Novartis Pharma Executive Production Post – Apply Online
Pharmaceutical Science Jobs. Applications are invited for the post of Executive – Production @ Novartis.Career @ Novartis. Pharma job opportunity at Novartis.vacancy at Novartis. Interested candidates may apply online. Check out all the details on Rasayanika.com
Job Title: Executive – Production
Job Id: 305647BR
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 the Production department.
Language: Marathi, Hindi & English.
Job Description
Novartis Technical Operations (NTO) brings billions of units of medicine to countries around the world.
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 the 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 the 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
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