Cleanroom Sanitation Team Lead

Job Description

Job Description

Job Posting Title

Cleanroom Sanitation Team Lead

Job Description

Company : OcyonBio is a partnership development and manufacturing organization focused on advancing gene and cell therapies.

OcyonBio provides dedicated autonomous manufacturing capacity with interconnected infrastructure and systems to support phased appropriate development for early development, pre-clinical, clinical, and commercial start. We behave more like a cGMP incubator space with all regulatory, systems capabilities, and resources to enable CMC data to support regulatory applications. Manufacturing and development spaces are designed to be autonomous while being interconnected to systems required to support clinical and commercial requirements.

We strive to create a space free of both explicit and implicit discrimination and harassment where everyone feels safe, heard, and valued. The character of our employees is as important as their talent, and we’re proud of the team and environment we’re assembling as we grow.

Place of Performance : CII George Sanders, Aguadilla Pueblo, Aguadilla P.R. 00603.

Job Overview:

Cleanroom Sanitation Team Lead will play a critical role in the start-up and ongoing support of OcyonBio’s GMP cleanroom operations. This individual will be responsible for establishing, executing, and maintaining compliant cleaning and sanitation programs for new cleanroom facilities supporting parenteral manufacturing operations. The role requires a strong hands-on presence, deep understanding of cleanroom behaviors, and the ability to build and lead a high-performing cleaning team in a startup environment. We are looking for a motivated, detail-oriented professional with strong cleanroom experience who is comfortable working hands-on while helping to build systems and teams in a fast-paced startup environment.

Key responsibilities:

• Lead the start-up and implementation of GMP-compliant cleaning and sanitation programs for newly constructed cleanrooms.

• Establish routine and non-routine cleaning schedules, procedures, and workflows for classified manufacturing areas (e.g., ISO 5–8).

• Perform hands-on cleaning activities within cleanroom environments in accordance with cGMPs, SOPs, and aseptic practices.

• Support cleaning validation activities, including execution of protocols, sampling activities, and documentation.

• Author, review, and execute SOPs, logbooks, and cleaning records in compliance with Quality Systems.

• Recruit, train, and develop the cleanroom cleaning team, setting expectations for performance, compliance, and cleanroom behavior.

• Train personnel on gowning practices, aseptic techniques, contamination control, and proper use of cleaning agents and equipment.

• Ensure proper handling, preparation, and storage of approved cleaning and disinfecting agents.

• Collaborate cross-functionally with Quality, Facilities, Engineering, and Manufacturing to support operational readiness and inspection preparedness.

• Support deviation investigations, CAPAs, and continuous improvement initiatives related to cleaning and contamination control.

• Demonstrate flexibility and a “roll-up-the-sleeves” mindset to meet evolving operational needs typical of a startup organization.

Basic Qualifications:

• Bachelor’s degree in Life Sciences, Engineering, Microbiology, Chemistry, or a related scientific discipline preferred. Equivalent combination of education and relevant GMP experience may be considered.

• Minimum of 5 years of hands-on experience in GMP-regulated cleanroom environments (ISO 5–8).

• Direct experience supporting cleaning and sanitation activities in classified areas.

• Strong understanding of cleanroom behaviors, gowning, and contamination control principles.

Preferred Qualifications:

• Experience in parenteral or aseptic manufacturing operations.

• Prior experience supporting cleanroom start-up or facility commissioning activities.

• Experience training and leading cleaning or facilities support personnel.

• Working knowledge of FDA cGMP regulations, aseptic processing guidelines, and industry best practices.

• Familiarity with cleaning validation concepts and environmental monitoring interfaces.

• Strong documentation skills and attention to detail.

• Ability to work independently, prioritize tasks, and adapt in a startup environment.

What we offer:

• Competitive salary (DOE.)
• Health, dental, and vision benefits.
• Professional training and development opportunities.
• Opportunities to participate in the company stock options program

We Are an Equal Opportunity Employer

OcyonBio provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

If you want to challenge yourself, accelerate your career, and give new hope to patients, there is no better place than here with our Cell Therapy team. Full of incredible and dedicated team members, those working on CAR-T and other forms of Cell Therapy are transforming patients' lives through science. From studying individualized cell lines to making brand new discoveries, this bold and personal discipline allows you to grow your career while making a lasting impact on the field of medicine. Join us today.

To learn more about us, please visit our website: