QC Scientist II: HPLC/GC (2nd Shift, Onsite)

Actalent; Westerville (OH); On-site; USD 39,000 - 41,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

PTO / Vacation / Sick Leave

Job summary

Actalent is hiring a Quality Control Scientist II in the Columbus, OH area to perform qualitative and quantitative testing of APIs, starting materials, packaging components, and finished products in a highly regulated environment.

Responsibilities include method validation, analytical investigations, and quality control activities using HPLC and GC, with a focus on supporting method transfer and optimization in a fast-paced pharmaceutical manufacturing setting.

Qualifications

• Bachelor’s or Master’s degree in a scientific field.
• 2–3+ years of industry laboratory experience with HPLC or GC.

Responsibilities

• Perform qualitative and quantitative testing of APIs, starting materials, packaging components, and finished products.
• Prepare samples, including dilutions, to support accurate analytical testing.
• Peer review analytical testing documentation and resolve discrepancies in a timely manner.
• Maintain laboratory data in notebooks and electronic systems with accuracy and compliance.
• Operate and maintain analytical instrumentation including HPLC and GC; perform routine and advanced testing.
• Author clear technical reports to support method improvements and investigations.

Education

Bachelor’s or Master’s degree in a scientific field

Tools

HPLC

GC

Job description

Actalent is hiring a Quality Control Scientist II in the Columbus, OH area to perform qualitative and quantitative testing of APIs, starting materials, packaging components, and finished products in a highly regulated environment.

Responsibilities include method validation, analytical investigations, and quality control activities using HPLC and GC, with a focus on supporting method transfer and optimization in a fast-paced pharmaceutical manufacturing setting.