Job for M.Pharm, MSc in Analytical Development, Formulation Development at JAMP group

The JAMP group is a proud Canadian owned company with its international headquarters located in Boucherville, 20 minutes from downtown Montreal, Quebec, Canada. The JAMP Pharma Group is active in all sectors of the pharmaceutical industry with our JAMP Pharma Generics, Orimed branded products, our Wampole and Laboratoire Suisse natural health supplements and our Cosmetic Import beauty and personal care products. The JAMP Pharma Group has also made a major investment in biosimilars which is one of the fastest growing markets in the pharmaceutical industry.

Post : Officer / Executive / Sr. Executive / Assistant Manager

Analytical Development (OSD) - Officer / Executive / Sr. Executive
Key Roles :
• Development of Analytical Methods for New Products.
• Responsible for Execution of Analytical Activities.
• Preparation & Review of SOP’s & Guidelines.
• Preparation & Review of STP, Test Methods & Specifications.
• Preparation & Review of Analytical Method Development Reports, Validation Protocols & Reports.
• Preparation & Review of Analytical Method Transfer Protocols & Reports.
• Responsible for Performance of Regular, Stability, Validation & Method Transfer Analysis.
• Should have sound knowledge of regulatory/ICH guidelines and GXPs i.e. GMP, GLP, GDP etc.
Experience : 3 - 6 yrs
Qualification : MSc. M.Pharmacy
Location : Hyderabad
Department : Analytical Development (OSD)

Formulation Development (Nasal) - Senior Executive / Assistant Manager / Manager
Key Roles :
• Should be well versed with nasal spray product development w.r.t.
• Regulatory requirements of US,EU,Canada & Australia markets.
• Lab experiments and Device selection.
• Project execution as per QbD based development.
• Fundamental understanding of Analytical instruments, techniques & interpretation of results.
• Worked in CDO/CDMO model
• Reference product characterization to decide the formulation strategy and to develop Prototype formulation.
• Formulation development with respect to QbD based concepts such as QTPP, CQA, CPP, CMA, etc and statistical
design to evaluate and establish the optimization of formulation.
• Device selection know how process and packaging material characterization to closely match with the reference product performance characteristics.
• Planning and execution of lab scale trials as per global regulatory guideline requirement of FDA, EMEA, Health Canada &
TGA - Australia.
• Preparation and execution of study protocols (In vitro, characterization, development studies etc.), MFC, PDR, scale-up & submission batch manufacturing, overall project management to achieve organizational timelines.
• Compilation and interpretation of analytical results. (Knowledge of analytical instruments / analysis techniques is required)
Experience : 5 - 14 yrs
Qualification : M.Pharm
Location : Hyderabad
Department : Formulation Development (Nasal)