What are the responsibilities and job description for the Senior Peer Reviewer position at Amneal Pharmaceuticals?
Job Description
Description:
Peer Reviewer III is responsible for reviewing and approving data that is generated by the laboratory to ensure accuracy and compliance with procedures and cGMP requirements. Complete audit tasks withing specified time frame without compromising quality of audit. Continuously improve the documentation system to increase efficiency and GLP compliance. Report all audit findings in audit reports and highlights as well as report any critical deficiencies.
Essential Functions:
Education:
Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at accommodations@amneal.com . Requests will be handled confidentially and in accordance with applicable laws.
Description:
Peer Reviewer III is responsible for reviewing and approving data that is generated by the laboratory to ensure accuracy and compliance with procedures and cGMP requirements. Complete audit tasks withing specified time frame without compromising quality of audit. Continuously improve the documentation system to increase efficiency and GLP compliance. Report all audit findings in audit reports and highlights as well as report any critical deficiencies.
Essential Functions:
- Review laboratory testing records with respect to written procedures/specifications, SOPS, and company policies.
- Review laboratory instrument calibration/qualification records, standard qualification records and records associated with investigations
- Review Raw-material, Excipients, Finished Product for data integrity, compliance with Specifications, Methods and USP monographs as applicable
- Review Analytical Method Validation/Verification data for compliance with Protocols and ICH guidelines
- Review stability data to identify any trends, alert limits and OOS
- Participation in audit of laboratory activities to determine improvement needs for maintenance of cGMP compliance
- Prepare for Pre-Approval Audits for Filed ANDAs
- Perform other duties as assigned.
Education:
- Bachelors Degree (BA/BS) - Required
- 6 years or more in scientist or group leader in pharmaceutical lab
Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at accommodations@amneal.com . Requests will be handled confidentially and in accordance with applicable laws.