Lab Technician

Piramal Pharma Ltd; Lexington (AL); Presencial; USD 42.000 - 52.000; Jornada completa

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

Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Lab Technician

Job Description

Business: Pharma Solutions

Department: Analytical Quality Control (AQC)

Location: Lexington

Job Overview

Reporting to the AQC Group Lead, the Lab Technician provides support the day-to-day activities of Chemists within the analytical quality control laboratory to ensure project timelines are met and cGMP standards are followed.

Reporting Structure

This position reports to the AQC Group Lead.

Key Responsibilities

• Sampling of incoming materials.
• Perform expired chemicals, reagents and supplies checks
• General laboratory and sampling room cleaning (daily, weekly and monthly) & maintaining respective areas in an organized manner.
• Perform testing as required and applicable (ex: TOC, pH, dimensional analysis, etc.)
• Document laboratory work according to, GDP, cGMPs, and SOPs.
• Preparation of stability summary reports as needed.
• Perform Glassware cleaning.
• Entering purchase requests for laboratory consumables and contract laboratory testing.
• Managing laboratory waste.
• Management and archival of laboratory data.
• Assistance with shipment paperwork for contract lab testing.
• Following safety procedures in laboratory and sampling areas.
• Use of systems including SAP, Ensur and S4HANA

Qualifications

• High School Diploma or equivalent
• 2+ years working with a laboratory or manufacturing environment
• Experience working with potent or cytotoxic materials preferred.
• Working experience in a GMP environment preferred.
• High level of proficiency operating all Microsoft Office applications
• Excellent communication skills, both verbally and in writing
• Detail oriented and organized
• Demonstrated ability to work within a team environment, supporting a continuous operation manufacturing facility
• Excellent problem solving, communication, and interpersonal skills
• Ability to follow written instructions
• Familiar with OSHA safety regulations