QC Associate Scientist

RESPONSIBILITIES

• Providing Quality Review/Oversight of site GMP documentation related to the operation of a vaccine manufacturing facility to ensure compliance
• Performs testing including, but not limited to clinical and/or commercial product, raw materials and validation samples.
• Analyzes and interprets results, makes decisions regarding the accuracy, completeness and compliance.
• Responsible for final authorization/approval/release of documentation/equipment/processes
• Assessing existing situations and suggesting improvements in the Quality systems to increase compliance throughout the facility
• Plans projects and may initiate and develop plans to ensure their timely completion

QUALIFICATIONS AND SKILLS NEEDED

WORK EXPERIENCE/SKILLS

MINIMUM

4 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry.

EDUCATIONAL BACKGROUND

MINIMUM

BS/BA Degree in Science/related field or other appropriate education/experience in biotech or pharmaceutical industry

OR

• 1-3 years of GMP Experience.

Ricky Bansal

732-429-1925