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Advanced Biotech Jobs in Indiana (NOW HIRING)

Merck & Co.

$79K - $124K/yr

... biotechnology, or medical devices. S2 Level: Bachelor's degree (BA/BS), or High school diploma or ... Proficient in using advanced analytics to generate customer insights and drive sales. Comfortable ...

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Advanced Biotech information

See Indiana salary details

$47.6K

$84.3K

$128.5K

How much do advanced biotech jobs pay per year?

As of Jul 17, 2026, the average yearly pay for advanced biotech in Indiana is $84,344.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,400.00 and $94,700.00 per year, depending on experience, location, and employer.

What is an Advanced Biotech professional?

An Advanced Biotech professional works in the biotechnology industry, specializing in the use of advanced technologies and biological systems to develop new products and solutions in fields such as healthcare, agriculture, and environmental management. Their work often involves genetic engineering, molecular biology, and bioinformatics to innovate and improve processes, medications, and sustainable practices. These professionals may work in research, product development, quality control, or regulatory compliance, and typically require a strong background in biological sciences and technology.

What is the difference between Advanced Biotech vs Laboratory Technician?

AspectAdvanced BiotechLaboratory Technician
Required CredentialsBachelor's degree in biotechnology, biology, or related field; sometimes certifications in lab techniquesAssociate's or bachelor's degree in laboratory science or related field; certification may be preferred
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsHospitals, research labs, manufacturing facilities
Employer & Industry UsageBiotech firms, pharmaceutical companies, research institutionsHospitals, diagnostic labs, biotech and research companies

Advanced Biotech professionals typically hold higher degrees and engage in complex research and development tasks, while Laboratory Technicians focus on conducting tests and supporting lab operations. Both roles are essential in biotech and healthcare industries, but they differ in responsibilities and qualifications.

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

Professionals in advanced biotech roles often encounter challenges such as rapidly evolving technologies, strict regulatory environments, and the need for interdisciplinary collaboration. Staying up-to-date with scientific advancements and regulatory changes is crucial, and many organizations support this through ongoing training and professional development. Effective communication and teamwork are also essential, as projects typically involve working closely with researchers, engineers, and business teams. Embracing a culture of continuous learning and open collaboration can help overcome these challenges and contribute to both personal and organizational success.

What are the key skills and qualifications needed to thrive as an Advanced Biotech Professional, and why are they important?

To thrive as an Advanced Biotech Professional, you need a strong background in molecular biology, genetics, and biochemistry, typically supported by an advanced degree in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), bioinformatics tools, and relevant certifications such as GLP or GMP compliance are highly valued. Analytical thinking, attention to detail, and strong teamwork skills set exceptional candidates apart. These competencies are crucial for ensuring accurate research, regulatory compliance, and successful collaboration in innovative biotech environments.
What are popular job titles related to Advanced Biotech jobs in Indiana? For Advanced Biotech jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Advanced Biotech jobs in Indiana look for? The top searched job categories for Advanced Biotech jobs in Indiana are:
Advanced Biotech jobs near you
Infographic showing various Advanced Biotech job openings in Indiana as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 17% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $84,344 per year, or $40.5 per hour.
Advisor - Molecular Biology, Analytical Development - BR&D

