Staff Validation Engineer

Performance Validation; Indianapolis (IN); On-site; USD 60,000 - 90,000; Full time

Job summary

An established industry player is looking for a Staff Validation Engineer to join their dynamic team. This role offers the chance to work on diverse projects within the pharmaceutical manufacturing sector, focusing on quality assurance and validation processes. The ideal candidate will possess a strong educational background in engineering or relevant experience in a regulated industry. With a commitment to employee growth and collaboration, this company provides an engaging work environment that values work-life balance and professional development opportunities. If you're passionate about quality assurance and eager to contribute to impactful projects, this is the perfect opportunity for you.

Benefits

Competitive salary

Profit sharing

Stock ownership

401(k) match

Paid vacation

Health coverage

Insurance

Training

Growth opportunities

Team building activities

Qualifications

• Bachelor's degree or 3 years experience in a regulated industry.
• Preferred degrees in Biomedical, Chemical, or Mechanical Engineering.

Responsibilities

• Develop understanding of technical, quality, and scientific principles.
• Create verification/qualification deliverables like Test Protocols.
• Manage change control activities across multiple projects.

Skills

Self-motivated

Interpersonal skills

Communication skills

Attention to detail

Microsoft Word

Microsoft Excel

Education

Bachelor's degree in Biomedical Engineering

Bachelor's degree in Chemical Engineering

Bachelor's degree in Mechanical Engineering

3 years experience in pharmaceutical or regulated industry

Tools

Microsoft Word

Microsoft Excel

Job description

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About Us

Here at Performance Validation, Inc (PV), we have been providing Commissioning, Qualification, and Validation services to the life science industries for over 30 years! We are a 100% employee-owned company with teams in Indiana, Michigan, Illinois, Kansas, Washington, and North Carolina, supporting clients throughout the US and overseas. PV is committed to providing growth opportunities through professional development, new services, and expanding into new geographical areas.

About The Job

Performance Validation is seeking a full-time Level I Validation Engineer/Specialist to join our teams in Indiana, Michigan, Illinois, Kansas, and North Carolina. The engineer will report to the Division Director or Manager and be assigned to project teams led by a Project Leader.

Responsibilities

1. Develop understanding of technical, quality, and scientific principles to meet industry and customer requirements.
2. Collaborate in a team environment to meet objectives within established timelines.
3. Create verification/qualification deliverables such as Requirements Documents, Specifications, Test Protocols (IQ/OQ/PQ), and Summary Reports.
4. Execute test protocols, identify and resolve non-conformances/deviations.
5. Manage change control activities across multiple projects.

Education & Requirements

• Bachelor's degree (BS/BA) or three years of experience in pharmaceutical or a regulated industry, not necessarily in validation.
• Preferred degrees in Biomedical, Chemical, or Mechanical Engineering.

Experience & Skills

• Self-motivated with professionalism, enthusiasm, and ability to work independently.
• Strong interpersonal skills for confident interaction with clients and team members.
• Excellent communication skills with high attention to detail.
• Proficiency with Microsoft Word and Excel.

What We Offer

• Competitive salary, profit sharing, stock ownership, 401(k) match.
• Paid vacation, holidays, training, health coverage, insurance, stipends, and growth opportunities.
• Team building activities and a collaborative work environment.
• Work/life balance and up to 20% travel availability.

Qualified candidates must be authorized to work in the US; sponsorship is not provided.

Additional Details

• Seniority level: Entry level
• Employment type: Full-time
• Job function: Quality Assurance
• Industry: Pharmaceutical Manufacturing