Manufacturing Validation Engineer

Ajulia Executive Search; Port Washington (WI); On-site; USD 55,000 - 60,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Paid time off

Job summary

A leading recruitment firm is seeking a Validation Engineer to join a rapidly growing company in the packaging industry. The position offers a competitive salary ranging from $55,000 to $60,000 per year, plus an excellent benefits package that includes healthcare and paid time off. The ideal candidate will possess a degree in a relevant field and have 1-2 years of relevant experience, with strong communication and project management skills. This is a full-time role in a dynamic environment.

Qualifications

• 1–2 years of experience in packaging, equipment validation, or technical writing.
• Ability to read and analyze technical documents and scientific materials.
• Experience in a regulated industry preferred.

Responsibilities

• Develop and execute IQ/OQ/PQ protocols and summary reports.
• Create and carry out product validation and cleaning validation protocols.
• Communicate technical information clearly across departments.

Skills

Strong mechanical aptitude

Excellent written and verbal communication skills

Project management skills

Familiarity with GMP

Education

Associate or bachelor's degree in a natural science or engineering discipline

Tools

Microsoft Office Suite

Google Suite

Job description

Pay Range

Base pay range: $55,000.00/yr - $60,000.00/yr

Are you looking to make a career change to a rapidly growing company in the manufacturing and packaging consumer products? This exciting opportunity as a Validation Engineer offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance, vision insurance, and paid time off. Does this position match your future career goals? Then this Validation Engineer opportunity could be the right fit for you.

Responsibilities

• Communicate technical information clearly across departments and project teams.
• Develop and execute IQ/OQ/PQ protocols and summary reports for manufacturing equipment, utilities, computerized systems, and lab equipment.
• Create and carry out product validation and cleaning validation protocols.
• Conduct training sessions related to validation procedures and GMP requirements.
• Write clear and accurate SOPs, Work Instructions, and other controlled documents.
• Support customer interactions and provide technical documentation as needed.
• Ensure all work follows Good Documentation Practices (GDP).
• Collaborate with cross-functional teams to meet regulatory requirements and production release deadlines.
• Assist with maintaining the Validation Master Plan (VMP) and Cleaning Validation Master Plan (CVMP).
• Perform additional duties assigned by leadership.

Qualifications

• Associate or bachelor's degree in a natural science or engineering discipline.
• 1–2 years of experience in packaging, equipment validation, engineering support, or technical writing.
• Strong mechanical aptitude and process comprehension; experience in a regulated industry is preferred.
• Ability to read, interpret, and analyze technical documents, regulations, and scientific materials.
• Excellent written and verbal communication skills, with the ability to present findings to all levels of management.
• Demonstrated project management skills and attention to detail.
• Familiarity with GMP and regulatory expectations for pharmaceutical or regulated manufacturing environments.
• Proficiency with Microsoft Office Suite, Google Suite, and relevant software tools (statistics, documentation, contract management).
• Strong commitment to confidentiality and data integrity.

Seniority Level

Associate

Employment Type

Full-time

Job Function

Manufacturing and Engineering

Industries: Engineering Services, Pharmaceutical Manufacturing, Manufacturing