Temporary QA Resource
About The Position
Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies. At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitable culture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai’s portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market. Your next role as a Miracle Maker Maravai LifeSciences is seeking a #MiracleMaker to join our Quality Assurance team as a Temporary QA Resource. As a Temporary QA Resource, you will be responsible for reviewing and approving material release specifications, raw materials, intermediates and consumables in compliance with cGMP regulatory requirements and ISO standards. Provide support for other functions performed by QA operations group.
Requirements
- BS degree or equivalent in a scientific discipline preferred.
- Quality professional with 1-3 years of hands on experience.
- Knowledge and experience working in ISO9001, ISO13485 or 21CFR210/211 preferred.
- Detail oriented professional with strong verbal and written communication skills.
- Good computer skills with working knowledge of MS office suite and Adobe Acrobat.
- Self-motivated and able to organize and prioritize multiple tasks.
Responsibilities
- Responsible for conducting raw material, component, in-process inspection and release in conformance to established product requirements.
- Response for assigning lot numbers, expiration dates, logging all materials in database and labeling materials appropriately.
- Review analytical test reports, certificates of analysis/origin in support of material specification approval and release.
- Sample raw materials according to current procedures for conformity with specifications and approve or reject accordingly.
- Oversee and assist in segregating and investigating non-confirming materials as required.
- Ensure quarantined materials are labeled and segregated from incoming raw materials until disposition is approved.
- Reviews and approves product documentation for disposition of finished goods.
- Provide backup support for final product release, non-conformance reports and other QA functions as required.
- Perform other functions and duties as required
Benefits
- 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 https://www.maravai.com/careers/benefits-and-growth/
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
11-50 employees
