Pharmaceutical Solid Dose Manufacturing Supervisor Job at Tedor Pharma Services, Cumberland, RI

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  • Tedor Pharma Services
  • Cumberland, RI

Job Description

Job description

Basic qualifications: 

  • BS/BA or Associates Degree with 5 or more years of directly related experience
  • 5-7 years experience in the Pharmaceutical industry-MUST
  • 3 years of manufacturing supervisory/manager experience or similar leadership role 
  • Good knowledge of Solid Oral Dosage/Tablet Manufacturing- REQUIRED
  • Warehouse Inventory Management experience -REQUIRED
  • Hot Melt Extrusion, Fluid Bed, Coating, and Granulation

Preferred qualifications: 

  • Strong quality/compliance orientation and track record 
  • Excellent interpersonal and leadership skills 
  • Strong influence and relationship building skills with an emphasis on teamwork 
  • Ability to lift 50 lbs. frequently and occasionally

Details:

Reporting to the Site Head, you will manage daily manufacturing operations of market entry and commercial manufacturing facility that produces pharmaceuticals for clinical and commercial purposes. Provides first line supervision to Manufacturing Associates, conduct granulations, tablet compression, encapsulation, tablet coating, hot melt extrusion, and putting finished product on stability. Serves as a leader in regards to process and system optimization, driving continuous improvement. Manage warehouse inventory.

Key Responsibilities

  • Manage and supervise all production and warehouse activities
  • Perform duties in a compliant manner and behave in accordance with site SOP’s, EHS standards and guidelines and relevant legal requirements and ensure that their teams do the same.
  • Supports successful implementation of new products and processes into the facility, including all appropriate equipment and area changeover activities.
  • Develops Manufacturing Associate work assignments to meet production schedules and to assure that resources are used efficiently and that product delivery targets are met. 
  • Review GMP documents i.e. SOP’s, BPR’s etc.
  • Accountable for Manufacturing Associate development and/or performance management though activities such as assignments and associated technical training programs.
  • Initiates/support/lead cross functional and cross departmental planning, learning, collaboration and teamwork to deliver high quality results.
  • Demonstrated higher level of leadership capability by optimizing manufacturing and process improvements and the capacity to stand in for the production manager.

Job Type: Full-time

Benefits:

  • 401(k)
  • Dental insurance
  • Health insurance
  • Paid time off
  • Vision insurance

Schedule:

  • 10 hour shift
  • 8 hour shift
  • Overtime
  • Weekends as needed

Work Location: In person

  • careers@tedor.com

Job Tags

Full time, Shift work, Weekend work,

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