6485 - Project Engineer / Project Engineer 2

Veristainc; Indianapolis (IN); On-site; USD 85,000 - 127,000; Full time

Benefits offered by this job

Medical, Dental & Vision insurances

401(k) Retirement Plan (Employer Match

Paid Time Off

Tuition Reimbursement

Life Insurance

Job summary

Verista seeks a Project Engineer to advance VHP decontamination for pharmaceutical isolators, developing and optimizing cycles and strategies for BI placement in collaboration with cross-functional teams.

The role involves analyzing validation data, drafting PQ protocols, and ensuring GMP and regulatory compliance. Strong technical writing and problem-solving are essential for success.

Join Verista’s growing team delivering solutions to life science clients and helping to improve lives.

Qualifications

• Hands-on experience with VHP cycle development and qualification for pharmaceutical isolators.
• 4295:oi?
• Strong knowledge of aseptic processing and contamination control principles.
• Experience authoring PQ protocols and final validation reports.
• Knowledge of GMP validation requirements in pharma/biotech manufacturing.
• Experience troubleshooting VHP cycle development and performance issues.
• Strong technical writing skills with SOPs, protocols, and risk assessments.

Responsibilities

• Develop and optimize VHP decontamination cycles for pharmaceutical isolators.
• Develop BI placement strategies including worst‑case locations and challenge studies.
• Execute VHP development cycles and troubleshoot cycle performance and decontamination issues.
• Author and execute PQ protocols for isolator decontamination systems.
• Analyze cycle and validation data; prepare final reports.
• Author, review, and revise validation documentation (qualifications, risk assessments, SOPs, lifecycle docs).
• Provide technical guidance on VHP implementation and lifecycle management.
• Ensure activities comply with cGMP and regulatory standards.
• Collaborate with Validation, Engineering, Manufacturing, Quality, and other stakeholders.

Skills

VHP cycle development

Aseptic processing knowledge

GMP validation understanding

Technical writing

Cross-functional collaboration

Analytical problem-solving

Regulatory knowledge

Job description

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

Project Engineer Responsibilities:

• Develop and optimize VHP (Vaporized Hydrogen Peroxide) decontamination cycles for pharmaceutical manufacturing isolators.
• Develop Biological Indicator (BI) placement strategies, including identification of worst‑case locations and execution of challenge studies.
• Execute VHP development cycles and troubleshoot cycle performance, distribution, and decontamination issues.
• Author and execute Performance Qualification (PQ) protocols for isolator decontamination systems.
• Analyze cycle and validation data, perform technical assessments, and prepare final reports.
• Author, review, and revise validation documentation, including:
  • Qualification protocols and reports
  • Risk assessments
  • SOPs
  • VHP cycle development documentation
  • Supporting validation and lifecycle documentation
• Provide technical guidance on VHP implementation, validation strategy, and lifecycle management.
• Ensure activities and documentation comply with cGMP requirements and applicable regulatory/industry standards.
• Collaborate with Validation, Engineering, Manufacturing, Quality, and other cross‑functional stakeholders.

Requirements:

• Demonstrated hands‑on experience with VHP cycle development and qualification for pharmaceutical isolators.
• Strong knowledge of aseptic processing and contamination control principles.
• Experience developing and executing BI placement and worst‑case challenge strategies.
• Experience authoring and executing PQ protocols and preparing final validation reports.
• Strong understanding of GMP validation requirements within pharmaceutical or biotechnology manufacturing.
• Experience troubleshooting VHP cycle development and performance issues.
• Strong technical writing skills with experience authoring protocols, reports, risk assessments, and SOPs.
• Knowledge of current regulatory expectations and industry best practices for VHP decontamination and isolator qualification.
• Strong analytical, problem‑solving, and cross‑functional communication skills.
• Experience supportingsterile/aseptic pharmaceutical manufacturing operations.
• Experience with VHP systems used infilling, packaging, or other aseptic manufacturing isolators.
• Familiarity with contamination control strategies and the qualification/lifecycle management of barrier systems.

Benefits

Why Choose Verista?

• High growth potential and fast‑paced organization with a people‑focused culture
• Competitive pay plus performance‑based incentive programs
• Company‑paid Life, Short‑Term, and Long‑Term Disability Insurance.
• Medical, Dental & Vision insurances
• FSA, DCARE, Commuter Benefits
• Supplemental Life, Hospital, Critical Illness and Legal Insurance
• Health Savings Account
• 401(k) Retirement Plan (Employer Matching benefit)
• Paid Time Off (Rollover Option) and Holidays
• As Needed Sick Time
• Tuition Reimbursement
• Team Social Activities (We have fun!)
• Employee Recognition
• Employee Referral Program
• Paid Parental Leave and Bereavement

National (US) Range

$85,470—$127,144 USD

*Verista is an equal opportunity employer.

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For more information about our company, please visit us at Verista.com