Summary

We are seeking an individual to assist our environmental monitoring group with sampling classified environments (Grades A, B, C and D). You will be part of the group that helps maintain our classified environments where pharmaceutical manufacturing occurs. You will be able to see firsthand all the activities that involve making sterile injectable drug products as well as gain a knowledge and understanding of aseptic technique and aseptic filling. You will be the owner of the environmental monitoring program and can escalate issues that are seen on the production floor and work alongside the QA department to ensure compliance.

Job description

Your Role

We are seeking an individual to assist our environmental monitoring group with sampling classified environments (Grades A, B, C and D). You will be part of the group that helps maintain our classified environments where pharmaceutical manufacturing occurs. You will be able to see firsthand all the activities that involve making sterile injectable drug products as well as gain a knowledge and understanding of aseptic technique and aseptic filling. You will be the owner of the environmental monitoring program and can escalate issues that are seen on the production floor and work alongside the QA department to ensure compliance.

Weekday Afternoons: Monday - Friday 10am - 6pm or 12pm - 8pm.

Minimum Qualifications

High School Diploma or GED.

Preferred Qualifications

Strong desire to learn new activities and make improvements to processes.
Able to adequately use tablets and software for environmental monitoring.
Experience with GMP, GDP or GLP procedures.
Ability to work cross-functionally with multiple departments including manufacturing, QA, maintenance and Sterility Assurance.
Knowledge of regulatory requirements for pharmaceutical products.

Requirements

High School Diploma or GED
Strong desire to learn new activities and make improvements to processes
Able to adequately use tablets and software for environmental monitoring
Experience with GMP, GDP or GLP procedures
Ability to work cross-functionally with multiple departments including manufacturing, QA, maintenance and Sterility Assurance
Knowledge of regulatory requirements for pharmaceutical products

Benefits

Health Insurance
Paid Time Off (PTO)
Retirement Contributions

Company overview

Merck Healthcare KGaA is the healthcare business sector of the Merck Group, a German multinational science and technology company headquartered in Darmstadt. Founded in 1668, Merck is the world's oldest operating pharmaceutical and chemical company. The Healthcare division focuses on developing innovative therapies across multiple therapeutic areas including oncology, neurology & immunology, fertility, and cardiovascular, metabolic, and endocrinological disorders. With approximately 62,557 employees globally, Merck Healthcare operates in more than 65 countries and generated 40% of the Group's sales in 2024. The company's oncology portfolio includes blockbuster products like Erbitux (cetuximab) for colorectal and head and neck cancers, Bavencio (avelumab) for urothelial carcinoma, and Tepmetko (tepotinib) for MET-altered cancers. In neurology, Mavenclad (cladribine) has achieved blockbuster status for treating relapsing multiple sclerosis, while the fertility division has helped bring over 6 million babies into the world through products like Gonal-f. Merck Healthcare combines a strong established business with specialty innovation, delivering a diversified portfolio of therapies to millions of patients worldwide.