Validation engineer Jobs in Indianapolis, IN
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Validation engineer • indianapolis in
Last updated: 5 hours ago
The Validation Engineer I will help support the Radiopharmaceutical facility and GMP operations in Indianapolis.The Validation Engineer I will be responsible for the drafting and executing commissi...Show moreLast updated: 16 days ago
Professional experience and strong knowledge with real time experience in IT Quality & Compliance, Computer System Validation / Software Testing / System Implementation in the Life Sciences industr...Show moreLast updated: 30+ days ago
At Advanced Accelerator Applications, a Novartis company, we are committed to leading innovation in nuclear medicine and delivering the next generation of targeted radioligand therapy to cancer pat...Show moreLast updated: 5 hours ago
Provide application / system validation expertise for standalone, enterprise, and integrated systems in a regulated (GxP) environment.
Lead OT system qualification and validation, including Client / DCS...Show moreLast updated: 30+ days ago
The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing heal...Show moreLast updated: 30+ days ago
Commissioning Qualification Validation Engineer (CQV).Responsibilities for the Commissioning Qualification Validation Engineer (CQV).
Commissioning : Lead commissioning activities for new laboratory ...Show moreLast updated: 30+ days ago
Required •Minimum of 10 years’ experience as a Computer System Validation Consultant in a regulated environment (preferably Pharma) and must have played a lead role (able to work independently with...Show moreLast updated: 30+ days ago
Job Title : Validation and Verification Engineer - AE Defense.Indianapolis, IN / Hybrid - 3 Office Days / Week)The AE Defense V&V Engineer is responsible for ensuring that Rolls-Royce has sufficient ove...Show moreLast updated: 30+ days ago
Welcome to the forefront of innovation in cutting edge patient treatments! We are thrilled to present an incredible opportunity to join our high performing organization.
As a leader within the life ...Show moreLast updated: 30+ days ago
A company is looking for a Validation Engineer to provide validation support for software systems in regulated environments.
Key Responsibilities Plans, executes, and documents validation activiti...Show moreLast updated: 30+ days ago
As a global leader in industrial automation, process control solutions and instrumentation, we serve clients in the life sciences, pharmaceutical, medical device, food & beverage, and util...Show moreLast updated: 30+ days ago
Commissioning Qualification Validation Engineer (CQV).Responsibilities for the Commissioning Qualification Validation Engineer (CQV).
Commissioning : Lead commissioning activities for new laboratory ...Show moreLast updated: 30+ days ago
This job is with Novartis, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.
Please do not contact the recruiter directly.At Advanced Acc...Show moreLast updated: 1 day ago
Increase your chances of an interview by reading the following overview of this role before making an application.Job Title : Validation and Verification Engineer - AE Defense.Indianapolis, IN / Hybri...Show moreLast updated: 30+ days ago
Our client, a global leader in industrial dispensing & flow drill systems, is seeking a Senior Field Service Validation Engineer to provide site support in Auburn Hills & New Hudson, MI to K-Flow d...Show moreLast updated: 30+ days ago
Creating Peace of Mind by Pioneering Safety and Security.Summer Intern – System Test / Validation Engineer, Hague Road Technical Center – Indianapolis, Indiana.
As an Allegion System Test / Validation E...Show moreLast updated: 30+ days ago
We’re hiring a Validation Engineer to support Computer System Validation (CSV) and system qualification activities in a regulated pharmaceutical environment.
This role is ideal for someone with stro...Show moreLast updated: 1 day ago
CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide.For mission-critical and regulated industries that need to deliver critical s...Show moreLast updated: 16 days ago
Must be legally authorized to work in the United States without sponsorship • •.You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in team...Show moreLast updated: 30+ days ago
Validation Engineer
STEM Diverse Talent SolutionsIndianapolis, Indiana, USAFull-time
Validation Consultant
KaygenIndianpolis, IN, USFull-time
- Promoted
- New!
