Alembic Pharma Released Job Openings On 03-06-2022.Alembic Pharmaceuticals Limited, with an established presence in the Indian pharma industry has a proud, historical track record going back 112 years.. Application form link provided at the end of post.
Vacancy Details:
Alembic Pharma Recruiting MSc,BSc,M.Pharm,B.Pharm,BTech,MTech Candidates with 2+ Years of Experience for QC (API/OSD/Injectable) & Production (API) Position.Complete Details for the QC (API/OSD/Injectable) & Production (API) as follows.
Important Details :
- Location:Vadodara (Gujarat)
- No of Vacancies:200
- Details of Salary:NA
- Opening date for online Application: 03-06-2022
- Mode of application :Walk In
- Time And Venue: 05th June 2022,9.30 AM – 4.30 PM,Hotel Express Inn Next to Big Bazar, Ostwal Empire, Boisar- Tarapur Road, Boisar – Maharashtra – 401501
Related Job: Viatris(Mylan) Excellent Opportunity For B.pharma,M.pharma,M.sc Graduates
For more Latest pharma jobs https://pharmajobscooin.wordpress.com/
Job Description/Skills Required
Executive/AM/DM – Quality Control (Injectable/OSD/API) –
Experience in performing analysis of RM, Intermediate, FP or stability samples on HPLC, GC or UV. Exposure in Method Validation, Verification & Transfer activities on analytical instruments. Handling online trouble shooting of all analytical instruments in QC lab during analysis. Calibration of instruments like HPLC, GC, GC-MS, XRD, Potentiometer. Handling of Laboratory Investigation Reports, OOS & OOT. Monitoring of Good Laboratory Practices.
Executive/Sr. Executive- Production (API) –
Must have handled critical equipment like Reactor, Centrifuge, Blender, Sifter, Multi-mill etc. To ensure that the products are manufactured as per the cGMP to achieve consistent results and documented accordingly. To highlight technical problems during manufacturing of API products concerning processes conditions and coordinate with Shift in-charge and resolve problems/take corrective actions where necessary. Having exposure of plant SOP’s and formats as well as daily & monthly reports and maintain documentation as per regulatory authorities requirement like change control, deviations or market complaints investigations, if any. Maintain safety practices.
Â

