GMP Cleaning Associate
Precigen, Germantown, MD, United States
Overview
GMP Cleaning Associate will require a professional who thrives in a dynamic team environment, brings meticulous attention to detail in the quality of their work and is proactive in implementing improvements. This position will perform professional cleaning of the GMP manufacturing clinical and commercial areas. Prior experience in cleaning GMP manufacturing areas and labs are required. GMP Cleaning Associate will maintain cleanliness in production, lab, and warehouse areas. This role focuses on adhering to safety and quality standards, with an emphasis on GMP cleaning operations.
Duties and Responsibilities
Performs sanitary cleaning activities as defined by established operating procedures and as directed by Manager/Supervisor
Perform stocking and staging of usable garments for multiple gowning rooms
Maintains accurate and complete records
Attends and completes all training required by company SOPs, procedures and policies
Maintains accurate and complete inventory of cleaning supplies ensuring supplies are never depleted
Works in a safe and effective manner in accordance with all company, state and federal rules and regulations
Perform any other tasks/duties as assigned by management
Education and Experience
Minimum of one to three (1-3) years’ experience in sterile or GMP cleaning operations within the pharmaceutical or biotechnology industry.
Physically capable to don and wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves
Ability to wear a respirator during use of certain cleaning chemicals
Perform operations within an ISO Class/Grade clean rooms
Employee must be able to occasionally lift and/or move up to 40 pounds
Must be able to squat, bend, kneel, and or reach for 80% of a shift
Must be able to stand, walk, and/or move about for 80% of a shift
Desired Key Competencies
Familiarity with cGMPs, regulatory guidelines, and standard operating procedures.
Clean Room sanitization experience a plus, Task breakdown (by %): 75% cleaning 15% documentation 10% other duties as assigned
#J-18808-Ljbffr
GMP Cleaning Associate will require a professional who thrives in a dynamic team environment, brings meticulous attention to detail in the quality of their work and is proactive in implementing improvements. This position will perform professional cleaning of the GMP manufacturing clinical and commercial areas. Prior experience in cleaning GMP manufacturing areas and labs are required. GMP Cleaning Associate will maintain cleanliness in production, lab, and warehouse areas. This role focuses on adhering to safety and quality standards, with an emphasis on GMP cleaning operations.
Duties and Responsibilities
Performs sanitary cleaning activities as defined by established operating procedures and as directed by Manager/Supervisor
Perform stocking and staging of usable garments for multiple gowning rooms
Maintains accurate and complete records
Attends and completes all training required by company SOPs, procedures and policies
Maintains accurate and complete inventory of cleaning supplies ensuring supplies are never depleted
Works in a safe and effective manner in accordance with all company, state and federal rules and regulations
Perform any other tasks/duties as assigned by management
Education and Experience
Minimum of one to three (1-3) years’ experience in sterile or GMP cleaning operations within the pharmaceutical or biotechnology industry.
Physically capable to don and wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves
Ability to wear a respirator during use of certain cleaning chemicals
Perform operations within an ISO Class/Grade clean rooms
Employee must be able to occasionally lift and/or move up to 40 pounds
Must be able to squat, bend, kneel, and or reach for 80% of a shift
Must be able to stand, walk, and/or move about for 80% of a shift
Desired Key Competencies
Familiarity with cGMPs, regulatory guidelines, and standard operating procedures.
Clean Room sanitization experience a plus, Task breakdown (by %): 75% cleaning 15% documentation 10% other duties as assigned
#J-18808-Ljbffr