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Quality Control Chemist

Melrose Park, IL

Job Title: QC Chemist

Reports To: QC Manager

Duties & Responsibilities:

1.Collects and analyzes samples for all incoming raw materials.

2.Oversee batch processes at production line based on quality control procedures

3.Assist in maintaining and modifying SLPs based on QC Control, ISO, FDA and OSHA guidelines.

4.Analyzes all production batches based on formulation specifications

5.Develops all MSDS, and COA’s

6.Work in Cooperation with other R&D Chemist to analyze competitive data

7.Laboratory testing and evaluation of new and existing raw materials

8.Laboratory testing and evaluation of new and existing products

9.Work with regulatory manager and other R&D Chemist to evaluate the efficacy and assist in

maintaining all OSHA, FDA, EPA, and ISO Regulations and quality standards of manufacturing

processes and raw materials.

10.Conduct instrumental product performance testing using the Rheometer, Particle Size Analyzer,

Polarized/Visible light Microscope, and other related equipment. This includes the calibration and

balancing of the instrument.

11.Perform computer work such as data entry and transformation using the Excel spreadsheets.

12.Maintain current technical awareness in hair/skin care technology particularly those that are

involved with Fiber Physics and skin Bio-engineering and image analysis techniques.

13.Maintain cleanliness in their respective work areas and observe proper work safety habits at all

times.

14.Handles other related duties as assigned and assists other R&D personnel as needed.

15.Must get involved in the process development of newly formulated product.

16.Writing of reports, status and progress of project assigned.

17.Continuously enhance his/her abilities and knowledge in the above fields through studying of books

and publications, attending seminars, and electronic databases.

18.Evaluate competitive products.

19.Performs other duties as assigned

Qualifications

BS Degree in Chemistry

2 Years in a laboratory environment

Must have experience in QC, QA, cGMP, ISO, FDA, EPA, and OSHA matters.

Must be detail oriented and meet deadlines while handling multiple tasks.

Computer proficient, Excel and Microsoft Word.

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