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.
Post : Associate Business Analyst
Job Description
About the department GSC QMS Support department was established in May 2015, with a purpose of delivering services related to quality processes such training coordination and document control (SOPs), NovoGloW (Quality & Complaince Management platform), Records Management to various internal clients within Novo Nordisk as per agreed SLA’s.
Key responsibilities:
This position is mainly responsible for providing functional support to various process experts working in Change Control, Non-conformity, Audits and CAPA processes in the use of novoGloW IT system(ETQ reliance platform for Quality and compliance management) in Novo Nordisk. Processes supported within novoGloW system,
1. Nonconformity handling
2. Change Control
3. Audit
4. CAPA Handling
Main job tasks:
Support
Advise and support subject matter experts and stakeholders globally in the supported quality processes in novoGloW
Perform workarounds and data corrections in novoGloW
Participate in novoGloW problem investigations
Master Data
Maintaining the master data, master keyword lists and profiles in novoGloW
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Experience:
- Minimum 4 years of experience working in a global corporate company
- 2 years of relevant working experience or thorough knowledge with nonconformity, Change Control, Audit, CAPA processes (At least 1 process)
- Prior experience working with ETQ Reliance platform or other similar “Quality and compliance management IT systems” will be an added advantage.
- Experience in supporting workflow-based IT systems and QMS processes
- Excellent communication skills (Both written and Oral)
- Experience within the pharmaceutical industry
- Understand the overall elements and regulatory requirements regarding the quality processes in novoGloW
- Demonstrated impact of knowledge about different cultures
Personal skills:
Support
Advise and support subject matter experts and stakeholders globally in the supported quality processes in novoGloW
Perform workarounds and data corrections in novoGloW
Participate in novoGloW problem investigations
Master Data
Maintaining the master data, master keyword lists and profiles in novoGloW
Additional Information:
Location Bangalore
Industry Type: Pharma/ Biotech/Clinical Research
End Date: 26th Sept, 2017
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