Senior Validation Engineer, GMP Radiopharma
Bristol-Myers Squibb
Bristol-Myers Squibb is seeking a Lead Validation Engineer in Indianapolis to support the Radiopharmaceutical facility. This position will lead commissioning, qualification, and validation activities, applying broad engineering and GMP knowledge. You will collaborate with teams to ensure the efficacy of validation protocols and drive continuous improvement in compliance and efficiency. Candidates should have extensive experience and strong leadership skills. #J-18808-Ljbffr Bristol-Myers Squibb
- Bristol-Myers Squibb is seeking a Lead Validation Engineer in Indianapolis to support radiopharmaceutical facility operations. This role leads validation activities and provides technical guidance on GMP compliance, ensuring quality in our mission to develop transformative...Suggested
- Bristol-Myers Squibb is seeking a Senior Automation/Controls Engineer for their facility in Indianapolis. This role focuses on designing and optimizing... ...commitment to compliance and continuous improvement in a GMP-regulated setting. #J-18808-Ljbffr Bristol-Myers SquibbSenior
$93.8k - $174.2k
Novartis Farmacéutica in Indianapolis, Indiana, is seeking an experienced engineer to support capital initiatives and manufacturing technologies in a GMP-regulated environment. Candidates should have a Bachelor's degree in engineering and at least 5 years of experience...Senior- ...Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on... ...- Bachelor’s degree (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience... ...industry - Essential experience in a GMP (Good Manufacturing Practice) environment...SeniorFor contractorsWorldwide
$66k - $171.6k
...better for people around the world. The Senior Principal Engineer - Automation Engineering will work as... ...processes required to support GMP operations, and build the site culture... ...related production data. Maintain the validated state of the site control system hardware...SeniorFull timeWork experience placementRemote workFlexible hours$66k - $171.6k
Eli Lilly and Company is seeking a Process Control and Automation Engineer for their new manufacturing facility in Lebanon, Indiana. The... ...involves managing application upgrades, ensuring compliance with GMP standards and collaborating on engineering initiatives. Qualified...Senior- E Solutions, LLC seeks a Validation Engineer in Indianapolis, IN to manage commissioning and qualification activities for new equipment. Candidates require a Bachelor's degree in a relevant field and at least five years of experience in a regulated environment. The role...
- Scorpion Therapeutics in Indianapolis, Indiana is seeking an engineer to monitor equipment performance, provide technical support for new... ...engineering and 3+ years in a manufacturing environment supporting GMP operations. The role involves ensuring compliance with safety...Senior
$144.7k - $261.3k
...Job Description The Senior ML Validation Research Engineer will lead applied machine learning research focused on improving verification and validation of ML components used in robotics and autonomous driving systems. This role centers on simulation-based evaluation...SeniorLocal areaWork from homeFlexible hours$4,500 - $5,000 per week
SQA Services is seeking a senior auditor with FDA experience for a 4-day mock FDA Pre-Approval Inspection in Indianapolis, Indiana. The... ...effectively. Applicants should have a strong background in GCP and GMP operations, and experience with regulatory audits. This role...Senior- SQA Services seeks a Senior Auditor in Indianapolis to conduct mock FDA Pre-Approval Inspections. The ideal candidate will have direct... ...Good Clinical Practices (GCP) and Good Manufacturing Practices (GMP). The role involves assessing inspection readiness, identifying...SeniorWeekly payPermanent employment
- ...Indianapolis, Indiana. The role involves reviewing quality documentation and partnering with manufacturing teams to ensure compliance with GMP regulations. Candidates should possess a Bachelor’s degree in a scientific discipline and have over 8 years of experience in GMP-...Senior
- A leading biopharmaceutical company in Indianapolis seeks a Senior Specialist in QA Operations. The role requires oversight of shop floor... ..., handling quality assurance tasks for clinical development and GMP operations. Candidates should possess a BS/MS in a science-...Senior
- ...implementation. This remote role requires expertise in configuring, validating, and supporting Empower chromatography systems for QC... ...operations. The ideal candidate must have over 5 years of experience in GMP environments and a strong understanding of chromatography...SeniorRemote job
- A biotech company seeks a Senior Process Engineer to lead technical excellence in radiopharmaceutical operations. This role requires mentorship and expertise in optimizing production processes. The successful candidate will work cross-functionally with teams, driving initiatives...Senior
$68.5k - $97.8k
Cardinal Health, Inc. is seeking a Senior Technical Operations Engineer in Indianapolis, Indiana, to enhance processes within radiopharmaceutical operations. This role ensures product quality, regulatory compliance, and operational efficiency, requiring 2-6 years of experience...Senior- ...Equipment Validation Engineer Non-Headquarters Valspec—a global provider of system validation and lifecycle services—provides commissioning... ...the discovery of new and innovative therapies. Job Title: GMP Equipment Validation Engineer – CQV Location: Indianapolis...
