QC Analytical Analyst, Raw Materials Testing

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.

Summary of role

We are seeking a Quality Control (QC) Analytical Analyst, to ensure that manufactured products meet established quality, safety, and regulatory standards. The daily QC activities include raw material, intermediate product and final drug product release testing of sterile injectable radiopharmaceutical products used to detect and treat cancer.  Additional laboratory duties include performing stability testing, analytical method transfers and analytical method validations.  Qualified Analysts are expected to provide training on testing protocols and safety measures for junior staff members.  The QC Analytical Analyst will have the opportunity to draft documents related to these efforts as well.

This position is based in Springfield, NJ and requires a presence on-site five days per week, and open to applicants authorized to work for any employer within the United States. This role will be on First Shift (approximately 8 AM – 5 PM).

Responsibilities

• Perform Raw Material Sampling
• Perform USP ID testing, both chemical and instrumentation
• Perform QC release and stability testing on drug products
• Execute experimental protocols, SOP’s, etc., consistent with cGMP/GLP.
• Validate analytical procedures to meet QC’s needs.
• Adapt, maintain, and operate analytical instrumentation.
• Develop and transfer analytical methods to and from QC and contract manufacturers as assigned by management.
• Adhere to all safety requirements.
• Conduct radiation safety duties conforming to regulations.
• Participate in department meetings via input, feedback, and execution of assigned tasks.
• Ensure the work environment is clean, safe and in compliance with safety and pharmaceutical regulations.
• Report monthly on supplies for QC orders involving devices and reagents.
• Participate in laboratory investigations and root-cause analyses.
• Prepare chemical reagents for manufacturing and QC.

Basic Qualifications

• Bachelor’s degree in Chemistry or Biochemistry required
• Minimum of 3+ years of applicable GMP laboratory experience required Radiopharmaceutical experience preferred.
• Experience using analytical techniques, such as High-Performance Liquid Chromatography (HPLC) and radio-Thin Layer Chromatography (rTLC).
• Strong organizational, and problem-solving skills while working under strict timelines.
• Ability to convey complex ideas in a simple manner to management and customers, exercise independent judgement during method development/transfer processes.
• Knowledge of analytical methods currently used for testing, release, and stability of sterile pharmaceutical products.
• Team oriented mindset and demonstrates ability to work easily with cross functional teams.
• Fluent in Microsoft Word and experienced in working with laboratory information management systems (LIMS).

Preferred Qualifications

• Strong written and oral communication skills, as well as the ability to critically review and interpret quality event investigations.
• Understanding of quality risk management strategies, as well as demonstrated ability to continuously improve the QMS and manufacturing/testing operations.
• Skilled at initial interpretation of issues and effectively communicating such issues to Upper Management for further consideration.
• Ability to lead quality initiatives that enhance site QMS, and adjacent activities.
• Ability to work efficiently when working independently on quality-related tasks.
• Ability to implement corrective and preventive actions on the shop floor, with assistance from cross-functional team members.
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