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Quality Control Scientist

Sanford, NC, United StatesPosted 130 months ago
ContractonsiteMid-Senior Level

Job Description

• Providing Quality Review/Oversight of site GMP documentation related to the operation of a vaccine manufacturing facility to ensure compliance with global regulatory agencies and quality standards.

• Performs testing including, but not limited to clinical and/or commercial product, raw materials and validation samples.

• Displays strong investigative or technological orientation with independence for design of projects/studies.

• Organizes and provides written and/or oral presentations of work with minimal input.

• 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 and leads projects to ensure their timely completion.

• Provide guidance/coaching to junior colleagues. 

• Minimum 5 - 8 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry.

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

• University Degree in the field of Engineering, Microbiology, Chemistry, Biotechnology, Biochemistry or Pharmacy or other appropriate education and experience in biotech or pharmaceutical industry is preferred.

Thanks

Warm Regards

Ricky Bansal

732-429-1925

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Quality Control Scientist at Integrated Resources INC | Renata