Titan Pharma India Pvt Ltd

Accountabilities I. Execute production activities in a shift by managing available resources to achieve production target II. Maintain standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality III. Prepare manufacturing records and update online documentation to meet production and cGMP requirements IV. Follow safe wor

Job Purpose Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift I. Operate the equipment efficiently without error and deviation as per SOP to meet shift targets II. Provide suggestions for optimization of processes to manufacture quality product III. Execute and update online documentation to meet cGMP requirements IV.

Accountabilities I. Prepare documents like SOPs, specifications and non-routine documentation and ensure timely availability across the site to provide support during the analysis II. Review the latest pharmacopeial updates, supplements and amendments by evaluating the updates required in the available document to ensure the compliance with the current pharmacopoeia through consent with regul

Job Purpose Operate & maintain packing machines to achieve quality product & shift wise targeted output with maximum utilisation I. Prepare the machine for packing operation as per production plan by using proper resources to ensure smooth operations II. Operate the packing machines by using minimum resources to get quality product III. Execute and update online documentation to meet cGM

Key Responsibilities: Building and maintaining MS Excel databases from source data Analysing client data using quantitative and qualitative methods to evaluate key performance indicators Collaborating with Project leaders and senior analysts to interpret data Produce high quality presentations and other deliverables for clients using powerpoint. Key Requirements: The ideal candidate m

Job Purpose Provide analytical support to API R&D, Regulatory Affairs, Manufacturing units and other analytical laboratories by method development of raw materials, intermediates and final API in order to ensure the drug development is carried out as per the project timelines and adheres to all regulatory requirements I. Provide method development and routine analysis under GLP environment

As MEDICAL REPRESENTATIVE where you will be at the grass root level, meeting doctors and chemists promoting company's brands and ensuring brand building. Eligibility criteria. Fresher/Experienced not more than 1.5yr Good Communication skill in English. Experience in pharma sales. Candidate will be responsible for Sales & Business development activities. Relationship building with doctors

Manufacturers pharmaceuticals, including liquids, tablets, and drug devices. Works closely with the laboratory manager and other pharmaceutical technicians. Collaborates with the quality assurance (QA) and quality control (QC) teams. Sterilizes all equipment and keeps a safe and hygienic work environment. Follows batch manufacturing records (BMR).

Designation name & Description: As an Associate Consultant / Consultant, you are expected to lead the offshore delivery and manage onshore / client communication. Consultant/Sr. Consultant designs and implement analyses over variety of pharma data sources like DDD, HCOS, Xponent, NPA, Patient data analytics, APLD, fingertip formulary, promotional datasets, and internal CRM commercial & salesforc

Ensuring country medical activities are aligned with WW strategies Implementing TA strategies and initiatives in line with the WW medical strategy Planning and implementing high quality medical educational activities, enabling HCPs best understanding on Immuno-Oncology Ensuring clinical trials within India are delivered to agreed standards of time, quality and costs in collaboration with RCO