Associate Principal Scientist, Small Molecule Analytical Research & Development

About the Role

The Small Molecule Analytical Research and Development (SMAR&D) group has an exciting opportunity for an Associate Principal Scientist based in Rahway, NJ. Join us and experience our culture firsthand - one of strong ethics & integrity, diversified experiences, exceptional science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

As an Associate Principal Scientist, you will be part of a team developing innovative analytical methodologies for medicines based on small molecules, peptides, mRNA, oligonucleotides and bioconjugates. Our responsibilities range from early stage up to commercialization for both drug substance and a broad array of oral, sterile and combination products. You will also contribute towards regulatory submissions to enable clinical trials.

Responsibilities

• Driving our Company's Pipeline: Leading or participating on analytical teams driving the development of drugs in our Company's pipeline, with a deep understanding of product development from early stage through commercialization
• Actively partnering with other functional areas to design scientific studies guiding product and process development
• Defining and implementing end-to-end analytical control strategies for clinical supplies under good manufacturing practices (including method development and validation as well as specification setting)
• Authoring investigational new drug (IND), investigational medicinal product dossier (IMPD), and new drug application (NDA)/ worldwide marketing application (WMA) submission documents across the project development lifecycle, as well as responding to agency questions
• Promoting our Company's scientific excellence and regulatory influence through leadership in the scientific community
• Advancing and expanding analytical capabilities via the adoption and implementation of novel technologies for product and process characterization
• Designing and executing the experiments needed to influence programs with data-driven decisions
• Mentoring and providing day-to-day oversight of junior analytical scientists
• Representing your team and/or department via presentations to governance committees and other internal audiences
• Proactively identifying and escalating program risks
• Fostering strong collaborations with internal stakeholders and external partners by actively engaging in two-way communication to build trusting relationships
• Applying a strong understanding of new product development and commercialization to analytical development challenges for small molecules, peptides, mRNA, oligonucleotides, and bioconjugates
• Using conventional and novel technologies through active collaboration with cross functional project teams and external vendors

Qualifications

Education

• Minimum Requirements

Applicants must hold one of:

• PhD Degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related fields with at least 3 years of pharmaceutical industry experience
• Master's Degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related fields with at least 7 years of pharmaceutical industry experience
• Bachelor's Degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related fields with at least 10 years of pharmaceutical industry experience

Required Experience and Skills

• Strong team player with excellent written and oral communication skills, as well as leadership and interpersonal skills
• Technical expertise and strategic experience in analytical control strategy development and execution
• Ability to develop talent through good mentoring skills
• Demonstrated ability for taking initiative, creativity, and innovation in problem solving
• Ability to design, execute and/or direct the development and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process development
• Strong technical problem-solving ability
• External scientific engagement demonstrated by scientific publications and presentations
• Ability to work both independently for development of analytical methodologies and cross-functionally for successful transfer methods
• Plan optimization and documentation to meet program deadlines
• Authoring and reviewing internal technical reports, sections of regulatory filings (e.g., IND, BLA) and external scientific publications
• Experience with matrix management and peer to peer coaching
• Ability to deliver complex objectives under aggressive timelines in a rapidly changing environment
• Accountability
• Adaptability
• Analytical Chemistry
• Analytical Method Development
• Assay Development
• Biochemistry
• Biological Assay Development
• Biopharmaceuticals
• Cell-Based Assays
• Chromatographic Techniques
• Clinical Trials
• Communication
• Cross-Functional Teamwork
• Experimental Methods
• External Collaboration
• High Resolution Mass Spectrometry (HRMS)
• Immunochemistry
• Liquid Chromatography-Mass Spectrometry (LC-MS)
• Mass Spectrometry Analysis
• Matrix Management
• Messenger RNA
• Optimistic Attitude
• Process Analytical Technology (PAT)
• Product Development

Preferred Experience and Skills

• Hands-on chromatography (e.g., LC, GC) method development, analysis and troubleshooting
• Other advanced analytical techniques such as mass spectrometry or dissolution
• Experience in development and characterization of small and/or large molecules, mRNA, and/or antibody drug conjugates
• Established scientific reputation supported by publications and external presentations
• Experience in high-throughput experimentation and data-rich experimentation, or data science

Hybrid Work Model

• Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday
• Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business needs require otherwise.

Application Information

• Current Employees apply HERE
• Current Contingent Workers apply HERE
• US and Puerto Rico Residents Only

Equal Opportunity Employment

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.

As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.

For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights, EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together talented and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.

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