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Otsuka Pharmaceuticals Ltd – Walk In Interview for Production/ Packing/ Maintenance Department on 19th September 2021

Otsuka Pharmaceuticals Ltd -Walk In Interview for Production/ Packing/ Maintenance Department on 19th September 2021

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Otsuka Pharmaceuticals Ltd : Walk In Interview for Production / Packing/ Maintenance Department on 19th September 2021

Production (Parenteral/Injectable exposure only):

Process In-charge: (B.Sc./M.Sc./B.Pharm./M.Pharm.)

– To ensure the cleanliness, environmental norms and other process of various area like Dispensing, Mixing, Filling and Terminal Sterilizer.

-To complete CIP, SIP and batch manufacturing process timely.

-To ensure the batch manufacturing process is done as per Batch Manufacturing record.

-To co-ordinate with other departments like QA, QC, Stores, Engineering, etc. as and when required.

Associate (Machine Operator): (ITI/Diploma)

-To monitor temperature / humidity of clean rooms, and if any deviation is found, inform the Engineering department.

-To ensure cleaning and disinfections of floor, ceiling, wall, pipeline, vessels and equipment as per frequency defined.

-To maintain the cleaning and lubrication of machine regularly.

-To ensure the machine is working smoothly and it is performing well..

 Packing (Parenteral/Injectable exposure only):

>Process In-charge: (B.Sc./M.Sc./B.Pharm.)

-To make sure that issued material is as per requirement and the material quality is as per specification.

-To check the availability of packing material with proper labels and status.

-To ensure that the packing activity does not start without line clearance.

-To check, verify and destroy the rejection generated during packing and ensure recording of all such material.

– To update the Batch Packing Record on line.

-To check the packing online at frequent intervals as defined in the Standard Operating Procedure.

-To train personnel for the critical operations like visual inspection and labeling.

Associate (Machine Operator): (ITI/Diploma)

-To maintain the machine in good condition by regular cleaning and lubrication.

-To ensure that machines are working smoothly and performing as per standards.

-To supervise the packing activities online at frequent intervals as defined in the Standard Operating Procedure (SOP).

-To ensure that the machine/s are started within time period & perform challenging test.

Plant Maintenance (Parenteral/Injectable exposure will be preferred):

>Process In-charge: (B.E./B.Tech./M.E. (Electrical/ Mechanical/ Intrumentation))

-To prepare monthly Preventive Maintenance (PM) Schedule.

-To verify spares.

-To observe PM activity and prepare PM review report.

-To verify PM checklist & equipment operation logbooks.

-To maintain documentation system in compliance with Current Good Manufacturing Practice (cGMP) norms.

>Associate (Fitter/Electrician/Welder): ( Diploma/ITI (Fitter/ Electrical/ Welder))

-To perform Preventive Maintenance (PM) of equipments as per schedule.

-To perform task as allocated.

-To escort supplier / service provider personnel for maintenance.

-To follow safety precautions during maintenance.

Candidate Profile :-

  • Ready to work in rotational shifts.

  • Excellent understanding about working area.

  • Initiator and Learner.

  • Decision making ability.

  • Team player and if required, can provide training to other team members.

  • Good communication.

Time and Venue

19th September , 9.30 AM – 3.00 PM

Otsuka Pharmaceutical India Pvt. Ltd. 21st Floor, B-Block, Westgate, Nr. YMCA, S.G. Highway, Ahmedabad, Gujarat – 380 015

Contact – Team HR 

The above positions are for experienced candidates only. Fresher candidates can share their resume on [email protected]

Apply for this position

Allowed Type(s): .pdf, .doc, .docx

About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 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

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