Legacy of Alembic Pharmaceuticals Limited (APL) dates back to over 100 years. Established in 1907 with an objective to develop and revolutionize the Pharmaceutical and Drug industry in the Indian subcontinent, Alembic Pharmaceuticals Limited today is one of the leading pharmaceutical companies in India.
Walk-In Drive for API sites at Panelav/Karakhadi near Vadodara.
Executive - Quality Assurance (API)
Email : quality@alembic.co.in
Qualifications :
• M.Sc / B.Pharm / M.Pharm
• 1 to 5 years of experience.
Job Responsibilities
• Perform sampling of saleable intermediates, APIs and maintain related documents
• Online Review of BMR, BPR, BCR.
• Perform IPQA activity and co-ordinate in the Change control, Deviation, Incident, OOS, CAPA etc. Quality related documents of plant.
• Collection of Process performance qualification samples and cleaning validation and verification samples.
Executive - Quality Control (API)
Email : quality@alembic.co.in
Qualifications :
• M.Sc. - Organic/ Analytical Chemistry
• 1 to 5 years of experience.
Job Responsibilities :
• Analysis of finished products, stability samples and raw materials.
• Handle instruments like HPLC, GC, UV-visible/ IR Spectrophotometer, Dissolution apparatus KF, IPC-OES.
Sr. Executive/ Executive - Production (API)
Email : apiproduction@alembic.co.in
Qualifications :
• M.Sc / B.E - B.Tech (Chemical Engg.)
• 1 to 7 years of experience.
• Experience in handling critical equipment like reactor, centrifuge, blender, sifter, multi-mill, etc.
Job Responsibilities :
• Ensure that the products are manufactured as per the cGMP.
• Maintain documentation as per regulatory authorities requirements like change control, and deviations.
• Highlight technical problems and take corrective actions.
Walk in Interview
Date & Day : 21st January, 2024 Sunday
Time : 9:30 AM to 3:30 PM
Venue : Alembic Pharmaceuticals Limited "M" Floor, Corporate House Opp. Bhailal Amin General Hospital Alembic Road, Vadodara.
For all positions, candidates having exposure to regulatory requirements of documentation cGMP/GLP in regulated plants shall be preferred.
Those who are unable to attend the Walk-In, may send their updated resume on provided email-ids.
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