Job Description
Job Description
Job Title: QC Chemist – Finish Products/Stability
Department/Division: Quality Control
Reports to: Director of Quality Control
About LTS:
LTS Lohmann Therapy Systems is a premier, global Contract Development and Manufacturing Organization (CDMO) and partner the pharma industry trusts most to deliver innovative oral, transdermal, and intradermal drug delivery systems. From concept to market, launch to lifecycle management, we deliver single source oral and transdermal drug delivery solutions that power partners’ market advantage. Every one of our 1,000 plus members of the LTS family, across three continents, is focused on utilizing our collective strength and innovation to explore new therapeutic opportunities, maximize partner value and improve patient outcomes.
We Care.
We Create.
We Deliver.
As a Quality Control Chemist, you'll perform routine analysis of raw materials, in-process goods, finished products, and stability testing. You'll work in a fast-paced laboratory and use a narrow spectrum of analytical techniques to maintain and troubleshoot instruments, as well as perform calibration procedures.
This is a full time, onsite position located in West Caldwell, NJ
What You Will Do:
- Perform routine and accurate analysis on submitted samples according to SOPs and pharmacopoeias.
- Document results in accordance with cGMP and LTS SOPs.
- Conduct basic maintenance, calibration, and troubleshooting of laboratory instruments.
- Immediately inform the supervisor of any deviations in results or procedures from established specifications.
- Adhere to all policies and procedures, including SOPs, cGMPs, and safety protocols.
- Provide input for laboratory investigations, corrective and preventive actions (CAPAs), and change controls.
- Identify areas for improvement and provide action plans, viable options, and alternatives to laboratory management.
- Abide by all cGMP, FDA, and DEA regulatory standards.
Qualifications:
- Bachelor’s degree in Chemistry or Biochemistry.
- Minimum of 1-2 years of experience in a laboratory or research environment.
- Proficiency in Microsoft Word, Excel, PowerPoint, and SAP.
- Experience in technical writing and documentation, including method writing.
- Experience with Chromatography Data Systems (CDS) such as Chromeleon or Empower.
- Excellent team player with good problem-solving abilities.
- Knowledge of cGMPs and pharmacopeial procedures, including USP testing and requirements.
If this sounds like you, we want to hear from you!
LTS is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.