1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
10.00 LPA TO 12.00 LPA
Pharma experience specialized in sales training with oncology segment background,
Create and execute learning strategies and programs
Evaluate individual and organizational development needs
Implement various learning methods companywide (e.g. coaching, job-shadowing, online training)
Design and deliver e-learning courses, workshops and other trainings
Assess the success of development plans and help employees make the most of ...
3 Opening(s)
2.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 3.00 LPA
Job responsivities are to assist Regulatory manager
Preparation, Compilation and review of registration dossier of tablet /capsule/injection in CTD, ACTD as well as country specific format for countries
Preparation, Compilation and review of registration dossier of capsule/syrup/balm in a Herbal products for country specific format in countries of African Region, Cambodia, Myanmar, ...
2 Opening(s)
10.0 Year(s) To 25.0 Year(s)
11.00 LPA TO 20.00 LPA
Designation
Manager - Production
Vacant Positions
2
Department
Production
Location
Vapi
Education
M.Sc / B.Tech / B.E (Chemical)
Required Experience
10 - 15 Yrs in Pharma Industry
Salary Range
11 - 20 Lakh
Job Description
1) Candidate shall having exposure of 11 to 18 yrs in pharma industry2) Should have worked as block lead for at least 3 - 5 yrs3) Shall have handled 60 ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 3.50 LPA
Duties and Responsibilities: • Hands on experience of all handling lab instrument like HPLC, GC and UV.• Checking Of Method of Analysis, Specification and Protocol.• Checking Of Finish Product Certificate of Analysis (COA).• Handling of daily and monthly calibration of all instruments.• Handling of Stability products.• Prepare and Maintain Reference Standard, ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Duties and Responsibilities :
Collect and coordinate information and prepare regulatory documentation for submission to regulatory agencies or to commercial partners, advise on the submission strategy
Timely compile materials for license renewals, updates and registrations
Maintain regulatory files/database and chronologies in good order. Establish and maintain system for tracking changes in documents submitted ...
5 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 6.00 LPA
Tech / BE Chemical — having 3 — 6 years of experience in Pharma industry, have exposure of Heat Transfer and Mass transfer calculation, P&lD, PFD, Process Design, Scale-Up activities, PrcRess Optimization.
Tech / BE Chemical — having 3 — 6 years of experience in Pharma industry, have exposure of Heat ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
12.00 LPA TO 16.00 LPA
Job Description Functional Responsibilities:• Provides strong and decisive project leadership and establishes an execution framework to ensurethe quality, schedule and profitability of the total project execution (EPCM, commissioning, start up,and operations as appropriate to the project scope).• Delivery of the project in accordance with the project deliverables & schedule.• Establishes ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
12.00 LPA TO 15.00 LPA
Experience : 10-15 Yrs
Designation : Manager
Qualification : Any post Graduate
Industry - Pharma
CTC - 15 LPA
JD:
SAP - SD Module: - To ensure the maintenance & required changes in SD module2. Streamline, testing & training CFAs for Value CN Process due to change in 194R rule.
3. Streamline, test & provide training to ...
3 Opening(s)
2.0 Year(s) To 4.0 Year(s)
1.00 LPA TO 2.40 LPA
Conducting tests to ensure that products meet federal regulations regarding safety, quality, and performance
Monitoring production processes to ensure that they are running smoothly
Evaluating the effectiveness of new methods or processes to ensure that they are producing desired results
Performing analyses of samples to ensure that they meet specific standards or specifications
Adjusting ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Job responsibilities :
Preparation, Compilation and review of registration dossier of tablet /capsule/injection in CTD,
ACTD as well as country specific format for countries
Preparation, Compilation and review of registration dossier of capsule/syrup/balm in a Herbal
products for country specific format in countries of African Region, Cambodia, Myanmar, CIS
To manage new registration / preregistration ...