RCI-GSK0-106425 Assistant Scientist - Zebulon, NC

Rangam; Zebulon (NC); On-site; USD 34,440 - 41,328; Full time

Benefits offered by this job

Medical insurance

Job summary

A leading company in pharmaceutical manufacturing is seeking an Assistant Scientist for their Zebulon, NC location. This fully onsite position focuses on conducting analytical and microbiological testing, ensuring compliance with GMP standards. Candidates should have a Bachelor's in a scientific discipline and experience with various lab instruments, including HPLC and GC.

Qualifications

• Experience with analytical testing and data documentation.
• Ability to operate laboratory instruments and software.
• Bachelor's degree in Chemistry or a related field preferred.

Responsibilities

• Conduct routine analytical testing of raw and finished products.
• Document and evaluate data according to GMP standards.
• Maintain laboratory instruments and assist in training personnel.

Skills

Analytical testing

Microbiological testing

Data analysis

Education

Bachelor's degree in a scientific field

Tools

HPLC

GC

Vitek

Job description

RCI-GSK0-106425 Assistant Scientist - Zebulon, NC

RCI-GSK0-106425 Assistant Scientist - Zebulon, NC

This range is provided by Rangam. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$25.00/hr - $30.00/hr

Fully onsite roles, 5 days per week.

Summary

• To ensure that the QC testing of all products is performed to GMP and company standards.
• This involves analytical/microbiological testing (as applicable), analysing samples, recording, evaluating and reporting data using prescribed procedures with limited or no supervision.

Duties:

• Conduct routine analytical testing of raw materials, packaging materials, finished products and environmental samples using approved methods and various instrumentation, (e.g., HPLC, Vitek, GC, UV, Microscope, Gram Stainer, and Robotics) while adhering to cGMP and established policy.
• Generate valid data at expected levels of productivity while adhering to cGMP.
• Interpret validity of own test data and generate accurate results.
• Advise immediate supervisor or designee of all important aspects of analytical testing including deviations.
• Evaluate data generated by others in the analytical group.
• Accurately document analytical data and review official laboratory documents (e.g., SOP’s, Technical reports, Methods, and specifications).
• Maintain and troubleshoot laboratory instruments.
• Assist in training other laboratory personnel on methods, instrumentation and computer systems.
• Participate in interdepartmental project teams or committees.
• Understand data integration and calculation of results

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Contract

Job function

• Job function

  Research

• Industries

  Chemical Manufacturing, Manufacturing, and Pharmaceutical Manufacturing

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Inferred from the description for this job

Medical insurance

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