Walk-in Interview For Women's For Multiple Departments At Alembic

Women's Special Walk-In Drive "Equal Rights, Equal Opportunities"

CITY 

VADODARA

DATE

08 December 2024

DAY

Sunday

TIME

9:30AM to 2:00PM

VENUE

Alembic Pharmaceuticals Ltd, "Sanskruti Hall" Alembic Colony, Opp. Bhailal Amin General Hospital, Alembic Road, Vadodara.

For all positions, candidateshaving 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 to relevant email-ids provided above.

Please note that Alembic Pharmaceuticals Limited does not hire consultants/agents who promise interviews/jobs for monetary

consideration/registration fees. Beware of such fraudulent calls

www.alembicpharmaceuticals.com

1)

Executive-Quality Control (OSD/Injectable/API)

Job Criteria:

M.Pharm/B.Pharm/ M.Sc

1 to 5 years of experience

Job Role:

Experience in handling QC instruments like HPLC, LCMS, GC, UV-spectrophotometer, dissolution apparatus, KF, IPC-OES, IR spectrophotometer

Handle QMS activities, maintaining lab records.

Exposure of QC compliance and GLP activities.

2)Technical Officer/Junior Executive/Executive-Production (OSD)

Job Criteria:

M. Pharm/B. Pharm/DME/ITI

1 to 5 years of experience

Job Role:

Email ID: prodform@alembic.co.in

Manage granulation, compression, coating, pelletization and capsule filling area.

3)Technical Officer/Junior Executive/Executive-Packing (OSD)

Job Criteria:

M. Pharm/B. Pharm/DME/D.Pharm/ITI

1 to 5 years of experience

Job Role:

Manage blister packing and bulk bottle, Track and Trace, serialization and documentation

Handle machines like CAM, BQS, HONGA & UHLMANN.

4)Junior Executive/ Executive/ Senior Executive-Production (API)

Job Criteria:

M.Sc./B.E-B.Tech (Chemical Engg.)/B.Sc. 1 to 5 years of experience.

Must have handled critical equipment like reactor, centrifuge, blender, sifter, multi-mill, etc.

Job Role:

Monitor and supervise production process to ensure compliance with SOP and cGMP.

Maintain documentation as per regulatory authorities requirement like change control, deviations.

Highlight technical problems and take corrective actions.