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Biotech Startup Jobs in Indiana (NOW HIRING)

CRA 1, IQVIA Biotech

Indianapolis, IN · On-site

$71K - $145K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...

... biotechnology, or similarly regulated manufacturing environment. * Working knowledge of Process Safety Management (PSM), Management of Change (MOC), and startup readiness processes. * Experience ...

PSSR Coordinator

Lebanon, IN · On-site

$70K - $85K/yr

... biotechnology, or similarly regulated manufacturing environment. * Working knowledge of Process Safety Management (PSM), Management of Change (MOC), and startup readiness processes. * Experience ...

... biotechnology, or similarly regulated manufacturing environment. * Working knowledge of Process Safety Management (PSM), Management of Change (MOC), and startup readiness processes. * Experience ...

... biotechnology, or similarly regulated manufacturing environment. * Working knowledge of Process Safety Management (PSM), Management of Change (MOC), and startup readiness processes. * Experience ...

... biotechnology, or similarly regulated manufacturing environment. * Working knowledge of Process Safety Management (PSM), Management of Change (MOC), and startup readiness processes. * Experience ...

Experience in one or more of the following industries: pharmaceutical, biotech, semiconductor, power generation, chemical processing, refining, or advanced manufacturing is a plus * Startup and ...

Experience in one or more of the following industries: pharmaceutical, biotech, semiconductor, power generation, chemical processing, refining, or advanced manufacturing is a plus * Startup and ...

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Showing results 1-20

Biotech Startup information

What is a biotech startup?

A Biotech Startup job involves working in an early-stage company that develops innovative biological or medical technologies. Roles can vary widely, including research, product development, regulatory affairs, and business operations. Employees often wear multiple hats, contributing to both scientific advancements and business growth. The fast-paced environment requires adaptability, problem-solving skills, and a passion for innovation.

What are the key skills and qualifications needed to thrive in a biotech startup?

To thrive at a biotech startup, you need a strong background in life sciences or bioengineering, paired with an entrepreneurial mindset and practical research experience. Familiarity with laboratory equipment, data analysis software, and, in many cases, regulatory compliance certifications like GLP or GMP are vital. Exceptional adaptability, problem-solving abilities, and teamwork skills are also crucial in this fast-paced, multidisciplinary environment. These competencies help ensure innovation, rapid iteration, and successful navigation of the complex challenges faced by emerging biotech companies.

What are some unique challenges of working at a biotech startup compared to larger organizations?

Working at a biotech startup often means taking on a wide variety of responsibilities, as teams are usually small and roles can be less narrowly defined than at established companies. You may regularly transition between lab research, project management, and business development tasks, which can be both challenging and rewarding. Limited resources, tight deadlines, and the pressure to rapidly produce results are common, but these challenges also provide opportunities for accelerated learning and career advancement. Many employees find the collaborative, innovative atmosphere and the ability to make a tangible impact particularly fulfilling in this setting.

What cities in Indiana are hiring for Biotech Startup jobs?

Cities in Indiana with the most Biotech Startup job openings:

Infographic showing various Biotech Startup job openings in Indiana as of August 2026, with employment types broken down into 91% Full Time, 7% Part Time, and 2% Contract. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution.

Pre-Startup Safety Review (PSSR) Coordinator

Indianapolis, IN

Part-time

Posted 4 days ago


Job description

Overview

The Pre-Startup Safety Review (PSSR) Coordinator position is an exciting opportunity to join PM Group’s quickly growing Outsourced Technical Services (OTS) team near Indianapolis, IN. Outsourced Technical Services (OTS) is an integral part of PM Group’s ability to support clients across the complete project life cycle. We have over 50 years’ industry experience, strong technical knowledge and integrated resources. Clients look to us to provide experienced technical professionals that complement their project teams. Together we are sharing knowledge, learning, growing and continuing to be an integral part of supporting PM Group’s ongoing expansion in the US.

PM Group is seeking an experienced Pre-Startup Safety Review (PSSR) Coordinator to support a client project within a regulated life sciences manufacturing environment. Embedded within the client’s project team, the PSSR Coordinator will plan, coordinate, and facilitate the Pre-Startup Safety Review process for new and modified equipment, utilities, facilities, and manufacturing systems. The role will work closely with Engineering, Construction, Commissioning and Qualification (CQV), EHS, Operations, Maintenance, Automation, and Quality to confirm that applicable safety, operational, engineering, and documentation requirements have been satisfied before startup.


The successful candidate will be highly organized, comfortable working across multiple disciplines, and capable of driving outstanding actions to closure in a fast-paced project environment.

PM Group is an employee owned, international project delivery firm with a team of 4,000+ people.  We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organizations. We are focused on growing a sustainable business centered on our people, our clients and trade partners. 


