On-Site GMP Pharmaceutical Technician – Solid Dose Manufacturing

Catalent Pharma Solutions

Winchester (KY)

On-site

USD 38,000 - 52,000

Full time

14 days+
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Benefits offered by this job

Diversity & Inclusion groups
Tuition reimbursement
401K match
PTO 152 hours + 8 holidays

Job summary

Catalent Pharma Solutions in Winchester, KY, is hiring a Pharmaceutical Technician for 100% on-site work. You will weigh, transfer, mix and process raw materials to produce finished goods, while maintaining strict GMP and batch records. Cleaning, equipment handling, and proper documentation are essential.

Strong teamwork and adherence to safety protocols are required. You will collaborate with Room Leaders and supervisors to ensure quality and regulatory compliance, with emphasis on accurate

Qualifications

  • High School Diploma or equivalent required.
  • Prior GMP-regulated manufacturing experience preferred.
  • Able to perform weighing, transferring, mixing and processing of materials.
  • Must follow cGMP, SOPs and maintain batch records.
  • Ability to lift up to 40 lbs and perform manual material handling.

Responsibilities

  • Weigh and transfer materials using calibrated scales and balances.
  • Assemble and disassemble machinery with hand tools.
  • Document tasks on batch records and cleaning records.
  • Clean manufacturing suites and equipment to keep an audit-ready environment.
  • Operate within cGMP and SOPs and interact professionally with coworkers and visitors.

Skills

GMP knowledge
Documentation
Team collaboration

Education

High School Diploma or Equivalent

Tools

Calibrated scales
Balances
Hand tools

Job description

Catalent Pharma Solutions in Winchester, KY, is hiring a Pharmaceutical Technician for 100% on-site work. You will weigh, transfer, mix and process raw materials to produce finished goods, while maintaining strict GMP and batch records. Cleaning, equipment handling, and proper documentation are essential.

Strong teamwork and adherence to safety protocols are required. You will collaborate with Room Leaders and supervisors to ensure quality and regulatory compliance, with emphasis on accurate

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