Chemex Global Walk-in Interview 2025.Chemex Global Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.
Important Details :
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Vacancy details:
- Department: Apprentice – Analytical Research & Development (ARD)
- Qualification: BPharm / MPharm degree
- Experience: Freshers
Job Description: Greeting from Milan Laboratories Pvt Limited.!!!!!
Greetings from Chemex Global!
We are urgently seeking 2 freshers male candidates with a BPharm / MPharm degree, under NATS/NAPS.
Key Details:
– Designation: Apprentice – Analytical Research & Development (ARD)
– Positions: 2
– Immediate Joiners: Preferred
If you’re interested, kindly send your updated CV to hr@chemex.global
Greetings from Chemex Global..
We are Hiring…
– Designation: Research Associate (API)
– Qualification: MSc in Analytical/Organic Chemistry
– Experience: 2-3 years of experience in R&D, HPLC, GC & Method Development
– Salary: Best in industry
Job Location: Guwahati, Assam
Interested candidates kindly mail your updated CV to hr@chemex.global
Greetings from Chemex Global..
We are hiring..
Position: Executive / Sr. Executive / Assistant Manager – Quality Assurance – API
Education: B.Pharm / M.Pharm
Experience: 3–6 years in Quality Assurance for API manufacturing
Location: Based in Guwahati or willing to relocate
Interested candidates kindly share your cv at hr@chemex.global
Job Description:
1. Preparation & amp; Review of Standard Operating Procedures.
2. Ensure that all activities comply with internal quality standards, regulatory requirements, and Good Manufacturing Practices (GMP).
3. To ensure the Preparation, Revision/Review and Retrieval of the documents.
4. Develop and prepare detailed protocols for various quality assurance and validation activities,
ensuring that all procedures and guidelines are followed.
5. Provide training to staff on Quality Assurance Procedures, GMP, SOPs, and other Quality-related topics.
6. Developing, Implementing, and Maintaining Quality Systems including Documentation
Control & Change Control.
7. Collaborating with cross-functional teams including Research & Development, Quality Control, Production, Maintenance & Utility, Safety Health and Environment , Purchase , Human Resource and Warehouse to ensure effective communication and to ensure GDP.
8. Ensure all quality-related documents, such as batch records, test results, CAPA reports, and audit reports etc. are accurately maintained and filed according to company procedures.
9. Assist in the Preparation and Submission of Regulatory reports.
10. Participate in supplier audits and evaluations to ensure vendors meet required quality standards and regulatory requirements.
11. Review and approve batch records, ensuring they are complete, accurate, and in compliance with applicable regulations before product release.
12. To ensure all the activities related to Process Validation , Hold Time & Stability Study.
13. Conduct internal audits of all the Departments to verify compliance with established standards.
14. Assist in preparing for External Audits and inspections by regulatory agencies.
15. To perform the IPQA related activities.
16. Support other departments in quality-related activities and ensure alignment with QA policies
17. Day to Day activities are reporting to Quality Head.
18. Any other work assign by the Quality Head
