Quality Control Laboratory Professional Jobs

Proven leadership capabilities and experience applying GMP requirements in a Quality Control setting.

Responsible for activities including analytical testing, data management and trend analysis, laboratory investigations, and change control in a dynamic team environment.

Collaborate cross functionally as needed to ensure the Quality Management System processes are implemented in accordance with established procedures.

Support internal/external audits and inspections as part of the audit/inspection management team.

Strong knowledge and understanding of GMP pharmaceutical production and associated testing methods experience.

Knowledge and experience with Quality Control testing and GMP laboratory operations for common pharmacopeia testing methods and associated equipment.

General Natural Resources Management And Biological Sciences

Department of Health and Human Services

Centers for Disease Control and Prevention

Center for Preparedness and Response

8/10/2023 4:57:58 PM to 8/16/2023 11:59:59 PM

CDC HELPDESK 1600 Clifton Road NE Atlanta GA US 30333

Project management experience is preferred.

Benefits on offer for this contract position:

2+ years of QC laboratory experience

Truvault, TrackWise, eLIMS experience preferred.

Write and edit detailed SOPs, validation protocols/reports, forms, analytical and technical documents and reports from conception to utilization.

MS Office Application (Word, Excel, Powerpoint) required.

Management Experience: 1 year of lead or supervisory experience.

Experience: Minimum 3 years of related experience or equivalent combination of education and related experience required.

Ensure monthly product QC requirements are met, and that accurate electronic and physical inventories for products are maintained.

MT (ASCP) certifications or equivalent certifications where required.

Knowledge of blood products and supplies is preferred

Ensure compliance with state and federal regulations, and regional policies and procedures.

Drafting equipment and method validation documents, management of the site Stability Program.

Applicant must have High School Diploma (or Equivalent) with 6 years of relevant experience

OR an Associate's degree with 4 years of experience

OR a Bachelor's degree with 0+ years of experience.

Demonstrated technical skills in method validation and testing.

Knowledge of Good Manufacturing Practices and its application standards, processes and policies.