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Principal Scientist, Analytical Research

Job in Cherry Hill Township, Cherry Hill, Camden County, New Jersey, 08034, USA
Listing for: Hikma Pharmaceuticals
Full Time position
Listed on 2026-03-09
Job specializations:
  • Research/Development
    Research Scientist, Clinical Research
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 92850 USD Yearly USD 92850.00 YEAR
Job Description & How to Apply Below
Location: Cherry Hill Township

Job Title: Principal Scientist, Analytical Research - Injectables

Location: Cherry Hill, NJ

Job Type: Full time

Req : 10943

About Us:

As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ mission is to bring Better Health. Within Reach. Every Day.® for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 800 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 32 manufacturing plants, eight R&D centers, and 9,500+ employees worldwide, we are always hard at work creating high-quality medicines and making them 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, Analytical Research - Injectables to join our team.

In this role, you will be responsible for providing chemistry laboratory support such as, but not limited to, preparing formulations, analyzing samples, developing analytical methods and conducting pre‑validation studies. Responsibilities primarily involve working in the lab with some guidance.

Key Responsibilities:
  • Operates, maintains and is responsible for lab equipment.
  • Designs and executes routine and non‑routine experiments associated with generic drug product development such as deformulation studies, analytical method development and prevalidation and formulation and process development.
  • Understands and applies scientific principles and technology, and demonstrates an in-depth knowledge of relevant regulatory requirements.
  • Demonstrates the ability to design novel experiments and to analyze and interpret subsequent experimental results.
  • Maintains proper records (notebooks, electronic records, study files, etc.) per relevant policies and procedures.
  • Assists in the review and approval of co‑worker laboratory notebook entries and provides guidance on notebook documentation practices to junior level staff.
  • Demonstrates proficiency in oral communication and technical writing.
  • Interfaces with enabling service teams such as Laboratory Services, Document Control, Logistics, and Environmental Health & Safety, regarding support needs and compliance requirements.
  • Maintains current technical and safety training.
  • Understands appropriate regulations and legal requirements as well as company policies and procedures relevant to areas of expertise.
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:

  • Bachelor’s degree in chemistry or other scientific discipline and a minimum 10 years of relevant hands‑on analytical method development experience; or
  • Master’s degree in chemistry or other scientific discipline and 8 years of relevant hands‑on analytical method development experience; or
  • PhD in chemistry or other scientific discipline and 6 years of relevant hands‑on formulation experience.
  • Expansive knowledge of analytical method development following QbD, materials characterization, process development, and scale up of sterile injectable products.
  • Computer literacy, technical writing, multi‑tasking, time management and work prioritization skills are required.
  • Thorough understanding and proficiency in the use of analytical glassware, syringes, pipettes, balances and other instrumentation.
  • In‑depth knowledge of lab techniques.
  • Proficiency in the use of Microsoft Office including Word and Excel. Project planning techniques and use of project planning software.
  • Advanced level of experience in instrumental analysis, especially HPLC and GC. Experience in pharmaceutical formulation development, analytical method development, research, problem‑solving, and experimental design.
  • Excellent communication skills, both oral and written.
Compensation:

Base Salary: $92,850.00 to $ annually. The compensation for this position will be determined…

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