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Quality Assurance Manager in Indianapolis
Takeda Pharmaceutical Company Limited
Quality Management Rep
Cgmp regulatory compliance knowledgePlasma center operations experienceQuality assurance audit execution$63,080.00 - $86,735.00 py
The role monitors all systems to ensure source plasma manufacturing is performed consistently according to current Good Manufacturing Practices (cGMP)
Indianapolis, IN, USFull timeExperience requiredJob Match ScoreCreate Profile
19 days agoRayzeBio
Manager, Qa Compliance
Bachelor's degree in engineering or life science5+ years quality assurance experienceKnowledge of us, eu, and rest-of-world cgmp regulations$124,449 - $150,803 py
The role involves managing site quality operations in accordance with RayzeBio policies and global cGMPs while leading the Change Control Review Board and Quality Council
Indianapolis, IN, USFully remoteFull time+5y experienceJob Match ScoreCreate Profile20 days agoRayzeBio
Manager, Qa Compliance
Bachelor's degree in engineering or life science5+ years quality assurance experienceKnowledge of us, eu, and global cgmp regulations$124,449 - $150,803 annually py
The role involves managing Site Quality Operations activities in accordance with RayzeBio policies and global cGMPs
Indianapolis, IN, USFully remoteFull time+5y experienceJob Match ScoreCreate Profile22 days agoRayzeBio
Manager, Qa Compliance
Bachelor's degree in engineering or life science5 years minimum quality assurance experienceKnowledge of us, eu, and global cgmp regulations$124,449 - $150,803 py
The role involves managing site quality operations in accordance with RayzeBio policies and global cGMPs while leading the Change Control Review Board and Quality Council
Indianapolis, IN, USFully remoteFull time+5y experienceJob Match ScoreCreate Profile22 days agoEli Lilly
Principal - Qa Api External Manufacturing Peptides
Cgmp regulatory compliance experienceExternal manufacturing site auditingApi manufacturing quality oversight$65,250 - $169,400 py
This role provides essential Quality Assurance oversight for API External Manufacturing operations to ensure compliance with cGMP and regulatory requirements
Indianapolis, IN, USFull time+5y experienceJob Match ScoreCreate Profile29 days agoLilly
Sr. Principal Associate For Analytical Quality Assurance - Foundry
Bachelor's degree in pharmacy chemistry or biologyMinimum 5 years technical laboratory experienceStrong knowledge of analytical method development and validation$65,250 - $169,400 py
The role ensures laboratory activities at the Lilly Medicine Foundry adhere to global quality standards and current Good Manufacturing Practice (cGMP)
Carmel, Indiana, USFull time+5y experienceJob Match ScoreCreate Profile29 days agoLilly
Principal Associate - Qa
Bachelor of science in stem field3-5 years pharmaceutical manufacturing experienceCgmp compliance knowledge$65,250 - $169,400 py
The role ensures appropriate execution of Quality Systems to sustain cGMP compliance for clinical trial materials
Indianapolis, Indiana, USOnsiteFull time+5y experienceJob Match ScoreCreate Profile29 days agoLiljamesofficial
Sr. Principal Associate For Analytical Quality Assurance - Foundry
Bachelor's degree in pharmacy chemistry or biologyMinimum 5 years technical laboratory experienceStrong knowledge of analytical method development$65,250 - $169,400 py
This role ensures laboratory activities at the Lilly Medicine Foundry comply with global quality standards and cGMP regulations
Carmel, Indiana, USFull time+5y experienceJob Match ScoreCreate Profile29 days agoEli Lilly
Principal - Qa Api External Manufacturing Peptides
Bachelor's degree in chemistry or related field5+ years qa experience in pharmaceutical industryCgmp regulations and global pharmacopeial requirements$65,250 - $169,400 py
This role provides essential Quality Assurance oversight for API External Manufacturing operations ensuring compliance with cGMP and regulatory requirements
Indianapolis, IN, USFull time+5y experienceJob Match ScoreCreate Profile29 days agoLilly
Sr. Principal Associate For Analytical Quality Assurance - Foundry
Bachelor's degree in pharmacy chemistry or biologyMinimum 5 years technical laboratory experienceStrong knowledge of analytical method development and validation$65,250 - $169,400 py
This role ensures laboratory activities at the new Lilly Medicine Foundry comply with global quality standards and cGMP regulations
Carmel, Indiana, USFull time+5y experienceJob Match ScoreCreate Profile29 days agoLilly
Principal Associate - Qa
Bachelor of science in stem field3-5 years pharmaceutical manufacturing experienceCgmp compliance and quality systems knowledge$65,250 - $169,400 py
The role ensures appropriate execution of Quality Systems to sustain cGMP compliance for clinical trial materials
Indianapolis, Indiana, USOnsiteFull time+5y experienceJob Match ScoreCreate Profile29 days agoEli Lilly
Principal - Qa Api External Manufacturing Peptides
Bachelor's degree in chemistry or related field5+ years qa experience in pharmaceutical industryExpertise in cgmp regulations and global pharmacopeia$65,250 - $169,400 py
This role provides essential Quality Assurance oversight for API External Manufacturing operations ensuring compliance with cGMP and regulatory requirements
Indianapolis, IN, USFull time+5y experienceJob Match ScoreCreate Profile29 days agoLilly
Principal Associate - Qa
