Sigma
cGMP Associate Production Scientist - Night Shift
Sigma, Saint Louis, Missouri, United States, 63101
Scientist/Associate Production GMP Night Shift
At MilliporeSigma, as a Scientist/Associate Production GMP on the Night Shift at our Cherokee site, you will be responsible for manufacturing active biopharmaceutical ingredients (APIs), chemicals, and bulk pharmaceuticals in compliance with Food and Drug Administration (FDA) regulations. Job duties include: Production shifts consist of 12-hour night shifts (6 PM - 6:30 AM) with a two-week rotation: Week 1 (Monday, Tuesday, Friday, Saturday) and Week 2 (Sunday, Wednesday, Thursday), including competitive shift differentials. Carry out production operations and communicate status to Manufacturing Supervision, possibly in front of the Customer. Provide technical leadership during the manufacturing process. Obtain equipment and ensure cleaning protocols are followed and recorded. Prepare production areas, chemicals, and equipment for operations. Conduct analytical tests and assess results during production. Advise chemical processors on key in-process decisions based on test results. Write and revise Master Manufacturing Formulas. Prepare and review Operating Procedures for FDA and cGMP compliance. Physical Attributes: Lift and carry up to 50 pounds while wearing personal protective equipment, including respirators, for an extended time. Perform tasks while wearing personal protective equipment, such as respirators or chemical protective clothing, for long durations. Who you are: Minimum Qualifications: Bachelor's Degree in Chemistry, Biochemistry, Chemical Engineering or other scientific discipline OR Associate Degree with 2+ years GMP production experience Preferred Qualifications: 1+ year GMP experience. Detail oriented with excellent organizational, written, and verbal communication skills. Logical approach to problem solving. Experience with customer interaction. Knowledge of Process Improvement methodology (e.g., PDSA, Lean Manufacturing, and/or Six Sigma). 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.
At MilliporeSigma, as a Scientist/Associate Production GMP on the Night Shift at our Cherokee site, you will be responsible for manufacturing active biopharmaceutical ingredients (APIs), chemicals, and bulk pharmaceuticals in compliance with Food and Drug Administration (FDA) regulations. Job duties include: Production shifts consist of 12-hour night shifts (6 PM - 6:30 AM) with a two-week rotation: Week 1 (Monday, Tuesday, Friday, Saturday) and Week 2 (Sunday, Wednesday, Thursday), including competitive shift differentials. Carry out production operations and communicate status to Manufacturing Supervision, possibly in front of the Customer. Provide technical leadership during the manufacturing process. Obtain equipment and ensure cleaning protocols are followed and recorded. Prepare production areas, chemicals, and equipment for operations. Conduct analytical tests and assess results during production. Advise chemical processors on key in-process decisions based on test results. Write and revise Master Manufacturing Formulas. Prepare and review Operating Procedures for FDA and cGMP compliance. Physical Attributes: Lift and carry up to 50 pounds while wearing personal protective equipment, including respirators, for an extended time. Perform tasks while wearing personal protective equipment, such as respirators or chemical protective clothing, for long durations. Who you are: Minimum Qualifications: Bachelor's Degree in Chemistry, Biochemistry, Chemical Engineering or other scientific discipline OR Associate Degree with 2+ years GMP production experience Preferred Qualifications: 1+ year GMP experience. Detail oriented with excellent organizational, written, and verbal communication skills. Logical approach to problem solving. Experience with customer interaction. Knowledge of Process Improvement methodology (e.g., PDSA, Lean Manufacturing, and/or Six Sigma). 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.