Validation Engineer II
Novartis Group CompaniesIndianapolis, IN, United StatesFull-time
Validation Engineer
Katalyst HealthCares & Life SciencesIndianapolis, INFull-time
- Promoted
5823 - Validation Engineer / CQV Engineer
Verista, Inc.Indianapolis, IN, USFull-time
Commissioning Qualification Validation Engineer
Piper CompaniesIndianapolis, INFull-time
Validation Lead
Tata Consultancy ServicesIndianapolis, INFull-time
Validation and Verification Engineer - AE Defense
Rolls-RoyceIndianapolisFull-time +1
Validation Engineer
Precision Medicine GroupIndianapolis, Indiana, United StatesFull-time
Validation Engineer
VirtualVocationsSouthport, Indiana, United StatesFull-time
- Promoted
Senior Validation Engineer - Project Lead
PACIVIndianapolis, IN, USFull-time
Commissioning Qualification Validation Engineer
Zachary Piper SolutionsIndianapolis, IN, USFull-time
Validation Engineer II
NovartisIndianapolis, Indiana, United StatesFull-time
- Promoted
Validation and Verification Engineer - AE Defense
Rolls RoyceIndianapolis, Indiana, USFull-time +1
Global Team – Validation Engineer
BrooksourceIndianapolis, Indiana, USFull-time +1
Summer Intern- System Test / Validation Engineer
AllegionHague Rd,IN,IndianapolisFull-time
- Promoted
Validation Engineer
Process AllianceIndianapolis, IN, United StatesFull-time
- Promoted
Senior Validation Engineer
CAIIndianapolis, IN, USFull-time
Sr. Validation Engineer
Barry-WehmillerIndianapolis, IN USAFull-time
- mail carrier (from $ 44,265 to $ 300,000 year)
- owner operator (from $ 78,770 to $ 250,000 year)
- chief medical officer (from $ 193,102 to $ 250,000 year)
- hospitalist (from $ 30,000 to $ 250,000 year)
- subcontractor (from $ 101,250 to $ 241,250 year)
- pediatrician (from $ 80,000 to $ 235,000 year)
- medical director (from $ 75,633 to $ 230,000 year)
- physician (from $ 50,000 to $ 230,000 year)
- crna (from $ 175,000 to $ 230,000 year)
- dentist (from $ 150,000 to $ 225,000 year)
- Santa Rosa, CA (from $ 112,099 to $ 191,614 year)
- Santa Clarita, CA (from $ 112,125 to $ 190,417 year)
- San Jose, CA (from $ 102,509 to $ 182,500 year)
- Allentown, PA (from $ 113,400 to $ 182,500 year)
- Palm Bay, FL (from $ 123,500 to $ 182,250 year)
- San Diego, CA (from $ 100,465 to $ 180,000 year)
- San Mateo, CA (from $ 102,168 to $ 180,000 year)
- San Francisco, CA (from $ 100,000 to $ 179,386 year)
- Fremont, CA (from $ 135,000 to $ 173,750 year)
- Daly City, CA (from $ 95,194 to $ 170,725 year)
The average salary range is between $ 85,008 and $ 146,340 year , with the average salary hovering around $ 104,994 year .
Validation Engineer
STEM Diverse Talent SolutionsIndianapolis, Indiana, USA16 days ago
Job type
- Full-time
Job description
Position Overview :
The Validation Engineer I will help support the Radiopharmaceutical facility and GMP operations in Indianapolis. The Validation Engineer I will be responsible for the drafting and executing commissioning qualification and validation (CQV) documents and protocols which support the use of highly specialized facility utility analytical and process equipment. The position will utilize a wide range of engineering disciplines to support the advancement from construction to clinical development and subsequent GMP commercial operations. Additional responsibilities may include the onboarding of new technologies process development GMP operations support deviation investigation CAPA management continuous improvement projects and future facility expansion projects.
Key Responsibilities :
- Work with the project team and / or General Contractor as required to support the commissioning and validation of a 60000 sq. ft. office warehouse and GMP Radiopharmaceutical production facility
- Develop and implement the CQV strategies for the GMP spaces including but not limited to office warehouse development quality control sterility / microbiology and GMP production areas
- Work with consultant(s) as required to support the implementation and execution of the CQV program
- Support the engineering QC and Operations team as required to improve and implement new processes
- Provide validation support for day-to-day development and GMP operations
- Provide engineering and operational support as required
- Develop expertise in areas of validation (process validation QC assets CSV cleaning validation etc)
- Apply technical knowledge and abilities to investigate manufacturing deviations
- Review data and documentation to support investigations
- Participate and drive projects and continuous improvement efforts
- Draft GMP documentation including but not limited to SOPs Forms Protocols Technical Documents Reports Deviations CAPAs Change Controls and reports.
- Support Health Authority Inspections
- Maintain department KPIs related to performance
- Provide support executing equipment and process validations as necessary.
Key Skills
Python,SOC,Debugging,C / C++,FDA Regulations,Minitab,Technical Writing,GAMP,OS Kernels,Perl,cGMP,Manufacturing
Employment Type : Full Time
Experience : years
Vacancy : 1