Microbiology In Ludhiana Bhatia International Ltd

0.0 - 3.0 years

0 Lacs

ludhiana, punjab

On-site

As a Microbiologist at our company, you will be responsible for ensuring the quality and safety of our products through rigorous testing. A successful candidate for this position should hold a degree in MSc/BSc (Microbiology) and have 1-2 years of experience in a similar role, although freshers are also welcome to apply. Your primary role will involve conducting various tests to assess the quality of input water, lotions, machines, production equipment, and final products for microbial contents. It is essential that you are FDA approved and have a solid understanding of microbiological testing procedures. Additionally, maintaining detailed records of all tests conducted is crucial for audit purposes. This position is based in Ludhiana, where you will play a key role in upholding our commitment to quality and safety standards. If you are passionate about microbiology and have the necessary qualifications and experience, we encourage you to apply for this exciting opportunity.,

Posted 6 days ago

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Quality Head Ankit Pulps & Board

10.0 - 15.0 years

10 - 12 Lacs

Nagpur

Work from Office

Role & responsibilities 1. Shall responsible to review implementation & maintain of the Quality Management system with the regulations. 2. Determining, negotiating, and agreeing on in-house quality procedures, standards and specifications 3. Checking & Maintaining of Master Documents related to the QMS system. 4. Shall responsible to review filled Batch Production control record & analysis report for batch release. 5. Responsible for coordinate validation activity and validation protocols. 6. Responsible for control and approve deviations whenever raised in the concerned department and record the deviations. 7. Review and approval of the standard operating procedures for other concerned departments. 8. Responsible to plan and carry out internal audits & MRM. 9. Responsible for Coordinate with QC/Production for handling and investigation of Market complaints. 10. Responsible for conducting on-going training programs for new recruits and retraining for existing employees of concern department on the topic of SOP, GTP, GLP cGMP, WHO, ISO, etc. whenever required or as per schedule & Responsible for verifying the effectiveness of training programs system. 11. To check and approve artworks in coordination. 12. Verification and approval of the change control whenever the change in the document, facility, process, and equipment. 13. Verification and approval of documents concern to the production process, analysis including quality system. 14. Responsible for verifying the effectiveness of corrective action and preventive action systems. 15. Responsible to review & maintain system represent in QA department SOPs like OOS, OOT, (document record, storage & retention), Document control, APQR, Calibration, Trend data, etc. 16. Should have better co-ordination with QA, Production, QC, Engineering & Maintenance, for implementation of cGMP and also the electrical department. 17. Responsible for complying with all regulatory queries during any inspection and audit. 18. Responsible for application to FDA, FSSAI, Kosher, Halal, ISO, and others for any approval like Technical person, License/Renewal License, and additional Product, GMP. 19. Also responsible to work on time and to ensure TAT (Turn Around Time) given by Directors, any other job assigned by Superior. 20. Ensuring the manufacturing processes comply with standards at both the national and international levels. Job Type: Full-time

Posted 2 months ago

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Production Chemist (FDA Approved) Crown Hr Services

2.0 - 5.0 years

3 - 4 Lacs

Vadodara

Work from Office

* Urgent job opening for Production Chemist for reputed Chemical Manufacturing Company with B.Sc. / M.Sc. ( Chemistry) near Vadodara Location. * Experience in FDA Approved in Bulk Drugs Manufacturing

Posted 2 months ago

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Production Officer - Executive - Tablet - Capsule - Injection - Liquid Perfect Placement Bureau

4 - 9 years

5 - 12 Lacs

Vapi, Ratlam, Thane

Work from Office

Help in Day To Day Production Of Pharmaceutical Products Manpower Allocation For Smooth Working In Shift Supervision Of Production Activity BMR And BPR Report Preparation Data Preparation For Internal And External Audit -IE. US FDA - EU GMP Etc Required Candidate profile B. Pharm - M. Pharm - B.Sc - M. Sc Experience In Production Or Packaging Working Experience US FDA Approved Plant is Desirable FDA Approval in Tablet - Capsule Or Any will be an added advantage

Posted 3 months ago

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Production Officer - Executive - Tablet - Capsule - Injection - Liquid Perfect Placement Bureau

4 - 9 years

5 - 12 Lacs

Dahej, Panaji, Mumbai

Work from Office

Posted 3 months ago

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