Plant Hygienist

GOJO, Makers of PURELL; Cuyahoga Falls (OH); On-site; USD 101,000 - 140,000; Full time

Benefits offered by this job

401(k) match

Parental leave

Onsite well-being care

Bonus eligible

Job summary

GOJO, Makers of PURELL, located in Cuyahoga Falls, Ohio, seeks a Plant Hygienist to prevent contamination risks and maintain GMP-compliant hygiene standards in OTC drug, cosmetics, and related manufacturing areas.

The role emphasizes hygienic design, cleaning, sanitization, and cross-functional collaboration to ensure product safety and regulatory compliance. Travel is sporadic with a strong emphasis on on-site work.

Qualifications

• Bachelor's degree in a technical field is required.
• Minimum ten years of manufacturing experience (preferred FDA-regulated).
• OTC drug, cosmetic, pharmaceutical, food, or medical device experience preferred.

Responsibilities

• Lead investigations of particulate, foreign material, plant debris, and microbiological contamination events.
• Identify contamination pathways and drive sustainable CAPA.
• Perform risk assessments (FMEA/HACCP) on manufacturing processes, equipment, suppliers, cleaning failures, and facility changes.
• Establish site cleanliness standards, metrics, and conduct routine audits.

Skills

Investigations leadership

CAPA

Risk assessment

Cross-functional influence

Education

Bachelor's degree in engineering/biology/chemistry/toxicology/pharma/food science

Job description

Information about #32830 Plant Hygienist

Work Location: this role works from our manufacturing and distribution facility in Cuyahoga Falls, Ohio

For more than 80 years, our company has been powered by people who are energized by helping the world experience greater health and well-being.

The positive impact of our PURELL hand and surface hygiene solutions is driven by our global community of highly collaborative and talented team members who love to learn, innovate, care for each other, and deliver our Purpose of Saving Lives and Making Life Better.

We look for people who are inclusive, results driven, customer-focused, and passionate about impacting the health and well-being of people, businesses, and communities around the world. If this inspires you, please join us at Clorox Purell.

Role Objective

Prevent contamination risks to OTC drug and cosmetic products through hygienic design, cleaning and sanitization effectiveness, contamination investigations, and risk-based manufacturing controls.

Essential Functions and Responsibilities

• Lead investigations of particulate, foreign material, plant debris, and microbiological contamination events
• Identify contamination pathways and drive sustainable CAPA

Risk Assessment & Continuous Improvement

• Perform risk assessments (FMEA/HACCP) on manufacturing processes, equipment, suppliers, cleaning failures, and facility changes
• Recommend engineering, procedural, and supplier corrective actions

Plant Cleanliness & Auditing

• Establish site cleanliness standards, performance metrics and conduct routine audits of operations

Hygienic Design & Cleanability

• Assess new and existing equipment and facility design for contamination risks
• Review pipe velocities, drainability, dead legs, cleanability, and CIP/COP effectiveness

Cleaning & Sanitization Assessment

• Evaluate cleaning and sanitization procedures for effectiveness and GMP compliance
• Review cleaning validation/verification strategies, swab locations, acceptance criteria, and inspection methods
• Assess contamination risks from raw materials, packaging, components, and contract manufacturers
• Support supplier audits and corrective action programs

Cross-Functional Influence & Technical Leadership

• Influence manufacturing, maintenance, engineering, quality, sanitation, and supplier partners to prioritize contamination control and hygienic design actions
• Provide subject matter expertise and practical recommendations that guide decision-making, risk reduction, and sustainable corrective actions
• Build alignment across teams by clearly communicating risks, connecting technical findings to business and compliance impacts, and driving accountability for follow-through
• Lead cross-functional problem-solving efforts when contamination, cleaning effectiveness, or facility/equipment design concerns require coordinated action

Education and Experience

Required:

• Bachelor's degree required in one of the following technical fields (i.e. engineering, biology, chemistry, toxicology, pharma, food science)
• Minimum ten (10) years of manufacturing company (preferred FDA-regulated)
• OTC drug, cosmetic, pharmaceutical, food, or medical device experience

Preferred Experience:

• FDA inspection

Supervision/Coordination

This role does not have direct reports; however, it requires the ability to provide technical leadership, build alignment, and influence cross-functional partners.

Role Type

Mostly On-Site - 80%+ on-site work

Travel Requirements

Overnight Travel - sporadic - required.

Travel between campus locations in Northeast Ohio as needed

The expected starting pay for this role is between $101,400.00 - $139,500.00 per year. Within this range, an offer will depend on factors such as level of experience and technical competencies relevant to this specific role, as well as internal equity considerations.

• 401(k) match
• parental leave
• onsite well-being care
• bonus eligible

Clorox Purell is the business name of GOJO Industries, LLC, and we are an affirmative action and equal opportunity employer. We value different backgrounds, experiences, and perspectives, and all qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability.

Applicants must be legally authorized to work in the United States.