GMP‑Compliant Lab Technician: QC & Sample Prep

Piramal Pharma Limited

Lexington (AL)

Presencial

USD 42.000 - 52.000

Jornada completa

Hace 6 días
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Descripción de la vacante

Piramal Pharma Solutions, Lexington site, is seeking a Lab Technician in the Analytical Quality Control (AQC) department. The role supports chemists in daily QC activities to ensure project timelines and cGMP standards are met. You will report to the AQC Group Lead.

Key duties include sampling, testing, documentation, and waste management, with exposure to SOPs and regulatory guidelines. Team-based environment and strong communication are essential.

Formación

  • High school diploma or equivalent required.
  • 2+ years in a lab or manufacturing setting.
  • Experience with potent or cytotoxic materials preferred.
  • GMP environment experience preferred.
  • Proficient with Microsoft Office applications.
  • Excellent written and verbal communication skills.
  • Detail oriented and organized; able to work in a team.

Responsabilidades

  • Sample incoming materials.
  • Check expiry of chemicals, reagents and supplies.
  • Maintain cleanliness and organization of the lab and sampling areas.
  • Perform testing as required (e.g., TOC, pH, dimensional analysis).
  • Document laboratory work according to GDP, cGMPs and SOPs.
  • Prepare stability summary reports as needed.
  • Clean glassware and manage waste.
  • Enter purchase requests for consumables and contract testing.
  • Assist with shipment paperwork for contract testing.
  • Follow safety procedures in lab areas.
  • Use SAP, Ensur and S4HANA systems.

Conocimientos

Communication
Detail oriented
Team player
Problem solving
Interpersonal skills
Written instructions

Educación

High School Diploma or equivalent

Herramientas

SAP
Ensur
S4HANA

Descripción del empleo

Piramal Pharma Solutions, Lexington site, is seeking a Lab Technician in the Analytical Quality Control (AQC) department. The role supports chemists in daily QC activities to ensure project timelines and cGMP standards are met. You will report to the AQC Group Lead.

Key duties include sampling, testing, documentation, and waste management, with exposure to SOPs and regulatory guidelines. Team-based environment and strong communication are essential.

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