Senior Analyst, QC Chemist

The Senior Analyst, QC Chemist is an individual contributor position performing complex analytical testing for various samples including but not limited to in process, finished product, stability, raw material, cleaning verification/validation, and development and validation samples.

Job Title: Senior Analyst, QC Chemist

Location: West Chester, OH (onsite)

Shift: 2-2-3 Nights | Monday-Thursday | 6:00pm-4:00am

Rate: $42/hour

Contract (6 months) to Hire

Training on Night Shift

Responsibilities

• Performs testing on a range of samples, including chemical raw materials, components (including packaging materials), finished products, stability samples, water, and environmental samples.
• Conduct GMP review of laboratory documentation including review of electronic data in a timely manner for compliance with applicable SOPs, test methods, regulations, and protocols. Communicate findings to analysts and follow up on corrections.
• Assist in authoring and finalizing departmental SOPs.
• Evaluates data trends and actively participates in the investigation of OOS and atypical events and/or quality issues placing particular attention to root cause analysis, technical completion and scope while ensuring accuracy of documentation contents.
• Provides and follows up on ideas for continuous improvements in laboratory processes.
• Maintains and troubleshoots testing equipment.
• Participates in investigations for PET process areas related to QC processes or data.
• Trains QC employees in good analytical techniques, methods and instrumentation based on expertise.
• Actively support the implementation of compendial changes for raw materials, chemical methods or finished products tests in accordance with applicable Pharmacopoeias such as USP/NF, European Pharmacopoeia, British, and Japanese Pharmacopoeia.
• Troubleshoots methods and processes. Senior Analyst, QC Chemist Effective Confidential. Retrieved from Veeva by Kelly Dixon on 25 Feb 2025. Before use the end user must confirm this document is the current version. TRAINING MATERIAL Document Number: D-56834 Version: 2.0 Effective Date: 03 Apr 2024 Page 2 of 5 Title: WCHJD Senior Analyst, QC Chemist
• Leads continuous improvements in laboratory processes.
• Trains QC employees in GMP, SHE, QC methods and processes.
• May serve as an expert in a specific area of laboratory equipment, process, or system and supports regulatory audits.
  
  

Minimum Requirements

Education, Qualifications, Skills, and Experience

• Analytical experience in a pharmaceutical GMP facility using various types of instrumentation (HPLC/GC required, including proficiency with chromatography software such as Empower)
• Proficient in math, laboratory, and computer skills. Understand basic statistics and quality control terminology.
• Working knowledge of laboratory equipment (including HPLC), operations, and safety.
• Good problem-solving skills
  
  

Preferred Background

• Bachelor’s degree in chemistry, biology or related field
• QC chemistry laboratory experience in pharmaceutical industry
• Working knowledge of cGXP requirements and a strong familiarity with production operation
  
  

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

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