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Entry Level Biopharma Jobs in Indiana (NOW HIRING)

INCOG

Senior Technical Transfer Engineer

Fishers, IN · On-site

Provide technical guidance and mentorship to Entry Level engineers and review their work * Author ... At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture ...

INCOG

QC Scientist, Weekend Nights

Fishers, IN · On-site

This entry-level role focuses on accurate execution, strong Good Documentation Practices (GDP), and ... At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture ...

Immune Biopharma

Pharmaceutical Detail Rep

Fort Wayne, IN · On-site

$89K - $119K/yr

Pharmaceutical Sales Representative (Specialty to entry level both available) Pharmaceutical Sales Rep Opening Summary: We are seeking driven, collaborative and positive sales leaders to build out ...

Immune Biopharma

Pharmaceutical Detail Rep

Carmel, IN · On-site

$89K - $119K/yr

Pharmaceutical Sales Representative (Specialty to entry level both available) Pharmaceutical Sales Rep Opening Summary: We are seeking driven, collaborative and positive sales leaders to build out ...

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All JobsBiopharma JobsEntry Level Biopharma JobsEntry Level Biopharma Jobs in Indiana

Entry Level Biopharma information

See Indiana salary details

$28.1K

$46.4K

$58.5K

How much do entry level biopharma jobs pay per year?

As of Aug 8, 2026, the average yearly pay for entry level biopharma in Indiana is $46,448.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,900.00 and $50,400.00 per year, depending on experience, location, and employer.

What are common daily responsibilities for someone in an entry level biopharma position?

In an Entry Level Biopharma role, your daily tasks typically involve conducting laboratory experiments, recording and analyzing data, preparing samples, and assisting more senior scientists with research projects. You may also be responsible for maintaining lab equipment, adhering to safety protocols, and documenting results for regulatory compliance. Collaboration is an important aspect, as you often work closely with scientists, quality assurance teams, and production staff to ensure study goals are met. This hands-on experience offers a solid foundation for understanding the intricacies of biopharmaceutical research and sets the stage for future advancement.

What is an entry level biopharma?

An Entry Level Biopharma job is a starting position in the biopharmaceutical industry, typically for recent graduates or individuals with limited experience. These roles can include positions in research, manufacturing, quality control, regulatory affairs, or clinical trials. Responsibilities may involve conducting experiments, analyzing data, ensuring compliance with industry regulations, or assisting in production processes. Employers generally look for candidates with degrees in biology, chemistry, biotechnology, or related fields. This role provides foundational experience for career growth in the biopharma industry.

What are the key skills and qualifications needed to thrive in an entry level biopharma position?

To thrive as an Entry Level Biopharma professional, you typically need a bachelor’s degree in biology, chemistry, or a related field, along with foundational laboratory skills and a detail-oriented mindset. Familiarity with laboratory equipment, data analysis software, and adherence to Good Laboratory Practices (GLP) are often required, while some roles may value experience with regulatory documentation. Key soft skills include effective communication, adaptability, and the ability to work collaboratively within cross-functional teams. These competencies ensure accurate experimental results, efficient workflow, and strong integration within dynamic biopharma projects.

What are the most commonly searched types of Biopharma jobs in Indiana? The most popular types of Biopharma jobs in Indiana are:
What job categories do people searching Entry Level Biopharma jobs in Indiana look for? The top searched job categories for Entry Level Biopharma jobs in Indiana are:
What cities in Indiana are hiring for Entry Level Biopharma jobs? Cities in Indiana with the most Entry Level Biopharma job openings:
Entry Level Biopharma jobs near you
Infographic showing various Entry Level Biopharma job openings in Indiana as of July 2026, with employment types broken down into 27% Locum Tenens, 67% Full Time, 4% Part Time, and 2% Contract. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $46,448 per year, or $22.3 per hour.

QC Scientist, Weekend Nights

INCOG BioPharma Services

Fishers, IN • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 10 days ago

Job description

Description
Weekend QC Scientist Summary
The Weekend QC Scientist supports GMP manufacturing and laboratory operations by performing routine microbiology and chemistry testing, sample handling, and laboratory support activities under approved procedures and supervision. This entry-level role focuses on accurate execution, strong Good Documentation Practices (GDP), and maintaining laboratory readiness during weekend operations.
Work Schedule
  • Friday-Sunday 12-hour shifts (36 hours/week)
  • Night Shift (7p - 7:30a)
  • Additional hours may be required to support operational needs, on-demand testing, or quality events.-demand testing, or quality events.

Essential Job Functions:
A) Laboratory Testing & Sample Support
  • Perform routine microbiology and chemistry testing in accordance with approved methods, SOPs, and GMP requirements.
  • Support testing of materials that may include raw materials, utilities, in-process samples, finished products, stability, environmental, or validation-related samples, as assigned.-process samples, finished products, stability, environmental, or validation-related samples, as assigned.
  • Perform sample receipt, labeling, log-in, tracking, storage, incubation/handling, and disposal activities per procedure.
  • Escalate atypical results, execution concerns, or equipment issues promptly to on-shift scientist and/or area leadership.

B) Laboratory Operations & Readiness
  • Support daily laboratory operations, including:
    • Glassware washing and preparation
    • Reagent preparation (as trained)
    • Consumables inventory management and restocking
    • Laboratory cleaning, waste handling, and 5S activities
  • Perform basic equipment checks, verifications, and routine maintenance activities within trained scope.
  • Ensure laboratory spaces, instruments, and documentation remain inspection-ready at all times.-ready at all times

C) Documentation & Data Integrity
  • Accurately complete laboratory forms, logbooks, and electronic records in compliance with GDP and data integrity principles.
  • Perform second-person verifications or peer reviews of data and documentation, as trained and assigned.-person verifications or peer reviews of data and documentation, as trained and assigned.
  • Support laboratory investigations and deviations by gathering documentation, performing authorized re-work, and assisting senior staff.

D) Safety, Compliance & Teamwork
  • Follow all GMP, safety, biosafety, and chemical hygiene requirements, including proper PPE use.
  • Work collaboratively with QC Scientists, Technicians, and cross-functional partners to ensure timely and compliant testing.-functional partners to ensure timely and compliant testing.
  • Demonstrate reliability and accountability as a weekend team member supporting ongoing manufacturing operations.
  • Participate in required training, cross-training, and continuous improvement activities.-training, and continuous improvement activities.

Special Job Requirements
• Bachelor's degree coursework in a scientific discipline (e.g., Biology, Microbiology, Chemistry).
• Minimum of 2 years of hands on experience performing Quality Control testing within a GMP/GDP environment.
• Ability to follow written procedures and perform routine laboratory tasks with accuracy and consistency.
• Strong attention to detail and commitment to documentation accuracy.
• Willingness and ability to work 12-hour weekend shifts.
Preferred Qualifications
  • Exposure to both microbiology and chemistry laboratory operations.
  • Familiarity with laboratory documentation systems (paper or electronic).
  • Experience supporting investigations, audits, or inspection readiness activities.

INCOG's Benefits:
• Paid time off, based on tenure.
• 11 observed holidays + 1 floating holiday.
• Choice to elect pet insurance.
• 401(k) plan with company match up to 3.5% of salary, vested immediately.
• Choice of health & wellness plans.
• FSA and HSA programs.
• Dental & vision care.
Additional info about INCOG BioPharma Services:
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 long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.
If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.
INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.
By submitting your resume and details, you are declaring that the information is correct and accurate.

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