Executive / Sr. Executive Job in Micro Labs Ltd

• DEPARTMENT : Production
• LOCATION : Bangalore
• MINIMUM QUALIFICATION REQUIRED : B.Pharm / M.Pharm
• MINIMUM EXPERIENCE REQUIRED : 2 to 6 Years in Formulation
• SKILLS REQUIRED : Experience in automatic compression machine with AWC controls, Experience in handling equipment like RMG, FBD, roll compactor in closed loop system with documentation,Experience in auto coater for film coating of tablets
• TYPE OF INTERVIEW : Walk-in Drive
• DATE & TIME : Monday till Saturday
• WALK-IN INTERVIEW :Plot No 16, Veerasandra Industrial Area, Electronic City Phase 2, Bangalore - 560100
• ROLE & RESPONSIBILITIES :
• Competent in the areas like Granulation, Coating, Compression , Capsule Filling, Palletisation, FBP & FBD & RMG.

ADVICE ABOUT REPORTING

• Report adverse experiences with medications
• Report serious adverse reactions. A reaction is serious when the patient outcome is:
  • Death
  • Life-threatening (real risk of dying)
  • Hospitalization (initial or prolonged)
  • Disability (significant, persistent or permanent)
  • Congenital anomaly
  • Required intervention to prevent permanent impairment or damage
• Report even if:
  • Youre not certain the product caused adverse reaction
  • You dont have all the details however point nos. 1, 5, 7, 8, 11, 15, 16 & 18 (see reverse) are essentially required.
• Who can report:
  • Any health care professional (Doctors including Dentists, Nurses and Pharmacists).
• Where to report:
  • After completing, please return this form to Micro Labs Ltd, Pharmacovigilance Cell
• What happens to the submitted information:
  • Information provided in this form is handled in strict confidence. PV cell at Micro Labs will carry out causality analysis and the data is statistically analysed and finally submitted to CDSCO.

Confidentiality:

The patients identity is held in strict confidence and protected to the fullest extent. Programme staff is not expected to and will not disclose the reporters identity in response to a request from the public. Submission of a report does not constitute an admission that medical personnel or manufacturer or the product caused or contributed to the reaction.