QC Scientist I – Bench Chemistry & Method Validation

Actalent; Columbus (OH); On-site; USD 27,000 - 39,000; Full time

Job summary

Actalent is seeking a QC Scientist I to perform hands-on bench testing and support the development and release of multisource pharmaceutical products in Columbus, OH. The role emphasizes chemical and physical analyses, sample preparation, standard weighing, and dilutions with progressive training on HPLC and GC techniques.

You will contribute to regulatory submissions, method validation and transfer activities, while maintaining data integrity and complying with cGXP standards in a fast-paced,

Qualifications

• Bachelor's degree in science required or equivalent laboratory experience.
• Chemistry or Biochemistry preferred; other sciences with strong chemistry experience considered.
• Hands-on lab experience, including sample prep and wet chemistry, is essential.

Responsibilities

• Perform routine bench testing including sample prep, wet chemistry and dilutions.
• Conduct chemical/physical analyses to support multisource product development.
• Provide analytical support for release of registration materials for regulatory submissions.
• Assist in analytical method validation and transfer activities to ensure robustness.
• Document activities and results with data integrity and compliance to cGXP guidelines.
• Collaborate with quality and manufacturing teams to complete tasks on schedule.

Skills

Bench testing

Wet chemistry

Data integrity

cGXP compliance

Analytical support

Education

Bachelor's degree in science

Chemistry or Biochemistry preferred

Other science with lab experience

Tools

HPLC

GC

Job description

Actalent is seeking a QC Scientist I to perform hands-on bench testing and support the development and release of multisource pharmaceutical products in Columbus, OH. The role emphasizes chemical and physical analyses, sample preparation, standard weighing, and dilutions with progressive training on HPLC and GC techniques.

You will contribute to regulatory submissions, method validation and transfer activities, while maintaining data integrity and complying with cGXP standards in a fast-paced,