Last updated: 2025-05-22

25 Quality Assurance And Engineering jobs in Indianapolis.

Hiring now: Manufacturing Spec 2Nd Sh @ Incog Biop, Consultant @ Project Fa, Technical Ops Consultant @ Precision , Sr Spec Quality Assurance @ Cardinal H, Quality Mgr @ Azenta Lif, Process Expert Comecer Li @ Novartis, Healthcare Quality Adviso @ Federal Ex, Manufacturing Team Leader @ Genezen, Cqv Engr @ Cai, Clinical Trial Labeling C @ Keywords.Explore more at at kaamvaam.com

🔥 Skills

GMP (9) continuous improvement (6) project management (5) Compliance (5) validation (4) compliance (4) pharmaceutical (3) aseptic processing (3) training (3) Project Management (3)

📍 Locations

Indianapolis (21) Fishers (4)

Incog Biopharma Services

Skills & Focus: manufacturing, GMP, pharmaceutical, aseptic, filling, equipment, validation, troubleshooting, continuous improvement, batch records
About the Company: At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs focused on building long-term value, technical excellence, and a service-cu…
Experience: High School diploma and 7 years of GMP pharmaceutical experience
Skills & Focus: visual inspection, packaging, cGMP requirements, technical support, leadership, quality inspection, process development, team management, pharmaceutical packaging, Aseptic techniques
About the Company: 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 lo…
Experience: 8 years related experience in the development or support of processes, quality inspection, or pharmaceutical packaging.
Type: Full-time
Skills & Focus: pharmaceutical manufacturing, GMP, aseptic processing, cleanrooms, production equipment, documentation, training, continuous improvement, collaboration, technical excellence
About the Company: 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 lo…
Experience: High School diploma and 3 years of GMP pharmaceutical experience

Project Farma

Consultant Indianapolis
Skills & Focus: biomanufacturing, project management, validation, quality/compliance, engineering, client management, business development, problem solving, teamwork, customer focused
About the Company: Project Farma (PF) is the leading advanced therapy technical operations consulting company in the life science industry, providing biomanufacturing strategy an…
Experience: A minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience
Salary: Competitive salary based on experience
Type: Full-time
Benefits: Aggressive bonus structure, Medical, Dental, and Vision insurance effective the first day of employment, 401k Plan with…
Skills & Focus: CQV Engineering, life science, project management, validation, quality compliance, technical documentation, mentoring, team development, business development, process validation
About the Company: Project Farma is the leading advanced therapy technical operations consulting company in the life science industry, committed to advancing manufacturing to ach…
Experience: A minimum of 3 years of Project Engineer, Consulting, and/or relevant industry experience.
Salary: $50,000 - $240,000 USD
Type: Full-time
Benefits: Competitive salary, aggressive bonus structure, medical, dental, and vision insurance, 401k plan with company match, pa…

Precision For Medicine, Manufacturing Solutions

Skills & Focus: technical operations, advanced therapy manufacturing, GxP best practices, project management, quality/compliance, validation protocols, cross-functional collaboration, engineering life cycle, client support, patient focused
About the Company: Precision for Medicine, Manufacturing Solutions is the leading advanced therapy technical operations consulting company in the life science industry, committed…
Experience: Bachelor’s degree in Life Science, Engineering, or related discipline and/or comparable military experience.
Salary: $58,000 — $63,000 USD
Type: Full-time
Benefits: Competitive salary based on experience, Aggressive bonus structure, Medical, Dental, and Vision insurance effective you…

Project Farma

Project Engineer Indianapolis
Skills & Focus: Technical Delivery, Biomanufacturing, Project Management, Cell and Gene Therapy, Validation Life Cycle, Quality, Regulatory, Compliance, Engineering Automation, Patient Focused
About the Company: Project Farma (PF) is the leading advanced therapy technical operations consulting company in the life science industry, providing biomanufacturing strategy an…
Experience: 0-3 years of consulting and/or project engineer experience
Salary: Competitive salary based on experience
Benefits: Competitive salary, aggressive bonus structure, Medical, Dental, and Vision insurance, 401k Plan with company match, Pa…