Advisor - Molecular Biology, Analytical Development - BR&D

Eli Lilly and Company

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 days ago

Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

10th of 74 rated pharmaceutical

Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
Position Overview:
The BRD Analytical Development team is seeking an Advisor to support analytical development for genetic medicines and advanced therapy medicinal products (ATMPs). This role is primarily laboratory-based, with responsibility for developing and qualifying analytical methods that characterize drug substance and drug product quality attributes across the genetic medicines portfolio, spanning early-phase IND-enabling studies through commercial BLA readiness. The successful candidate will have practical expertise in molecular biology and nucleic acid analytics and will contribute to GMP analytical activities within a cross-functional CMC development environment.
Key Responsibilities:
  • Develop, qualify, and execute PCR-based methods (qPCR, ddPCR/dPCR) for viral vector genome titration, residual DNA quantitation, and related nucleic acid analytes in support of genetic medicine programs.
  • Experience with immunoassay platforms (ELISA, MSD, Gyrolab) for residual host cell protein or impurity testing.
  • Apply molecular biology techniques including 1- and 2-D gel electrophoresis, blotting, and restriction enzyme analysis for product characterization.
  • Contribute to analytical control strategies for genetic medicine drug substance and drug product, including identification of critical quality attributes (CQAs) and appropriate test methods.
  • Support assay qualification, verification, and validation activities per ICH Q2(R2) and applicable regulatory expectations for genetic medicine and ATMP products.
  • Contribute analytical data and technical content supporting stability study design and execution across DS and DP matrices.
  • Ensure all analytical work is conducted in compliance with GMP, GLP, and applicable HSE requirements; maintain awareness of internal quality procedures and regulatory expectations.
  • Author and review analytical methods, protocols, qualification/validation reports, method transfer packages, and technical summaries with high scientific accuracy and clarity.
  • Maintain rigorous electronic laboratory notebook (ELN) practices and documentation standards for all experimental records.
  • Support technology transfer of analytical methods to CRO/CMO partners and Lilly manufacturing sites; participate in cross-site qualification or co-validation studies.
  • Provide technical input during interactions with external analytical partners; review and interpret externally generated data packages.
  • Maintain awareness of emerging analytical technologies, regulatory guidance updates, and industry best practices relevant to genetic medicine analytical development.
  • Collaborate within cross-functional project teams including process development, quality, regulatory affairs, and clinical operations to deliver analytical support for clinical trials and regulatory submissions.
  • Communicate analytical results, timelines, and technical challenges clearly to team members and project stakeholders in oral and written formats.
  • Contribute to a positive, inclusive, and scientifically rigorous team culture; share technical knowledge and support the growth of colleagues.

Basic Qualifications:
  • Ph.D. in Molecular Biology, Biochemistry, Biology, or Analytical Chemistry; with 0-5+ years of relevant pharmaceutical or biotech industry experience; or
  • M.S. in Molecular Biology, Biochemistry, Biology, or Analytical Chemistry; with 6+ years of relevant pharmaceutical or biotech industry experience; or
  • B.S. in Molecular Biology, Biochemistry, Biology, or Analytical Chemistry; with 12+ years of relevant pharmaceutical or biotech industry experience.
  • Practical proficiency with qPCR and/or ddPCR/dPCR for quantitative nucleic acid analysis in a pharmaceutical or biotech development context.
  • Practical proficiency with immunoassay platforms (ELISA and/or related technologies) for quantitative analysis of process-related impurities or product quality attributes in a pharmaceutical or biotech development context.
  • Hands-on experience with molecular biology techniques (gel electrophoresis, blotting, restriction analysis) applied to biopharmaceutical or genetic medicine characterization.
  • Demonstrated ability to independently design experiments, generate high-quality data, and interpret results in a development environment.
  • Familiarity with GMP/GLP requirements and their application to analytical method development and documentation.

Additional Skills & Preferences
  • Experience with viral vector (AAV, LVV) or cell therapy analytical programs, including genome integrity, residual DNA, and encapsidation efficiency assessments.
  • Familiarity with NGS workflows (library preparation, sequencing, bioinformatic interpretation) as an orthogonal characterization approach for genetic medicine products.
  • Knowledge of FDA/EMA regulatory expectations for nucleic acid-based CQA testing in genetic medicine CMC submissions.
  • Experience supporting analytical aspects of IND or BLA/MAA submissions, including contributing to Module 3 analytical sections.
  • Experience with method transfer to external CRO/CMO organizations and participation in inter-laboratory comparability studies.
  • Proficiency with electronic laboratory notebooks (e.g., Benchling) and data management systems.
  • Effective oral and written communication skills; ability to present complex technical information to multidisciplinary audiences.
  • Demonstrated ability to manage multiple priorities and work productively in a fast-paced, collaborative team environment.

Additional Information
  • Travel: 0 to 15%.
  • Potential exposure to chemicals, allergens, and loud noises.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$126,000 - $244,200
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
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About Eli Lilly

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Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876

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