Analytical Chemist II: QC, Validation & LIMS

RXinsider LTD.; Bedford (OH); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Annual bonus

401(k) with company match

Paid time off 20 days plus holidays

Tuition reimbursement

Parental leave

Job summary

Hikma Pharmaceuticals USA Inc. in Bedford, OH is seeking a Chemist II to perform chemical and physical analyses across all stages of manufacturing. The role includes executing validation studies, maintaining LIMS data, and supporting QA with documentation and audits.

The candidate will use HPLC, GC, FTIR, and other instruments, write SOPs, and mentor QA staff as needed. A chemistry degree with relevant experience is required, with flexibility for shift schedules to meet production needs.

Qualifications

• Proficient in wet and instrumental analyses.
• Advanced laboratory skills with knowledge of statistics.
• Strong technical problem-solving abilities.
• Ability to multitask and meet deadlines.
• Computer literate and effective communicator.
• Ability to train and lead junior staff as needed.
• Flexibility to work weekends or shifts for business needs.

Responsibilities

• Perform analyses on raw materials, in-process materials, and finished products using laboratory instrumentation.
• Maintain data integrity and document results in LIMS.
• Validate processes and test methods; write SOPs and exception reports.
• Support stability, reference standards, and calibration activities.
• Ensure compliance with USP, Ph.Eur, FDA, GLP, GDP, and cGMP.

Skills

Wet methods

Instrumental analyses

Statistical methods

Problem solving

Multitasking

Communication

Training/leadership

Flexibility

Education

Bachelor’s Degree in Chemistry or Biological Sciences with Analytical Chemistry

Master’s Degree in Chemistry or Biological Sciences

Tools

LIMS

HPLC/GC

Job description

Hikma Pharmaceuticals USA Inc. in Bedford, OH is seeking a Chemist II to perform chemical and physical analyses across all stages of manufacturing. The role includes executing validation studies, maintaining LIMS data, and supporting QA with documentation and audits.

The candidate will use HPLC, GC, FTIR, and other instruments, write SOPs, and mentor QA staff as needed. A chemistry degree with relevant experience is required, with flexibility for shift schedules to meet production needs.