Aykon Bioscience Hiring Fot Regulatory Affairs/ QA/ QC/ Production/ Warehouse and Microbiology
Aykon Biosciences Pvt. Ltd. is Hiring!
How to Apply: Send your CV to hr@aykon.in
1) Dept: Regulatory Affairs
Experience: 2-3 years
Number of Openings: 2
Job Description: Experienced in parenterals with strong knowledge of pharmaceutical regulations, CTD/ACTD submissions, and country-specific guidelines. Detail-oriented, excellent at communication, and skilled in handling multiple projects.
2) Dept: Quality Assurance (QMS)
Position: Officer/ExecutiveExperience: 2-3 years
Number of Openings: 3
Job Description: Ensure GMP and quality compliance in injection manufacturing through in-process checks, line clearance, documentation review, deviation investigation, and CAPA support.
3) Dept: Quality Control
Position: Officer/ExecutiveExperience: 1-3 years
Number of Openings: 2
Job Description: Handle sampling and testing of raw, in-process, and finished injectable products. Ensure cGMP and pharmacopoeial compliance, and manage analytical documentation and reports.
4) Dept: Production
Position: Officer/ExecutiveExperience: 0-3 years
Number of Openings: 5
Job Description: Oversee injectable manufacturing per GMP, ensuring equipment operation, cleaning, and maintenance. Manage BMRs and ensure timely production as per plan.
5) Dept: Warehouse
Position: Officer/Executive
Experience: 0-3 years
Number of Openings: 2
Job Description: Manage receipt, storage, and issuance of materials for injectables. Ensure GMP/SOP compliance, accurate documentation, labeling, and inventory control.
Experience: 0-3 years
Number of Openings: 2
Job Description: Manage receipt, storage, and issuance of materials for injectables. Ensure GMP/SOP compliance, accurate documentation, labeling, and inventory control.
6) Dept: Microbiology
- Position: Officer/Executive
- Experience: 2-3 years
- Number of Openings: 3
- Job Description: Perform microbiological testing of raw materials, water, environment, and injectables. Handle sterility tests, microbial limits, and cleanroom monitoring as per GMP, GLP, and regulatory standards.
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