Cardinal Health

Skills & Focus: quality systems, compliance, GMP, root cause analysis, investigations, regulatory, FDA, cGMP, batch documentation, corrective actions
Experience: 2+ years’ experience in related field preferred
Salary: $67,500 - $95,000
Type: Full time
Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. Medical, dental and vi…
Skills & Focus: quality assurance, compliance, regulations, root cause analysis, corrective actions, gap assessments, analytical metrics, training, audits, radiopharmaceutical
About the Company: Cardinal Health is responsible for developing and implementing a compliant and cost-effective quality system that assures products and services are reliable, s…
Experience: 4+ years experience in related field
Salary: $79,300 - $113,800
Type: Full time
Benefits: Medical, dental and vision coverage, Paid time off plan, Health savings account (HSA), 401k savings plan, Access to wag…

Azenta Life Sciences

Quality Manager Indianapolis
Skills & Focus: Quality Manager, Quality Assurance, QMS, Compliance, Internal Audit, Continuous Improvement, Performance Management, Team Management, Regulatory Requirements, Life Sciences
About the Company: Azenta Life Sciences is a global leader in the life sciences space with headquarters in Burlington, MA, and offices and operations worldwide. We provide unpara…
Experience: 4 years of Quality Assurance related work experience required. Life sciences preferred.
Type: Full-time

Novartis

Skills & Focus: manufacturing, GMP, SOPs, process improvement, quality, safety, training, documentation, deviation investigations, continuous improvement
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Experience: 1+ years of experience in a manufacturing environment, preferably in pharmaceutical manufacturing
Type: Full-time

Federal Express Corporation

Skills & Focus: healthcare, quality assurance, management, project management, continuous improvement, business, transportation, logistics, supply chain, compliance
Experience: Five (5) years’ minimum experience required in healthcare quality
Salary: Indianapolis Pay Range: $6,511.62/month - $8,627.89/month; Newark Pay Range: $7,882.48/month - $10,444.28/month
Type: Full Time
Benefits: health, vision and dental insurance, retirement, and tuition reimbursement

Project Farma

Skills & Focus: Project Management, Validation, Engineering, Quality/Compliance, Technical Documents, GxP Best Practices, Troubleshooting, Client Support, Manufacturing Processes, Patient Focused
About the Company: Leading advanced therapy technical operations consulting company in the life science industry.
Experience: Bachelor’s degree in Life Science, Engineering, or related discipline and/or comparable military experience
Salary: $50,000 - $240,000 USD
Type: Full-time
Benefits: Competitive salary based on experience, Aggressive bonus structure, Medical, Dental, and Vision insurance, 401k Plan wi…

Genezen

Skills & Focus: gene therapy, GMP, vector manufacturing, aseptic processing, process improvements, compliance, EHS, performance management, supervisory experience, cleaning/sanitization
About the Company: Genezen is a fast-growing company in the field of gene therapy, providing process development, GMP viral vector production, and cell transduction for gene and …
Experience: 3 years of related work experience in a GMP environment; 1 year of supervisory experience
Type: Full-time
Benefits: Paid vacation days, paid sick time, observed holidays, 401(k) plan with company match, Share Appreciation Rights, choic…

Cardinal Health

Skills & Focus: Quality Assurance, GMP compliance, root cause analysis, corrective actions, regulatory requirements, FDA, pharmaceutical, working knowledge, Document Management software, relevant regulations
Experience: 2+ years’ experience in related field preferred
Salary: $64,000 - $92,500
Type: Full time
Benefits: Medical, dental and vision coverage, Paid time off plan, Health savings account (HSA), 401k savings plan, Access to wag…
Skills & Focus: Quality Control, Chemistry, cGMP compliance, SOPs, analytical testing, laboratory investigations, regulatory requirements, technical writing, pharmaceutical, medical device
About the Company: At Cardinal Health, we’re developing the innovative products and services that make healthcare safer and more productive. Join a growing, global company genuin…
Experience: 2+ years of relevant work experience working with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device) preferred.
Salary: $67,500- $92,400
Type: Full time
Benefits: Medical, dental and vision coverage, Paid time off plan, Health savings account (HSA), 401k savings plan, Access to wag…

