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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: 80000 - 110000 USD Yearly USD 80000.00 110000.00 YEAR
Job Description & How to Apply Below
Location: Cherry Hill Township

Job Title: Scientist, Analytical Research

Location: Cherry Hill, NJ

Job Type: Full time

Req : 10911

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 continue to be committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Scientist, Analytical Research
. In this role, you will be responsible for providing chemistry laboratory support and work with more senior R&D scientists performing duties such as, but not limited to, evaluating methods for transfer, analyzing samples, developing analytical methods and conducting pre‑validation/validation studies. Responsibilities primarily involve working in the lab with moderate supervision.

Key Responsibilities
  • Operates, maintains, and is responsible for lab equipment.
  • Performs routine procedures in an efficient manner with minimal direction. Assists in the execution of non‑routine experiments and procedures with supervision.
  • Understands and applies basic scientific principles and technology and builds knowledge of relevant regulatory requirements.
  • Has the ability to correctly analyze and interpret the outcome of experiments.
  • 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.
  • Communicates own work orally/in writing and demonstrates an aptitude for developing technical writing expertise.
  • Interfaces with enabling service teams such as Technical Services, Document Control, Quality Control Chemistry, 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 another scientific discipline and at least 5 years of pharmaceutical or related laboratory experience, or
  • Master’s degree in chemistry or closely related field with 3 years of pharmaceutical or related laboratory experience, or
  • Ph.D. in chemistry or pharmaceutical science or closely related field.
  • Computer literacy, technical writing, and multi‑tasking skills are required.
  • Requires basic understanding and proficiency in the use of analytical glassware, syringes, pipettes, balances and other instrumentation.
  • Understanding of lab techniques.
  • Proficiency in the use of Microsoft Office including Word and Excel. Project planning techniques and use of project planning software.
  • Demonstrated proficiency with chromatographic, spectrophotometric and titrimetric instruments, especially HPLC, GC and volumetric/potentiometric titrations. Experience in basic pharmaceutical formulation concepts, analytical method development, research, and problem‑solving.
  • Good communication skills, both oral and written.
Compensation

Base Salary
: $80,000 to $110,000 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…

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