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Ceek recruitment solutions
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
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Offered SalaryNegotiable
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Experience*N/A
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Qualification*Bachelor Degree
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Job Reference*546