Sr. Director, Gmp Quality Assurance Operations
By Moderna At Norwood, MA, United States
Family care benefits, including subsidized back-up care options and on-demand tutoring
Generous Paid Leave offerings, including 18 weeks of 100% paid parental leave for all new parents
Moderna-paid Life, LTD and STD insurance coverages, as well as voluntary benefit options
Ensure the quality policy and objectives are understood, implemented, and maintained at all levels of the organization.
Develop short and long-term plans to achieve both quality and business objectives.
Provide guidance, support and oversees all activities related to batch record review and product disposition for internal Manufacturing at Moderna Inc.
Quality Assurance Specialist - Gmp
By Integrated Resources, Inc ( IRI ) At San Diego, CA, United States
Strong interpersonal skills, time management, and organizational skills
Strong Document Control skills and knowledge
May include other duties as defined by the Document Control department management.
Bachelors degree, equivalent college courses or equivalent experience
Years (3+) of related work experience preferred
Experience using Oracle Agile PLM software preferred
Gmp, Quality Assurance Associate Ii
By Duke University At , Durham, 27710, Nc
Demonstrate leadership, organizational, and time management skills and the ability to handle a multitude of tasks.
With minimal oversight by management or independently
OR ANY OTHER EQUIVALENT COMBINATION OF RELEVANT EDUCATION AND/OR EXPERIENCE
5 years of experience in a GXMP or similar regulated environment.
Experience training users on implementing Quality Systems.
Experience in preparing for external audits and/or site visits.
Gene Therapy Quality Control Lab Aid/ Gmp Contractor
By Sarepta Therapeutics At , Andover, 01810, Ma
Working experience in a cGMP environment is preferred.
Experience in general laboratory experimentation, documentation with adherence to cGMP is necessary.
Must have effective written and verbal communication skills.
Monitor, compile, and review analytical and QC data individually and with team members.
Assist broader Analytical Development/Quality Control team with coordination of sample pulls, set downs, and tracking critical reagents.
Create and maintain clear, concise records and documentation.