Maravai LifeSciences
Document Control Associate I
Maravai LifeSciences, San Diego, California, United States, 92189
Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within nucleic acid production and biologics safety testing to many of the world\'s leading biopharma, vaccine, diagnostics, and cell and gene therapy companies.
About the role
Maravai LifeSciences is seeking a
#MiracleMaker
to join our document control team as a
Document Control Associate I . The Document Control Associate I is responsible for maintaining the document and record control systems and ensuring they meet Quality Management System (QMS) requirements. This position coordinates the issuance, revision, review, and approval of SOPs and other documents. How you will make an impact
Issue document change order numbers, route and track new and revised documents for approval, file controlled documents and other documentation provided to QA, and ensure that all documentation follows the change control procedures Review documents for completeness, adherence to company guidelines on formatting, and authorization for approvals Monitor status of in-process document changes to ensure timely completion Organize filing systems for electronic and paper based GMP/research documents Support the establishment and improvement of quality systems Facilitate continuous improvements efforts of quality systems Assist in quality audits, including document preparation and record retrieval Update and maintain quality metrics as needed Support after hours and weekends as needed Perform other functions and duties as required The skills and experience that you will bring
BS Degree in scientific area preferred Minimum of 1-2 years hands-on experience with document control management, preferably in a life science industry Experience with ISO 9001, ISO 13485, 21CFR820, 21CFR 211, or other regulated industry a plus Experience with MasterControl or other document management system a plus but not required Demonstrated ability to work independently and as part of a team Good writing skills, high degree of organization and excellent attention to detail Good computer skills with working knowledge of MS office suite and Adobe Acrobat Must be able to support after hours and weekend as needed Self motivated and able to organize and prioritize multiple tasks Salary information
The anticipated salary range for this position is $27.87 - $32.63 per hour. The salary offer will depend on multiple factors which may include the successful candidate\'s skills, experience and other qualifications, as well as the location of the role. The benefits of being a #MiracleMaker
You have the potential to change, improve, and save lives around the world. You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans. We offer comprehensive medical plans and HSA/FSA options. Fertility & family planning assistance. A variety of additional optional benefits and insurance options, including pet insurance. Retirement contributions. Holidays & Paid Time Off. Benefits may vary by region and employment type and do not apply to temporary employees or contractors. See a comprehensive list of benefits at our Benefits & growth site at Maravai.com/careers/benefits-and-growth/ Equal opportunity
Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
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Maravai LifeSciences is seeking a
#MiracleMaker
to join our document control team as a
Document Control Associate I . The Document Control Associate I is responsible for maintaining the document and record control systems and ensuring they meet Quality Management System (QMS) requirements. This position coordinates the issuance, revision, review, and approval of SOPs and other documents. How you will make an impact
Issue document change order numbers, route and track new and revised documents for approval, file controlled documents and other documentation provided to QA, and ensure that all documentation follows the change control procedures Review documents for completeness, adherence to company guidelines on formatting, and authorization for approvals Monitor status of in-process document changes to ensure timely completion Organize filing systems for electronic and paper based GMP/research documents Support the establishment and improvement of quality systems Facilitate continuous improvements efforts of quality systems Assist in quality audits, including document preparation and record retrieval Update and maintain quality metrics as needed Support after hours and weekends as needed Perform other functions and duties as required The skills and experience that you will bring
BS Degree in scientific area preferred Minimum of 1-2 years hands-on experience with document control management, preferably in a life science industry Experience with ISO 9001, ISO 13485, 21CFR820, 21CFR 211, or other regulated industry a plus Experience with MasterControl or other document management system a plus but not required Demonstrated ability to work independently and as part of a team Good writing skills, high degree of organization and excellent attention to detail Good computer skills with working knowledge of MS office suite and Adobe Acrobat Must be able to support after hours and weekend as needed Self motivated and able to organize and prioritize multiple tasks Salary information
The anticipated salary range for this position is $27.87 - $32.63 per hour. The salary offer will depend on multiple factors which may include the successful candidate\'s skills, experience and other qualifications, as well as the location of the role. The benefits of being a #MiracleMaker
You have the potential to change, improve, and save lives around the world. You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans. We offer comprehensive medical plans and HSA/FSA options. Fertility & family planning assistance. A variety of additional optional benefits and insurance options, including pet insurance. Retirement contributions. Holidays & Paid Time Off. Benefits may vary by region and employment type and do not apply to temporary employees or contractors. See a comprehensive list of benefits at our Benefits & growth site at Maravai.com/careers/benefits-and-growth/ Equal opportunity
Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
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