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3.0 - 7.0 years

0 Lacs

navi mumbai, maharashtra

On-site

As an integral part of the team, you will be responsible for inspecting materials, managing inventory, overseeing product manufacturing, conducting testing, coordinating installation and commissioning processes, managing sales and after-sales services, handling procurement activities, and effectively managing customer relationship management (CRM) tasks. Your role will involve ensuring the quality and efficiency of various operational processes related to the aforementioned areas. A keen attention to detail, strong organizational skills, and the ability to effectively multitask will be essential in successfully fulfilling these responsibilities.,

Posted 2 weeks ago

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0.0 - 1.0 years

2 - 2 Lacs

bengaluru

Work from Office

Key Responsibilities: Assist in the manufacture of devices Organize workflow to meet specifications and deadlines. Manage stocks of Raw materials, in process and finished goods Estimate costs and prepare budgets for procurement of Raw materials Taking care of packaging and dispatching the product Ensure output meets quality standards. Provide Demonstration of the products to the clients when required Preparing scientific literature for the product Maintaining sterility of the production lab with appropriate microbiological testing

Posted 3 weeks ago

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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 Novartis sites and Contract Manufacturing Organizations. Collaboration with external Supply organization, Novartis sites, and Country pharma organizations for continuous improvement is essential for this role. 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, support continuous improvement initiatives, manage ad-hoc p...

Posted 1 month ago

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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...

Posted 1 month ago

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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 ...

Posted 1 month ago

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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 Industrializatio...

Posted 2 months ago

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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 3 months ago

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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/ Inter...

Posted 4 months ago

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