QA Lead Technical Operations
QA Lead Technical Operations
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
- Provides Quality Assurance (QA) support to Devens Site and reporting Manger through quality review and approval of Investigations and Corrective Actions.
- Decision making of non-conformance through a deep understanding of Quality Systems Regulatory expectations.
- Reviews and approves Quality Quality Control Validation and Automation related documents.
- Review and approves Standard Operating Procedures (SOPs).
- Review and approval of Validation related documentation such as risk assessments protocols and test scripts and summary reports.
- Review and approval of change proposals as well as associated deliverables ensuring the change deliverables meet external regulatory and internal WWQC guidelines and requirements.
- Ability to coach across different departments within the subject matter of Investigations CAPAs general risk assessments and Validation.
- Ability to self-manage and prioritize work across multiple competing deliverables in a remote working environment.
- Able to interpret complicated data and make sound decisions independently.
- Knowledge of science generally attained through studies resulting in a B.S; in biological science Engineering biochemistry or related discipline or its equivalent is preferred.
- Advanced Level of relevant experience in a GMP GCP or GXP with at least 8 years focused on product quality. Preferred Active member of ASQ or ISPE.
- Prior experience of QC equipment Qualification and some project management experience.
- Knowledge of biotech bulk drug substance or finished product manufacturing medical device analytical testing is highly desirable.
- Extensive knowledge of US and EU cGMP regulations and guidance and GAMP 5.
- Knowledge of electronic systems including any of the following: SAP LIMS Track Wise Veeva Vault and electronic or paper-based batch records desirable.
- Excellent Technical writing and oral communication skills are required.
- Background in problem solving.
- Knowledge of Data integrity principles.
- Proven attention to details.
- Comfortable working in an FDA regulated environment.
- Quality Control Equipment experience preferred.
- Technical Writer.
- Investigations/Deviation experience preferred.
Employment Type
Full Time
