5868 - Project Engineer / Risk Management (Pharma / Med Device) Indianapolis, IN

5868 - Project Engineer / Risk Management (Pharma / Med Device)

Indianapolis, IN

Description

Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values :

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do the right thing
• We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
• We constantly acquire new skills and learn from our experiences to enhance our collective expertise

We are seeking a highly motivated Project Engineer with proven experience in risk management within the pharmaceutical or medical device industry . This role will be responsible for leading and supporting cross-functional projects that ensure product and process compliance while minimizing risks throughout the product lifecycle. Candidates with experience or familiarity in Turbo AC (Air Conditioning or Turbo Compressor) systems are highly desired.

Project Engineer – Risk Management (Pharma / Med Device) Responsibilities :

Coordinate with cross-functional teams (QA, Regulatory, Manufacturing, R&D) to ensure risk mitigation strategies are effectively implemented

Drive the development, execution, and documentation of engineering project plans, timelines, and deliverables

Analyze and interpret engineering specifications, user needs, and technical drawings to support risk assessments and product safety evaluations

Manage technical issues and provide solutions that align with project objectives and compliance standards

Prepare and deliver clear project updates, risk reports, and design documentation to stakeholders

Support product verification and validation (V&V) efforts, ensuring alignment with regulatory and industry standards

Contribute technical expertise, especially where Turbo AC systems are applicable in the design or manufacturing environment

Requirements :

Bachelor's degree in Engineering (Mechanical, Biomedical, Electrical, or related field)

Minimum 3–5 years of experience in risk management within the pharmaceutical or medical device industry

Deep understanding of relevant FDA / EMA regulations

Strong project engineering and cross-functional collaboration skills

Excellent problem-solving and analytical skills

Experience or working knowledge of Turbo AC systems (e.g., turbo compressors, air conditioning systems in regulated environments)

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.

National (US) Range

$80,465 - $132,593 USD

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