Pharma Packaging Team Lead - GMP/cGMP Expert

Clinigen Group

Malvern (Chester County)

On-site

USD 55,000 - 75,000

Full time

7 days ago
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Job summary

Clinigen in Malvern, PA, is seeking a Production Team Lead to head the packaging team, overseeing packaging, labeling and documentation of clinical trial material. This is an on-site role that requires commitment to 5 days/week.

The ideal candidate has a high school diploma and some office/medical experience; familiarity with SOPs, cGMP or GDP is preferred. You will mentor staff, coordinate day-to-day tasks, support the supervisor, and work with the CEMS inventory system while seeking process

Qualifications

  • High School Diploma or GED is required.
  • 6 months office or medical field experience preferred.
  • 6 months Clinigen packaging experience preferred.
  • Familiar with SOPs, cGMP, or GDP preferred.

Responsibilities

  • Acts as lead to the packaging team by coordinating and directing the day-to-day tasks of the packaging team.
  • Supports the Packaging team by sharing knowledge, skills and information related to the tasks and requirements of the position.
  • Acts as a subject matter expert for the CEMS inventory system
  • Acts as a subject matter expert on all primary packaging operations, including machine set ups and trouble shooting.
  • Makes proactive recommendations and present/offer solutions to improve quality and work efficiently.
  • Trains new packaging employees on packaging processes, procedures, and works with supervisor to ensure a mentor is assigned.
  • Performs all Packaging Specialist tasks and duties alongside other team members.
  • Provides support to their direct supervisor as needed.
  • Suggests improvements to processes and is a knowledge resource for other team members

Skills

Detail-oriented
Time management
Communication
Teamwork
Confidentiality

Education

High School Diploma or GED

Job description

Clinigen in Malvern, PA, is seeking a Production Team Lead to head the packaging team, overseeing packaging, labeling and documentation of clinical trial material. This is an on-site role that requires commitment to 5 days/week.

The ideal candidate has a high school diploma and some office/medical experience; familiarity with SOPs, cGMP or GDP is preferred. You will mentor staff, coordinate day-to-day tasks, support the supervisor, and work with the CEMS inventory system while seeking process

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