QC Chemist Job
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Employer: ScieGen Pharmaceuticals, Inc
SpiderID: 13703859
Location: HAUPPAUGE, New York
Posted: 3/21/2024
Wage:
Priority Review Date: 6/19/2024
Job Code / NOC / SOC:
Category: Medical/Health
Job Description:
QC Chemist is needed to perform the following duties:
• Scientifically analyze and test raw materials, in-process and finished product samples using modern quality control techniques like UV-Vis, ICP etc. under supervision of experienced chemists/scientists;
• Work with advanced analytical equipment like HPLC, GC, DSC and IR and apply knowledge of broad variety of quality control and analytical techniques;
• Validate and analyze results as per USP, BP, EP, ICH and USFDA;
• Assist experienced chemists/scientists to develop, implement and maintain quality control systems and activities by collecting/researching scientific data/reports, recording scientific evidence/results from lab/development activities etc.;
• Compile data for documentation of test procedures and prepare reports;
• Perform in-process inspection, document results and perform a wide variety of inspections, checks, tests and sampling procedures for the manufacturing process while working as part of a group of chemists/scientists and following established guidelines;
• Calibrate/check critical laboratory equipment and instrumentation and assist in drafting/updating inspection procedures and checklists as necessary;
• Assist scientists in developing and implementing validation protocols and test procedures by performing lab experiments, chemical analysis of materials, preparing test solutions, conducting QC tests etc. to ensure products meet with appropriate regulatory agency validation requirements, internal company standards and industry current practices; and
• Approximately 85% of the time will be spent in scientifically analyzing raw materials, in-process and finished product samples and validating results using modern quality control and analytical methods under supervision of experienced chemists/scientists in our Quality Control team and while following established guidelines. Approximately 15% of the time will involve preparing reports, documents and papers and conferring/interacting with scientists and maintaining ICH guidelines and US FDA regulations
Bachelor’s degree in Chemistry or Molecular Sciences & Nanotechnology
• Scientifically analyze and test raw materials, in-process and finished product samples using modern quality control techniques like UV-Vis, ICP etc. under supervision of experienced chemists/scientists;
• Work with advanced analytical equipment like HPLC, GC, DSC and IR and apply knowledge of broad variety of quality control and analytical techniques;
• Validate and analyze results as per USP, BP, EP, ICH and USFDA;
• Assist experienced chemists/scientists to develop, implement and maintain quality control systems and activities by collecting/researching scientific data/reports, recording scientific evidence/results from lab/development activities etc.;
• Compile data for documentation of test procedures and prepare reports;
• Perform in-process inspection, document results and perform a wide variety of inspections, checks, tests and sampling procedures for the manufacturing process while working as part of a group of chemists/scientists and following established guidelines;
• Calibrate/check critical laboratory equipment and instrumentation and assist in drafting/updating inspection procedures and checklists as necessary;
• Assist scientists in developing and implementing validation protocols and test procedures by performing lab experiments, chemical analysis of materials, preparing test solutions, conducting QC tests etc. to ensure products meet with appropriate regulatory agency validation requirements, internal company standards and industry current practices; and
• Approximately 85% of the time will be spent in scientifically analyzing raw materials, in-process and finished product samples and validating results using modern quality control and analytical methods under supervision of experienced chemists/scientists in our Quality Control team and while following established guidelines. Approximately 15% of the time will involve preparing reports, documents and papers and conferring/interacting with scientists and maintaining ICH guidelines and US FDA regulations
Bachelor’s degree in Chemistry or Molecular Sciences & Nanotechnology
Job Criteria:
Start Date:
Position Type: Full-Time Permanent
Experience:
Education: Bachelors
Travel:
Vacation:
Contact Information:
| Contact Name: ScieGen Pharmaceuticals, Inc | Type: Employer |
| Company: |