About this role

Company Description

Job Description

Candidates should have exp with tablets and capsule formulations, clinical products stage I - III, working with contract manufacturing organizations, they are a virtual company so the candidate will give documentation feedback to external manufacturing organizations.

Job Description:

  • Performs a wide variety of activities to ensure compliance with applicable regulatory requirements.
  • Participates in developing Standard Operating Procedures (SOPs) to ensure quality objectives are met.
  • Maintains routine programs and processes to ensure high quality products and compliance with current Good Manufacturing Practices (GMPs) and Good Laboratory Practices GLPs)
  • Reviews manufacturing, environmental monitoring and quality control data for in-process and finished products.
  • Works directly with operating entities to ensure that inspections, statistical process control analyses and audits are conducted on a continuing basis as specified to enforce requirements and meet specifications.
  • May participate in the writing of annual product reviews and the development of training programs regarding all aspects of producing quality products.
  • May conduct or serve as a lead/coordinator of investigations and corrective and preventive action (CAPA) recommendations related to manufactured products.
  • Works with Research and Development during new product start-ups, and identifies checkpoints for new products and processes.
  • Normally receives very little instruction on routine work, general instructions on new assignments.

Qualifications

Additional Information

All your information will be kept confidential according to EEO guidelines.

Frequently Asked Questions

Is the salary disclosed for the QA Specialist - Formulation position at integratedresourcesinc?
The salary for this QA Specialist - Formulation role at integratedresourcesinc is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the QA Specialist - Formulation position at integratedresourcesinc located?
This QA Specialist - Formulation role at integratedresourcesinc is based in CA, Foster City, Foster City, CA, United States, us. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the QA Specialist - Formulation role at integratedresourcesinc full-time or part-time?
This is listed as a Contract position. It is posted as a QA Specialist - Formulation role at integratedresourcesinc.
How do I apply for the QA Specialist - Formulation position at integratedresourcesinc?
Click the "Apply Now" button on this page. You will be redirected to integratedresourcesinc's official application portal hosted on smartrecruiters where you can submit your application directly.
When was the QA Specialist - Formulation job at integratedresourcesinc posted?
This QA Specialist - Formulation position at integratedresourcesinc was posted on Jul 14, 2017. Apply as soon as possible โ€” early applications are often reviewed first.
QA Specialist - Formulation
integratedresourcesinc
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