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2.0 - 6.0 years
0 Lacs
goa
On-site
The main purpose of the role is to follow established procedures and guidelines to manufacture the organization's products according to production specifications and schedules, volume, cost, and wastage targets, and quality standards. You will be responsible for operating machines and production equipment safely and in accordance with instructions. It is important to monitor the quality of output to identify, discard, or re-manufacture faulty products. Additionally, maintaining accurate daily production records is essential so that manufacturing performance can be analyzed. To qualify for this role, you should have a Technical Diploma (12 years) education and a minimum of 2 years of relevant experience/background.,
Posted 4 days ago
5.0 - 9.0 years
0 Lacs
hyderabad, telangana
On-site
Handle market complaints received from across the globe. You will be responsible for reviewing the investigation reports received from the Novartis sites and Contract Manufacturing Organizations. You will collaborate with external Supply organization, Novartis sites, Country pharma organizations for continuous improvement. As a Specialist - Product Complaints - QOP based in Hyderabad, your key responsibilities will include performing day-to-day activities of processing market complaints assigned as per the relevant SOPs, business matrix, and SLA timelines. You will assist in data collection and reporting of KPIs, participate in continuous improvement initiatives, manage ad-hoc projects, and proactively report all deviations through timely escalations. Your role will also involve implementing continuous process improvement projects to enhance quality & productivity, ensuring that the service dashboard, order management framework, and time sheet are always kept updated. You will receive training on relevant procedures before taking up any GxP activities and report deliverable status while continuously acquiring process knowledge. The essential requirements for this role include having 5-8 years of relevant experience in Quality Operations, a thorough understanding of Quality Management Systems, and the ability to review market complaints investigation reports. You should have a basic understanding of product manufacturing, Pharma products and lifecycle events, Trackwise, performance KPIs, MS Excel, and awareness of GXP. Strong communication skills are essential, with fluency in verbal and written English; knowledge of other languages is an added advantage. A graduate or post-graduate degree in Pharmacy would be a desirable requirement for this position. Novartis is committed to building an outstanding, inclusive work environment with diverse teams representative of the patients and communities served. If you are looking to be part of a mission to reimagine medicine and improve lives, consider joining Novartis. To learn more about the benefits and rewards offered at Novartis, please refer to the Novartis Life Handbook. If this role does not align with your current experience or career goals, you can stay connected and learn about other career opportunities within Novartis by joining the Novartis Network. Novartis values the contribution of its associates in driving the company towards becoming the most valued and trusted medicines company in the world.,
Posted 4 days ago
1.0 - 6.0 years
4 - 8 Lacs
Thane, Maharashtra, India
On-site
PURPOSE OF THE ROLE, RESPONSIBILTIES AND DELIVERABLES: Responsible for Localization, Development Vendor Development activities. Master Data Maintenance. Knowledge in SAP similar system is mandatory. Digitization/Automation for O AIS Products manufacturing. Development of Tools, fixtures other infrastructure at vendors place New Product Introduction Localization Projects. Supplier development Layout optimisation Contribution to evaluation of design, existing new for manufacturing processes. Identification execution of Benchmarking projects. Digitalization/Automation of existing process systems Conduct production readiness review with compliance to the process. Prototyping and Industrialization of products. Implementation of Engineering change management process Self-driven, personality with self-assertion in a multi-cultural environment. Coordinates with Production and Quality for continuous improvement on value engineering initiatives, cost efficient and robust manufacturing processes. EDUCATION EXPERIENCE: Academic degree in Mechanical / Production / Industrial Engineering or other compatible technical areas Early or mid professional.
Posted 2 weeks ago
1.0 - 5.0 years
2 - 3 Lacs
Faridabad
Work from Office
Minimum Education Qualification : B Pharma Experience: 1.5 to 4 Years in Finished Pharmaceuticals Product Manufacturing (IPQA) Age: 21-30 Years Line Clearance. Dispensing, In-process checks at different stages as per defined frequency and filling of BMR/BPRs. Collection of In-process, Finished, Control samples as well as Stability samples. Review of Filled BMR/BPRs and release of product to next stage. To ensure online recording of BMR/BPR, log books etc. and QC Report must be obtained prior to release any batch for next stage. Calibration of IPQA Instruments.
Posted 2 months ago
2 - 6 years
3 - 7 Lacs
Bharuch, Vapi
Work from Office
Develop and implement production plans, schedules, and budget. Analyze production needs, identify areas of improvement, and recommend solutions. Plan personnel activity, assign tasks and adjust workflow and schedules accordingly. Monitor production costs and discuss changes with the management team to ensure cost efficiency. Ensure compliance with safety guidelines and company regulations. Supervise a team of production personnel to meet production targets. Ensure that production activities comply with the quality standards set by the organization. Conduct performance reviews and provide employees with feedback to help them improve and meet targets. Required Skill Set / Keywords : API/ Intermediate and Multi product manufacturing Candidates Location: Gujrat, Maharashtra
Posted 2 months ago
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