Alembic Pharma – Walk-In Interviews on 20th Aug’ 2023 @ Vadodara

Alembic Pharma – Walk-In Interviews on 20th Aug’ 2023 @ Vadodara

Walk-In-Interview at Vadodara
We are inviting you to join a Great Place to Work at API sites at Panelav and Karakhadi near Vadodara (Gujarat).
Sr. Executive/ Executive – Production (API)
Job Criteria:
M.Sc./B.E-B.Tech (Chemical Eng.)
⚫ 01 to 07 years of experience.
• Handled critical equipment like reactor, centrifuge, blender, sifter, multi-mill, etc.
Job Role:
• Ensure that the products are manufactured as per the cGMP.
• Maintain documentation as per regulatory authorities requirement like change control, deviations. • Highlight technical problems and take corrective actions.
• Maintain safety practices

August 20, 2023 Sunday
Time 9.30AM to 3.30PM
Venue
Alembic Pharmaceuticals Limited,
“Sanskruti Hall” Alembic Colony,
Opp. Bhailal Amin General Hospital, Alembic Road, Vadodara.

Candidates who have appeared for an interview at Alembic Pharmaceutical Limited in last three months are requested not to appear for interview. Those who are unable to attend Walk-in may send their resume with details of total experience, current CTC, expected CTC and notice period on apiproduction@alembic.co.in
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

Job Category: pharma
Job Type: Full Time
Job Location: vadodara

Apply for this position

Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

Check Also

MICROBIOLOGICAL CONTROL FOR EXCIPIENTS, DRUG PRODUCT AND DRUG SUBSTANCE

MICROBIOLOGICAL CONTROL FOR EXCIPIENTS, DRUG PRODUCT AND DRUG SUBSTANCE PURPOSE: To describe microbiological test controls …