Tuesday, October 19, 2021

Otsuka Pharmaceutical Walk In 23rd Oct 2021 for QA(IPQA/Validation/QMS/Doc Cell)/QC-Chemical Analysis/ADL

 Otsuka Pharmaceutical India Pvt Ltd Walk-in Interview 2021 B.sc,M.sc,B.pharma,M.pharma for QA(IPQA/Validation/QMS/Doc Cell)/QC-Chemical Analysis/ADL At Ahmedabad( Moraiya ).Otsuka Pharmaceutical India Pvt Ltd Notification full detailes below.Interested and eligible candidates can attend interview on scheduled time and venue.


  • Vacancy details:
  • Post Name: QA(IPQA/Validation/QMS/Doc Cell)/QC-Chemical Analysis/ADL
  • Qualification: B.sc,M.sc,B.pharma,M.pharma
  • Experience:2 to 7 years

Job Description: Otsuka Pharmaceutical India Pvt Ltd Hiring For QA(IPQA/Validation/QMS/Doc Cell)/QC-Chemical Analysis/ADL ! 

Important Details :

  • Location:Ahmedabad( Moraiya )
  • Post of date: 19/10/2021
  • NoteThe above positions are for shift (rotational) operations and only for experienced candidates while fresher candidates can share their resume on hrm.opmf-amd@otsukapharma.in
  • Selection ProcessThe selection will be on the basis of Interview.

Walk-in Interview QA(IPQA/Validation/QMS/Doc Cell)/QC-Chemical Analysis/ADL, Otsuka Pharmaceutical India Pvt Ltd

  • Date :23 October , 9.30 AM – 3.00 PM
  • Venue : Otsuka Pharmaceutical India Pvt. Ltd. 21st Floor, B-Block, Westgate, Nr. YMCA, S.G. Highway, Ahmedabad, Gujarat – 380 015

For QA(IPQA/Validation/QMS/Doc Cell):-

  • 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.

For ADL:

  • Responsible for Analytical Method Validation and Method Development activity.
  • To perform F&D sample analysis.
  • Responsible for Good Lab Practices (GLP) activities and its complies.
  • Responsible for Calibration of lab instruments.
  • Preparation and review of Validation Protocols/Reports and Analytical Reports including data.
  • Preparation/Review of SOP and its compliance.
  • Responsible for Procurement of analytical and Lab requirements.
  • To maintain the Documents of Analytical Protocols and Reports including Validation and Development.
  • Responsible for maintain the stock of Laboratory requirements including chemicals and other analytical requirements.
  • To maintain all data and log book records with Online as per GLP Requirement.

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.
  • Exposure in Parenteral Formulation.

About Company

Otsuka Pharmaceutical India Private Limited primarily manufacture & market products across multiple therapeutic segments. To keep pace with our growth plans, we require young and skilled employees with experience in Parenteral/ Injectable formulation for our manufacturing facility at Ahmedabad, Gujarat.

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