Manufacturing Supervisor- 3rd Shift

Cleveland, TN, United States
May 09, 2018
Required Education
Bachelors Degree
Position Type
Full time
Your tasks and responsibilities

The primary responsibilities of this role, Manufacturing Supervisor- 3rd Shift, are to:

  • Supervise multi-skilled personnel as assigned, to ensure that performance meets established safety, quality/Good Manufacturing Practices (cGMP), quantity and cost standards;
  • Manage, coordinate and directly supervise employees including coaching, counseling, performance reviews and feedback/initiating corrective action as needed, in a timely fashion;
  • Collaborate with other area supervision and Human Resources in ensuring consistency in situations requiring corrective action with employees;
  • Provide leadership and support to personnel in solving technical problems or contacting other resources as appropriate to solve problems;
  • Ensure compliance of local, state and federal regulations and guidelines (e.g., Good Manufacturing Practices (CGMP), Occupational Safety and Health Administration (OSHA), Environmental Protection Agency (EPA), etc.). Ensure SOPs for areas of responsibility are updated, accurate, and complete;
  • Ensure formal and informal training occurs in employee technical skill development as well as other training initiatives including safety, CGMP, teamwork, etc.;
  • Support the Director Manufacturing and Formulations/Compounding Superintendent in the timely completion of assigned projects;
  • Participate in cost reduction programs with respect to waste and other inefficiencies;
  • Perform other supervision duties and responsibilities as assigned.

Who you are

Your success will be driven by your demonstration of our LIFE values. More specifically related to this position, Bayer seeks an incumbent who possesses the following:

Required Qualifications:

  • Bachelor's degree with at least one year of experience in a government regulated industry using QA procedures or a Master's degree with at least two years of experience or a PhD and at least one year of experience;
  • In lieu of a degree, candidate must have at least five years of supervisory/leadership experience in a government regulated industry using QA procedures (FDA, pharmaceutical industry) and must commit to starting/continuing a college degree/certification program;
  • Strong personal computer skills;
  • Demonstrated ability to communicate positively with personnel at all levels;
  • Demonstrated ability to collaborate with others in cross-functional settings;
  • Proven organizational, analytical and problem solving skills are required to appropriately balance short-term business demands;
  • Demonstrated ability to provide developmental opportunities to subordinates and provide constructive feedback in a timely fashion.

Preferred Qualifications:

  • FDA, pharmaceutical industry experience;
  • experience with windows environment, Microsoft WORD and Excel;
  • Knowledge of automated Materials Requirement Planning (i.e. MES) system.

Your application

Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and you have the "Passion to Innovate" and the "Power to Change", we encourage you to apply now. Job postings will remain open for a minimum of ten business days and are subject to immediate closure thereafter without additional notice. To all recruitment agencies: Bayer does not accept unsolicited third party resumes.

Bayer is an Equal Opportunity Employer/Disabled/Veterans

Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below.

Country: United States
Location: TN-Cleveland