Senior Pharmaceutical Technician

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Irfa******

  • United States 
  • Last Update: 18.12.2018 at 12:00

Job Type
Full Time
Start
ASAP
Duration
11 Month +
Place
Kansas City, MO, US
Country
United States

Category


Clinical and medical development

Description


The Role
  • Responsible for ensuring cGMP compliance and generally good housekeeping.
  • Responsible for collaborating with Senior Pharmaceutical Technician or Pharmaceutical Manufacturing Lead to request work orders be placed for processing rooms and equipment (Roller Compactors) within core group.
  • Ensures product is visually inspected to ensure quality requirements are thoroughly met.
  • Responsible for requesting work orders to be placed for processing rooms and equipment within core group.
  • Drives reductions in unplanned deviations and focuses on troubleshooting identified equipment malfunctions.
  • Senior Pharmaceutical Technician should have high ability to trouble shoot and repair. Partners with scientists and Pharmaceutical Manufacturing Lead on batch record template issues to ensure clarity and drive accuracy for processing.
  • Ensure that the facility is kept “tour ready” at all times and people/material/flow/cleaning and zone concepts are maintained at all times.
  • Set up and tear down of equipment
The Candidate The minimum level of total work-related experience required to perform the job’s responsibility is: High school diploma – five to seven years of experience with a minimum of three years in a Pharma or cGMP manufacturing environment. Technical degree/certification – three to five years of experience with a minimum of three years in a Pharma or cGMP manufacturing environment. Knowledge/Skills Requirements
  • Previous experience with Roller Compaction technologies required.
  • Must have thorough equipment process and framework knowledge
  • Must have a minimum of advanced operator qualification per supervisor / manager specified equipment train(s). Must be basic on all equipment within work zone.
  • Must have a thorough knowledge of cGMP, FDA, MHRA and DEA guidelines and how to apply them effectively.
  • Thorough knowledge of Solid Dosage manufacturing preferred.
  • Excellent computer skills.
  • Must be able to manage priorities and projects prioritizing effectively.
Physical Requirements
  • Handling of raw materials for product assembly
    • Manipulation of drums to and from 6-inch pallets
    • Drum weight <10kg. (Empty) to 150kg (max. full weight) multiple times per shift
    • Maneuvering of drums in manufacturing area consisting of rolling, scooting, pushing and pulling (up to 80 lbs. of force)
    • Utilization of scoops and other hand held implements
    • Lifting boxes and/or containers from waist to chest height
  • Loading product of various amounts of completion to counters and quality control devices
    • Overhead lift and reach (?15 lbs.)
  • Handling of finished product
    • Manipulation of drums to and from 6-inch pallets (up to 80 lbs. of force)
  • Push and pull ingredient canisters
  • Cleaning of area and equipment
    • Utilizing hand held brushes, wands, hoses, and other cleaning utensils
    • Operating in various postures
    • Overhead reach, squatting, kneeling, and forward bending
  • Transport of materials to and from designated lab space
Successful Applicants Will Display Catalent’s Standard Leadership Competencies
  • Leads with Integrity and Respect
  • Delivers Results
  • Demonstrates Business Acumen
  • Fosters Collaboration and Teamwork
  • Champions Change
  • Engages and Inspires
  • Coaches and Develops
Position Benefits
  • Medical, Dental, Vision and 401K are all offered from day one of employment
  • 19 days of paid time off annually
  • Potential for career growth within an expanding team
  • Defined career path and annual performance review and feedback process

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