Analytical Method Development Scientist at Ajulia Executive Search
Rock Hill, SC 29730, USA -
Full Time


Start Date

Immediate

Expiry Date

15 Oct, 25

Salary

110000.0

Posted On

16 Jul, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Working Environment, Analytical Techniques, Method Development, Pharmaceutical Industry, Raw Materials, Gc Ms, Validation, Calibration, Icp Ms, Equipment Qualification, Ftir, Icp, Hptlc, Chemistry, Microsoft Office, Communication Skills, Biotechnology, Biochemistry

Industry

Hospital/Health Care

Description

Analytical Method Development Scientist

  • Familiarity with laboratory instrumentation, including FTIR, HPLC, ICP, GC, UV-Vis, LC-MS, GC-MS, ICP-MS, and HPTLC.
  • Experience in analytical method validation and development

Are you looking to make a career change to a rapidly growing company? This exciting opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance and paid PTO. Does this position match your future career goals? Then this opportunity could be the right fit for you

EDUCATION AND EXPERIENCE REQUIREMENTS:

  • Master’s degree in Chemistry ,Biochemistry, Biotechnology or related field.
  • Must have prior experience working in the Pharmaceutical industry, using analytical techniques including HPLC and GC as well as experience with Method Development and Validation of these techniques.
  • Troubleshoots equipment
  • Expertise in developing analytical methods for chromatographic, spectroscopic, titrimetric, and wet chemistry analyses.
  • Strong understanding of routine laboratory operations.
  • Strong knowledge of analytical method development strategies and specification setting for raw materials and finished products.
  • Familiarity with laboratory instrumentation, including FTIR, HPLC, ICP, GC, UV-Vis, LC-MS, GC-MS, ICP-MS, and HPTLC.
  • Experience with Method development and Method validation
  • Coordinates equipment qualification and calibration.
  • Maintains a clean and safe working environment.
  • Must have knowledge of cGMPs, Quality Concepts, and Microsoft Office.
  • Excellent written and verbal communication skills.
  • Proficiency in MS Office.
  • Strong attention to detail.
    Job Type: Full-time

Schedule:

  • 8 hour shift

Work Location: In perso

Responsibilities

Please refer the Job description for details

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