Analytical Lab Chemist - 6 Months Temporary
- Employer
- Englewood Lab, Inc
- Location
- Totowa, NJ
- Closing date
- Nov 29, 2021
View more
- Sector
- Science, Chemistry, General Chemistry, Pharmaceutical, Laboratory
- Organization Type
- Corporate
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1. Perform material and product testing using approved Methods and Official Compendia.
2. Conduct analytical testing of raw materials, stability samples, bulk and finished products in compliance with all regulatory standards for OTC Skincare and Cosmetic products.
3. Review daily instrument calibration and verifications; and review of logbooks.
4. Review testing with other analysts and supervisor.
5. Perform calibration and system suitability using approved Methods.
6. Problem solve with colleagues regarding OOS results, discuss additional testing, operation of equipment, meeting to share ideas. CAPA responsibility.
7. Review Investigations prior to submission to Lab Manager, check calculations, possible cause with review of batch records.
8. Perform analytical testing using HPLC, GC, ICP-OES, UV-VIS, Karl Fischer, etc., (as applicable).
9. Compliance to US FDA Data Integrity requirements.
10. Assist with investigation of quality issues such Out of Specification (OOS), Out of Trends (OOT), etc.
11. Execute testing methods, protocols and other work instructions
12. Assist in managing of chemical and consumable stocks
Requirements
1. Familiarity with USP/NF Compendia, ASTM, ISO Stds
2. Familiarity with US FDA 21CFR Part 210 & 211 (Drug Product) and Cosmetic GMPs is MANDATORY.
3. Bachelors degree in Chemistry or related field.
4. Laboratory management experience preferred, with experience in Cosmetic or Pharmaceuticals desired.
5. 1+ years Quality Control Analytical Lab experience with HPLC and/or GC, ICP-OES, UV-VIS, Karl Fischer, etc.
Benefits
* Medical, dental, and vision insurance after 3 months
* Life insurance paid by the Company after 3 months
* NJ Sick Leave
2. Conduct analytical testing of raw materials, stability samples, bulk and finished products in compliance with all regulatory standards for OTC Skincare and Cosmetic products.
3. Review daily instrument calibration and verifications; and review of logbooks.
4. Review testing with other analysts and supervisor.
5. Perform calibration and system suitability using approved Methods.
6. Problem solve with colleagues regarding OOS results, discuss additional testing, operation of equipment, meeting to share ideas. CAPA responsibility.
7. Review Investigations prior to submission to Lab Manager, check calculations, possible cause with review of batch records.
8. Perform analytical testing using HPLC, GC, ICP-OES, UV-VIS, Karl Fischer, etc., (as applicable).
9. Compliance to US FDA Data Integrity requirements.
10. Assist with investigation of quality issues such Out of Specification (OOS), Out of Trends (OOT), etc.
11. Execute testing methods, protocols and other work instructions
12. Assist in managing of chemical and consumable stocks
Requirements
1. Familiarity with USP/NF Compendia, ASTM, ISO Stds
2. Familiarity with US FDA 21CFR Part 210 & 211 (Drug Product) and Cosmetic GMPs is MANDATORY.
3. Bachelors degree in Chemistry or related field.
4. Laboratory management experience preferred, with experience in Cosmetic or Pharmaceuticals desired.
5. 1+ years Quality Control Analytical Lab experience with HPLC and/or GC, ICP-OES, UV-VIS, Karl Fischer, etc.
Benefits
* Medical, dental, and vision insurance after 3 months
* Life insurance paid by the Company after 3 months
* NJ Sick Leave
You need to sign in or create an account to save a job.
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