FORMULATION SUPERVISOR

Department: Manufacturing

We are looking for a Formulation Supervisor to lead day-to-day formulation activities in the manufacturing area. You will delegate tasks to appropriate subordinates, interact and communicate effectively with manufacturing management, QA/QC personnel and other formulation chemists to produce quality products following all applicable regulatory and good manufacturing guidelines.

RESPONSIBILITIES INCLUDE:

  • Delegates duties to staff on a day-to-day basis.
  • Maintains the formulation laboratory in the condition required by GMP and ISO guidelines.
  • Ensures that employees in the Manufacturing area are working in a safe manor wearing appropriate PPE and following the Code of Safe Practices.
  • Ensures that direct reports are properly trained and that that training is documented and current.
  • Trains new formulators in the duties and requirements of the position.
  • Creates and maintains a positive work environment.
  • Performs the duties of a formulation chemist as required.
  • Works with other departments, particularly R&D in the development of new products.
  • Writes, reviews, revises and or updates manufacturing documents, SOPs, or any other necessary technical documents.
  • Responsible for using appropriate equipment to run assays and verify results.
  • Work with scheduling and management to determine workflow through the area.
  • Interacts with the ERP system to report work orders and monitor raw material inventory.
  • Performs other tasks and duties as directed by management and supervisory personnel.
  • Assists in maintaining Quantimetrix quality system.
  • Exhibits and maintains Quantimetrix values.

QUALIFICATIONS:

  • Bachelor’s degree (BS) in science plus 2+ years in a supervisory role in a related industry.
  • Excellent soft skills and experience leading a diverse workforce.
  • Needs to be a motivator of staff.
  • Excellent technical writing and problem-solving skills are also essential.
  • Competency with MS Office.
  • Knowledge of Good Laboratory Practices.
  • Have experience working in a quality system environment and cGMP. Experience using ERP software.

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