5+

M.Sc Chemistry, B.Pharm, M.Pharm ; Preparation of IPQA SOPs, IPQA Checks, AQL, Line Clearance, Review of BPR, Audit & Compliance, Sampling of API & Drug Product, Document & Data Control, Control Sample Management.

The person should require minimal guidance when determining methods and procedures on new assignments. Decisions often impact the team in which they reside and occasionally impact other teams.

Bachelors degree in Engineering (B.Tech/B.E.), Pharmacy (B.Pharma), Life Sciences, or a related discipline. A Masters degree such as M.Tech, M.Pharma, MBA, or equivalent is highly preferred

Doctorate degree in life sciences, pharmacy, biomedical sciences, or a related field

Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads and line manager as appropriate

Supplier qualification: Ensures a valid Quality Agreement in line with the requirements of the Novartis global template is in place and continuously amended to the business needs.

Review of specification, Method of analysis Protocol, handling of OOS and OOT, Investigation and lab event, review and approval of QC documents.

This role involves researching, writing, and adapting scientific information into accurate, compliant, and engaging materials for healthcare professionals, patients, and other stakeholders.

Candidate should be B.Sc./ M.Sc./ B.Pharma/ M.Pharma with 3 to 6 years of experience working with Pharma Industry