Associate Director, MSAT

Lantheus Brand • Springfield, NJ

9d • Onsite

About The Position

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. This role will be based at Evergreen Theragnostic, a Lantheus company, located in New Jersey, requires a presence on-site four days per week, and is and open to applicants authorized to work for any employer within the United States.

Requirements

• B.S. or M.S. in relevant scientific/technical disciplines, advanced degrees (e.g., PhD) or technological certificates preferred but not required.
• 5+ years of experience in the radiopharmaceutical industry, including 3+ years focused on technology development and tech transfer activities.
• If no prior radiopharmaceutical experience, 10+ years of work experience within pharmaceutical or medical device industry, 5+ years of technology development and transfer experience, within a matrixed pharmaceutical, medical device, or biotechnology organization.
• Previous experience working with aseptically filled/finished drug products, medical device, radiopharmaceuticals and CDMO management strongly preferred.

Nice To Haves

• Subject matter expert (SME) in parenteral operations: aseptic processing, sterilization, sterile filtration, isolator technology operations.
• Strong knowledge of global regulatory requirements related to the design and control of these processes.
• Knowledge of SOPs, cGMPs and GLPs and the ability to work and manage within a regulatory environment.
• Demonstrated experience with the execution of technology transfer and scale up programs for commercial drug product manufacturing processes.
• Ability to work within and lead different technical teams.
• Familiarity with Design of Experiments, Quality by Design, and Quality Risk Management concepts commonly employed in pharmaceutical manufacturing.
• Excellent organizational skills and the ability to successfully manage a multitude of technical projects.
• Ability to work in a prompt, complex and changing environment.
• Excellent analytical, technical and experiences.
• Proactive mindset with strong leadership, facilitation, teamwork, and influence management/negotiation skills.
• Understanding of FDA and/or EMA quality and regulatory processes.
• Prior experience with regulatory filings is highly desired.
• Experience working with external partners is highly desirable.
• Ability to work independently in decision-making and resolution of program obstacles and conflicts.
• Keen insight, independent judgment and tactful discretion are required.
• Ability to function autonomously, with an appreciation of detail while being cognizant of “the big picture”.
• Proficiency with Microsoft Word, Excel, PowerPoint, and Project is required.
• Candidate represents Evergreen Theragnostics’ to external organizations and must exhibit the highest levels of personal integrity, quality, and professionalism.
• Travel may be required and is dictated by product needs and project deliverables, including overnight travel to CDMO locations.

Responsibilities

• Acts as a technology development and transfer lead in the Tech Ops organization.
• Leads and manages the Manufacturing Science and Technology (MSAT) team at Evergreen.
• Accountable for the technical work between internal and external stakeholders to ensure design, development, and transfer of robust manufacturing processes for new products and key lifecycle injectable pharmaceutical finished products.
• Principal expert and process owner for the end-to-end manufacturing process for injectable pharmaceutical finished products.
• Ensures processes are designed and validated per applicable cGMPs, Evergreen Theragnostics’ procedures, and that processes are defined consistent with regulatory filings.
• Complies with all Security guidelines, Environmental Health and Safety regulations and the current Good Manufacturing Practices.
• Responsible for review and authoring of key CMC submissions, along with setting relevant standards and creating /maintaining associated tech development transfer business processes.
• Leads technology development and transfer projects for key lifecycle injectable radiopharmaceutical products, including the establishment of the process/parameters for each unit operation of the process, and up until the completion of process performance qualification and subsequent CMC filing activities.
• Leads a team of engineers/scientists to execute the development, characterization, optimization and troubleshooting product and manufacturing processes of parenteral dosage forms.
• Leads a team of engineers/scientists to Perform Design of Experiments and Process Risk Assessment (FMEA) activities to establish appropriate process control strategies (PCS).
• Designs, prepares, and reviews technology transfer protocols, methods/processes, experimental or authoring plans or templates as appropriate.
• Responsible to create, maintain and harmonize key tech transfer business processes with internal and external stakeholders.
• Partners with the Internal and CDMO management team in the identification of best practices in industry related to technology transfers, pharmaceutical technology to create a competitive advantage.
• Partners with Business Development (BD) team in identifying and evaluating new technological platforms and pipeline products for business growth.
• Partners with site operations to provide a parenteral manufacturing process that is sustainable for future product supply.
• Partners with existing sites in the network to incorporate lessons learned from ‘sending’ sites for an optimized manufacturing process.
• Leads, motivates, mentors, and develops team members to exceed and meet company goals.
• Develops and maintains effective working relationships with other division groups and external partners in support of technology transfer, validation, and process support activities.
• Leads a team of engineers/scientists to own QEs (i.e. Change controls, Investigations, CAPAs, Protocol & report writing)
• Responsible to review and co-author key CMC sections with external partners and cross functional stakeholders.
• Requires approximately ~20% travel.
• Actively promotes safety rules and awareness.
• Always demonstrates good safety practices including the appropriate use of protective equipment.
• Reports and takes initiative to correct safety and environmental hazards.
• Actively demonstrates company values.

Benefits

• 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 for this position include a comprehensive health benefits package that includes medical, prescription drug, dental, and vision coverage.
• Other offerings include life and disability benefits, pre-tax accounts, a 401(k) with company contribution, and a variety of other benefits.
• In addition, employees are eligible for a generous time off package including paid vacation, holidays, sick days, and paid parental leave.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 501-1,000 employees