insurance
Quick Apply
6d
Software Engineer I
Sonablate Corp. —Indianapolis, IN
- $75,000 - $80,000 a year
- Full-time
- Background check
- Computer Science
- English
- AD&D insurance
- Health insurance
Quick Apply
Validation Engineer II
E2i Inc. —Indianapolis, IN
- $85,000 - $110,000 a year
- Full-time
- Engineering
- Laboratory experience
- Mid-level
- Health insurance
- Dental insurance
Process Validation Engineer
INCOG BioPharma Services —Fishers, IN
- Full-time
- Engineering
- Office
- Analysis skills
Sr. Validation & Compliance Engineer
Katalyst Healthcares & Life Sciences —Indianapolis, IN
- Contract
- 5 years
- Engineering
- Senior level
Quick Apply
6505 - Validation Engineer / CQV Engineer - Change Control & Deviations
Verista, Inc. —Indianapolis, IN
- $69,300 - $95,358 a year
- Engineering
- Mid-level
- Continuous improvement
- Commuter assistance
- Paid parental leave
Quick Apply
10d
Validation Engineer, Sterility & CQV
Bristol-Myers Squibb —Indianapolis, IN
- $96,148 - $116,508 a year
- Email
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Paid holidays
- Disability insurance
Validation Engineer II
Design Group —Indianapolis, IN
- Full-time
- Background check
- Bachelor of Science
- Pass drug screening
Principal Validation Engineer
INCOG BioPharma Services —Fishers, IN
- Full-time
- Office
- Master's degree
- Bachelor's degree
4d
Process Validation Engineer
Katalyst Healthcares & Life Sciences —Indianapolis, IN
- Contract
- Hybrid work
- Engineering
- Mid-level
- Communication skills
Quick Apply
Embedded Software Engineer
Endress+Hauser Level+Pressure USA —Greenwood, IN
- Temporary
- Computer science
- Computer Science
- Writing skills
- Paid parental leave
- Paid holidays
CQV Engineer - Commissioning, Qualification & Validation
PACIV —Indianapolis, IN
- Full-time
- Engineering
- Mid-level
- Bachelor's degree
- Health savings account
- Paid time off
Quick Apply

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Process Engineer

Yoh, A Day & Zimmermann Company -
Noblesville, IN

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Job Details

$95,000 - $110,000 a year

Benefits

Health savings account
Disability insurance
Health insurance
Dental insurance
401(k)
Employee assistance program
Vision insurance
Referral program

Qualifications

Incident investigation techniques for hazard identification
Performance monitoring
Record keeping
Project development phase management
Project engineering
Content creation for technical audiences
Defect resolution root cause analysis
Document control experience within pharmaceutical industry
Pharmaceutical regulatory compliance
Preventive action implementation
Design of manufacturing processes
Technical writing experience within manufacturing
Production deviation management
Engineering process optimization
Reliability analysis
Equipment troubleshooting
Quality control preventive actions
Corrective and preventive actions (CAPA)
Metrics Reporting
Manufacturing standard operating procedures
Manufacturing facility experience
Key Performance Indicators
Bachelor's degree in engineering
Quality standards in production
Collaboration with manufacturing teams
Technical troubleshooting support
Quality improvement programs in engineering
Cross-functional communication
Failure analysis
Pharmaceutical manufacturing facility experience

Full Job Description

Yoh is hiring a Process Engineer for our Pharmaceutical Manufacturing client in Noblesville, Indiana. This position will support a fast-paced sterile drug-product manufacturing operation. The Process Engineer will lead process and equipment improvements, troubleshoot manufacturing issues, establish performance metrics, investigate failures, and support new products and manufacturing lines within a cGMP environment.

What You Will Do

Lead process improvement, equipment reliability, troubleshooting, and remediation initiatives across manufacturing operations.
Establish and monitor process KPIs related to reliability, quality, throughput, yield, downtime, and operational performance.
Evaluate, design, and implement robust manufacturing processes for new products using existing or new equipment.
Support product launches, technology transfers, and implementation of new manufacturing lines.
Lead formal root-cause investigations involving manufacturing processes and equipment.
Author deviations, determine root causes, and develop corrective and preventive actions to prevent recurrence.
Write and execute technical documentation, including engineering protocols, reports, risk assessments, and process-improvement documentation.
Initiate and support change controls associated with equipment and process improvements.
Partner with Quality, Manufacturing, Validation, Technical Services, R&D, and other functions to ensure compliant implementation of cGMP practices.
Provide input into project-cost forecasts and track project activities against established milestones.
Develop and maintain manufacturing procedures, batch records, equipment documentation, and training materials.
Provide hands-on manufacturing-floor support during equipment issues, process changes, startup activities, and project implementation.

Education and Experience Requirements

Bachelor’s degree in Engineering required. Mechanical Engineering is preferred; Chemical, Biochemical, Biotechnology, Manufacturing, or another engineering discipline may be considered based on relevant experience.
Five or more years of relevant engineering experience in a cGMP manufacturing environment.
Demonstrated experience optimizing manufacturing processes and establishing or monitoring process KPIs.
Hands-on experience troubleshooting manufacturing processes or equipment and implementing sustainable reliability or quality improvements.
Experience leading formal root-cause analysis using structured problem-solving methodologies.
Experience authoring deviations, CAPAs, change controls, protocols, technical reports, or comparable controlled documentation.
Working knowledge of cGMP requirements, validation, quality systems, document control, and the regulatory impact of engineering changes.
Experience supporting cross-functional projects from evaluation and design through implementation and operational handoff.
Strong project-management, organizational, technical-writing, and communication skills.
Ability to work independently while collaborating effectively within multidisciplinary project and manufacturing teams.

Preferred Experience

Automated visual inspection systems
Vial inspection or vial-labeling equipment
Pharmaceutical packaging equipment or packaging lines
Sterile injectable, aseptic, or fill-finish manufacturing
New-product introduction, technology transfer, or manufacturing-line startup
Medical-device or other highly regulated manufacturing environments may also be considered when accompanied by strong process-engineering, validation, and quality-system experience

Additional Requirements

Must be able to work fully onsite in Noblesville, Indiana, Monday through Friday from 8:00 a.m.–5:00 p.m.

#IND-SPG

Estimated Min Rate: $95000.00
Estimated Max Rate: $110000.00

What’s In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:

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 Programs
Certification 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

Stay Safe During Your Job Search
Fraudulent recruiting communications have become increasingly common. Emails from Yoh recruiters will only come from an @yoh.com email address. Yoh will never ask candidates to pay fees, purchase equipment, send gift cards, or transfer funds as part of the recruiting or hiring process. If you receive a communication that appears suspicious or requests payment, contact Yoh directly before responding or sharing personal information.
IND-SPG

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Refine Your Search

validation engineer jobs in indianapolis in

Process Engineer

Sr. Equipment Engineer

Systems Engineer

Senior Platform Controls Software Engineer

Validation Engineer, Sterility & CQV

Lead Validation Engineer

Validation Engineer

Application Support Engineer

Senior Validation Engineer

Software Engineer I

Validation Engineer II

Process Validation Engineer

Sr. Validation & Compliance Engineer

6505 - Validation Engineer / CQV Engineer - Change Control & Deviations

Validation Engineer, Sterility & CQV

Validation Engineer II

Principal Validation Engineer

Process Validation Engineer

Embedded Software Engineer

CQV Engineer - Commissioning, Qualification & Validation

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