Daicel chiral technologies Walk In Interview 2022.Daicel chiral technologies Notification full details below.Interested and eligible candidates can Send Resume.Chiral Technologies, a subsidiary of DAICEL CORPORATION, serves pharmaceutical and other life science industries and offers the largest portfolio of chiral stationary phases and analytical and preparative chiral columns for the separation of racemic mixtures into single enantiomers.
- Vacancy details:
- Department: Executive/ senior Executive – Quality Assurance (Bioassay)
- Qualification: Post Graduate in biotechnology or pharmaceutical sciences
- Experienced: 4 to 6 years
Job Description: Greeting from Daicel chiral technologies !!!!!
- Important Details :
- Location: Turkapally, Hyderabad (Genome Valley)
- Post of date: 12/09/2022
- Selection Process: The selection will be on the basis of Interview.
- Interested candidates share across your updated resume to kesavapani@chiral.daicel.com
Job description:
Daicel chiral technologies is looking for Executive/ senior Executive – Quality Assurance (Bioassay)
Quality Assurance personnel is responsible for implementing Daicel Quality Policy and Quality Management Systems. The day-to-day work includes enforcement of quality standards and routine process checks.
Experience Required : 4 to 6 years
Job Location : Turkapally, Hyderabad (Genome Valley)
Desired Skills Set:
1. Proven work experience (4-6 years) in Quality assurance
2. Post Graduate in biotechnology or pharmaceutical sciences
3. Good knowledge of relevant regulatory standards
4. Good communication skills, both verbal and written
5. Good knowledge of Microsoft office tools like MS word, MS excel and PowerPoint
6. Previous experience with software related to handling of documents.
Job Responsibilities:
1. Review of Bioassay method development and method validation.
2. Ensure effective implementation of Quality Policy & Quality Objectives.
3. Issuance and review of all applicable logbooks, forms and formats.
4. Preparing, Controlling and issuing of Quality System Manual and other systems related documents.
5. Responsible for compliance monitoring , and implementations of DCTI’s Quality Management System, Policies and procedures in applicable areas.
6. Review of Equipment Qualification data and calibration data.
7. Responsible for participation in investigations and review of incidents , deviations, OOC, OOS and shall follow up on effectiveness of CAPA where applicable.
8. To ensure document control and Data Integrity in applicable areas.
9. To support during the audits conducted by Regulatory bodies, statutory bodies and customers.
10. Review the changes through change controls and implementation.
11. Quality Management System Orientations to applicable new Joiners.
12. Responsible for ensuring archival and retention of all the documents and records as per the procedure.
13. Review and maintenance of external calibration certificates.
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