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As of Aug 29, 2026, the average hourly pay for senior associate scientist in the United States is $35.92, according to ZipRecruiter salary data. Most workers in this role earn between $27.88 and $40.87 per hour, depending on experience, location, and employer.

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Senior Associate Scientist jobs near you
A map of the United States highlighting the number of Senior Associate Scientist job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Senior Associate Scientist job openings in each state, with California having the most at 2 and Hawaii the least at 0.

Sr. Associate Scientist, Analytical Research

Hikma Pharmaceuticals PLC

Columbus, OH • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.

Hikma Pharmaceuticals rating

7.8

Company rating: 7.8 out of 10

Based on 31 frontline employees who took The Breakroom Quiz

49th of 86 rated pharmaceutical

Job description

Job Title: Sr. Associate Scientist, Analytical Research
Location: Columbus, Ohio
Job Type: Full time
Req ID: 12298
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 Sr. Associate Scientist, Analytical Research to join our team.
In this role, you will be responsible for conducting chemical and physical analyses in support of the development of a manufacturable multisource pharmaceutical product. Providing analytical support for the release of registration materials in support of regulatory submissions. Assisting analytical method validation and transfer activities. You will work closely with Senior and Principal Scientists in the Analytical Research team and Formulation Development team.
Key Responsibilities:
  • Regular and predictable onsite attendance and punctuality.
  • Performs the assigned analytical tasks in support of product development, registration lot release, pre and post regulatory submission activities. Performs activities within the assigned timelines and in compliance with cGXP's, and company practices and procedures.
  • Follows work instructions, SOPs and company practices.
  • Documents analytical activities and results accurately, in a timely manner and right-first time and maintains integrity of data.
  • Performs assigned tasks in support process changes (e.g. processes, procedures, etc...) within the assigned timelines.
  • Communicates effectively with peers and supervisor about the status of the assigned tasks, maintaining supervisor constantly updated.
  • Follows written analytical procedures. Identifies execution challenges of analytical methods and support trouble shooting activities.

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 scientific discipline such as chemistry, pharmacology.

Preferred Qualifications:
  • 6 months+ relevant work experience in pharmaceutical industry including but not limited to the following:
    1. Experience with the following analytical techniques:
      1. For API: UV/Vis, IR, pH meter, wet chemistry techniques, GC and HPLC.
      2. For Product: UV/VIS, dissolution, pH meter, wet chemistry techniques, and HPLC
  • Experience in c-GXP analytical laboratories.
  • Inhalation Testing experience.

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 4% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute
  • A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries
  • 3 personal days (prorated based on hire date)
  • 11 company paid holidays
  • Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits
  • Employee discount program
  • Wellbeing rewards program
  • Safety and Quality is a top organizational priority
  • Career advancement and growth opportunities
  • Tuition reimbursement
  • Paid maternity and parental leave

*Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.
Recruiters:
Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.
Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.
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