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Project Manager Biotech Jobs in Indiana (NOW HIRING)

Engineering Project Manager

Indianapolis, IN ยท On-site

$110K - $160K/hr

Demonstrated experience managing engineering or capital projects in pharmaceutical, biotechnology, medical device, or another regulated manufacturing environment. * Experience with CAPEX planning ...

CAPITAL PROJECT MANAGER

Mount Vernon, IN ยท On-site

$100K - $150K/yr

... biotechnology, medical device, chemical, or other regulated manufacturing environments. * Demonstrated experience managing projects involving facility expansion, manufacturing equipment, process ...

CAPITAL PROJECT MANAGER

Mount Vernon, IN ยท On-site

$100K - $150K/yr

... biotechnology, medical device, chemical, or other regulated manufacturing environments. * Demonstrated experience managing projects involving facility expansion, manufacturing equipment, process ...

... biotechnology, medical device, chemical, or other regulated manufacturing environments. * Demonstrated experience managing projects involving facility expansion, manufacturing equipment, process ...

... pharma, biotech, academic and research institutions, that support critical life science ... We are looking for a project management professional who can lead with structure, collaborate ...

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Showing results 1-20

Project Manager Biotech information

See Indiana salary details

$20

$44

$72

How much do project manager biotech jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for project manager biotech in Indiana is $44.00, according to ZipRecruiter salary data. Most workers in this role earn between $38.22 and $48.27 per hour, depending on experience, location, and employer.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.
What are popular job titles related to Project Manager Biotech jobs in Indiana? For Project Manager Biotech jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Project Manager Biotech jobs? Cities in Indiana with the most Project Manager Biotech job openings:
Infographic showing various Project Manager Biotech job openings in Indiana as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $91,525 per year, or $44 per hour.

Engineering Project Manager

Genovice

Indianapolis, IN โ€ข On-site

$110K - $160K/hr

Contractor

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Engineering Project Manager – CAPEX
Location: Indianapolis, IN
Duration: 6-month contract
Department: Engineering
Industry: Pharmaceutical Manufacturing
Position Summary

Our client is seeking an experienced Engineering Project Manager to support engineering and capital projects within a regulated pharmaceutical manufacturing environment. This individual will report directly to Engineering leadership and coordinate the planning, execution, and delivery of CAPEX initiatives.

The ideal candidate has experience managing engineering projects involving equipment, facilities, utilities, or manufacturing infrastructure and can effectively coordinate internal stakeholders, vendors, contractors, budgets, schedules, and project documentation.

Key Responsibilities
  • Manage engineering and CAPEX projects from planning through execution and closeout.
  • Develop and maintain project scopes, schedules, budgets, milestones, and resource plans.
  • Coordinate activities across Engineering, Manufacturing, Quality, Validation, Facilities, EHS, and other stakeholders.
  • Manage external vendors, engineering firms, contractors, and equipment suppliers.
  • Track project costs, commitments, forecasts, risks, and schedule performance.
  • Lead project meetings and provide clear status updates to Engineering leadership.
  • Identify project risks, constraints, and dependencies and coordinate timely resolution.
  • Support equipment procurement, installation, commissioning, qualification, and turnover activities.
  • Ensure projects comply with site procedures, safety requirements, change-control processes, and applicable GMP expectations.
  • Maintain accurate project records, decisions, action items, and closeout documentation.
  • Help manage project changes while minimizing impacts to budget, schedule, and operations.
Required Qualifications
  • Bachelor’s degree in Engineering, Construction Management, Project Management, or a related technical field.
  • Demonstrated experience managing engineering or capital projects in pharmaceutical, biotechnology, medical device, or another regulated manufacturing environment.
  • Experience with CAPEX planning, budgeting, forecasting, and cost tracking.
  • Strong experience managing project schedules, vendors, contractors, and cross-functional teams.
  • Understanding of GMP environments and engineering change-control processes.
  • Strong communication, organization, problem-solving, and stakeholder-management skills.
  • Ability to manage multiple priorities and independently drive projects to completion.
Preferred Qualifications
  • Experience supporting pharmaceutical manufacturing facilities, laboratories, utilities, or process equipment.
  • Familiarity with commissioning, qualification, and validation activities.
  • PMP certification or comparable project-management training.
  • Experience with radiopharmaceutical manufacturing or similarly complex regulated operations.
  • Proficiency with project-management and scheduling tools such as Microsoft Project, Smartsheet, or equivalent platforms.