QA Specialist - Document Management - Site based Seattle WA
QA Specialist - Document Management - Site based Seattle WA
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Job Description
Position
This role is responsible for the of daytoday QA responsibilities for GMP manufacturing along with building and enhancing the quality assurance systems. The role incumbent works both independently and collaboratively with Manufacturing Quality and Facilities staff to ensure compliance with cGMPs and internal procedures. The responsibilities of the employee is based on the assigned QA organization as outlined below.
Document Management
Issue production batch records and labels to support manufacturing operations.
Serve as primary point of contact for site functional areas regarding documents and label controls.
Responsible for issuance of final product labels batch record and other controlled documentation.
Support the development and deployment of document control tools.
Responsible for the management of document control room at site and archival of documentation.
Execute the scanning and true copies process for the production batch records.
Support internal and external client audits and regulatory inspections including but not limited to SME for document control and document retrieval.
Perform routine and ad hoc labeling and issuance metric reporting and analysis for the local site data.
Qualifications:
Bachelors degree in biological or engineering science& Minimum of 3 years relevant experience in a biopharmaceutical/Pharmaceutical cGMP manufacturing or similar environment OR Associates degree and 5 years of relevant quality experience OR High school diploma / GED and 7 years of relevantquality experience.
Ability to collaborate and communicate crossfunctionally.
Proven attention to detail
This job description is intended to describe the general content of the job and to identify the essential functions of and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties responsibilities or requirements. Because job requirements evolve with the changing needs of JustEvotec Biologics business this description is subject to change and may be modified at any time whether formally or informally.
The base pay range for this position at commencement of employment is expected to be $83000 to $86250; Base salary offered may vary depending on the individuals skills experience and competitive market value. Additional total rewards include discretionary annual bonus comprehensive benefits to include Medical Dental and Vision shortterm and longterm disability company paid basic life insurance 401k company match flexible work generous paid time off and paid holiday wellness and transportation benefits.
Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race gender age disability genetic information gender expression gender identity national origin religion sexual orientation or veteran status.
Required Experience:
Unclear Seniority
Employment Type
Full-Time
