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)/ (Stability)/ (Micro)
- Qualification: B.Sc in Chemistry, B.Pharma in Pharmacy/MS/M.Sc(Science) in Chemistry, M.Pharma in Pharmacy
- 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 Anee.Silas@otsukapharma.in
Walk-in interview details Below
Time and Venue
26 April , 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
