Alembic Pharmaceutical, vadodara 

Walk-In Drive at Vadodara

For our Injectable & OSD Formulations site at Karakhadi & Panelav

We are inviting you to join a Great Place to Work

Vacancy Details :- 

1)

Department Name :- Jr. Executive/Technical Officer - Production (Injectable

Criteria

• Diploma/IT

• 2 to 10 years of experience

• Exposure to aseptic practices and good documentation practices are must

Job Role

Email: injectable@alembic.co.in 

• Handle manufacturing skids, Fedegari autoclaves, Isolator, lyophilizers, vial washing and tunnel, vial/ ophthalmic/PF

filling and aseptic filtration, FFS, CIP/SIP, filters, microsphere refiner, active freeze drying System

• Execute manufacturing activities as per SOP

2)

Department Name :- Sr. Executive/Executive - IPQA (OSD

Criteria :-

M.Pharm/B.Pharm

• 1 to 7 years of experience

Job Role

Email: qualityform@alembic.co.in 

• Perform area and equipment line clearance/certification at manufacturing and packing stages

• Ensure to various in process test, sampling at intermediate and finished product stages

• Prepare and update the batch record review and calibration of routine IPQA instruments

3)

Department Name :- 

Position :- Trainee - Production (Formulations

Criteria:-

Diploma in Mechanica

 2022-23 Batch only with no backlog or ATK

• Proficient in English (written & oral communication

• Willing to work in rotational shift

Process of Recruitment

• Written Test (Candidates must clear technical and English proficiency tests.

Those who are unable to attend the Walk In, may send their updated resume on above provided email-ids respectively

Email: trainee@alembic.co.in

Important Details :-

Job Location :- Karakhadi, Panelav 

Interview Date :- 08 July 2023, Saturday

Interview Time :- 9:30 to 3:30

Interview Location :-Alembic Pharmaceuticals Limited

"Alembic Research Centre"

Opp. Alembic City, Besides Inorbit Mall, Alembic-Gorwa Road, Vadodara

Contact Person: Ms. Ashwini Adhyar

For all the positions, candidates having exposure to regulatory requirements of documentation cGMP/GLP in regulated plants