Otsuka Pharma Ahmedabad jobs for Quality Assurance Bsc Msc Bpharm Mpharm apply now
🔶 Reference - Industrial Guide Always write reference for better attention.
Otsuka Pharmaceuticals Hiring B.Sc, M.Sc, B.Pharm, M.Pharm for QA ( Parenteral )
Important Vacancy details:Interested candidates can share their resumes on hrm.opmf-amd@otsukapharma.in[ads id="ads1"] A. Post Name: Quality Assurance ( Parenteral )
B. Education: B.Sc./M.Sc./B.Pharm. /M.Pharm.
C. Experience:01 to 5 years
D. Location: Ahmedabad
Job Description:Urgent opening at Otsuka Pharmaceutical India Pvt. Ltd, for Ahmedabad.
Roles and Responsibilities
For IPQA/QMS :-[ads id="ads2"] 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.[ads id="ads1"] Review critical quality attributes of products, review trend analysis and keep track of OOT results.
To review Preventive Maintenance, Breakdown maintenance and perform risk assessment, suggest immediate corrective actions, report conclusion of the same.
To maintain stability general quarantine area/ record and issue stability batch samples in case of any requirement received.
For QA-Process Validation :-[ads id="ads2"] 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.[ads id="ads1"] 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.
Interested candidates can share their resume on hrm.opmf-amd@otsukapharma.in
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Otsuka Pharma Ahmedabad jobs for Quality Assurance Bsc Msc Bpharm Mpharm apply now
🔶 Reference - Industrial Guide Always write reference for better attention.Otsuka Pharmaceuticals Hiring B.Sc, M.Sc, B.Pharm, M.Pharm for QA ( Parenteral )
Important Vacancy details:Interested candidates can share their resumes on hrm.opmf-amd@otsukapharma.in
[ads id="ads1"]
A. Post Name: Quality Assurance ( Parenteral )
B. Education: B.Sc./M.Sc./B.Pharm. /M.Pharm.
C. Experience:01 to 5 years
D. Location: Ahmedabad
Job Description:Urgent opening at Otsuka Pharmaceutical India Pvt. Ltd, for Ahmedabad.
Roles and Responsibilities
For IPQA/QMS :-
[ads id="ads2"]
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.
[ads id="ads1"]
Review critical quality attributes of products, review trend analysis and keep track of OOT results.
To review Preventive Maintenance, Breakdown maintenance and perform risk assessment, suggest immediate corrective actions, report conclusion of the same.
To maintain stability general quarantine area/ record and issue stability batch samples in case of any requirement received.
For QA-Process Validation :-
[ads id="ads2"]
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.
[ads id="ads1"]
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.
Interested candidates can share their resume on hrm.opmf-amd@otsukapharma.in
🔶 Our Free Courses for Chemical Plant persons
Basic Industrial Concepts
Technical Interview Questions
Pharma Interview Questions
Reactors
Distillation
Heat exchangers
Pumps - All type
Centrifugal Pump
Industrial Equipments
Industrial Valves
Compressors | All types
Safety Blogs
Piping and Equipment's
Utility Blogs
Chemical Storage Blogs
Instrumentation Blogs
Electrical Blogs
Industrial Policies
HR Interview Questions
Career Blogs
Cooling Tower
Efficient Equipment Operation
🔶 Jobs we are Offering
Production
Gulf Jobs
QC
QA
R&D
Mechanical
Electrical
Instrumentation
Safety
Utility
Boiler operator
HR
Civil.
MR
ASM
RSM
TSM
ZSM
We had prepared Interview Questions book which Contains Chemical, Pharma, Safety, HR, Interview Questions asked frequently in interviews.
We are developing Interview Questions book Please submit your interview question
When we get job suitable to you we can contact you. Please upload your updated Resume