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How much do biopharma jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for biopharma in Indiana is $45.41, according to ZipRecruiter salary data. Most workers in this role earn between $28.84 and $55.66 per hour, depending on experience, location, and employer.

What is a biopharma?

A Biopharma job involves working in the biotechnology and pharmaceutical industries to research, develop, manufacture, or market biological drugs and therapies. Professionals in this field may work in roles such as research scientist, regulatory affairs specialist, manufacturing associate, or quality control analyst. Their work focuses on creating innovative treatments using biotechnology, like monoclonal antibodies, gene therapies, or vaccines. Careers in biopharma require expertise in biology, chemistry, engineering, or related fields and often involve collaboration with regulatory agencies to ensure product safety and efficacy.

What are the key skills and qualifications needed to thrive in biopharma?

To thrive in the biopharma industry, a strong background in life sciences, such as biology, chemistry, or pharmaceutical sciences, and relevant advanced degrees or experience are essential. Familiarity with laboratory techniques, regulatory compliance systems (like FDA or EMA guidelines), and specialized software for data analysis or clinical trials is typically required. Excellent analytical thinking, teamwork, and strong communication skills help professionals collaborate effectively and drive successful project outcomes. These abilities are important because the field demands rigorous scientific support, precise regulatory adherence, and effective multidisciplinary teamwork to advance new pharmaceutical products.

What are some typical career advancement opportunities in the biopharma industry?

The biopharma industry offers a range of career advancement paths, starting from entry- or associate-level scientific roles to more senior positions like project manager, lead scientist, or regulatory affairs specialist. With experience, professionals can transition into leadership roles overseeing research teams, clinical trial management, or move toward specialized areas like quality assurance, business development, or medical affairs. Many companies also support ongoing professional development through training, certifications, and opportunities to participate in high-impact projects. Advancement is often based on expanding technical expertise, strong performance, and the ability to successfully deliver results within cross-functional teams. This dynamic field rewards continuous learning and offers clear pathways for growth within both scientific and business tracks.

What are the most commonly searched types of Biopharma jobs in Indiana?

The most popular types of Biopharma jobs in Indiana are:

What are popular job titles related to Biopharma jobs in Indiana?

For Biopharma jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Biopharma jobs in Indiana look for?

The top searched job categories for Biopharma jobs in Indiana are:

What cities in Indiana are hiring for Biopharma jobs?

Cities in Indiana with the most Biopharma job openings:

Biopharma jobs near you
Infographic showing various Biopharma job openings in Indiana as of August 2026, with employment types broken down into 95% Full Time, 3% Part Time, 1% Contract, and 1% Nights. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $94,450 per year, or $45.4 per hour.

Senior Manager of Validation Engineering

INCOG BioPharma

Fishers, IN • On-site

$130 - $185/hr

Other

Posted yesterday

New

Job description

The Senior Manager of Validation Engineering is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing and packaging facility. The ideal candidate has practical experience in qualification and validation as well as leadership experience. The Senior Manager of Validation Engineering will partner with internal and external customers to meet the needs of client projects, capital expansion projects, and maintenance of the validated state. They will possess a demonstrated ability to influence positive outcomes and have direct reporting authority.Additionally, they must thoroughly understand and be able to adapt to the changing needs of a manufacturing environment.

Essential Job Functions:
  • Lead the Validation department with Commissioning, Qualification and Validation (CQV) activities for utilities, equipment and associated systems. This includes, but is not limited to, clean utilities, steam sterilization and depyrogenation, manual and automated cleaning, filling, inspection, packaging and labeling, etc.
  • Review and approve CQV lifecycle documentation.
  • Support and oversee development and maintenance of validation lifecycle documents, document templates, validation strategies and policies.
  • Support site change management program, including risk assessment and evaluation of required testing and GMP activities.
  • Assess risks involved in processing steps related to equipment, developing and/or reviewing validation requirements and design deliverables.
  • Interact with clients to provide validation support including, but not limited to, customer product launches, new equipment qualifications, audits, etc.
  • Review and provide technical expertise to regulatory filings, and support health authority inspections.
  • Support and provide validation oversight for capital expansion projects/build outs. This includes development and maintenance of CQV schedule for capital projects.
  • Engage in a cross functional team and work closely with other supporting groups including Engineering and Operations to support and monitor validation and process improvement efforts.
Special Job Requirements:
  • Bachelor's degree or higher in a STEM discipline, preference in an engineering or life science discipline
  • 10+ years of experience in Validation or related discipline
  • 8+ year GMP experience required or other regulated industry
  • 5+ years of supervisory experience
  • Physically capable of working onsite
Additional Preferences:
  • Aseptic Fill and Finish Experience
  • Experienced with cleaning validation, steam and dry heat sterilization and depyrogenation, inspection and packaging
  • Strong working knowledge of regulatory requirements, risk-based guidance, and industry expectations
  • Continuous improvement certification, i.e., Lean Six Sigma, or similar practices
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.

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.

Qualified applicants must be authorized to work in the United States on a full-time basis. INCOG will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

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