Sandoz
is a global leader in generic pharmaceuticals and biosimilars. As a division of
the Novartis Group, our purpose is to discover new ways to improve and extend
people’s lives. We contribute to society’s ability to support growing
healthcare needs by pioneering novel approaches to help people around the world
access high-quality medicine. Our portfolio of more than 1000 molecules,
covering all major therapeutic areas, accounted for 2015 sales of USD 10.1
billion. In 2015, our products reached more than 500 million patients and we
aspire to reach one billion.
is a global leader in generic pharmaceuticals and biosimilars. As a division of
the Novartis Group, our purpose is to discover new ways to improve and extend
people’s lives. We contribute to society’s ability to support growing
healthcare needs by pioneering novel approaches to help people around the world
access high-quality medicine. Our portfolio of more than 1000 molecules,
covering all major therapeutic areas, accounted for 2015 sales of USD 10.1
billion. In 2015, our products reached more than 500 million patients and we
aspire to reach one billion.
We
are recruiting to fill the position of:
are recruiting to fill the position of:
Job
Title: Supply
Chain Manager
Job ID: 222014BR
Location: Lagos
Functional Area: Technical Operations
Job Type: Full Time
Employment Type: Regular
Title: Supply
Chain Manager
Job ID: 222014BR
Location: Lagos
Functional Area: Technical Operations
Job Type: Full Time
Employment Type: Regular
Job
Description
Description
- Leading
the demand and supply management processes and ensuring that they are in
line with the agreed business targets. - Ensure
effective inventory management in the local organizations. - Inventory
and write off management of the country/region. - Ensuring
commercial/site team compliance of the invoicing policy. - Negotiation
of supply plan with suppliers. - Ensuring
demand forecasting data generated in finance, marketing and sales with
support of the Country Head. - Support
site registration processes in countries - Support
new markets development - Responsible
for measuring forecasting accuracy and feeding trends to marketing. - Drive
improvements in working capital management. - Facilitate
best practice sharing/standardized processes. - Monitor
and improve Global SCM KPI’s for country/region (such as PA, Sales
Forecast Accuracy, stock out, write-off). - Ensuring
demand analysis and consumption tracking is carried out on behalf of the
business. - Support
launches and new products supply set ups - Pricing
negotiations for (TPC, SPR requests) private and tenders pricing - Provide
link between 3rd party customer and sites, payment and LC follow-up - Identify,
kick-off and support SC projects to improve the regional performance. - Implementation,
support as well as training of new tools within the region (e.g. NRC).
Ensure proper tool usage in operational environment. - Process
owner and Expert of dedicated supply chain and forecasting processes to
ensure process adherence within supply chain and related functions.
Minimum
Requirements
Requirements
- University
degree in Business, Finance, Statistics, Economics, or related degree
English 5 – 7 years Experience in Supply Chain Management & Logistics
or a related role
How to Apply
Interested and qualified candidates should:
Click here to apply
Job
Title:
RA Associate
Job ID: 222009BR
Location: Lagos
Division: SANDOZ
Business Unit: Commercial Ops SZ
Functional Area: Research & Development
Title:
RA Associate
Job ID: 222009BR
Location: Lagos
Division: SANDOZ
Business Unit: Commercial Ops SZ
Functional Area: Research & Development
Job
Description
Description
- New
Product Registrations: Prepares and submits documentation for application
of drug registration in a timely manner and monitoring of the application
during the evaluation phase to achieve a favourable outcome within agreed
timeframes - Ensures
the implementation of Company corporate Quality Standards in the RO to be
compliant with Novartis Quality standards/Sandoz Standards. - Ensures
full QA support for all QA related activities. - Assist
in ensuring that all aspects of the handling and distribution of
pharmaceutical products at the site/in the country and all other QA
related activities comply with the requirements of the Novartis Quality
Manuals (QM), Sandoz GOPs and internal company SOPs - Ensures
implementation of relevant Sandoz d.d. SOP to the RO organisation - Ensures
that compliance is maintained for Quality System and all Standard
Operating procedures (SOPs) are in place for all GXP related activities - Maintenance
of registered products: Support the DRA Manager, Sandoz in maintaining
registration of currently approved products and timely submission of
documentation for renewal of registration. - Prepares,
submits and monitors variation packages to the health authority and
ensures timely approval - Prepares
& submits CDS update and PSUR to the health authority and ensures
safety update is implemented if required - Prepares
text master and final artwork master in accordance with local labelling
regulations and Sandoz internal requirement - Assists
in ensuring adequate escalation process up to the management according to
escalation management - Maintains
knowledge of local and international regulatory and legislative
requirements and trends to ensure technical support on all quality related
aspects to the RO - Ensures
all product specific annexes and QA agreement with each sites are updated
and approved - Assists
in ensuring that all activities related to complaints, market
action/recalls are performed in accordance with the relevant QM and are in
compliance with the local regulations and Sandoz standards - In
case of any local third party coordination of the following activities
with Sandoz d.d. responsible person: Audit and Quality Agreements with 3rd
parties. Ensures coordination of third party activities (re-packaging,
re-labelling , storage and/or distribution in way that all activities on
3rd party site are in compliance with Sandoz standards
Minimum
Requirements
Requirements
- Bachelors
Degree in Pharmacy English 2 – 5 years experience in Regulatory Affairs or
a similar role
How to Apply
Interested and qualified candidates should:
Click here to apply