Pharma Jobs

To prepare and review new product documents like material requirement sheet, master formula card, bill of material, risk assessment reports, scale up protocol and reports, exhibit/ trial batch manufacturing record and exhibit protocols and reports etc.

Demonstrated experience managing, coaching, and developing clinical and medical professionals within a matrixed and cross-functional environment

Develops and maintains clinical software Risk Management Files that include risk management plans, hazard analyses, risk assessments and post market surveillance.

Design and develop innovative formulations for solid oral dosage forms (Tablets / Capsules / Pellets) and injectable dosage forms. 

As a subject matter expert, you would be leading the workshop discussions on configurations with concerned business leads, understand & document business requirements. Solution designing, problem solving and working closely with other leads / consultants on a project assignment would be part of core responsibilities in this role.

Gathers, analyzes and documents user requirements for various business initiatives. Liaisons with IT and ensures requirements are appropriately translated into design specifications for systems and reports. Thermo Fisher Scientific

Applicants who meet the following criteria are invited to apply for this fellowship. South African, Permanent Resident, citizen from SADC countries/foreign

Ph.D or equivalent degree OR having 3 years of research, teaching, and design/development experience after M.Pharm with at least one research paper in a Science Citation Indexed (SCI) journal. PGIMER

Degree or Diploma Pharmacy & Registration in Pharmacy Council. National Health Mission, District Sarangarh-Bilaigarh