Environmental Support Technician

*US AMR-Jones Lang LaSalle Americas, Inc.; Thousand Oaks (CA); On-site; USD 46,000 - 52,000; Full time

Benefits offered by this job

401(k) plan with matching

Comprehensive Medical, Dental & Vision

Paid parental leave

Paid Time Off

Daily Pay

Job summary

Jones Lang LaSalle Incorporated (JLL) seeks an Environmental Support Technician to sanitize GMP-controlled areas and ensure cleanroom standards in Thousand Oaks, CA. You will follow SOPs, maintain meticulous records, and support cross-functional teams in a fast-paced biopharmaceutical environment.

The role emphasizes adherence to cGMPs, GDPs, and proper PPE, with training provided. Strong attention to detail and teamwork are essential for successful daily operations in ISO-cleanroom settings.

Qualifications

• High School Diploma or equivalent
• English usage, spelling, grammar and punctuation
• Business computer hardware and software applications
• Attention to detail
• Must follow work instructions
• Excellent attendance record
• Professional attitude with Client and Peers

Responsibilities

• Routine sanitization in GMP areas (daily, weekly, monthly, quarterly)
• Non-routine sanitization during excursions or maintenance
• Verify proper sanitization disinfectant rotation for each cleaning task
• Complete GMP documentation accurately
• Mixing and disposal of sanitization solutions daily
• Dispose of GMP waste daily in accordance with procedures
• Maintain sanitization supply area organization and inventory
• Collaborate with Manufacturing and Quality to meet GMP requirements
• Participate in training on sanitization disinfectants and equipment
• Follow SOPs and cGMPs (21CFR Part 211)
• Pass sterile gowning qualification to access GMP rooms
• Control entry and materials into GMP areas
• Perform cleaning with mops and PPE as required

Skills

GMP documentation

Clear communication

English literacy

Teamwork

Customer service

GDPs emphasis

Education

High School Diploma or equivalent

Job description

Environmental Support Technician - JLL

JLL empowers you to shape a brighter way. Our people at JLL are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are committed to hiring the best, most talented people and empowering them to thrive, grow meaningful careers and to find a place where they belong. Whether you’ve got deep experience in commercial real estate, skilled trades or technology, or you’re looking to apply your relevant experience to a new industry, join our team as we help shape a brighter way forward.

What this job involves:

The GMP Environmental Support Technician works in activities associated with the sanitization of controlled areas in accordance with internal procedures, protocols, and cGMP's. The incumbent will follow all applicable standard operation procedures (SOP), guidelines and policies to ensure sanitary conditions are maintained, that appropriate room and equipment sanitization records are neat and accurate, and that professional behavior is displayed within the controlled areas. The incumbent will receive daily production schedule direction from the Lead and/or area management. The incumbent plays a critical role in assuring sanitary conditions of the controlled areas is maintained to manufacture biopharmaceuticals. A hospitality mindset is fundamental to delivering exceptional workplace experiences for our client. We seek candidates who excel in collaborative environments, communicate effectively with diverse stakeholders, manage multiple priorities simultaneously, maintain high standards of accuracy, and adapt quickly to resolve challenges.

What your day‑to‑day will look like:

• Responsible for routine daily, weekly, monthly, quarterly, and additional frequency room sanitization in GMP manufacturing process areas
• Responsible for non‑routine sanitization in the GMP manufacturing process areas due to environmental excursion, process requirements, or facility maintenance and/or construction
• Responsible for verifying that the proper sanitization disinfectant rotation is followed and that the proper sanitization disinfectant is used for each cleaning assignment
• Responsible for completing required GMP documentation to ensure records are properly and accurately maintained
• Responsible for mixing and disposal of sanitization solutions on a daily basis
• Responsible for disposal of waste from GMP manufacturing process area waste receptacles on a daily basis
• Responsible for organization and upkeep of sanitization supply areas
• Responsible to participate in cycle counting and inventory of sanitization supplies and gowning articles in order to maintain inventory levels for timely reordering

Other Responsibilities Include:

• Collaborate with Manufacturing, GMP Operations Manager, and Quality teams to manage schedules necessary to clean the GMP controlled environment and support areas to comply with GMP requirements
• Participate in required training on the use of sanitization disinfectants and equipment
• Strictly follow Standard Operating Procedures
• Follow cGMPs as outlined in 21CFR Part211
• Must pass a sterile gowning qualification test in order to enter and sanitize the GMP process rooms
• Control what enters the GMP process areas
• Adhere to procedures while performing cleaning and sanitization activities
• Sanitation activities will be performed with ceiling mops, wall mops, floor mops, and wipers
• Understands and follows proper solvent handling procedures (EHS) and personal protective equipment (PPE)
• Performs related duties as assigned

Skills In:

• Accurate GMP documentation and sign off on work performed with an emphasis on Good Documentation Practices (GDPs)
• Communicating clearly and concisely, both orally and in writing
• Ability to read, write and understand documentation in English
• Ability to work in a team environment and independently
• Establish and maintaining collaborative working relationships with internal and external customers
• Providing excellent customer service with both internal and external customers

Required Qualifications:

High School Diploma or equivalent

Company policies and practices, including safety rules and regulations

English usage, spelling, grammar and punctuation

Business computer hardware and software applications

Attention to detail

Must have a professional attitude with Client and Peers

Excellent attendance record

Must follow work instructions

Preferred Qualifications:

Prior experience of cleaning a biopharmaceutical GMP controlled environment is a plus but not required

Current Good Manufacturing Practices (cGMP)

Good Documentation Practices (GDP)

Physical Requirements and Working Environment:

No make‑up, nail polish, and/ or jewelry may be worn in the GMP process areas. Incumbent is subject to extended periods of standing, walking, pushing and pulling, bending and crouching, climbing, and lifting of equipment and/or materials weighing up to 50pounds. Continuous mental and visual attention to manufacturing functions. Continuous standing and walking throughout work day. Majority of time spent in ISO8 (Class100K) or ISO7 (Class10K) cleanroom, fully gowned including head covering, facemask, gloves, plant shoes, safety glasses/goggles and/or face shield. Working in the ancillary support space adjacent to the ISO areas described above to ensure cleanliness.

This position requires strict adherence to current Good Manufacturing Practices (cGMPs), established cleaning practices and procedures, and compliance with quality standards and regulations. The purpose of the cleaning and sanitization program is to control microbial contamination and to serve as a corrective action for the loss of control for viable excursion contamination. Standard Operating Procedures (SOPs) must be followed and strictly enforced to ensure acceptable environmental monitoring results of the cleaned GMP environment.

Compensation:

Expected compensation for this position: 45,760.00 – 52,000.00USD per year. Final compensation packages are determined by various considerations including but not limited to candidate qualifications, location, market conditions, and internal considerations.

Location:

100% Onsite - Thousand Oaks, CA

Location: On‑site – Thousand Oaks, CA

Benefits:

• 401(k) plan with matching company contributions
• Comprehensive Medical, Dental & Vision Care
• Paid parental leave at 100% of salary
• Paid Time Off and Company Holidays
• Early access to earned wages through Daily Pay

Equal Opportunity and Inclusion Statements:

JLL is an Equal Opportunity Employer committed to diversity and inclusion.

Jones Lang LaSalle (“JLL”) is an Equal Opportunity Employer and is committed to working with and providing reasonable accommodations to individuals with disabilities.

This position does not provide visa sponsorship. Candidates must be authorized to work in the United States without sponsorship.

For any portion of the employment process – including the online application and/or overall selection process – you may email us at [e-mail]. This email is only to request an accommodation.

Due to background checks for any convictions directly related to its duties and responsibilities, this position is subject to a background check for any convictions directly related to its duties and responsibilities.