QC Physical Testing Analyst

Lantheus (NASDAQ: LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease to deliver better patient outcomes. Headquartered in Massachusetts with offices in New Jersey, Canada, Germany, Sweden, Switzerland and United Kingdom, Lantheus has been providing radiopharmaceutical solutions for nearly 70 years.

Today, we’re expanding our portfolio and pipeline across oncology, neurology and cardiology. Through recent acquisitions, along with strategic partnerships across the life sciences ecosystem, we are accelerating our efforts to advance precision medicine and improve patient outcomes around the world.

At Lantheus we are purpose-driven, and every employee plays a vital role in our success. We’re dedicated to cultivating a high-growth, forward-thinking culture where innovation thrives and diverse perspectives drive meaningful progress.

Join us and be part of a company where your contributions make a real impact, because we know someone’s health is in our hands.

We are seeking a strong candidate to:
Perform routine and advanced testing on incoming materials, reference standards, solutions, finished product release and stability in QC Laboratory following cGMP standards. This is a site-based role requiring an onsite presence 5 days a week in Billerica, MA.

• Perform routine QC testing in accordance with SOPs and cGMP guidelines. SME who can troubleshoot, may require assistance. Minimal supervision required.
• Perform a variety of basic to complex methods utilizing lab equipment such as calipers, rulers, microscope, and Raman Spectrometer and material sampling.
• Perform verification of data to ensure accuracy. Perform approval upon discretion of supervisor.
• Assist with audit readiness of laboratory area and calibration and maintenance of laboratory equipment.
• Utilize a range of electronic systems such as ERP, QMS, LIMS, and equipment management software.
• Author and review SOP changes; participate in change controls, CAPAs, etc.
• Resolve routine and advanced problems by utilizing appropriate resources. Provide problem solving skills to support & possibly lead investigations.
• Participate in protocols for procedural validations and instrumentation qualifications.
• Work on special projects as needed. Contribute towards continuous improvement.
• Train on and maintain knowledge of current regulatory requirements and relevant internal procedures.
• Actively promote safety rules and awareness. Demonstrate good safety practices at all times including the appropriate use of protective equipment. Report and takes initiative to correct safety & environmental hazards.
• Work individually and as a team with quality and attention to detail. Good communication skills both oral and written. Effectively and efficiently participate in assigned tasks in a quality manner.
• Demonstrate & adhere to Lantheus corporate Values. Actively demonstrate quality, accountability, customer service, efficiency, collaboration, and safety, as well as appropriate workplace behaviors and professionalism, including respect, flexibility, and a positive attitude toward work and others.

• Requires an Associate’s degree and typically 5 years of related experience; or a BS degreee and 3 years related experience; or an equivalent combination of education and work experience. Degree in a scientific discipline and experience in the pharmaceutical industry, related GMP environment, or equivalent highly preferred.
• Must be able to pass pre-placement eye exam for color and have correctable vision. Vision acuity capable of particulate detection required.
• Must be able to lift/move materials up to 50 lbs, e.g. gas cylinders, chemicals,…