Senior Validation Engineer
Fishers, IN · On-site
The Senior Validation Engineer is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing facility. The ideal candidate has subject matter ...
Fishers, IN · On-site
The Senior Validation Engineer is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing facility. The ideal candidate has subject matter ...
Fishers, IN · On-site
The Senior Validation Engineer is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing facility. The ideal candidate has subject matter ...
The Senior Validation Engineer is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing facility. The ideal candidate has subject matter ...
The Senior Validation Engineer is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing facility. The ideal candidate has subject matter ...
Fishers, IN · On-site
The Senior Validation Engineer is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing facility. The ideal candidate has subject matter ...
Quick apply
Fishers, IN · On-site
The Senior Validation Engineer is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing facility. The ideal candidate has subject matter ...
Fishers, IN · On-site
The Senior Validation Engineer is a key individual contributor role within the INCOG BioPharma Validation Department. The Senior Validation Engineer is responsible for understanding and implementing ...
Fishers, IN · On-site
The Senior Validation Engineer is a key individual contributor role within the INCOG BioPharma Validation Department. The Senior Validation Engineer is responsible for understanding and implementing ...
Indianapolis, IN · On-site
$107K - $130K/yr
Summary The Senior Validation Engineer will help support the Radiopharmaceutical facility and GMP operations in Indianapolis The Senior Validation Engineer will be responsible for the drafting and ...
Indianapolis, IN · On-site
$107K - $130K/yr
Summary The Senior Validation Engineer will help support the Radiopharmaceutical facility and GMP operations in Indianapolis The Senior Validation Engineer will be responsible for the drafting and ...
Indianapolis, IN · On-site
$107K - $130K/yr
The Senior Validation Engineer will be responsible for the drafting and executing commissioning, qualification, and validation (CQV) documents and protocols which support the use of highly ...
Indianapolis, IN · On-site
$107K - $130K/yr
The Senior Validation Engineer will be responsible for the drafting and executing commissioning, qualification, and validation (CQV) documents and protocols which support the use of highly ...
$107K - $130K/yr
The Senior Validation Engineer will be responsible for the drafting and executing commissioning, qualification, and validation (CQV) documents and protocols which support the use of highly ...
$107K - $130K/yr
The Senior Validation Engineer will be responsible for the drafting and executing commissioning, qualification, and validation (CQV) documents and protocols which support the use of highly ...
Job Summary The Senior Engineer, Manufacturing oversees and project manages large engineering ... Ensure all validation activities and documentation comply with cGMP, pharmaceutical regulatory ...
Job Summary The Senior Engineer, Manufacturing oversees and project manages large engineering ... Ensure all validation activities and documentation comply with cGMP, pharmaceutical regulatory ...
Job Summary The Senior Engineer, Manufacturing oversees and project manages large engineering ... Ensure all validation activities and documentation comply with cGMP, pharmaceutical regulatory ...
Job Summary The Senior Engineer, Manufacturing oversees and project manages large engineering ... Ensure all validation activities and documentation comply with cGMP, pharmaceutical regulatory ...
Job Summary The Senior Engineer, Manufacturing oversees and project manages large engineering ... Ensure all validation activities and documentation comply with cGMP, pharmaceutical regulatory ...
Job Summary The Senior Engineer, Manufacturing oversees and project manages large engineering ... Ensure all validation activities and documentation comply with cGMP, pharmaceutical regulatory ...
Job Summary The Senior Engineer, Manufacturing oversees and project manages large engineering ... Ensure all validation activities and documentation comply with cGMP, pharmaceutical regulatory ...
Job Summary The Senior Engineer, Manufacturing oversees and project manages large engineering ... Ensure all validation activities and documentation comply with cGMP, pharmaceutical regulatory ...
Job Summary The Senior Engineer, Manufacturing oversees and project manages large engineering ... Ensure all validation activities and documentation comply with cGMP, pharmaceutical regulatory ...
Job Summary The Senior Engineer, Manufacturing oversees and project manages large engineering ... Ensure all validation activities and documentation comply with cGMP, pharmaceutical regulatory ...
Job Summary The Senior Engineer, Manufacturing oversees and project manages large engineering ... Ensure all validation activities and documentation comply with cGMP, pharmaceutical regulatory ...
