Job Summary:
To fulfil varying quality control tasks and assignments, including product
analysis and implementing procedures in order to detect any defects or issues
in products before they are released into the market.
Duties & Responsibilities:
* Performs a variety of routine and basic tests in support of routine testing for commercial raw materials, production of intermediate and bulk samples, finished products, and process / cleaning validation samples to ensure that materials comply with the standards.
* Assists in reviewing technical documents to ensure the documents are up to standards and comply with regulations.
* Implements procedures and systems to develop an appropriate level of expertise in order to ensure the successful execution of project work within the current pharmaceutical industry technical standards in addition to maintaining compliance with cGMP's.
* Assists in troubleshooting basic technical issues to support in efficiently solving these problems.
* Supports activities related to analytical method transfers for the assigned projects to ensure efficient transfer of projects between sites.
* Assists in standardizing of processes throughout the laboratory to ensure compliance to cGMP's and current SOP's.
Qualifications:
* Bachelor's degree in Pharmacy or Science with grade Very good or Excellent.
* Minimum Experience: 1-3 years of experience in a Quality role.
* Good documentation practices and technical writing
* V. Good English language.
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