Alembic Pharmaceuticals Limited, with an established presence in the Indian pharma industry has a proud, historical track record going back over 100 years.
To realize our ambitious plans, we call upon dynamic, result oriented team members to join our API & Formulation manufacturing unit located at PANELAV, near Vadodara (Gujarat).
Post: Executive/Sr. Executive/Asst. Manager/ Dy. Manager/Manager - Production, QA, QC
Executive/Sr. Executive/Asst. Manager/ Dy. Manager/Manager - Production Injectable (Oncology)
Candidates should be M.Pharm/ B.Pharm with 2 to 12 years of experience in working with Containment facility (Oncology Parenteral manufacturing) at OEL level 3 & 4. Experience with process equipment like Aseptic filling, Vials, lyophilisation. Sterilization is must.
Executive/Sr. Executive/Asst. Manager/ Dy. Manager/Manager- Production Solid Orals (Oncology)
Candidates should be M.Pharm/ B.Pharm with 2 to 12 years of experience in working with OSD oncology manufacturing facility with experience on process equipment like Granulation. Compression. Coating Capsules. Blister Packing, Bottle line. Knowledge and experience with Documentation like BMR. BPR, SOPs & other documents involved in machine qualification is necessary. Knowledge of cGMP & SAP is essential.
Executive/ Sr. Executive/Asst. Manager - Production Solid Oral (General Formulation)
Preferred candidates would be M. Pharm / B. Pharm / M.Sc with 2 to 9 years of expenence in manufacturing operations, e.g. Granulation / Compression / Coating / Packaging, etc.. Experience of working in a facility catering to Regulated market will be beneficial. Knowledge and experience of documentation practices as required for Regulatory agencies and Multinational customers would be desired. Knowledge of cGMP& SAP are essential.
Executive/Sr. Executive/Asst. Manager/ Dy. Manager/ Manager • QC/ QA (Formulation or API)
Candidate should be M.Pharm/ B.Pharm/ M.Sc / B.Sc for QC/ OA Formulation & M.Sc/ B.Sc for QC/ QA API with 2 to 12 years of relevant experience in formulation in area of oral solid dosage, injectable, sterile & oncology products/ Active substance from manufacturing site catering to regulated market. Responsibility includes operation and documentation for chromatography & spectroscopy instruments, wet chemistry analysis for RM. intermediates & finished Products. Exposure to regulatory inspections and customer audits. Experience of documentation submission for US, EU regulatory agencies. Working knowledge of analytical instrumentation related software & database. Good written & communication skills are required.
Executive/Sr. Executive/ Asst. Manager/ Dy. Manager/ Manager • Microbiology (Oncology)
Candidates should be M.Sc/ B.Sc with 2 to 12 years of Experience & knowledge of method validation, equipment, autoclave. LAF area, water system. Bioassay. BET test. Stenlity test & Microbiological activities of pharmaceutical industry. Experience of regulatory inspection is desirable.
Technicians / Plant Operators (Formulation)
Candidates should be Diploma in Pharmacy / Diploma in Engineering / ITI (Fitter) v/ith 2 to 7 years experience of operating machines like FBD, RMG, Compression, Coating, Capsule filling, BQS Blister Packing, Bulk Packing, etc.
WALK-IN INTERVIEW
Date: 23-04-2016 (Saturday)
&
24-04-2016 (Sunday)
Time: 9.00 AM to 5.00 PM
Venue: HOTEL SITARA GRAND 15-24-20/21/22, ME 1st PHASE, ROAD NO. 1, KPHB COLONY, HYDERABAD.
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