Manufacturing and Facility Cleaning Support Technician 4 - 2nd Shift

Merck•Saint Louis, MO

21d•$24 - $41•Onsite

About The Position

At MilliporeSigma, Manufacturing and Facility Cleaning Support Technician 4 – 2nd Shift at our Cherokee Site/ 3300 S. Second Ave, St Louis, will be expected to safely execute, develop new approaches, and perform support operations in a cGMP regulated environment for the support of API (Active Pharmaceutical Ingredients) manufacturing teams, including maintaining equipment, preparation of solutions, staging of equipment and supplies, and other various manufacturing support activities. Job duties include: Shift Hours: Monday – Friday, 2:00pm – 10:30pm, including a 10% shift differential Clean manufacturing equipment and facilities before, during and after operations Support functions of the facility (e.g., maintain equipment, prepare cleaning solutions, and restock supplies, waste disposal) Safely perform operations to meet quality expectations. Safely and properly dispose cleaning and process waste per approved procedures Maintain required training to perform tasks/assignments Support functions of the facility (e.g., maintain equipment, prepare reagents, and restock supplies, waste disposal) Communicate the status of operations and convey concerns to the supervisor Provide complete and accurate records consistent with quality guidelines. Utilize quality approved operating procedures and document activities with adherence to GDP standards Ensure all applicable logbooks are completed as required by current procedures Interact with other departments as needed and performs procedures independently and part of a team Improve processes through application of experience and principles, in compliance with change control Develop and assist in the implementation of process improvement, safety, quality, and 6S Take action to resolve unsafe conditions Physical Attributes Stand for extended periods of time Lift, push, and or pull up to 50lbs. Wear mask, safety shoes, gloves, Tyvek suits, respirator, and related personal protective equipment

Requirements

High school diploma or GED.
6 + months of experience working in a pharmaceutical GMP operations environment (Manufacturing, Quality, MSAT)

Nice To Haves

GDP experience
Prior experience in an API manufacturing environment
Strong mechanical aptitude
Demonstrated process improvement experience
Familiarity with FDA, EMA, and other regulatory standards
Demonstrated knowledge and experience in various computer skills, including Windows (Word, Excel, PowerPoint, etc .
2 + years of experience working in a pharmaceutical GMP operations environment (Manufacturing, Quality, MSAT)

Responsibilities

Clean manufacturing equipment and facilities before, during and after operations
Support functions of the facility (e.g., maintain equipment, prepare cleaning solutions, and restock supplies, waste disposal)
Safely perform operations to meet quality expectations.
Safely and properly dispose cleaning and process waste per approved procedures
Maintain required training to perform tasks/assignments
Support functions of the facility (e.g., maintain equipment, prepare reagents, and restock supplies, waste disposal)
Communicate the status of operations and convey concerns to the supervisor
Provide complete and accurate records consistent with quality guidelines.
Utilize quality approved operating procedures and document activities with adherence to GDP standards
Ensure all applicable logbooks are completed as required by current procedures
Interact with other departments as needed and performs procedures independently and part of a team
Improve processes through application of experience and principles, in compliance with change control
Develop and assist in the implementation of process improvement, safety, quality, and 6S
Take action to resolve unsafe conditions