Quality Control Chemist at LTS Lohmann Therapy

West Caldwell, New Jersey, United States -

Full Time

Start Date

Immediate

Expiry Date

05 Aug, 26

Salary

80000.0

Posted On

07 May, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Routine Analysis, cGMP Documentation, Instrument Maintenance, Calibration, Troubleshooting, FDA/DEA Regulatory Standards, CAPA, Change Control, Wet Chemistry, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Computerized Data Acquisition Systems, Communication Skills, Basic Math

Industry

Pharmaceutical Manufacturing

Description

ABOUT THE COMPANY LTS Lohmann Therapy Systems is a global leader in transdermal and oral thin‑film drug delivery technologies. Our teams have pioneered breakthroughs such as the first contraceptive patch, nicotine patch, oral active ingredient film, and Parkinson’s patch. When you join LTS, you become part of a team that continues to shape the future of patient care and bring life‑changing therapies to market. At LTS, our purpose drives everything we do: We CARE. We CREATE. We DELIVER. We’re committed to fostering an employee experience that reflects our innovation — supportive, collaborative, and empowering. Across our New Jersey and Minnesota locations, you’ll work alongside knowledgeable experts on diverse projects in an environment where every day is different and your contributions truly matter Job Summary: LTS is hiring a QC Chemist to join our Quality Control team in West Caldwell, NJ. This position supports routine testing of raw materials, in-process, finished products, and stability samples in a cGMP laboratory environment. Shift/Schedule: 7:30 AM – 4:00 PM (Mon-Fri) Work Setting: On-site laboratory and office environment (West Caldwell, NJ) What You Will Do: * Perform routine analysis of raw materials, in-process samples, finished products, and stability samples according to SOPs and pharmacopoeias * Document results in accordance with cGMP requirements and LTS SOPs * Perform basic instrument maintenance, calibration, and troubleshooting * Notify your supervisor of any deviations from established specifications or procedures * Follow all applicable policies and procedures (SOPs, cGMPs, safety protocols), including FDA/DEA regulatory standards * Provide input for lab investigations, CAPAs, and change controls; identify improvement opportunities and propose viable options * Support other Quality Control unit functions as needed Qualifications: * Bachelor’s degree * 1–2 years of experience in a laboratory or research environment * Above average reading, writing, and verbal communication skills * Basic math skills * Basic use of tools/equipment * Proficiency in Word, Excel, and PowerPoint * Experience with computerized data acquisition systems Preferred Qualifications: * Basic wet chemistry techniques * Above average knowledge of chemistry and/or biochemistry 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.

Responsibilities

Perform routine analysis of raw materials, in-process, finished products, and stability samples in a cGMP laboratory. Document results according to SOPs and support lab investigations, CAPAs, and instrument maintenance.