Work Location: St. Louis, Missouri Shift: Department: LS-SC-POKMC1 Cherokee Protein Purification 1 Recruiter: Erin Wilson
This information is for internals only. Please do not share outside of the organization.
Your Role:
At MilliporeSigma, Manufacturing Technician 4 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.
The Manufacturing Technician is a key role within our GMP Manufacturing. Expectations is to ensure "Compliance "and "Readiness" within our GMP Operations teams, enabling high manufacturing success. Standard operations involve facility preparations, on-the-floor formulations, automated/manual ultrafiltration, and chromatography. Job duties include:
Rotating schedule Monday- Friday (1st, 2nd and 3rd shift (including evenings and nights). This role will eventually be rolled into a 24/7 schedule
Evaluate products according to established protocols and perform operations in support of the group and department
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
Perform routine processes and unit operations. Buffer formulation, ultrafiltration, and chromatography are standard
Clean equipment and working areas during and after operations
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
Who you are:
Minimum Qualifications
High school diploma or GED.
6 + months of experience working in a cGMP environment
Preferred Qualifications
cGMP 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.
RSREMD
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.