Responsibilities
  • Plan, schedule, and facilitate multidisciplinary PSSR meetings and field reviews involving Engineering, Construction, CQV, EHS, Operations, Maintenance, Automation, and Quality representatives.
  • Coordinate PSSR activities for new installations, equipment modifications, facility upgrades, and systems returning to service following significant maintenance or shutdown activities.
  • Verify that installed equipment and systems align with approved design documentation, including P&IDs, engineering drawings, specifications, equipment data sheets, and applicable change-control records.
  • Confirm that required safety, operational, and regulatory documentation is complete and current before startup, including SOPs, operating manuals, emergency procedures, training records, risk assessments, and maintenance requirements.
  • Ensure applicable Management of Change (MOC), Process Hazard Analysis (PHA), HAZOP, What-If, and other risk-assessment actions are appropriately addressed and documented.
  • Develop, maintain, and manage PSSR checklists, readiness trackers, dashboards, action logs, and supporting documentation.
  • Document, categorize, assign, and track PSSR findings through closure, with particular focus on safety-critical items that must be resolved before startup.
  • Perform field walkdowns to verify equipment installation, system labeling, guarding, access, emergency controls, safety devices, and general operational readiness.
  • Coordinate closely with commissioning, qualification, and turnover teams to align PSSR activities with system completion and startup schedules.
  • Escalate overdue, safety-critical, or schedule-impacting actions to the appropriate project and client stakeholders.
  • Assemble final PSSR packages and support the client’s formal review and startup-authorization process.
  • Participate in project planning and readiness meetings, providing clear updates on PSSR status, risks, constraints, and upcoming milestones.
  • Identify opportunities to improve PSSR templates, workflows, reporting tools, and lessons-learned processes.
  • Perform all work in accordance with client procedures, PM Group standards, applicable EHS requirements, and current Good Manufacturing Practices (cGMP).

Qualifications
  • Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Occupational Health and Safety, or another relevant engineering or technical discipline.
  • 3–5+ years of relevant experience within the pharmaceutical, biotechnology, medical-device, or other regulated manufacturing industry.
  • Experience coordinating PSSR, startup-readiness, commissioning, turnover, EHS, or process-safety activities.
  • Working knowledge of Management of Change, risk assessments, HAZOP, What-If analysis, and other process-safety methodologies.
  • Familiarity with engineering and project documentation, including P&IDs, equipment specifications, SOPs, turnover packages, commissioning documentation, and action-tracking systems.
  • Strong organizational and documentation skills, with the ability to manage multiple systems, priorities, deadlines, and stakeholders simultaneously.
  • Effective communication, leadership, facilitation, and conflict-resolution skills.
  • Ability to work collaboratively within an integrated client and project-delivery team.
  • Proficiency with Microsoft Office applications and electronic document-management or action-tracking platforms.
  • Ability to work on-site and participate in field walkdowns in active construction and manufacturing environments.

Preferred Qualifications:

  • Professional certification such as Certified Safety Professional (CSP), Associate Safety Professional (ASP), or an equivalent EHS or process-safety credential.
  • Experience supporting commissioning, qualification, validation, or operational-readiness programs in a cGMP environment.
  • Previous experience coordinating plant shutdowns, turnarounds, outages, or large-scale project turnover activities.
  • Familiarity with OSHA Process Safety Management requirements and applicable life sciences industry standards.
  • Experience using electronic MOC, PSSR, commissioning, turnover, or project-management systems.
  • Knowledge of pharmaceutical manufacturing equipment, clean utilities, process utilities, automation systems, and facility infrastructure.

All of your information will be kept confidential according to EEO guidelines.

Why PM Group?

As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2026 business strategy. Click here to read more in our 2025 Environmental, Social and Governance Report.

Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.

PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.

RECRUITMENT AGENCIES NEED NOT APPLY

#LI-CV1

#hybrid

Qualifications:
  • Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Occupational Health and Safety, or another relevant engineering or technical discipline.
  • 3–5+ years of relevant experience within the pharmaceutical, biotechnology, medical-device, or other regulated manufacturing industry.
  • Experience coordinating PSSR, startup-readiness, commissioning, turnover, EHS, or process-safety activities.
  • Working knowledge of Management of Change, risk assessments, HAZOP, What-If analysis, and other process-safety methodologies.
  • Familiarity with engineering and project documentation, including P&IDs, equipment specifications, SOPs, turnover packages, commissioning documentation, and action-tracking systems.
  • Strong organizational and documentation skills, with the ability to manage multiple systems, priorities, deadlines, and stakeholders simultaneously.
  • Effective communication, leadership, facilitation, and conflict-resolution skills.
  • Ability to work collaboratively within an integrated client and project-delivery team.
  • Proficiency with Microsoft Office applications and electronic document-management or action-tracking platforms.
  • Ability to work on-site and participate in field walkdowns in active construction and manufacturing environments.

Preferred Qualifications:

  • Professional certification such as Certified Safety Professional (CSP), Associate Safety Professional (ASP), or an equivalent EHS or process-safety credential.
  • Experience supporting commissioning, qualification, validation, or operational-readiness programs in a cGMP environment.
  • Previous experience coordinating plant shutdowns, turnarounds, outages, or large-scale project turnover activities.
  • Familiarity with OSHA Process Safety Management requirements and applicable life sciences industry standards.
  • Experience using electronic MOC, PSSR, commissioning, turnover, or project-management systems.
  • Knowledge of pharmaceutical manufacturing equipment, clean utilities, process utilities, automation systems, and facility infrastructure.

All of your information will be kept confidential according to EEO guidelines.

Why PM Group?

As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2026 business strategy. Click here to read more in our 2025 Environmental, Social and Governance Report.

Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.

PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.

RECRUITMENT AGENCIES NEED NOT APPLY

#LI-CV1

#hybrid

Education:UNAVAILABLEEmployment Type: PART_TIME