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How much do biopharma jobs pay per hour?

As of Jul 18, 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 job?

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 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 key skills and qualifications needed to thrive in the Biopharma position, and why are they important?

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 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
Senior Manager Site Security

Senior Manager Site Security

INCOG BioPharma Services

Fishers, IN • On-site

$16.75 - $20.50/hr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Description
This position will serve as INCOG's leader for managing and executing the site security program at INCOG Biopharma, a contract development and manufacturing organization (CDMO). This role ensures the safety and security of employees, visitors, facilities, intellectual property and biopharmaceutical product supporting GMP operations for its clients.
The Site Security Manager partners cross-functionally with Operations, Quality, EH&S, Facilities, People and Culture and IT to ensure security controls are effective, compliant, and aligned with business needs in a regulated biopharmaceutical manufacturing environment. This role is accountable for driving continuous improvement of site security processes, controls, and systems and delivering security enhancements that meet or exceed biopharmaceutical industry standards and best practices.
Essential Job Functions:
Site Security Operations & Continuous Improvement
  • Manage day-to-day site security operations, ensuring consistent coverage and adherence to established policies and procedures.
  • Serve as the primary site contact for all security-related matters.
  • Maintain site security SOPs in alignment with GMP expectations and corporate standards.
  • Proactively identify opportunities for security process improvement, risk reduction, and operational efficiency.

Physical Security & Access Control
  • Oversee physical security systems including access control, CCTV, badging, alarms, and visitor management.
  • Manage employee, contractor, and visitor access privileges based on role and authorization.
  • Conduct routine security inspections, risk assessments, and vulnerability reviews.

GMP & Client Compliance
  • Ensure security practices support GMP compliance and inspection readiness.
  • Support regulatory inspections and client audits by providing documentation and site security walkthroughs.
  • Partner with Quality to address security-related deviations, investigations, and CAPAs when applicable.

Incident Response & Investigations
  • Lead response to security incidents, including unauthorized access, theft, safety concerns, or workplace disruptions.
  • Conduct investigations, document findings, and implement corrective actions.
  • Maintain incident logs and trend security events to identify improvement opportunities.

Vendor & Contract Management
  • Manage contracted security services and vendors, including performance monitoring and issue resolution.
  • Coordinate guard coverage, schedules, and post orders as required by site operations.
  • Assist with security budget planning and cost control.

Training & Awareness
  • Deliver site security orientation and awareness training for employees and contractors.
  • Promote a strong security culture while minimizing disruption to manufacturing and laboratory operations.
  • Provide guidance to site leadership on security best practices and emerging risks.

Emergency Preparedness
  • Support site emergency response plans and drills in coordination with EH&S and Facilities.
  • Serve as a security representative on the site emergency response or crisis management team.
  • Coordinate with local emergency services as needed.

Special Job Requirements:
  • Bachelor's degree in Security Management, Criminal Justice, Risk Management, or related field, or equivalent experience.
  • 10+ years of experience in public law enforcement or federal agencies.
  • Experience managing physical security systems and contract security vendors.
  • Working knowledge of GMP environments and inspection readiness.
  • Strong incident investigation and report-writing skills.

Additional Preferences:
  • Prior site security experience within pharmaceutical, biotech, or other regulated manufacturing environments.
  • Security certifications such as CPP, PSP, or similar.
  • Experience supporting FDA or client audits.

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.
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.
By submitting your resume and details, you are declaring that the information is correct and accurate.

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