Scientist II, QC Labs

Scientist II, QC Labs Location: Columbus, OH Job Type: Full time Req ID: 11678 Description We are seeking a talented and motivated Scientist II, QC Labs to join our team. Key Responsibilities Perform qualitative, quantitative chemical and physical testing of API's, starting materials, packaging components and finished products as specified by compendia or specification. Perform peer review of analytical testing documentation and resolve discrepancies. Complete and/or conduct required training according to the laboratory curriculum. Maintain laboratory data in an orderly manner in laboratory notebooks, worksheets, and documents. Re-validate microbiological methods. Author technical reports for analytical methods improvement. Perform investigational, troubleshooting and advanced analytical techniques to troubleshoot approved commercial analysis. Possess knowledge of the critical functions/variables for each type of equipment as well as instrument trouble‑shooting ability. Work independently using a team approach to accomplish tasks assigned, and manage multiple projects in a fast‑paced environment. Possess good written and verbal communication skills. Qualifications High school diploma or equivalent with 7 years GMP analytical pharmaceutical laboratory experience, including execution of analytical methods with supervision for evaluation and release of Active Pharmaceutical Ingredients (API) or pharmaceutical products. Able to perform compendia and non‑compendia testing for multiple projects concurrently. Preferred Qualifications Bachelor’s of Science in Chemistry or a scientific‑related discipline with 2+ years of pharmaceutical laboratory experience, including execution of analytical methods with supervision for evaluation and release of API or pharmaceutical products. Experience with Empower data analysis software and peer review of data. Ability to perform compendia and non‑compendia testing for multiple projects concurrently. 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 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)8lli>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. 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. #J-18808-Ljbffr Hikma Pharmaceuticals