Lab Technician

Piramal Pharma Limited; Lexington (KY); On-site; USD 42,000 - 54,000; Full time

Job summary

Piramal Pharma Solutions in Lexington, KY is hiring a Lab Technician to support daily analytical quality control activities and ensure cGMP compliance. The role reports to the AQC Group Lead and involves sampling, testing, and documentation in a GMP lab.

Ideal candidates have 2+ years in a lab/manufacturing setting, proficiency in Microsoft Office, and strong communication skills. Safety and accuracy are essential in this team-oriented environment.

Qualifications

• High School Diploma or equivalent.
• 2+ years in a laboratory or manufacturing environment.
• Experience with potent or cytotoxic materials preferred.
• GMP environment experience preferred.
• Proficient with Microsoft Office applications.
• Detail oriented and organized.
• Excellent communication and interpersonal skills.

Responsibilities

• Sampling of incoming materials.
• Perform routine checks on chemicals, reagents and supplies.
• Maintain clean and organized laboratory 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.
• Enter purchase requests for laboratory consumables.
• Manage laboratory waste and data archival.
• Assist with shipment paperwork for contract lab testing.
• Follow safety procedures in laboratory and sampling areas.

Skills

Communication

Detail oriented

Teamwork

Problem solving

Education

High School Diploma

Tools

SAP

Ensur

S4HANA

Job description

Lab TechnicianThis website contains strictly necessary cookies. These cookies are necessary for the website to function and cannot be switched off in our systems. These cookies do not store any personally identifiable information.# Careers## Lab TechnicianApply: Lexington: Full time: Posted Today: R00004945***Be the First to Apply*****Division**Piramal Pharma SolutionsPiramal 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.comJob TitleLab TechnicianJob DescriptionBusiness: 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