Scientist III, QC Labs

Hikma Pharmaceuticals; Columbus (OH); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Annual performance bonus

401(k) with company match

PTO 20+ days + milestones

Health, dental, vision benefits

Tuition reimbursement

Job summary

Hikma Pharmaceuticals USA Inc. is seeking a Scientist III, QC Labs in Columbus, OH. The role involves performing complex analytical testing to support raw materials and finished products, ensuring regulatory compliance in a fast-paced QC lab.

You will review data, maintain compliant records, and contribute to method improvements while coordinating with cross-functional teams to meet quality targets.

Qualifications

• Experience performing qualitative and quantitative analytical testing in GMP labs.
• Proficient use of HPLC/UPLC and data review against specifications.
• Familiarity with GMP, SOPs, and laboratory record keeping.

Responsibilities

• Perform qualitative and quantitative testing for APIs and finished products per compendia or specification.
• Review analytical documentation against specification and procedures.
• Maintain laboratory data in notebooks, worksheets, and documents; author improvement reports.
• Troubleshoot analytical techniques and operate lab equipment per methods.
• Approve batch records and release analytics per procedures.

Skills

Analytical testing

HPLC

GMP

Data review

Laboratory procedures

Education

High School Diploma with GMP experience

BS in Chemistry

Tools

Empower

LabWare

Chromatographic Data Systems

Job description

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 Title

Scientist III, QC Labs

Location

Columbus, OH

Job Type

Full time

Req ID

12890

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 Scientist III, QC Labs to join our team. In this role, you will be responsible for performing workflow processes within the quality control laboratory to meet customer requirements by supporting the testing of raw materials and finished products while ensuring regulatory compliance standards is met.

Key Responsibilities

• Perform qualitative, quantitative chemical and physical testing and as specified by compendia or specification for API's, starting materials, packaging components and finished products. Meet core department goals and site metrics for RFT and productivity (testing turn-around, throughput time, QSDB).
• Perform peer review of analytical testing documentation and resolve discrepancies. Review analytical documentation against specification, analytical procedures, and laboratory practices (training and procedures).
• Maintain laboratory data in an orderly manner in laboratory notebooks, worksheets, and documents. Accurate use of current DPs, SOPs, cGMP regulations. Author technical reports for analytical methods improvement.
• Perform investigational, troubleshooting, and advanced analytical techniques. Proper use of laboratory equipment, techniques, and documentation according to laboratory methods and standards.
• Approval of batch records. Review and release analytical documentation as per specification, analytical procedures, and laboratory practices (training and procedures).

Experience with the following analytical analyses and processes is required

• For APIs: UV, HPLC, GC, UPLC, KF, FTIR, Advanced Data Review, Lead Investigator, Disposition (Packaging / Labeling).
• For Pharmaceutical products: HPLC, UPLC, Chromatographic Data Systems (Empower preferred), Laboratory Information Management Systems (LabWare preferred), Advanced Data Revies, Lead Investigator.

Additional experience with the following analytical techniques is highly desired

• For APIs: Particle size, ICP, AA, Viscosity, XRD, packaging component testing.
• For Pharmaceuticals: GC, IC, Droplet Size Distribution, Automated Actuators, FTIR, Microscopes.
• Knowledge of the critical functions/variables for each type of equipment is also highly desired as well as instrument/method troubleshooting ability.
• Must be able to work independently using a team approach to accomplish tasks assigned. Must possess the ability to work on multiple projects in a fast-paced environment.
• Must possess excellent written and verbal communication skills. Must be able to organize and lead RRRFTT meetings to discuss laboratory deviations with stakeholders.
• The candidate must have the ability to work with supervision using scientific judgment and professional competency. This position has no direct reports but does require training lower-level scientists in various analytical techniques and evaluating their skills.

Qualifications

• High School Diploma or equivalent with ten years GMP pharmaceutical analytical chemistry experience. The work-related experiences required include the execution of analytical methods, with supervision for evaluation and release of Active Pharmaceutical Ingredients (APIs) or Pharmaceutical Finished Products (FPs). The candidate must be able to perform compendia and non-compendia testing for multiple projects at one time.

Preferred Qualifications

• BS in Chemistry or in a science-related field with five years GMP pharmaceutical analytical chemistry experience. The candidate must be able to perform compendia and non-compendia testing for multiple projects at one time.

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.