Bachelor of science in stem field3-5 years pharmaceutical manufacturing experienceKnowledge of cgmps and fda regulations$65,250 - $169,400 py
The role involves ensuring quality oversight of all materials used in clinical trials and maintaining compliance with current Good Manufacturing Practices
Indianapolis, IN, USOnsiteFull time+5y experienceJob Match ScoreCreate Profile29 days agoGoodwill Legacy Group
Manufacturing Quality Assurance (qa) Supervisor- 38th And Sheridan
Iso 9001 and iso 13485 compliance expertiseInternal audit program leadershipCapa and ncr investigation management$50-$60k annually ph
This leadership position provides oversight of the Quality Management System ensuring alignment with ISO 9001 and ISO 13485 standards
Indianapolis, IN, USFull time+15y experienceJob Match ScoreCreate Profile29 days agoGoodwill Legacy Group
Manufacturing Quality Assurance (qa) Supervisor- Tremont
Iso 9001 and iso 13485 compliance expertiseInternal audit program leadershipCapa and ncr investigation management$50-$60k annually ph
This leadership position provides oversight of the Quality Management System in alignment with ISO 9001 and ISO 13485 requirements
Indianapolis, IN, USFull timeExperience requiredJob Match ScoreCreate Profile29 days agoGoodwill Legacy Group
Manufacturing Quality Assurance (qa) Supervisor- 38th And Sheridan
Iso 9001 and iso 13485 compliance expertiseInternal audit program leadershipCapa and ncr investigation management$50-$60k ph
This leadership role provides oversight of the Quality Management System ensuring alignment with ISO 9001 and ISO 13485 standards
Indianapolis, IN, USFull timeExperience requiredJob Match ScoreCreate Profile29 days agoGoodwill Legacy Group
Manufacturing Quality Assurance (qa) Supervisor- Tremont
Iso 9001 and iso 13485 compliance expertiseInternal audit program leadershipCapa and ncr investigation management$50-$60k annually ph
This leadership role provides oversight of the Quality Management System ensuring alignment with ISO 9001 and ISO 13485 standards
Indianapolis, IN, USFull timeExperience requiredJob Match ScoreCreate Profile29 days agoRayzeBio
Manager, Gmp Inspection Management
Bachelor's degree in engineering or life science5-7 years qa experience minimum4 years direct gmp audit/inspection leadership$124,449 - $150,803 py
The role leads site inspection readiness efforts for the Indianapolis site and manages the Self-Inspection Program
Indianapolis, IN, USFully remoteFull time+7y experienceJob Match ScoreCreate Profile29 days agoEli Lilly
Sr. Principal Associate For Analytical Quality Assurance - Foundry
Bachelor's degree in pharmacy chemistry or biologyMinimum 5 years technical laboratory experienceStrong knowledge of analytical method development$65,250 - $169,400 py
This role ensures laboratory activities at the Lilly Medicine Foundry comply with global quality standards and cGMP regulations
Carmel, Indiana, USFull time+5y experienceJob Match ScoreCreate Profile30 days agoEli Lilly UK
Principal - Qa Api External Manufacturing Peptides
Bachelor's degree in chemistry or related field5+ years qa experience in pharmaceutical industryApi manufacturing and external supply expertise$65,250 - $169,400 py
This role provides essential Quality Assurance oversight for API External Manufacturing operations ensuring compliance with cGMP and regulatory requirements
Indianapolis, IN, USFull time+5y experienceJob Match ScoreCreate Profile30 days agoRayzeBio
Manager, Gmp Inspection Management
Bachelor's degree in engineering or life science5-7 years qa experience minimum4 years direct gmp audit/inspection leadership$124,449 - $150,803 py
The role involves leading site inspection readiness efforts for the Indianapolis facility and managing the annual inspection readiness plan
Indianapolis, IN, USFully remoteFull time+7y experienceJob Match ScoreCreate Profile30 days agoRayzeBio
Senior Supplier Quality Auditor
7 years qa auditing experienceCgmp gxp regulatory knowledgeOnsite supplier audit execution$96,148 - $116,508 py
The Senior Supplier Quality Auditor leads the planning, execution, and reporting of audits to ensure compliance with cGMP/GxP regulations
Indianapolis, IN, USFully remoteFull time+7y experienceJob Match ScoreCreate Profile30 days agoRayzeBio
Manager, Quality Systems
Bachelor's degree in engineering or life science5 years quality assurance experienceKnowledge of us, eu, and global cgmp regulations$124,449 - $150,803 py
The role involves establishing and maintaining a Quality Management System in accordance with global cGMPs and RayzeBio policies
Indianapolis, IN, USFully remoteFull time+5y experienceJob Match ScoreCreate Profile31 days agoRayzeBio
Manager, Quality Systems
Maintain gmp-compliant quality management systemReview and approve change controls and protocolsOversee deviation investigations for quality systems$124,449 - $150,803 py
The role is responsible for establishing, maintaining, and continuously improving the Quality Management System in accordance with global cGMPs
Indianapolis, IN, USFully remoteFull time+5y experienceJob Match ScoreCreate Profile31 days agoRayzeBio
Senior Supplier Quality Auditor
7 years qa auditing experienceCgmp gxp regulatory knowledgeSupplier audit execution skills$96,148 - $116,508 py
This role leads the planning, execution, and reporting of supplier audits to ensure compliance with cGMP/GxP regulations within a pioneering oncology biotech
Indianapolis, IN, USFully remoteFull time+7y experienceJob Match ScoreCreate Profile31 days ago
