Validation/CSV Engineer

Pyramid Consulting, Inc; Round Lake (IL); On-site; USD 80,000 - 100,000; Full time

Job summary

An established industry player is seeking a talented Microbiologist/Sterilization/Process Engineer for a contract role in Round Lake, IL. This position offers the chance to work on critical projects within the pharmaceutical sector, focusing on product development and sterility assurance. You'll apply your microbiology expertise to design and improve processes while ensuring compliance with GxP regulations. Join a forward-thinking company where your contributions will directly impact the quality and safety of pharmaceutical products. If you're passionate about making a difference in the industry, this is the opportunity for you.

Benefits

Health Insurance (Medical, Dental, Vision)

401(k) Plan

Paid Sick Leave

Qualifications

• 3-5 years of experience in microbiology and sterilization.
• Understanding of GxP regulations and aseptic techniques.

Responsibilities

• Design and improve products and processes for sterility assurance.
• Write and review validation protocols and reports.

Skills

Microbiology

Sterilization

Bioburden Testing

Bacterial Endotoxin Testing

Data Analysis

Education

B.S. in Engineering

Job description

Microbiologist/Sterilization/Process Engineer

Pyramid Consulting, Inc provided pay range

This range is provided by Pyramid Consulting, Inc. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$40.00/hr - $45.00/hr

Immediate need for a talented Microbiologist/Sterilization/Process Engineer. This is a 12+ months contract opportunity with long-term potential and is located in Round Lake, IL (Onsite). Please review the job description below and contact me ASAP if you are interested.

Job ID: 25-69753

Pay Range: $40 - $45/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities:

• Design, develop, or improve products and processes under the supervision of the sterility assurance focal point.
• Apply technical knowledge to various projects within sterility assurance with minimal assistance.
• Understand sterilization modalities and related disciplines.
• Use engineering tools to solve straightforward problems.
• Perform routine engineering tasks and provide technical recommendations.
• Complete assignments independently within deadlines.
• Understand GxP regulations and guidance.
• Support product development and change controls related to sterility assurance.
• Write, execute, and review validation and qualification protocols and reports.
• Interpret technical data and test results.
• Apply engineering principles to small projects.

Key Requirements and Technology Experience:

• Skills in microbiology, sterilization, bioburden, and bacterial endotoxin testing.
• Basic understanding of sterilization methods (Moist Heat, Aseptic, Irradiation).
• Experience with microbiological validation protocols.
• Ability to analyze technical data.
• B.S. in Engineering with 3-5 years of related experience.
• Understanding of aseptic techniques.
• Ability to conduct experiments independently.
• Knowledge of GxP and related regulations.

Our client is a leading Pharmaceutical Industry. Interested candidates are encouraged to apply online for immediate consideration.

Pyramid Consulting, Inc. is an equal opportunity employer and prohibits discrimination and harassment of any kind.

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