QC Documentation Officer

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Ceek recruitment solutions
  • Post Date: 30/03/2022
  • Listing Expire Date: 14/04/2022
  • Views 134
Job Overview

Do you thrive on creating structure and modus operandi? Are you attentive to detail and a result-oriented individual? If so, our client, an international player in the within a pharmaceutical industry is seeking to recruit a motivated QC Document Officer. If you are looking for a new challenge, we at Ceek would love to hear from you!


What is expected of you?

  • Write/prepare analytical methods and specifications, including but not limited to the status of analysis, chromatographic proformas, and analytical records
  • Support in the documentation related to method validation studies, process, cleaning, and stability validation
  • Assist the QC Manager in drafting SOPs relevant to the Quality Control’s Operation
  • Participate in the management, coordination, execution/closure of change controls, deviations and CAPAs
  • Enter analytical results in MRP system and issue COAs
  • Co-ordinate and manage sample requests


What are you expected to bring?

  • In possession of a Diploma/Degree in Chemistry or related scientific subject
  • Ideally experienced with working in a pharmaceutical environment
  • Extremely organised and possess excellent communications skills
  • Able to think critically and a good problem solver
  • Able to work independently as well as in a team environment
  • Results-oriented and will display an attitude that reflects the company values


What’s in it for you?

  • Continuous opportunity for professional growth and training
  • Competitive salary
  • Health insurance
  • Medical check-ups
  • Culture where teamwork is a priority
  • Positive working environment with an employee-focused approach
Job Detail
  • Offered SalaryNegotiable
  • Experience*N/A
  • Qualification*Bachelor Degree
  • Job Reference*546
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