Walk-In Interview @ Otsuka Pharmaceutical, Ahmedabad On 28th Aug’ 22

Walk-In Interview @ Otsuka Pharmaceutical, Ahmedabad On 28th Aug’ 22- Production, Packing, QA, QC, QC-Micro

Otsuka Pharmaceutical India Private Limited (OPI)  is a Joint Venture between Otsuka Pharmaceutical Factory, Inc., Japan and Mitsui & Co. Ltd., Japan for Infusion Business in India and Emerging Markets. We primarily manufacture & market products across multiple markets and therapeutic segments

Experience : 2 – 7 Years

Date : 28th Aug, 2022

For 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.

*For 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).

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

For QA(IPQA/Validation/QMS):-

• Execution of All IPQA related activities within manufacturing unit.
• Line clearance, in-process dispensing and sampling activities.
• BMR/BPR issuance, review and preparation under the guidance of seniors.
• Issuance of Standard Formats and submitting the documents.
• Preparation of SOP as per the current organization norms and cGMP guidelines under the observation of seniors.
• Execute routine IPQA monitoring.
• Review and approve on-line documentation of manufacturing, testing and packing activity.
• Investigation of any deviation / abnormal observation.
• Review the GDP issues in Production / QC / QA and in logbooks.
• Execute CAPA defined by management/QMS.
• Review critical quality attributes of products, review trend analysis and keep track of OOT results.
• Execution of All Process Validation related activities within manufacturing unit.
• Review process validation, qualification planner.
• Conduct Material issuance for validations activities.
• Sample withdrawal during process validation.
• Record observations in observation sheets for process validation.
• Coordinate and execute process validation, qualification activities & inform about deviation from planning.
• New equipment qualification & validation.
• To help in identification of any deviation and report further.
• To support in investigation of any product deviation and Out of Specification (OOS).
• To suggest / recommend the changes in the Standard Operating Procedure (SOP).
• To help in investigation of OOS and Documentation of the same.
• To be updated about the new changes in all international and local regulatory requirements.
• To monitor and implement the Good Manufacturing Practice (GMP) standards in the plant.
• To help in conducting monthly Corrective and Preventive Action (CAPA) meetings and preparation of CAPA summary report and gather CAPA details generated from individual quality sub-systems (e.g. Deviation, Change Control, OOS, Complaint, External inspection, Self-inspection).

For QC-Chemical Analysis(RM/PM & IPPT/FP):-

• To carry out the sampling of all the materials according to Standard Operating Procedure (SOP).
• To carry out the testing of Raw Material and Packing Material according to approved procedure.
• To release Raw Material and Packing Material.
• To carry out the calibration of instruments as per the schedule.
• To prepare the working standards as per the guidelines and various pharmacopoeias.
• To ensure the status tag on the released material and transfer such material in the released area.
• To analyze the artworks as per the guidelines.
• To follow the Good Laboratory practices and Good Manufacturing practices (GMP).
• To prepare requirement list of chemical & reagent for procurement.
• To perform the analysis of stability sample as per current specification.
• To compile the data required for internal quality audit in the plant, as and when required.
• To implement the cGMP standards.

For QC-Micro:-

• To ensure the clean environment for sterile preparation by implementing the Good Manufacturing Practice (GMP) norms as per the international standards and guidelines.
• To do sampling of Water for Injection (WFI), Double Reverse Osmosis (DRO), Single Reverse Osmosis (SRO), Raw water and pure steam.
• To analyze water samples for pH, conductivity, Bacterial Endotoxin Test (BET), bioburden, Total Organic Carbon (TOC), pathogens, chlorides, hardness, silt density index and other testing as per the requirements.
• To analyze the samples of water system after maintenance work .
• To observe and record the results the microbiological plates and test tubes after analysis as well as supervise discarding method of same.
• To perform the timely microbiological testing of finished product samples, pre-sterile samples, Raw material as well as Packing material sample as per the requirements and SOPs and record the results for the same.

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.

The above positions are for experienced candidates and for rotational shifts only. Fresher candidates have to share their resume on hrm.opmf-amd@otsukapharma.in

Time and venue :

28th Aug, 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