USA - Scientist

The Fountain Group; Thousand Oaks (CA); On-site; USD 69,000 - 91,000; Full time

Job summary

The Fountain Group is seeking a QC Scientist for a prominent client in Newbury Park, CA. The role focuses on transferring, developing, validating and executing analytical methods within a cGMP QC setting.

It is a 6 ½ -month assignment with Monday-Friday schedule, offering responsibilities in investigations, instrumentation troubleshooting, and CAPA reviews, plus material testing and documentation support.

Qualifications

• Bachelor's degree required.
• 3+ years in analytical development or validation in GMP/pharma/biopharma.
• Knowledge of analytical methods, validation and cGMP/regulatory requirements.
• Experience with statistical analysis, QC data trending, investigations preferred.
• Experience with instrument qualification, troubleshooting and raw material qualification preferred.

Responsibilities

• Transfer, develop, validate and execute analytical methods in a cGMP QC environment.
• Support analytical investigations, troubleshooting methods and instrumentation, review OOS/OOT results, deviations and CAPAs.
• Support instrument qualification, raw material testing/qualification, QC data analysis, technical documentation and special projects.

Skills

Analytical methods

Method validation

GMP knowledge

Statistical analysis

Laboratory investigations

Troubleshooting

Data analysis

Raw material qualification

Instrument qualification

Education

Bachelor's degree in a relevant field

Tools

Instrument qualification

Job description

We are a national staffing firm and are currently seeking a QC Scientist for a prominent client of ours. This position is located in Newbury Park, CA Details of the position are as follows:

Job Description

• $50-66/hr
• Schedule: Monday-Friday
• This position is a 6 ½-month assignmentwith the possibility of extension.
• Position will be mainly responsible for transferring, developing, validating, and executing analytical methods in a cGMP Quality Control environment.
• Position will be responsible for supporting analytical investigations, troubleshooting methods and instrumentation, and reviewing OOS/OOT results, deviations, and CAPAs.
• Position will also be responsible for supporting instrument qualification, raw material testing and qualification, QC data analysis, technical documentation, and special projects.

Qualifications

• Bachelor's degree at a minimum is Required!
• Minimum of 3 years of analytical development or validation experience in a GMP pharmaceutical, biopharmaceutical, or related manufacturing environmentis Required!
• Knowledge of analytical methods, method validation, and cGMP/regulatory requirementsis Required!
• Experience with statistical analysis, QC data trending, and laboratory investigationsis Preferred!
• Experience with analytical instrumentation qualification, troubleshooting, and raw material qualificationis Preferred!