Clinical Packaging Operations Lead

CamWebDir

West Point (PA)

On-site

USD 64,000 - 100,000

Full time

6 days ago
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Benefits offered by this job

Medical, dental, vision benefits
401(k) retirement plan
Paid holidays and vacation
Annual bonus and long-term incentive

Job summary

Merck & Co., Inc. in West Point, PA is seeking an Operations Packaging Room Lead to supervise Clinical Packaging Technicians for GMP-compliant packaging and labeling of clinical study materials. You will manage room setup, training, documentation in SAP, and ensure GDP practices are followed.

This is an on-site, first-shift role with leadership responsibilities. Required is GMP experience, strong communication, coaching ability, and a focus on safety and quality in a fast-paced manufacturing

Qualifications

  • High School Diploma or equivalent required.
  • Minimum 1 year experience in GMP regulated environment.
  • Leadership experience to enable accountability for daily operations for a team of packaging technicians.

Responsibilities

  • Facilitate and oversee the execution of filling, labelling, and packaging of clinical packaging jobs.
  • Coordinate, perform and document de-packaging, packaging, labeling and sampling activities.
  • Ensure team members perform tasks according to GMP/SOP, batch records, and safety requirements.
  • Accountable for daily output and product quality in packaging of clinical studies per SOPs.
  • Report and prevent potential quality events and GMP non-conformances.
  • Overtime and weekend work may be required.
  • Train new employees and coach junior staff.

Skills

Coaching
Communication
GMP Compliance
GMP Training
Master Batch Records
Operations Support
Pharmaceutical Manufacturing
Production Scheduling
Teamwork
Technical Support
Continuous Improvement
Packaging

Education

High School Diploma or equivalent

Tools

SAP
MES

Job description

Merck & Co., Inc. in West Point, PA is seeking an Operations Packaging Room Lead to supervise Clinical Packaging Technicians for GMP-compliant packaging and labeling of clinical study materials. You will manage room setup, training, documentation in SAP, and ensure GDP practices are followed.

This is an on-site, first-shift role with leadership responsibilities. Required is GMP experience, strong communication, coaching ability, and a focus on safety and quality in a fast-paced manufacturing

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