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Specialist , Quality Assurance

Job in Columbus, Franklin County, Ohio, 43224, USA
Listing for: Hikma Pharmaceuticals
Full Time position
Listed on 2026-02-17
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist / Manager, Quality Control / Manager, Quality Technician/ Inspector
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Specialist I, Quality Assurance

Title:

Specialist I, Quality Assurance

Job Title: Specialist I, Quality Assurance

Location: Columbus, OH

Job Type: Full time

Req : 10661

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.

Job Summary

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 Specialist I, Quality Assurance to join our team.

In this role, you will be responsible for supporting Quality Assurance to ensure quality and compliance with regulations regarding product complaints and product/process deviations. The entry‑level position will mainly support QA Complaints (e.g., complaint inbox management, complaint intake, complaint follow‑up, etc.) and QA Investigations (e.g., fact‑check investigations, investigation triage, etc.) for investigation intake and closure activities.

Key Responsibilities
  • Regular and predictable onsite attendance and punctuality.
  • Supports Complaint Intake (enter complaints into QMS and support follow‑ups with complainant as needed) and QA Investigation triage (complete deviation details, follow up on supporting documents, etc.)
  • Conducts simple investigations on complaints and deviations and documents accordingly.
  • Applies investigative techniques to uncover problems, recommend corrective actions, and partners with operations to implement preventative programs for sustained improvement.
  • Receives phone calls, voicemails, email, or other inbound communications from product customers and documents product complaints as directed by Standard Operating Procedures.
  • Communicates clearly with internal and external customers, peers, and management.
  • Actively listens to gain accurate understanding and obtain necessary information to document within investigation records (complaints and deviations).
  • Supports incoming (returned product) and outgoing mail (DEA forms, complainant letters, etc.) requirements through mailroom or warehouse as needed.
  • Participates in meetings/discussions with process owners to discuss findings, obtain resolution commitments, and develop recommendations for CAPAs as part of investigations.
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:

  • High school diploma or GED required and 1+ year of industry‑related experience (pharmaceuticals, food, or bio‑science) which provides background for compliance and quality orientation.
  • Attention to detail/quality mindset.
  • Ability to multi‑task to meet deadlines and work quickly under short timelines.
  • Demonstrates problem‑solving skills or troubleshooting skills, ability to identify root cause and assign corrective and preventative actions.
  • Demonstrated proficiency in verbal and written communication skills.
  • Demonstrated technical writing skill.
  • Flexibility to a changing work environment and deliverables.
  • Standard business computer skills, MS Word, MS Excel, etc., as required.
  • Ability to work within a team setting and provide information and assistance to co‑workers and supervisors.
Preferred Qualifications
  • Two (2) years or more of pharmaceutical experience highly desired.
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…
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