Otsuka Pharmaceutical India Private Limited Walk In Interview 2025.Otsuka Pharmaceutical India Private Limited Notification full details below. Interested and eligible candidates can attend interview on scheduled time and venue.
Vacancy details:
- Department : Quality Control (IPPT/FP, RM/PM)/Quality Control (Stability)/Quality Control (Micro)
- Qualification: Bsc,Msc,Bpharm,Mpharm
- Experienced: -2-7 years
Important Details :
- Location: Ahmedabad( Moraiya )
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face interview
Job Description: Greeting from Otsuka Pharmaceutical India Private Limited!!!
*For Quality Control (IPPT/FP, RM/PM):-
- To perform all test for in process product & finish product as per the specification and schedule.
- To investigate failure of FP / Out of specifications (OOS) and take the corrective and preventive actions (CAPA).
- To perform and ensure the calibration of instruments as per the schedule.
- To perform and ensure preparation of reagent / volumetric solution as per schedule.
- To perform and ensure observation of FP retained samples.
- To ensure that all documents related to the testing data and related papers are maintained properly.
- To implement Corrective and Preventive Action (CAPA).
- 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 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.
*For Quality Control (Stability):-
- To implement the change in procedure as per change control note.
- To check and verify the sampling of respective samples as per defined intervals for testing.
- To check and verify that the samples are kept at appropriate temperature and humidity as per defined procedure, which is as per the Standard Operating Procedure.
- To verify results of analysis conducted in respective period, and to carry out trend analysis.
- To coordinate with Purchase department for routine requirement and follow up for the procurement.
- To sign the documents related to stability studies data.
- To select product batches for the stability studies.
- In the absence of Officer, Executive will ensure his roles and responsibilities.
- In the absence of Executive, Sub-department Manager will ensure these roles and responsibilities.
- To file deviation in case of non-compliance
*For Quality Control (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 mentioned requirement is for Male Candidate Only. Hence can be ready to work in rotational Shift. Candidate having Parenteral /Injectable exposure would be preferable.
Candidates having Pharma exposure will only be considered for interview process.
Fresher can also email their CV on [email protected]
Time and Venue
21st June , 9.30 AM – 3.30 PM
Venue: Otsuka Pharmaceutical India Pvt Ltd 21st Floor, B-Block, Westgate, Nr. YMCA, S.G Highway, Ahmedabad – 380 015