Position for Experience Candidates.
Position: QA/ AR&D / QC / FR&D/ Microbiology - Officer to Team Leader.
Qualification: Must be M.Sc/M.Pharm/B.Sc/B.Pharm/B. Tech/M. Tech.
Experience : Total experience from 2 to 6 years in Pharma Industry R&D.
Qualification: Must be M.Sc/M.Pharm/B.Sc/B.Pharm/B. Tech/M. Tech.
Experience : Total experience from 2 to 6 years in Pharma Industry R&D.
Position For Fresher Candidates.
Position: QC / AR&D / QA / FR&D/ Microbiology -Trainee to Officer.
Qualification: Must be M.Sc / M.Pharm/B.Sc/B.Pharm/B. Tech/M. Tech
Service Agreement: Service Agreement for 2 year for fresher.
Qualification: Must be M.Sc / M.Pharm/B.Sc/B.Pharm/B. Tech/M. Tech
Service Agreement: Service Agreement for 2 year for fresher.
Position for Fresher Candidates for Corporate Office.
Qualification : Ph.D / M.Sc / M.Pharm / B.Pharm & MBA / BBA / B.com / BBM Marketing.
Service Agreement: Service Agreement for 2 year for fresher.
JOB DESCRIPTION FOR QC/ARD.
Specific eligibility M.SC / M. Pharm / B. SC / B.Pharm
Present knowledge of GLP requirements and all analytical instruments and adequate knowledge of HPLC, UPLC, GC, Dissolution tester and UV- Spectrophotometer etc.
Examining in-process testing and products containing technical exposures such as assay, related matter / compounds, Dissolution, Content uniformity and GDP.
Method validation and methods transfer experience for the analytical methods of drug products like drug, content uniformity and residual solvents by present ICH guidelines and pharmacopia according to HPLC, GC and UV-Visible Spectrophotometer.
There is enough knowledge to prepare and review analytical method authentication / methods verification protocol, method transfer / regular / stability documentation for drug products such as assay.
Having an adequate knowledge for analytical raw data and stability sample review.
Generating ability to work in multi-task environments and high quality production.
JOB DESCRIPTION FOR QA.
M.Sc. / B. Pharm. / M. Pharm. /B.Sc
For implementation, continuous monitoring and review of quality management system and responsible for obtaining updated regulatory information and implementation of the laboratory.
Management review responsible for meeting management and deviation of deviation.
Responsible for internal audit, customer grievances, inspection and quality inspection.
To comply with the new quality system procedures for issuing deviation, OOS, OOT, CAPA, and change control forms and to pursue relevant departments and responsible for repeating the existing procedures according to regulatory requirements.
Not providing timely reporting to the customer, conducting training on the latest regulatory requirements. (SOP training, job-training and classroom room training)
Responsible for allocation of work and supervision of regular activities, assuring analytical results and leaving COA for regular samples and stabilization samples.
Responsible for granting certification master plans and eligibility protocols for laboratory equipment, review and approval of method transfer protocols and reports and reports of work
To approve analytical method development and method authentication protocols and reports, responsible for the review and approval of all records and protocol related to stability studies management.
To fully implement and monitor the effectiveness of the stability process, to activate stability studies in LIMs and to approve stability.
Responsibility is given to the QA-manager in the absence of duties.
JOB DESCRIPTION FOR FR & D
Specific eligibility M. Pharma / B. Pharm and Pharmaceutical Technology.
Creation of groups created from literary surveys, material reports such as preparation of documents, pre-product development strategy reports.
Displaying, Preparation of Appraisal and Batch Displays, Preparation, Optimization and Implementation of Scale-Up Processes.
Preparation of stability management bench and lab scale, preparation of summary report and preparation of stage product reports.
Known Knowledge in USFDA and ICH Guidelines.
MFC (Master Formula Card), BMP (Batch Production Protocol), BMR (Batch Production Records), Product Details (IP-FP), Protocol etc. To prepare
To create SOPs, IQs, OQs and PQs for R & D equipment and logbooks.
QBD concepts indicate tremendous knowledge and important process
Knowledge needed to create TTD and components for product development.
JOB DESCRIPTION FOR MICROBIOLOGY
Specific eligibility M.Sc. / B.Sc. Microbiology
Review and report for microbiology department, work allocation and ERP, preparation, performance and all microbiological methods are responsible for reviewing the report through verification documents.
Verifying and reviewing all microbiological samples, responsible for SOP review for microbiol related equipment / analysis. Raw data report, microbiology customer compliance.
To initiate deviation for microbiology-related equipment / analysis, responsible for starting monitoring control for microbiology related equipment / analysis. If anything.
New microbiology is responsible for the implementation of technical requirements, audit compliance.
Responsible for coordinating with new vendors / instrument installation with vendors for IQ, OQ, PQ.
Responsible for testing and verification of responsible documents for environmental monitoring.
Media growth promotion test, supervision of sub-culture maintenance, maintenance of GLP, responsible for maintaining GDP in the microbiology lab.
JOB PROFILE FOR BD.
Specialized Eligibility MBA / BBA / BBM Marketing.
Current GLP Pharmaceuticals Current Market Knowledge Required.
Handling technical potential and commercial potential business activities.
A mix of technical exhibition related products / business development and marketing.
Knowledge of pharmaceutical license and customer agreement.
The ability to work in multi-task environments and create high-quality output.
Job Profile for Research Administrator - Innovation.
Specific eligibility - M Pharma / B Pharma Pharmaceuticals / UG or PG in Life Sciences.
Coordinate the technical team with the help of innovation project and management.
Review project progress and related remedies.
Coordinate with the applicable organizational staff, local business / industry and community partners for the project.
All support activities, data entry, and filing of correspondence, purchasing and reporting.
VENUE
Stabicon Life Sciences Pvt. Ltd.
R&D Centre: Plot No. 28, Bommasandra Industrial Area (Sub layout), 4th Phase,
Jigani hobli, Anekal Taluk, Bangalore 560099, Karnataka, India.
Date & Time: 29th September - 30th September, 10 AM onwards
For More Information please visit: www.stabicon.com
