Opening for Various Position in Intas
At Intas, people are the most valuable assets. It boasts of having one of the most charismatic pools of employees with incredible achievement orientation. The human resource development strategies at Intas invariably focus on incessant improvement of professional and interpersonal skills and abilities, fostering team spirit and enhancing the knowledge base of its employees. Through numerous training and development programs, Intas continuously invests to bring out the best out of its human assets.
Intas believes in the spirit of "growing together". Through excellent career development opportunities, it provides a platform for carving a high trajectory of accomplishments to all people. Work-life balance is its winning formula, ensuring effectiveness across all spheres of life.
As a fast paced, Indian multinational Intas is growing at a tremendous pace. Young and dynamic professionals with a "CAN DO" attitude are welcome to become Intas' "Partners in Success".
Job Description for Manager
Required Experience : 4 to 7 years
Education Qualification : B.Sc. / M.Sc. / B.Pharm. / M.Pharm.
Job Profile :
- Implementation of Vendor Management System.
- Maintaining Vendor schedules and documents.
- Candidate should have Bulk Drugs / API facility experience.
- Should have experience of API / SM / Excipient Vendor Audit.
NO.Of Post: 02
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hrd_matoda@intaspharma.com
Job Description for Sr. Executive / Executive
Required Experience : 1 to 5 years
Education Qualification : B.Sc. / M.Sc. / B.Pharm. / M.Pharm.
Job Profile :
- Candidate should have Bulk Drugs / API facility experience
- Should have experience of API / SM / Excipient Vendor Audit
NO.Of Post: 01
send your resume
Job Description for Research Associate
Required Experience : 2 years
Preference : Male candidate
Education Qualification : M.Pharm. (Pharmaceutics)
Job Profile :
- Candidate should have experience in NDDS Product Development of Parenteral, Solid oral and Semi solid dosage forms for Regulated and Domestic Markets.
- Execution of Scale-up and Clinical Trial Batches for NDDS projects. Candidate should be competent for troubleshooting of the allotted projects.
- Responsible for exhibit / validation batches in co-ordination with process development lab
- Should care for documentation and compilation of necessary regulatory submission data
- Should have experience in technology transfer from R&D to manufacturing site
- Monitoring stability of products during development and validation batches
- Should co-ordinate with various functions like Analytical, QA, PDL & Plant etc.
Job Description for Research Associate
Required Experience : 2 years
Preference : Male candidate
Education Qualification : M.Pharm. (Pharmaceutics)
Job Profile :
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NO.Of Post: 01
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Job Description for Senior Research Scientist
Required Experience : 3 to 9 years
Preference : Male candidate
Education Qualification : M.Pharm.
Job Profile :
- Can initiate to collect, review & archive all technical information related to product registration for oral solid products in the Europe market. Person can take responsibility to coordinate with team members for dossier compilation, query responses activity and care of the assigned products for the EU countries
- Acquaint the filling requirements for the veterinary oral solid drug products in the Europe market
- Capable to provide the regulatory support to the various departments and regulatory system up gradation in context with the new regulatory requirements with respect to EU filling
- Carry out activities associated with installing the dossier on web and its access by clients
- Carry out additional activities related to the regulatory department as and when required
Job Description for Senior Research Scientist
Required Experience : 3 to 9 years
Preference : Male candidate
Education Qualification : M.Pharm.
Job Profile :
- Can initiate to collect, review & archive all technical information related to product registration for oral solid products in the Europe market. Person can take responsibility to coordinate with team members for dossier compilation, query responses activity and care of the assigned products for the EU countries
- Acquaint the filling requirements for the veterinary oral solid drug products in the Europe market
- Capable to provide the regulatory support to the various departments and regulatory system up gradation in context with the new regulatory requirements with respect to EU filling
- Carry out activities associated with installing the dossier on web and its access by clients
- Carry out additional activities related to the regulatory department as and when required
NO.Of Post: 03
send your resume
Job Description for Research Associate
Required Experience : 3 to 5 years
Education Qualification : M.Sc. (Biotech/Biochemistry) / M.Tech. (Bioprocess/Chemical/Biotech)
Job Profile :
- Downstream Process Development and Protein Purification for Microbial and Mammalian Products
- Understanding of Process characterization and QbD approach
- Provide technical support for designing experiments and facilitating technology transfer activity to manufacturing
Job Description for Research Associate
Required Experience : 3 to 5 years
Education Qualification : M.Sc. (Biotech/Biochemistry) / M.Tech. (Bioprocess/Chemical/Biotech)
Job Profile :
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NO.Of Post: 01
send your resume
Job Description for Officer / Sr. Officer / Executive
Required Experience : 1 to 5 years
Preference : Male candidate
Education Qualification : M.Sc. / B.Sc. / B.Pharm.
Job Profile :
- Should be well-versed with operation of sophisticated instruments like HPLC, GC, AAS & UV Spectrophotometer
- Should possess knowledge of GLP, GDP and various regulatory procedures
- To perform method validation / method transfer
- Knowledge of SAP will be an added advantage
Job Description for Officer / Sr. Officer / Executive
Required Experience : 1 to 5 years
Preference : Male candidate
Education Qualification : M.Sc. / B.Sc. / B.Pharm.
Job Profile :
- Should be well-versed with operation of sophisticated instruments like HPLC, GC, AAS & UV Spectrophotometer
- Should possess knowledge of GLP, GDP and various regulatory procedures
- To perform method validation / method transfer
- Knowledge of SAP will be an added advantage
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