Chemical analystGrowrich Manufacturing Inc
Salary: Agreement
Work form: Full time
Posting Date: 21/09/2025
Deadline: 20/10/2025
JOB DESCRIPTION
1. Develops and validates methods for testing of batches for manufactured products.
2. Develops and validates methods for new or existing bespoke products on the stability program.
3. Prepares analytical method development, validation and test reports.
4. Writes/Reviews of specification. Supports on all analytical activities.
6. Participates in self-inspection and regulatory inspections.
7. Prepares quality reports and submit to immediate superior
8. Performs the daily operations of the Stability Program.
9. Performs responsibilities for the organization, maintenance, operation, and date review required for the Drug Stability Program which is utilized for the evaluation of the stability of pharmaceutical drug products.
15. Develops and maintain the stability protocols for all products according to FDA guidelines and approved submissions/commitments.
16. Assures that all stability samples have been properly placed on stability at the correct stability conditions.
17. Follows the requirements of the Stability Protocols and helps maintain all required timelines (sample maintenance and documentation of test results)
18. Maintain stability documentation and stability chambers as required.
19. Interacts with the QC and RAD as well as with the appropriate Quality Assurance, Technical Operations and Regulatory areas.
20. Interacts with members and development teams, bringing the Stability perspective to bear on planned activities including study scheduling versus other studies planned within the function.
21. Tracks effectively stability data and perform trend analysis of this data.
22. Review analytical data to recognize potential trends and alert.
23. Maintain the activities of the Stability Area in compliance with cGMPs, SOPs, good documentation practices and safety standards I accordance with corporate, regulatory and timeline expectations.
24. Maintains productive communications with co-workers and internal colleagues in Quality Control, Quality Assurance, RAD Assurance, RAD, Technical Operations and Regulatory Affairs.
JOB QUALIFICATION
College graduate or equivalent
OTHER JOB REQUIREMENTS
Education
Bachelor's/College Degree
Field of study
Chemistry
Specialization
Chemistry
Chemistry, chemical, chemistry
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1. Develops and validates methods for testing of batches for manufactured products.
2. Develops and validates methods for new or existing bespoke products on the stability program.
3. Prepares analytical method development, validation and test reports.
4. Writes/Reviews of specification. Supports on all analytical activities.
6. Participates in self-inspection and regulatory inspections.
7. Prepares quality reports and submit to immediate superior
8. Performs the daily operations of the Stability Program.
9. Performs responsibilities for the organization, maintenance, operation, and date review required for the Drug Stability Program which is utilized for the evaluation of the stability of pharmaceutical drug products.
15. Develops and maintain the stability protocols for all products according to FDA guidelines and approved submissions/commitments.
16. Assures that all stability samples have been properly placed on stability at the correct stability conditions.
17. Follows the requirements of the Stability Protocols and helps maintain all required timelines (sample maintenance and documentation of test results)
18. Maintain stability documentation and stability chambers as required.
19. Interacts with the QC and RAD as well as with the appropriate Quality Assurance, Technical Operations and Regulatory areas.
20. Interacts with members and development teams, bringing the Stability perspective to bear on planned activities including study scheduling versus other studies planned within the function.
21. Tracks effectively stability data and perform trend analysis of this data.
22. Review analytical data to recognize potential trends and alert.
23. Maintain the activities of the Stability Area in compliance with cGMPs, SOPs, good documentation practices and safety standards I accordance with corporate, regulatory and timeline expectations.
24. Maintains productive communications with co-workers and internal colleagues in Quality Control, Quality Assurance, RAD Assurance, RAD, Technical Operations and Regulatory Affairs.
JOB QUALIFICATION
College graduate or equivalent
OTHER JOB REQUIREMENTS
Education
Bachelor's/College Degree
Field of study
Chemistry
Specialization
Chemistry
Chemistry, chemical, chemistry
=timeAgo('2022-07-02 11:26:45');?>
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Growrich Manufacturing Inc
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Growrich Manufacturing Inc jobs
Lot. 10, Blk. 29, Alibangbang St. Brgy. 179, Zone 16, Amparo Village, Caloocan City
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About the company
Growrich Manufacturing Inc jobs
Lot. 10, Blk. 29, Alibangbang St. Brgy. 179, Zone 16, Amparo Village, Caloocan City