Genezen

Skills & Focus: maintenance, calibration, GMP, equipment, ISO standards, support, metrics, qualification, validation, continuous improvement
About the Company: Genezen provides process development, GMP viral vectors production, and cell transduction for gene and cell therapy clinical trials, focusing on innovative hea…
Skills & Focus: gene therapy, engineering projects, project management, continuous improvement, EHS compliance, change management, CQV, GMP, collaboration, workflow optimization
About the Company: Genezen is a company that provides process development, produces GMP viral vectors, and offers cell transduction for gene and cell therapy clinical trials, con…
Experience: 3+ years of engineering/project management experience
Type: Full-time
Benefits: Paid vacation days, paid sick time, observed holidays, 401(k) plan with company match, Share Appreciation Rights, healt…

Cai

CQV Engineer Indianapolis
Skills & Focus: CQV, Commissioning, Qualification, Validation, Manufacturing process equipment, Filling, Packaging, Inspection equipment, Problem-solving, Team management
About the Company: CAI is a 100% employee-owned company established in 1996 that has grown to more than 800 people worldwide. We provide commissioning, qualification, validation,…
Experience: 2-4 years' experience with commissioning, qualification and/or validation preferred
Salary: Competitive compensation
Type: Full-time
Benefits: Competitive compensation and benefits which include: up to 15% retirement contribution, 24 days PTO and 5 sick days per…

Keywords

Skills & Focus: Change Management, Deviation Management, Compliance, CAPA, Project Management, Root Cause Analysis, Quality Standards, Communication, Process Improvement, Multi-tasking
About the Company: Keywords provides a competitive compensation package, good benefits and a casual, fun, productive and supportive working environment. We empower people to perf…
Salary: $24/hr
Type: Full-time
Benefits: Medical, dental and vision benefits, Paid time off (including sick and select holidays), 401(k) enrollment with 3% empl…

Baxter

Skills & Focus: Quality, Compliance, Hospital, Products, Medical, Healthcare, Manufacturing, Regulatory, Testing, Engineering
About the Company: Baxter provides a broad portfolio of essential renal and hospital products, as well as a leading presence in the changing markets.
Type: Full time

Novartis

Skills & Focus: Quality Management, GMP, Biopharmaceuticals, Compliance, Health Authority Inspections, Quality Assurance, Training, Data Integrity, Quality Systems, Continuous Improvement
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Experience: 6 years of experience in a GMP Biopharmaceutical environment, including at least 2 years of experience in a Quality Assurance role.

Cai

CQV Engineer Indianapolis
Skills & Focus: CQV Engineering, Commissioning, Qualifications, Validation, Protocol writing, Field verification, Project management, ISPE Baseline Guide 5, Regulated Industry, Troubleshooting
About the Company: CAI is a 100% employee-owned company established in 1996, that has grown year over year to more than 800 people worldwide. We provide commissioning, qualificat…
Experience: 4-8 years in commissioning and/or qualification activities in a regulated industry
Type: Full-time
Benefits: Competitive compensation and benefits include: up to 15% retirement contribution, 24 days PTO, 5 sick days per year, he…

Genezen

Skills & Focus: GMP, viral vector production, aseptic technique, chromatography, clarification, TFF, cell culture, SOPs, batch records, downstream manufacturing
About the Company: Genezen is a company in the gene therapy field that provides process development, produces GMP viral vectors, and provides cell transduction for gene and cell …
Experience: Minimum 2 years of post-graduation experience in a GMP environment; 2 years of experience operating in a GMP laboratory using aseptic technique; 2 years of experience with at scale Clarification, Chromatography, and TFF platforms.
Type: Full-time
Benefits: Paid vacation days, paid sick time, 10 observed holidays + 2 floating holidays + 1 volunteer day, 401(k) plan with comp…