About the Company
The firm is more than 200 years of experience in producing the quality standards helping major bio-pharmaceutical firms in delivering high quality medicines to relieve many diseases. This is an organization supplying methods at free of cost for the product development and maintaining the standards. This is distributed across the globe serving mankind.
About the Job :
Qualification : Masters in Pharmacy or M. Tech ( Biotech/Bio process engineering) with 7-8 years experience in Biologics with product based mass spec using mass spec based studies
Experience need to be with strong technical knowledge and practical experience of mass spec
Need to have experience in cGLP/cGMP environment is desirable
Required to have experience on techniques like HPLC UPLC and mass spectrometry
able to plan execute comply compile the company and verification, R&D projects for products such as proteins antibiotics peptides vaccines monoclonal antibodies.
quiet to demonstrate the expertise in biological methods the areas of mass spectrometry and handling of HPLC UPLC
Required to perform located by the supervisor and a able to complete the task on time
required to prepare the protocols and project reports as per the organizational quality systems and procedures
need to achieve and align with the organizational goals and objectives along with the along with the guidelines and other requirements
Required to follow the procedures related to safety ethics and compliance resist the group leader in implementing the process improvements
able to have support and collaboration best performance team in biologics lab under the supervision or as per the requirement
should be well worst with the workflow like bottom-up, top -down label free, DDA libraries targeted proteinomics approaches