About the Company:
JAMP Pharma Gathering is a confidential Canadian organization that was sent off in 1988. Initially an agreement producing organization1 (CMO), the organization currently gives great medications and wellbeing answers for patients and shoppers.
Our exercises are upward coordinated at our central command right beyond Montréal, in Canada; from business activities to the conveyance of drug items. With quite possibly of the biggest deal powers in the Canadian nonexclusive industry, as well as a committed deals force for our marked items, we are exceptional to offer customized help to accomplices and medical services experts across Canada. Besides the fact that we supply in excess of 11,500 drug stores from one coast to another, yet doctors additionally show their confidence in us by deciding to endorse our marked items.
About the Job
Job Role: Senior Manager/AGM/DGM/GM
Cadre for Technical Services department for our API Division.
Qualification B.Tech Chemical Engineering
Required experience: 10-20 years of experience.
Location - Hyderabad.
Interested candidates can share their profiles to [email protected]
For Formulation development
Company: JAMP India Pharmaceuticals Pvt. Ltd.
Location: Ahmedabad
Department: Product Development (Solid orals)
Designation: Executive / Senior Executive
Experience: 4 - 5 years
Key Roles:
Co-ordination & execution R&D project’s bigger scale batch & capable to resolve it’s trouble shooting at R&D.
Successful project transfer from R&D to plant and its co-ordination for timely meeting targeted timeline.
Need complete involvement to resolve the trouble shooting at plant for Scale up and Exhibit batches execution.
Tracking the project status and update the project tracker on regular basis for R&D projects.
Involvement for APIs and reference products procurement.
Need sound knowledge on F&D and basic analytical concepts understanding.✔Literature search: DPD database, Patent database, NOC database, Pharmacopeias and related ICH and regulatory guidelines.
Primary review of draft manufacturing documents like MFR, BMR, Spec and stability protocols in accordance with development data and regulatory requirements.
Share your profile at [email protected] subject line "Profile for Product Development"