Sipra Labs Hiring MS/M.Sc(Science) in Agriculture, Bio-Chemistry, Biology, Botany, Chemistry, Zoology, Environmental science Graduates

Sipra Labs Released Job Openings On 18/07/2022.SIPRA LABS LIMITED is a global Contract Research Organization (CRO) offering Regulatory Compliant Research and Developmental Services to Pharma, Biotech and Medical Device Companies since two decades. Sipra is USFDA registered & DSIR approved R & D center..Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Sipra Labs Recruitment 2021 are provided below. Interested and eliible candidates can  submit application along with resume. 

Vacancy Details:

Sipra Labs Recruiting MS/M.Sc(Science) in Agriculture, Bio-Chemistry, Biology, Botany, Chemistry, Zoology, Environmental science for QA / QC Manager Position.Complete Details for the QA / QC Manager as follows.

Important Details :

• Location :Hyderabad/Secunderabad( Sanath Nagar )
• No of Vacancies:NA
• Details of Salary:NA
• Opening date for online Application: 18/07/2022
• Mode of application :Online
  
• How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps

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Freshers & experience B.sc,M.sc,B.pharm,M.pharm,ITI,Diploma,D.Pharm,B.tech,M.tech,Any Graduate Jobs In QC, QA, Production, Engineering, R&D, Micro, Store ,Sales,Medical Coding All Departments In Multiple Locations 

Job Description/Skills Required

• The main purpose of the role is to enhance our regulatory requirements , and Quality Assurance (QA) professional is to assure management of the compliance with the GLP regulations within their departments.
• Knowledge about QMS, CAPA and GMP.
• Knowledge of about Preparation of SOPs and guideline. Knowledge of about Change control management.
• Handling of incidents, Deviations, Out of specification and OOT.
• Preparation and review of risk assessment reports.
• Exposure to regulatory audits. Review and preparation of master calibration schedule.
• Experience in conducting internal audits and audit preparedness.
• Implementation of good documentation practices.
• Knowledge about the qualification of equipment and instruments.
• Knowledge about regulatory guidelines and requirements.
• Knowledge about preparation and review of Development reports, validation reports and Dossier.
• Should have sound knowledge on USFDA , and must have attended at least one USFDA audit.

Click here for notification and Apply