Senior QMS Support
Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy. Headquartered in Denmark, Novo Nordisk employs approximately 33,300 employees in 75 countries, and markets its products in more than 190 countries Novo Nordisk’s B shares are listed on NASDAQ OMX Copenhagen (Novo-B).
Post: Senior QMS Support
Job Desciption
The main job responsibilities include:
• Perform continuous monitoring of compliance to internal SOP requirements.
• Maintain and update business critical documentation.
• Prepare training material and deliver effective training session on quality related topics.
• Support in handling change requests, deviations, training management system, records management, and other quality related activities.
• Provide inputs to SOP revisions, new QMS requirements, risk assessment and impact analysis.
• Contribute to the smooth conduct of audits and inspections.
The main job responsibilities include:
• Perform continuous monitoring of compliance to internal SOP requirements.
• Maintain and update business critical documentation.
• Prepare training material and deliver effective training session on quality related topics.
• Support in handling change requests, deviations, training management system, records management, and other quality related activities.
• Provide inputs to SOP revisions, new QMS requirements, risk assessment and impact analysis.
• Contribute to the smooth conduct of audits and inspections.
Qualifications
Bachelor’s/Master’s degree, preferably in Pharmacy or Life Sciences or equivalent professional experience.
You should have,
• Must have 1-3 years’ experience in quality management system.
• Good knowledge of clinical development and ICH-GCP guidelines
• Prior experience in Clinical Research/Pharmaceutical domain.
• Good communication and presentation skills.
You should have the ability to communicate, plan and coordinate multiple simultaneous activities.
You should be a strong team player who adapts easily to a changing environment with tight deadlines, and you should be good at planning, coordinating and reaching consensus.
Bachelor’s/Master’s degree, preferably in Pharmacy or Life Sciences or equivalent professional experience.
You should have,
• Must have 1-3 years’ experience in quality management system.
• Good knowledge of clinical development and ICH-GCP guidelines
• Prior experience in Clinical Research/Pharmaceutical domain.
• Good communication and presentation skills.
You should have the ability to communicate, plan and coordinate multiple simultaneous activities.
You should be a strong team player who adapts easily to a changing environment with tight deadlines, and you should be good at planning, coordinating and reaching consensus.
Additional Information:Requisition ID: 37482BR
Experience: 1-3 years
Qualification: Bachelor’s or Master’s degree
Location: Bangalore
Industry Type: Pharma/ Biotech/Clinical Research
End Date: 25th March,2016
Experience: 1-3 years
Qualification: Bachelor’s or Master’s degree
Location: Bangalore
Industry Type: Pharma/ Biotech/Clinical Research
End Date: 25th March,2016
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