Job Title: Quality Inspector - Final
Department/Division: Quality Assurance
Reports to: Quality Assurance Supervisor
About LTS:
LTS Lohmann 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 2,000 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.
Job Summary
Lohmann Therapy Systems North America is seeking a Quality Assurance Inspector to join our team. As a critical member of our organization, you will inspect, audit, and report on materials, processes, and products to ensure compliance with our standards and customer requirements.
This is a full time, onsite role located in West St. Paul, MN.
* 2nd shift: 2:00pm to 10:30pm, Monday-Friday
What You Will Do:
Conduct inspections to verify product conformance to specifications.Operate various test and measurement equipment such as calipers, rulers, Instron and Nikon.Perform in-process and final inspections on pharmaceutical and medical device products.Review and release production lines.Monitor environmental systems for compliance.Collect and review finished product retain samples.Review controlled records throughout the production process.Perform specialty measurements to support cross-functional departments.Your Background:
High School Diploma or GED.Basic math skills (addition, subtraction, multiplication, division, fractions, decimals, metric conversion).Ability to read and interpret instructions, drawings, and specifications.Experience with basic measuring and testing equipment.Good color discrimination.Proficiency with personal computers and Microsoft software.Physical ability to bend, squat, kneel, and lift up to 45 pounds.Excellent interpersonal skills.Willingness to work overtime as needed.Preferred Qualifications
Associate's or Technical degree in Quality Control.2+ years of experience in quality inspection in a pharmaceutical or medical device environment.Experience working in an ISO and cGMP environment.We Offer
Competitive compensation and benefits packageOpportunities for professional growth and developmentA collaborative and supportive work environmentThe chance to contribute to improving patient livesIf 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.
LTS 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.
LTS is hiring a Slitting Operator II in West Caldwell, NJ. In this role, you will operate slitting and spooling equipment to process raw materials, medical tape components, and coated non-active/active drug laminates and films while following MBRs, SOPs, cGMP requirements, and safety standards. This is a great opportunity for a skilled production professional who takes pride in quality, accuracy, and teamwork.
Location: West Caldwell, NJSchedule: 6:15 AM - 2:30 PM (1st Shift)- Monday-Friday; occasional overtime availableWe Offer
Competitive compensation and benefits packageOpportunities for professional growth and developmentA collaborative and supportive work environmentThe chance to contribute to improving patient lives
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.
About LTS:
LTS Lohmann 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.
Job Summary:
The Manufacturing Operator II - Mix Coat is a skilled role responsible for executing manufacturing tasks with increased independence. This role requires competence in basic equipment setup, initial troubleshooting, and material handling, performed under the guidance of senior Operators and supervision. The Manufacturing Operator II works to ensure production efficiency and compliance with GMP, FDA, and DEA standards while supporting process improvements.
This role is located is West St. Paul, MNThis role is 2nd shift- 2:00pm - 10:30pm M-FDuties/Responsibilities:
Technical Operations & Equipment Expertise
Perform equipment setup, operation, and troubleshooting with moderate supervision.Execute weighing, dispensing, and mixing operations.Assist with equipment changeovers, including cleaning and material movement.Conduct in-process control (IPC) sampling and testing during mixing and/or coating operations with moderate supervision.Maintain 5S standards, ensuring a clean and organized workspace.Manufacturing Documentation & Compliance
Understand and follow GMP, FDA, and DEA regulations.Complete basic documentation tasks accurately, including downtime tracking and material labeling.Support final production closing and material reconciliation of batch records.Leadership & Training
Embrace and promote LTS’s cultural values of Teamwork, Entrepreneurship, Accountability, and Leadership.
Education and Experience:
High school diploma or GED required; some college coursework preferred.1-3 years of experience in a manufacturing environment.Strong verbal and written communication skills.Basic computer literacy skills (e.g., MS Word, Excel).Preferred Skills/Abilities:
Standing for extended periods, performing physically demanding tasks.Lifting up to 50 lbs as required.Exposure to chemicals, solvents, and production machinery in a controlled environment.Flexibility to work various shifts, including nights, weekends, and overtime when necessary.We Offer
Competitive compensation and benefits packageOpportunities for professional growth and developmentA collaborative and supportive work environmentThe chance to contribute to improving patient livesIf 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.
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