• Working as Trainee/ Jr. Analyst/ Analyst/Research Associate at INDOCO REMEDIES LTD.

    • May 18, 2018
    • Posted By : admin
    • 0 Comment
    Post Name : Quality Control,Quality Assurance,Production
    Management Trainee/ Jr. Officer/ Officer
    Department: ARD
    Description: M.Sc. Graduate, who has 2-4 years of experience in handling HPLC & GC instruments and in chromatographic techniques and has basic understanding of raw material analysis.
    Management Trainee/ Jr. Analyst/ Analyst
    Department: AMD
    Description: M.Sc./ M.Pharm. Graduate with 2-5 years of experience in validation of analytical methods of finished dosage forms using HPLC, GC, Disso & UV.Manager/ Sr. Manager
    Department: AMD
    Description: M.Sc./ M.Pharm graduate 12-15 years of experience. Team Leader: Handling team of 25 chemists, ensuring activities as per defined SOPs. Handling projects pertaining to US, EU & other Regulatory market. Overall responsibility of ANDA & EU products.Jr. Research Associate/ Research Associate
    Department: Formulation development
    Description: M.Pharm graduate with 2-5 years of experience in Formulation & Development of OSD, Pellets & Ophthalmics. Preparation and issuance of formulation documents like MFC, MPC, BMR/ BPR, Stability protocols, coordination with plants & other related departments. Technology Transfer to site.
    Jr. Officer
    Department: Planning & Operations
    Description: B.Pharm Fresher. Should have good communication skills and computer knowledge.
    Officer / Executive (EU Market)
    Department: Regulatory Affairs
    Description: B.Pharm/ M.Pharm graduate with 3-6 years of experience in review of documents required for dossier compilation for EU & Canada. Assessment and evaluation of documents required for variation.
    Officer / Executive (ROW Market)
    Department: Regulatory Affairs
    Description: B.Pharm/ M.Pharm graduate with 2-4 years of experience in product dossier compilation and submission in ASEAN, LATAM and FWA/ Africa market. Knowledge of ACTD/ CTD compilation is a must. Review of documents viz., MFC, BMR, Stability Data etc., required for dossier compilation. Knowledge of ICH guidelines and Product Lifecycle Management.

    Time and Venue- 20th May , 9 AM onwards
    Venue –  INDOCO REMEDIES LTD- Plant I, L-14, Verna Industrial Estate, Verna- Salcette, Goa-403722
    Website: http://www.indoco.com/m/
    Telephone: 8379943497

    Apply Online


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