Job Summary The Senior Engineer, Manufacturing oversees and project manages large engineering ... Ensure all validation activities and documentation comply with cGMP, pharmaceutical regulatory ...
Indianapolis, IN · On-site
$107K - $130K/yr
Senior Validation Engineer #J-18808-Ljbffr
Indianapolis, IN · On-site
$107K - $130K/yr
Senior Validation Engineer #J-18808-Ljbffr
Bloomington, IN · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Bloomington, IN · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Carmel, IN · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Quick apply
Carmel, IN · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer Responsibilities: * Lead and drive end-to-end CQV and validation projects for pharmaceutical manufacturing, facility, utility, and equipment systems, from planning through ...
Senior Validation Engineer Responsibilities: * Lead and drive end-to-end CQV and validation projects for pharmaceutical manufacturing, facility, utility, and equipment systems, from planning through ...
Indianapolis, IN · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Indianapolis, IN · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Carmel, IN · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Carmel, IN · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Bloomington, IN · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Quick apply
Bloomington, IN · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
$33.17 - $38.70
4% of jobs
$38.70 - $44.23
10% of jobs
$48.70 is the 25th percentile. Wages below this are outliers.
$44.23 - $49.76
14% of jobs
$49.76 - $55.29
13% of jobs
The median wage is $59.44 / hr.
$55.29 - $60.82
13% of jobs
$60.82 - $66.36
17% of jobs
$68.43 is the 75th percentile. Wages above this are outliers.
$66.36 - $71.89
13% of jobs
$71.89 - $77.42
9% of jobs
$77.42 - $82.95
3% of jobs
$82.95 - $88.48
2% of jobs
$88.48 - $94.01
3% of jobs
$33
$61
$94
| Aspect | Senior Validation Engineer | Validation Specialist |
|---|---|---|
| Credentials | Bachelor's or Master's in Engineering, Life Sciences, or related fields; often with certifications like GxP or CSV | Similar educational background; certifications like GxP or CSV are common |
| Work Environment | Designs and oversees validation protocols in manufacturing, biotech, or pharmaceutical settings | Executes validation tasks, tests, and documentation in similar environments |
| Employer & Industry | Pharmaceutical, biotech, medical device companies | Same industries, often working under validation teams |
| Search & Comparison | Often compared for experience level and responsibilities | Commonly searched together for validation roles |
The main difference is that a Senior Validation Engineer typically leads validation projects, designs protocols, and oversees validation activities, while a Validation Specialist focuses on executing validation tests and documentation. Both roles require similar credentials and work in comparable environments, but the Senior Validation Engineer has more responsibility for planning and oversight.
The most popular types of Validation Engineer jobs in Indiana are:
For Senior Validation Engineer jobs in Indiana, the most frequently searched job titles are:
The top searched job categories for Senior Validation Engineer jobs in Indiana are:
Cities in Indiana with the most Senior Validation Engineer job openings:
For Senior Validation Engineer jobs in IN, the most frequently searched job titles are:

Fishers, IN • On-site
Full-time
This job post has expired today. Applications are no longer accepted.
INCOG BioPharma is seeking a highly motivated Senior Validation Engineer with validation expertise to join our team. The Senior Validation Engineer is a key individual contributor role within the INCOG BioPharma Validation Department. The Senior Validation Engineer is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing facility. The ideal candidate has subject matter expertise and practical experience in qualification and validation.
The Senior Validation Engineer will partner with internal customers to meet the needs of client projects, facility upgrades, capital expansion projects, and laboratory systems. They will possess a demonstrated ability to influence positive outcome without direct reporting authority. Additionally, they must thoroughly understand and be able to adapt to the changing needs of a manufacturing environment.
Essential Job Functions:
Special Job Requirements:
Additional Preferences:
INCOG is hiring for both Validation Engineer and Senior Validation Engineer opportunities. The final level will be determined based on the candidate’s qualifications, relevant industry experience, technical expertise, and demonstrated independence. Candidates may be considered for the Validation Engineer or Senior Validation Engineer level as appropriate.
Additional info about INCOG BioPharma Services:
At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.
If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.
INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.
Qualified applicants must be authorized to work in the United States on a full-time basis. INCOG will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
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Biotechnology research and development
51 - 200 Employees
Fishers, IN, US
2020