About the Job
Work experience/ Required qualification:
Need to have Abilities/Abilities listed below
Relational abilities (reliable, understanding)
Possible potential for development
Work/Item/Specialized Information/Pharma area information
Show and Relational abilities (If material)
Administrative or Individuals The executives abilities
Security mindfulness (If material)
Significance of Past Experience
Cognizance, Logical and Critical abilities to think
Efficiency and Result Direction (If material)
Disposition
Capability fitment
Deals drive (If material)
Character attributes (Individualistic/Cooperative person, Out spoken, Development level and so on.)
Work Area
Goa
Openings in Sun Pharma for Manager/ Sr. Manager for Bio-analytical
Sun Pharmaceutical Inds Limited - Baroda
Designation : Manager/Sr. Manager - Bio analytical for Biologics
Qualification : M.Sc./ Ph.D in immunology /Biochemistry / Life Sciences / Biotechnology
Experience : 12 - 15 years
Job Location: Baroda
Department: Proteomics
Key Responsibilities:
1) Work in close partnership with contract research organizations (CROs) for Bio analytical assay development.
2) Responsible for TK, PK, ADA & NAB assay development, validation at external contract organizations (CROs) in a regulated (GLP, GCLP) environment to support pre-clinical and clinical studies.
3) Responsible for assay development to detect innate immune response modulating impurities (IIRMIs) in therapeutic peptides and proteins at external contract organizations (CROs) in a regulated (GLP, GCLP) environment.
4) Responsible for assay development to detect adaptive immune response in therapeutic peptides and proteins at external contract organizations (CROs) in a regulated (GLP, GCLP) environment.
5) Serve as the bioanalytical representative at project team meetings and provide scientific and operational oversight of bioanalytical activities conducted at CROs including reagent generation, assay development and validation.
6) Work independently and in collaboration with a subject matter expert (SME) representative of the clinical & non-clinical group.
7) Identification & screening of CROs for Bioanalytical services.
8) Provide guidance to contract organizations (CROs) on assay development, experimental design, troubleshooting and sample analysis.
9) Review of method development reports (MDRs), validation reports and bio analytical test procedures (ATPs).
Send in your resume to [email protected]