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Jobs · Quality Assurance · New Jersey

QC Analytical Analyst, Raw Materials Testing

Lantheus · Springfield, NJ · 2 wk ago
On-siteQuality Assurance$72k–$107k/yrFull-time

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 the 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.

About the role

We are seeking a Quality Control (QC) Analytical Analyst to ensure that manufactured products meet established quality, safety, and regulatory standards. The role involves daily QC activities including raw material, intermediate product, and final drug product release testing of sterile injectable radiopharmaceutical products used to detect and treat cancer. Additional duties include stability testing, analytical method transfers, and validations. The QC Analytical Analyst will also provide training on testing protocols and safety measures for junior staff and draft related documents. This position is based in Springfield, NJ, requires on-site presence five days per week, and is open to applicants authorized to work for any employer in the United States. The role operates on First Shift (approximately 8 AM – 5 PM).

Responsibilities

  • Perform raw material sampling.
  • Conduct USP ID testing, both chemical and instrumentation.
  • Perform QC release and stability testing on drug products.
  • Execute experimental protocols, SOPs, 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.
  • Adhere to all safety requirements, including 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 compliant 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.

Requirements

  • Bachelor’s degree in Chemistry or Biochemistry required.
  • Minimum of 3+ years of applicable GMP laboratory experience.
  • 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 simply to management and customers, and exercise independent judgment during method development/transfer.
  • Knowledge of analytical methods for testing, release, and stability of sterile pharmaceutical products.
  • Team-oriented mindset with the ability to work easily with cross-functional teams.
  • Fluent in Microsoft Word and experienced in working with Laboratory Information Management Systems (LIMS).
  • Safety-first mindset, as the role involves working in proximity to radiation.

Preferred Qualifications

  • Strong written and oral communication skills, with the ability to critically review and interpret quality event investigations.
  • Understanding of quality risk management strategies and demonstrated ability to continuously improve the QMS and manufacturing/testing operations.
  • Skilled at initial interpretation of issues and effectively communicating them to upper management.
  • Ability to lead quality initiatives that enhance site QMS and adjacent activities.
  • Ability to work efficiently independently on quality-related tasks.
  • Ability to implement corrective and preventive actions on the shop floor with cross-functional team members.
  • Ability to quickly recognize conflicts/issues and notify management with proposed recommendations for resolution.
  • Clear verbal communication of updates, problems, projects, and required information to all audiences.

Core Values

The ideal candidate will embody Lantheus core values:

  • Let people be their best.
  • Respect one another and act as one.
  • Learn, adapt, and win.
  • Know someone’s health is in our hands.
  • Own the solution and make it happen.

Pay

The pay range for this position is between $72,000 and $107,000 annually. Actual base pay offered may vary depending on job-related knowledge, skills, and experience. Employees in this position are eligible for a discretionary performance-based cash incentive and, depending on the level of the role, may be eligible for a discretionary annual equity award.

Benefits

  • Comprehensive health benefits package including medical, prescription drug, dental, and vision coverage.
  • Life and disability benefits.
  • Pre-tax accounts.
  • 401(k) with company contribution.
  • Generous time off package including paid vacation, holidays, sick days, and paid parental leave.

Schedule

This role operates on First Shift (approximately 8 AM – 5 PM), five days per week.

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