Quality Control Analyst II - Method Dev/Validation (12mo)

Biopharma-Consulting-Jad-Group; Fort Worth (TX); Sur place; USD 34 000 - 48 000; Plein temps

Résumé du poste

Biopharma-Consulting-Jad-Group in Fort Worth, TX, seeks a laboratory professional to support testing, method development and quality operations at a global pharmaceutical manufacturer site. The role involves running routine and non-routine analyses across raw materials, in-process, environmental, finished goods and stability samples.

You will develop, qualify, validate and transfer analytical methods, interpret results against specifications, and contribute to release decisions.

Qualifications

• Bachelors in Chemistry, Biochemistry, Biology, or related field.
• Experience in analytical method development, validation and transfer.
• Familiarity with GMP/GDP and OOS investigations.

Responsabilités

• Run routine and non-routine analyses of materials, in-process, environmental, finished goods and stability samples.
• Develop, qualify, validate and transfer analytical methods.
• Interpret results against specifications and recommend release.
• Participate in OOS investigations; write reports, protocols and SOPs.
• Calibrate and troubleshoot lab equipment; coordinate with contract labs.

Connaissances

Analytical method development

Validation

OOS investigations

Lab equipment calibration

SOP writing

Data interpretation

Formation

Bachelor's degree in Chemistry, Biochemistry, Biology or related

Outils

HPLC/GC

Capillary electrophoresis

Description du poste

Biopharma-Consulting-Jad-Group in Fort Worth, TX, seeks a laboratory professional to support testing, method development and quality operations at a global pharmaceutical manufacturer site. The role involves running routine and non-routine analyses across raw materials, in-process, environmental, finished goods and stability samples.

You will develop, qualify, validate and transfer analytical methods, interpret results against specifications, and contribute to release decisions.