Novartis Hiring Technical Operations B.Pharma / B.Sc, M.Pharma Apply Now
Your responsibility
includes, but not limited to -
•To provide
expertise to improve process control and optimize production processes to full
satisfaction of our customers.
•Ensure
compliance to all relevant GxP and safety standards and Ensure that all
activities and documentation comply with the requirement of safety, GDP/GMP,
Data Integrity standards -Share knowledge and develop expertise of others and
understanding of applied practice and processes in own area/field -Follow up
production equipment to work accurately with planned capacity in his/ her
responsibility area -Ensure accurate critical issue of all matters related with
HSE, quality, supply and production, implement decisions and act as responsible
for continuity of production -Identify, assure and implement continuous
improvement initiatives which sustain Novartis competitive advantage
-Participate in a trouble-shooting team to Ensure that the potential or actual
process problems are correctly identified, and efficient resolved Responsible
for personal and professional development -Support building interpersonal
culture in line with Novartis values and behaviors 1.Ensure the integrity of
data at workplace. To follow current Good Manufacturing Practices and Good
Documentation Practice. SOP’s Revision and implementation, Change control &
deviation w.r.t. System SOP's. Managing of market complaints and investigation.
Follow Standard Operating Procedures of Manufacturing activity and their
documents.
•Maintain
cleanliness in the work area, equipment and Machine. To supervise the work as
per allocated job in respective department as per Production norms and Quality
norms adhering to GMP. Material manage activity follow-up as per cGMP
•Filling
Batch Manufacturing records, Maintain the shop floor records; carry out in
process checks, Co-ordination with cross-functional department. Support for
technical deviation investigation, CAPA and any product process related
investigations including complaints, OOE, OOS. To initiate CR and Deviation and
to involve in production compliance activity. Tracking of open compliance
activities owned by Production.
•Manufacturing
KPI: Output, yield, cycle time, Compliance with cGMP, HSE Audits etc.
•Operational
Perfection Continuous enhancing the skills (Dyn. Knowledge Development) Interpersonal
Savvy Breakthrough Analysis
•Operations
Management and Execution Collaborating across boundaries Functional Breadth
People Challenge English Transportation Manufacturing Process Execution General
HSE Knowledge Managing business continuity Knowledge of relevant tools and
system
Minimum requirements
Education :
B.Pharma / B.Sc, M.Pharma is added advantage.
Skills : Team
handling of 4 to 5 people, Leadership quality, able to operate different
machines in Production department.
TO APPLY CLICK HERE
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