Medley Pharmaceuticals Ltd Walk-in interview 2021 for R&D Officer,QA Officer At Tarapur.Medley Pharmaceuticals Ltd Notification full detailes below.Interested Candidates Apply Now.
- Important Vacancy details:
- Company Name:Medley Pharmaceuticals Ltd
- Post Name: R&D Officer,QA Officer
- Qualification: MS/M.Sc(Science) in Any Specialization,B.Sc in Any Specialization,B.Pharma in Any Specialization
- Experience; 2-8 Years
- Location: Tarapur
- Salary:₹ Not Disclosed by Recruiter
- Openings:NA
- Contact Number:NA
- Selection Process: The selection will be on the basis of Interview.
Job Description: We have Hiring For R&D Officer,QA Officer in Medley Pharmaceuticals Ltd !
Send Your resume corphr3@medleylab.com
Roles and Responsibilities
1. To perform reactions in the lab for the development of Process for Intermediates and API.
2. Process development, process optimization, process validation, determination of critical reaction parameters.
3. Synthesis, Isolation and Characterization of Impurities.
4. Handling of various types of chemical reaction in the laboratory
5. Optimization of Existing processes
6. Proper handling of Lab equipment and Document.
7. Hands on experience in Chromatographic techniques like TLC and Column Chromatography.
8. Write technical papers and reports; and prepare standards and specifications for processes, facilities, products, and tests.
9. Carry out calibration of equipments.
10. Conduct validation of batches.
11. Carry out pilot plant studies after standardization of batch in R&D.
12. Conduct scale up experiments from pilot plant to commercial level.
13. Conduct literature survey of molecules.
14. Should be able to conduct various reactions such as Hydrogenation, epoxidation, wittig reaction, friedal crafts reaction, aldol condensation, coupling reactions etc.
15. Prepare test solutions, compounds and reagents for laboratory to conduct test.
16. Carry out different chemical reactions in the laboratory as per the given protocol.
17. Analyze organic and inorganic compounds to determine chemical and physical properties, composition, structure, relationships and reactions, utilizing chromatography, spectroscopy and spectrophotometry techniques and other analytical techniques.
Roles and Responsibilities
- To maintain and control an overall quality management system documentation.
- Responsible for the preparation planning, coordination and execution of QA training programme. Assessment of other departments training
- Issuance of batch number, batch manufacturing record, Register, SOP’s, format, protocols, Analytical protocols to departments
- To review the Analytical records, Batch manufacturing record and batch packing record
- Preparation of QA-SOP’s, Validation protocol aPQR, summary reports based on the Analytical results and Batch documents data.
- To coordinate for the validation activities with other department for successful completion
- Submit customer questionnaire along with declarations, management of free samples.
- Maintaining vendor approval process
- Daily assessment of site to ensure GMP compliance level of site through round.
- Management of regulatory and customer audit at site
- Management of Deviation, Incident. Change control, OOS, Recall, Market complaint, Investigation, CAPA, Risk assessment etc
- Interpretation of sales order and overall management of dispatch
- Reviewing stability data and sharing inference with management.
- Providing data to Regulatory patent or any other authorities
How to Apply :
Step 1: Click on below link and you will be redirected to Career Page of Recruiting Company or Career portal.
Step 2. Register on Career Page of the Company or Career Portal by giving log in credentials and other personal or education details .
Step 3.Upon successful registration .User need to log in with credentials.
Step 4.Once logged in, User need to fill the all relevant personal ,educational , Work experience details ,attach resume and submit application form.
Click here for notification and Apply
About Company:
