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Medical Biotech Jobs in Indiana (NOW HIRING)

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Cleanroom Technician

Indianapolis, IN · On-site

$15 - $18/hr

Required Skills * 3+ years of cleanroom cleaning experience in pharmaceutical, biotech, or medical device environments * Experience with ISO Class 7/8 (Grade C) cleanrooms * Knowledge of GMP/GDP ...

Futures Consulting

Electrical Engineer EIT

Indianapolis, IN · On-site

$85K - $115K/yr

... medical, laboratory, commercial, public buildings such as healthcare, biotech, higher education, office, and large mixed-use residential buildings and hotels. Full knowledge and understanding of ...

AllSTEM Connections

IT Business Analyst

Indianapolis, IN · On-site

$140K - $145K/yr

Biotechnology Equal Opportunity Employer / Disabled / Protected Veterans The Know Your Rights ... medical, dental, vision, 401k and any statutory sick pay where required. We are committed to ...

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All JobsMedical Biotech JobsMedical Biotech Jobs in Indiana

Medical Biotech information

See Indiana salary details

$34.7K

$156.8K

$320.7K

How much do medical biotech jobs pay per year?

As of Aug 14, 2026, the average yearly pay for medical biotech in Indiana is $156,752.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,900.00 and $255,500.00 per year, depending on experience, location, and employer.

What can I do with a medical biotechnology degree?

A medical biotechnology degree prepares individuals for roles in research and development, clinical laboratories, and pharmaceutical companies. Graduates can work as research scientists, laboratory technicians, quality assurance specialists, or regulatory affairs professionals, often utilizing skills in molecular biology, cell culture, and data analysis. Certification and familiarity with laboratory tools and protocols enhance employment opportunities in healthcare and biotech industries.

What are the key skills and qualifications needed to thrive as a medical biotech professional?

To thrive as a Medical Biotech professional, you need a solid background in molecular biology, genetics, and laboratory techniques, often supported by a degree in biotechnology or a related field. Familiarity with lab equipment, PCR, data analysis software, and sometimes certifications like GLP (Good Laboratory Practice) are typically required. Strong problem-solving abilities, attention to detail, and effective communication skills help professionals excel in research and teamwork. These skills and qualities are crucial for ensuring scientific accuracy, regulatory compliance, and successful innovation in medical biotechnology.

What is a medical biotech professional?

Medical biotech professionals are scientists and technicians who use biological processes and technologies to develop products and solutions that improve human health. They work in areas such as developing new drugs, gene therapies, diagnostic tools, and vaccines. These professionals may be involved in laboratory research, clinical trials, regulatory affairs, or manufacturing. Their work often bridges the gap between scientific discovery and practical medical applications, contributing to advances in healthcare and treatment options.

Is medical biotechnology a good career?

Medical biotechnology is a growing field that involves developing medical products, therapies, and diagnostics using biological systems and organisms. It offers opportunities in research, development, and manufacturing, often requiring strong scientific skills and knowledge of laboratory techniques. The career can be rewarding for those interested in advancing healthcare and biotechnology innovations.

What are some common challenges faced by medical biotech professionals, and how can they be addressed?

Professionals in medical biotech often encounter challenges such as keeping pace with rapidly evolving technologies, navigating complex regulatory requirements, and managing cross-disciplinary collaboration. Staying current with scientific advancements requires continuous learning and adaptability. Regulatory compliance can be addressed through regular training and close coordination with quality assurance teams. Additionally, success in this field often depends on strong communication skills to effectively collaborate with research scientists, clinicians, and regulatory specialists.

What does a medical biotechnologist do?

A medical biotechnologist researches and develops technologies to improve healthcare, such as creating diagnostic tools, developing new treatments, and studying disease mechanisms. They often work in laboratories, using techniques like molecular biology and cell culture, and may require specialized training or certifications. Their work supports advancements in medical diagnostics, therapeutics, and personalized medicine.

What is the difference between Medical Biotech vs Clinical Research Associate?

AspectMedical BiotechClinical Research Associate
Required CredentialsBiotech degree, lab skills, sometimes advanced degreesLife sciences degree, clinical trial knowledge, certifications
Work EnvironmentLaboratories, biotech companies, research facilitiesClinical sites, hospitals, research organizations
Employer & Industry UsageBiotech firms, pharmaceutical companies, research institutionsPharmaceutical companies, CROs, hospitals

Medical Biotech professionals focus on developing and testing biotechnological products, often working in labs and research settings. Clinical Research Associates oversee clinical trials, ensuring compliance and data integrity at trial sites. While both roles require a background in life sciences and related certifications, Medical Biotech emphasizes product development, whereas Clinical Research Associates concentrate on trial management and regulatory adherence.

Medical Biotech jobs near you
Infographic showing various Medical Biotech job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $156,752 per year, or $75.4 per hour.

Quality Assurance Specialist

Stark Pharma Solutions Inc

Indianapolis, IN • On-site

Contractor

Re-posted 20 days ago

Job description

Job Title: Quality Assurance Specialist

Location: Indianapolis, IN
Duration: Long Term

Job Summary

We are seeking a detail-oriented Quality Assurance Specialist to support quality agreement management activities within a GMP-regulated pharmaceutical/biotech environment. The ideal candidate will be responsible for drafting, reviewing, negotiating, and maintaining quality agreements to ensure compliance with GxP regulations and internal quality standards.

The Quality Assurance Specialist will collaborate with internal cross-functional teams and external partners to support supplier qualification, regulatory compliance, and manufacturing readiness activities.

Key Responsibilities

  • Draft, review, revise, and maintain quality agreements in alignment with internal SOPs, GxP regulations, and company quality standards
  • Manage the full lifecycle of quality agreements from initiation through negotiation, execution, renewal, and closure
  • Partner with Quality Assurance, Procurement, Legal, Regulatory, and Manufacturing teams to resolve open items and obtain required approvals
  • Coordinate with external vendors, suppliers, and business partners to negotiate agreement terms and address redline comments
  • Maintain accurate tracking of agreement status, milestones, approvals, and version history within document management systems
  • Identify, communicate, and escalate risks or delays that may impact supplier qualification, product quality, regulatory compliance, or manufacturing operations
  • Support deviation investigations, CAPA activities, and change control processes related to quality systems documentation
  • Ensure compliance with FDA, cGMP, GDP, and internal quality management system requirements
  • Assist with internal audits, supplier audits, and regulatory inspections by providing quality documentation and support
  • Participate in continuous improvement initiatives related to quality agreement processes, templates, and document workflows

Experience

  • 3–5+ years of experience in a regulated pharmaceutical, biotechnology, medical device, or life sciences environment
  • Direct experience managing quality agreements, supplier quality documentation, or GxP-controlled records
  • Strong understanding of FDA regulations, cGMP, GDP, and quality systems requirements
  • Experience with document management systems, change control, CAPA, and deviation management processes
  • Strong technical writing, communication, negotiation, and organizational skills
  • Ability to manage multiple projects and deadlines within a fast-paced regulated environment