Validation Engineer Job at Woodstock Sterile Solutions, Woodstock, IL

  • Woodstock Sterile Solutions
  • Woodstock, IL

Job Description

Position Summary

The Validation Engineer II is responsible for the design, scheduling, execution, and evaluation of scientifically and statistically sound qualification and validation studies. This role demonstrates that critical cleaning, controls, equipment, facilities, processes, and utilities function consistently and repeatably in compliance with regulatory requirements, product license restrictions, and policies affecting final product integrity.

The Validation Engineer II prepares concise technical documentation, provides validation support to Business Development, Engineering, Manufacturing, Quality Assurance, Quality Control, and Regulatory Affairs, and may lead or provide validation oversight for small- to medium-sized project initiatives.

Key Responsibilities

  • Serve as a validation representative and, when assigned, Validation Project Manager on cross-functional project teams.
  • Research applicable governmental and regulatory requirements for assigned projects and ensure study subjects meet required specifications.
  • Prepare scientifically sound validation study protocols incorporating defined specifications, acceptance criteria, and assessment procedures.
  • Schedule and coordinate validation study execution with the appropriate departments.
  • Provide validation oversight for small- and medium-sized project initiatives.
  • Prepare detailed documentation dossiers summarizing experimental results, specifications, and conformance to defined acceptance criteria.
  • Develop and execute complex procedures and methods with a high level of quality.
  • Prepare test plans as required by Equipment Change Orders.
  • Maintain close communication with Business Development, Engineering, and Manufacturing regarding validation challenges and opportunities.
  • Provide technical support to Business Development, Engineering, Manufacturing, Quality Assurance, Quality Control, and Regulatory Affairs as needed.
  • Assist with development of validation policies, programs, SOPs, and quality standards that meet industry, quality, and external regulatory requirements.
  • Support the facility during internal and external inspections.
  • Work directly with management, contract customers, and contract engineers.
  • Maintain the effectiveness of Quality System components relevant to the position.
  • Identify, evaluate, and manage risk to ensure product quality.
  • Perform other duties as assigned.

Qualifications

Education

  • Bachelor of Science degree in Engineering or a related science discipline preferred.

Experience

  • Bachelor’s degree in Engineering or a closely related physical science with at least three years of directly related experience, or an equivalent combination of education, experience, and training.
  • A master’s degree with at least two years of related experience may be considered.
  • Knowledge of current Good Manufacturing Practices (cGMPs), direct pharmaceutical manufacturing methods, and validation principles.

Knowledge & Skills

  • Ability to interpret written, oral, diagram, and schedule-based instructions.
  • Ability to work independently on multiple projects and meet deadlines with limited supervision.
  • Strong documentation, problem-solving, analytical, and mechanical aptitude.
  • Detail-oriented with demonstrated initiative, sound judgment, ethical decision-making, and investigative ability.
  • Strong verbal, written, and interpersonal communication skills.
  • Ability to interact effectively with individuals and personalities across departments.
  • Proficiency with business computer applications, including word processing, spreadsheets, and database software.
  • Familiarity with cGMP and safe work practices.
  • Ability to read, write, and speak clear English.

Physical Requirements & Work Environment

  • Frequent sitting, standing, walking, reading written documents, using a computer monitor, reaching, talking, writing, and listening.
  • Occasional bending, grasping, carrying, stooping, kneeling, and crouching.
  • Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 30 pounds.
  • Fast-paced, performance-driven, customer-focused, collaborative, and inclusive work environment.

Job Tags

Full time, Contract work

Similar Jobs

Info Way Solutions

Copy Editor Job at Info Way Solutions

 ...Copy Editor Preferred Location : Austin.// SF Bay area Onsite Job Description: Provide editorial services for various content types, including but not limited to eLearning/SGT modules, Live Classes, Knowledge base articles, Internal documentation (technical... 

Johnson Controls International Plc

HVAC Mechanical Engineer Job at Johnson Controls International Plc

 ...within the region, primarily working with building mechanical equipment and building automation systems (MEP, HVAC mechanical, HVAC controls and automation, lighting, utilities, etc). As a Project Development Engineer, you will: Conducts site visits and develops... 

KT/ JP Group Inc

Fashion & Textile Designer Job at KT/ JP Group Inc

 ...customer service. We are a fast-growing, innovative company that values creativity, collaboration, and a passion for fashion and textiles. Role: Fashion & Textile Designer We are seeking a full-time, on-site Associate Designer in Manhattan, NY. You will design... 

Advantage Technical

Refinery Project Manager IV Job at Advantage Technical

Our client is seeking an experienced Project Manager IV to lead multi-disciplinary engineering capital projects from planning through successful closeout. This is an excellent opportunity for a seasoned Project Manager with a strong mechanical or civil/structural engineering...

Modern Woodmen

Data Analyst Intern Job at Modern Woodmen

Data Analytics Intern As a Data Analytics Intern at Modern Woodmen, you'll help turn data into meaningful insights that support business decisions and strengthen the way we serve our members. You'll gain hands-on experience with analytics, reporting and process improvement...