- ...leading global healthcare firm in Indianapolis is looking for a Senior Principal Engineer - Automation Engineering. This role involves providing... ...pharmaceutical manufacturing. Strong problem-solving skills and GMP knowledge are essential. Competitive salary and benefits are...SeniorFull time
- ...Description Position Overview: The Computer Systems Validation Engineer supports validation lifecycle activities for automation and control... ...for automation and control systems in a pharmaceutical or GMP regulated environment. Strong knowledge of GAMP 5...
- VALIDATION ASSOCIATES LLC is seeking a Utility Engineer in Indianapolis, Indiana, to optimize and maintain utility systems for pharmaceutical manufacturing. Responsibilities... ...2-7 years of experience in facilities engineering, GMP expertise, and AutoCAD skills. #J-18808-Ljbffr...
$59.95k - $102.62k
...from our experiences to enhance our collective expertise Validation/CQV Engineer Responsibilities: Authoring, editing, and executing technical... ...and time management skills Strong attention to detail GMP and Good Documentation Practice training (may be completed...Temporary workWork experience placementWork at office- ...Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective... ...high-quality, on-time delivery of analytical services. The Senior Manager is responsible for driving operational performance, building...SeniorContract workWork at officeDay shift
$107.9k - $130.75k
## Lead Validation EngineerIndianapolis - RayzeBio - INFind out how well you match with this jobAt RayzeBio,... ...patients. Learn more about RayzeBio: Lead Validation Engineer will support the Radiopharmaceutical facility and GMP operations in Indianapolis and serve as a...Hourly payFull timeTemporary workPart timeFor contractorsWork experience placementSummer workLive inWork at officeLocal areaImmediate startRemote workFlexible hours- Novartis Farmacéutica is looking for a Validation Lead in Indianapolis to ensure product quality and regulatory compliance. In this role... .... The position requires a Bachelor’s degree in Biomedical Engineering or related fields and a minimum of 5 years’ experience. Novartis...Relocation
- Bristol-Myers Squibb is seeking a Senior Supplier Quality Auditor in Indianapolis. This role involves leading the planning, execution, and reporting of audits for suppliers to ensure compliance with cGMP/GxP regulations. You will work collaboratively in a multidisciplinary...SeniorFlexible hours
- CBRE Group, Inc. is seeking a Project Manager in Indianapolis, Indiana, to coordinate multi-discipline real estate project solutions for pharmaceutical clients. The ideal candidate will manage project delivery from start to finish, requiring over 5 years of experience in...Senior
- A leading pharmaceutical company is seeking a Senior Associate Scientist I in Indianapolis to support Quality Control Microbiology activities. Responsibilities include conducting microbiological release testing and ensuring compliance with cGMP requirements. The ideal...SeniorFlexible hours
$123k - $180.4k
Scorpion Therapeutics is seeking a Plant Engineering Manager for their Indianapolis Parenteral Manufacturing facility. This role focuses on maintaining site facility infrastructure and ensuring compliance with regulatory standards. The ideal candidate will have a Bachelor...Senior- Initial Therapeutics, Inc. is seeking a Quality Assurance Representative in Indianapolis, Indiana. This role involves ensuring the quality and compliance of drug products through effective oversight, batch disposition, and leadership in quality matters. The ideal candidate...Senior
- ...ideal candidate should possess at least 10 years of CQV experience in Life Sciences or advanced manufacturing and hold a Bachelor’s degree in an engineering field. Benefits include competitive salary, comprehensive health coverage, and paid time off. #J-18808-Ljbffr JacobsSenior
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