Company
Stiefel, a GSK Company
stiefel.com
Designation
Chemistry and Chemical Engineering Interns
Job Type
Entry Level / Junior Executive
Job Period
Between June - Dec 2012
Profession
Engineering
Industry
Location Name
103 Gul Circle
Allowance / Remuneration
$800 monthly
Job Description
Stiefel, a GSK company, is a global leader in dermatology. Healthcare professionals around the globe prescribe and recommend formulations from Stiefel brand portfolio that include prescription medications, over-the-counter treatments and signature skin care products designed to treat a wide range of dermatologic conditions. With more than 180 product families globally, Stiefel now reaches patients and consumers in nearly every market around the world.
===Job Scope===
This role will be working with the Quality Officer and will be involve in the following aspects of the business:
• Training Management System: Assist the Quality Team in maintaining the compliance status of training program on-site. Will get to understand the importance of compliance training, as well as developing people skills.
• Document Control Management: Assist the Quality Team in maintaining the documents on-site to ensure that they are in good control. Will get to learn and apply the good documentation practices, which are essentials in the pharmaceutical industry.
• CAPA coordination: Assist the Quality Team in coordinating the CAPA on-site, as well as to update visual trackers. Will get to understand the importance of major Quality Systems, such as Internal Audit, Deviation Management etc.
• CofA (Certificate of Analysis) Verification: Verify the CofAs generated, which are critical to meet market regulatory requirements. Help maintain the CofA templates, as well as updating Product Specifications, under the supervision of a Quality personnel.
===Job Requirements===
Students from the field of Chemistry may apply.
We are looking for an individual that is able to work independently with minimal guidance. He/She needs to be meticulous and have great organizational skills. Must be IT savvy, with good competency level in Microsoft Words, Excel and Power Point.
===Job Scope===
This role will be working with the Quality Officer and will be involve in the following aspects of the business:
• Training Management System: Assist the Quality Team in maintaining the compliance status of training program on-site. Will get to understand the importance of compliance training, as well as developing people skills.
• Document Control Management: Assist the Quality Team in maintaining the documents on-site to ensure that they are in good control. Will get to learn and apply the good documentation practices, which are essentials in the pharmaceutical industry.
• CAPA coordination: Assist the Quality Team in coordinating the CAPA on-site, as well as to update visual trackers. Will get to understand the importance of major Quality Systems, such as Internal Audit, Deviation Management etc.
• CofA (Certificate of Analysis) Verification: Verify the CofAs generated, which are critical to meet market regulatory requirements. Help maintain the CofA templates, as well as updating Product Specifications, under the supervision of a Quality personnel.
===Job Requirements===
Students from the field of Chemistry may apply.
We are looking for an individual that is able to work independently with minimal guidance. He/She needs to be meticulous and have great organizational skills. Must be IT savvy, with good competency level in Microsoft Words, Excel and Power Point.
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