Principal Scientist

Job Title: Principal Scientist 

Location:Cherry Hill, NJ

Job Type: Full-time

 

 

About Us:

As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them.

 

Description:

We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds.  We are seeking a talented and motivated Principal Scientist to join our team.  In this role, you will be serve as a key member of the Cherry Hill Technical Services Team, responsible for developing, implementing, and governing validation strategies for new launch, and validation lifecycle management. This role focuses on global alignment, standardization of validation approaches, and strategic oversight of Tech Transfer, PPQ campaigns, launch & lifecycle management programs, and product release readiness. This role partners closely with regional R&D, Equipment, Quality, Regulatory, and Engineering teams to ensure consistent, compliant, and innovative validation practices globally.

 

Key Responsibilities:

• Author harmonized validation standards and templates across the global network.

• Provide strategic oversight for PPQ campaigns implemented at multiple sites, ensuring consistency and compliance

• Responsible for generation and execution of Batch size increase, Bulk Hold Extension, Process Validation, Room Transfer and Validation as a result of CAPA/Investigation.

• Support lifecycle improvement initiatives and evaluate digital for process optimization.

•  Partner with regional and site teams to assess validation readiness for new technologies and platforms.

• Support and author regulatory submissions with globally aligned validation documentation and strategies.

• Able to coach mentor new hires and team members to drive consistency and compliance in documentation and execution practices.

 

Qualifications:

We value the skills and experiences candidates bring to the table.  While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:

 

Education :

Bachelor's degree in Chemistry, Engineering, biotechnology or related scientific field is require.

 

Skills & Experience:
• 7+ years proven experience within a regulated pharma industry
• Experience in global process validation strategy, governance, and regulatory compliance for ATMPs.
• Strong understanding of risk-based validation principles and Health Authority expectations.
• Demonstrate the ability to work effectively in cross-functional environment and influence global teams.

 

Compensation:

Base Salary: $ 66,600 to $ 133,750 annually.  The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring proces

 

 

What We Offer*:

• Annual performance bonus, commission, and share potential
• Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay.  Hikma will match 100% of the first 6% of eligible pay that you