Medley Pharmaceuticals Ltd Hiring for R&D Officer,QA Officer

Medley Pharmaceuticals is Hiring for R&D Officer,QA Officer and has issued notification to accept Applications.We are progressive WHO-GMP, MHRA-UK and USFDA certified company beside approval by several other countries and one of the fastest growing amongst the top 40 pharmaceutical companies in the country as per IMS. We are currently present in about 30 countries including UK, European countries & ROW.Application form link provided at the end of post. 

Vacancy summary details :

• Company Name: Medley Pharmaceuticals
• Location : Tarapur
• PostName: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
• No of Vacancies: Not Disclosed by Recruiter
• Details of Salary:Not Disclosed by Recruiter
• Date of examination: NA
• Time and Venue :NA
• Contact: corphr3@medleylab.com
• Mode of application : online
• Selection Process: Shortlisted candidates may called for selection process (  Personal interview , Group discussion , etc…,)

Job Description/Skills Required: 

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

1. To maintain and control an overall quality management system documentation.
2. Responsible for the preparation planning, coordination and execution of QA training programme. Assessment of other departments training
3. Issuance of batch number, batch manufacturing record, Register, SOP’s, format, protocols, Analytical protocols to departments
4. To review the Analytical records, Batch manufacturing record and batch packing record
5. Preparation of QA-SOP’s, Validation protocol aPQR, summary reports based on the Analytical results and Batch documents data.
6. To coordinate for the validation activities with other department for successful completion
7. Submit customer questionnaire along with declarations, management of free samples.
8. Maintaining vendor approval process
9. Daily assessment of site to ensure GMP compliance level of site through round.
10. Management of regulatory and customer audit at site
11. Management of Deviation, Incident. Change control, OOS, Recall, Market complaint, Investigation, CAPA, Risk assessment etc
12. Interpretation of sales order and overall management of dispatch
13. Reviewing stability data and sharing inference with management.
14. Providing data to Regulatory patent or any other authorities

Click here for notification and Apply