665 Job openings found

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, ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

Major Responsibilities: Ø  Quality Management System Implementation and Modification control. Ø  Document Control. Ø  Approval for batch release. Ø  Review and approval of Qualification Document. Ø  Review and approval of Calibration and Validation document. Ø  Planning, execution and compliance of both internal and external audits. Ø  Preparation of audit compliance report.   Job description Minor Responsibilities:   Ø  Review and approval of SMF, VMP and Quality manual. Ø  Review and approval of ...

  Job Description Heading the regulatory department of the company and leading a team of executives/Senior executives/Asst.Manager.- Must be aware of the latest country specific guidelines for ROW market and capable of planning and implementing,guiding, supporting, reviewing and finally approving the dossiers and implementing the other defined activities of thedepartment.- Coordination with ...

  Job description QC/QA/Senior Project Executive Male 6 1 to 8 B.Sc Ci pet /Diploma/Plastic Collect/receive samples of raw materials, Material in process, finished products, waste water at different stage of ETP/STP/RO plant solid waste generated from the manufacturing process, segregate to different groups. Responsible to carry out test all the samples collected/received as per the provided slandered ...