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Analytical Chemistry (2-4 Yrs of Req Exp in pharmaceutical) - Onsite

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Location
Vernon Hills, IL
Workplace
Onsite
Type
Contract
Source
ApplicantStack

Description

Position : Analytical Chemistry (Req Exp in pharmaceutical)

Location : Vernon Hills, IL

Duration : 12 Months

1st Shift

Total Hours/week : 40.00

Client : Medical Devices Company

Job Category : Industrial

Employment Type : Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT

 

Rate of pay $35.79 Onsite

 

Segment/Department Name:  Infection Prevention, Analytical Chemistry

 

Job Description -

Purpose of Position:

  • This position provides analytical chemistry support and/or remediation to all chemistry-related projects for BD products currently on the market as well as new product development.  This position will also participate in the conduct of the stability testing program to support the approval of process and/or product design changes. As needed, this position also supports the development and validation of analytical methodologies for incoming raw materials, in-process, and finished product release testing.

 

General Functions, Specific Responsibilities, and Authority:

  • Chemistry & performance testing, data review and entry, protocol/report generation, laboratory maintenance and support.

 

Knowledge, Education, and Skills Required:

Education

  • BS/MS in Chemistry / Pharmaceutics with related science experience

 

Skills

  • Demonstrates developed knowledge of respective scientific discipline and standard scientific method and techniques.
  • Excellent scientific writing skills.
  • Ability to multi-task various activities.
  • Troubleshoot issues that arise and solve problems.
  • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

 

Experience

  • 2-4 years’ experience in pharmaceutical analytical chemistry is essential.
  • Hands-on experience with wet-chemistry and instrumental techniques (i.e. pH, tritration, UV-Vis, GC, HPLC).
  • Experience in working within an FDA regulated environment and GMP documentation requirements.

 

Specialized Knowledge

  • Ability to discuss scientific strategies/results and interact with other functional areas, including Regulatory, Manufacturing, and Quality.
  • Previous experience with writing scientific protocols and reports.

 

Skills

GMPFDA