Appcure Labs Released Job Openings On 27/10/2021.Appcure Labs Private Limited Notification full detailes below.Interested and eligible candidates can attend interview on scheduled time and venue.
Vacancy Details:
Appcure Labs Recruiting M.Sc or M.Pharm Candidates with 2 – 4 Years of Experience for Executive Quality Assurance Position.Complete Details for the Executive Quality Assurance as follows.
Important Details :
- Location :Hyderabad/Secunderabad
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application: 27/10/2021
- Mode of application :Online
- Contact Number:Admin ( 8008338808 )
- Time & Venue: 27 October – 4th November , 9.30 AM – 5.30 PM , Appcure Labs Private Limited, PLOT NO 2 SURVEY NO 93, SATYAM ENCLAVE, PETBASHEERABAD, JEDIMETLA VILLAGE, OPP RENOVA HOSPITAL, QUTHBULLAPUR MANDAL AND MUNICIPALITY, HYDERABAD – 500055 TELANGANA, INDIA
Job Description/Skills Required
M.Sc or M.Pharm candidate with relevant QA experience to ensure cGMP/GLP in the Formulation development and Analytical development Lab as per regulatory requirement.
- Review of standard operating procedures and specification.
- Initiation, Monitoring, implementation and Closing of the Change Controls.
- To support in investigation and review of incidents and deviations.
- Supporting to QMS governing documents tracking and close out compliance.
- To assist internal training programs.
- Monitoring of Issuance, distribution, retrieval and Obsolete/ uncontrolled of all documents at R&D level and maintenance of Archival Room.
- To monitor and ensure that the environment condition of the respective processing, and stores area is maintained as per the recommended environment conditions.
- Review of all online documents like equipment logs and environment conditions and balance logs in-processing, and stores area.
- Handling of Equipment Qualification activities.
- Preparation of quality overview documents and Quality Assurance relevant standard operating procedures.
- Review of Lab Notebooks, MFC, PDR and Method Validation Protocols and its Report.
- Review and archival of technology transfer documents.
- Coordination of maintenance relevant activities compliance wherever it is authorized.
- Review and monitoring of Annual calibration schedule and its addendum as and when required.
