1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
9.60 LPA TO 10.80 LPA
GST Compliances (GST-3B, GSTR-1) & Annual Return TDS Entries & file Returns
Preparing MIS Reports, Accounts Finalize, Adjustment Entries, Party’s Reconciliation
Imprest Accounts
Bank Reconciliation
Coordinated with all HR activities
Documents financial transactions by entering account information.
Challan Payment like TDS, GST
Analyze Reports, Financial Forecasting & risk analysis
Prepare Cash Book & Reconciliation
Provides financial information to management ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
8.40 LPA TO 9.60 LPA
Managing a team of designers. Closely monitoring the designers in executing the tasks in the given time frame. Scheduled Team Review meetings and performance audit every quarter to improve deliverables Responsible for the design process from conception through to final styling for assigned product category Responsible for product design ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
12.00 LPA TO 15.00 LPA
To understand, communicate and prepare a system to meet the desired production of each product as per the plan agreed by SCM team.
To manufacture all products of high quality by complying with CGMP and safety systems at Udaipur Plants.
To Plan and set production targets and ensure achieving the same for ...
3 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.60 LPA TO 6.00 LPA
Role –
Customer Care Representative
KPI –
Customer satisfaction score
Conversion percentage
KRA –
Customer communication
Coordination with logistics / finance / quality departments for resolution.
Maintaining CRM tools / reports
Job Description:
Manage incoming phone calls
Generate sales leads
Identify and assess customers’ needs to achieve satisfaction
Build sustainable relationships and trust with customer accounts through open and interactive communication
Provide accurate, valid ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.40 LPA TO 3.00 LPA
Ensure the quality and consistency of products on the production line.Conduct inspections and quality checks at various stages of the production process.Maintain accurate and detailed records of inspection results.Identify and report defects or inconsistencies in the production process.Strong understanding of quality control processes and standards.Should be familiar working on excel.
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 17.00 LPA
Preparation of techno-commercial proposals, cost estimation of WTP/STP/ETP & water supply & sewerage scheme in meeting the client’s requirement.
Preparation of basic engineering package (BEP) and assist the design team in preparation of drawings related to the projects awarded.
Meetings with the clients to explain our offer / scheme that we suggest.
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
12.00 LPA TO 15.00 LPA
The role is that of HOD of Electrical and Instrumentation (E&I) Department which shall include all responsibilities including proposals and planning, supervision and co-ordination of contracts for electrical and control & instrumentation works in water supply and sewage schemes including WTPs / STPs/ Pumping station etc.
In depth knowledge and experience ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.00 LPA TO 3.00 LPA
We are seeking a dynamic and motivated Business Development Associate to join our sales team. The ideal candidate will have a passion for sales, excellent communication skills, and a strong understanding of digital marketing services such as SEO, PPC, and web design/development. This role involves identifying new business opportunities, building and maintaining ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
15.00 LPA TO 18.00 LPA
Experience in Business Development / Sales / Marketing / In licensing / Out licensing of pharmaceutical formulations (ideally Injectable & Sterile) with a minimum of 10+ years . Must have worked in similar role with a reputed pharma company.
Build contacts with potential clients to create new business opportunities
Keep prospective client ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
12.00 LPA TO 14.00 LPA
A "QC Manager - Sterile Formulation" job description entails overseeing all quality control operations within a sterile injectable drug manufacturing facility, ensuring that all products meet stringent regulatory standards by managing testing procedures for raw materials, in-process samples, and finished products, while maintaining compliance with cGMP guidelines and conducting thorough ...