Axelia Laboratories Private Limited Walk In Interview 2023.Axelia Laboratories Private Limited Notification full details below.Interested and eligible candidates can attend interview on scheduled time and venue.Axelia Laboratories Private Limited. is one of the leading contract manufacturing pharmaceutical company, manufacturing more than 12% of India’s domestically consumed medicines.
Vacancy details:
- Department:– Quality Assurance
- Role: Quality Assurance
- Qualification – B.Sc in Microbiology, Chemistry, B.Pharma in Any Specialization
- Experienced: 5 – 10 years
- Salary: 2-3.25 Lacs P.A.
Job Description: Greeting from Axelia Laboratories Private Limited !!!!
Important Details :
Location: Palghar,Maharashtra
Post of date:12/12/2023
Selection Process: The selection will be on the basis of Interview.
Mode of Interview: Face To Face Interview
Interview Rounds of Interview: HR
Walkin Interview Details:
Role & responsibilities
Responsible to conduct chemical & instrumental analysis of all raw materials and finished products.
Responsible for ensuring that the quality of drugs being manufactured meet prescribed quality levels.
Handle daily scheduled quality control functions.
Intimating the out of specification results to the QC manager & Quality Assurance Department.
Perform scheduled Calibration & Validation of lab instruments.
Co-ordination with production department for smooth day to day production activity.
Preparation of analysis reports for COA preparation.
Preparation and Revision of all QC related documents, records and data, which are in agreement with the Quality system.
Co-ordination with PTL for outside test reports, sample collections etc.
Keep track for material requirement and request the same as per the requirement.
Maintain data as per requirement of Quality System.
Provide training on analysis, GMP, GLP for internal audits.
Maintain training records as per requirement of Quality System.
Attend the queries related to QC dept during audits.
Preferred candidate profile
Chemical & Instrumental Analysis approval from Maahrashtra FDA is a must for this job.
Looking for male candidates who can do later shift wise jobs.
Candidate must be a team player and able to work with his other team members and superiors.
Candidate must be punctual and well organized in documentation.
Must have good knowledge of GLP and good exposure to regional aswell as international regulatory norms and practices.
Candidate must add value to the QC teams efforts for timely delivery of results.
