Sunrise Systems
QA Lead Technical Operations, Projects
Sunrise Systems, Devens, Massachusetts, us, 01434
Job Title: QA Lead Technical Operations, Projects
Job ID:
24-02756
location: Devens, MA
Duration: 03 Months contract on W2
Job Description/ Responsibilities: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 expectationsReviews and approves Quality, Quality Control, Validation and Automation related documentsReview 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 environmentAble to interpret complicated data and make sound decisions, Independently
This position will regularly interact with:
Reporting Manager
Sometimes will interact with departments listed below:
Quality ControlManufacturing OperationsManufacturing EngineeringManufacturing Science and Technology (MS&T)ValidationSite EngineeringDigital Plant
Education, Experience, and Qualifications:
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 experienceKnowledge 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, TrackWise, Veeva Vault and electronic or paper based batch records desirable.Excellent Technical writing and oral communication skills are required.Background in problem solvingKnowledge of Data integrity principlesProven attention to detailsComfortable working in an FDA regulated environment.
Contractor must be able to come onsite Monday through Friday - 1st shift
Job ID:
24-02756
location: Devens, MA
Duration: 03 Months contract on W2
Job Description/ Responsibilities: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 expectationsReviews and approves Quality, Quality Control, Validation and Automation related documentsReview 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 environmentAble to interpret complicated data and make sound decisions, Independently
This position will regularly interact with:
Reporting Manager
Sometimes will interact with departments listed below:
Quality ControlManufacturing OperationsManufacturing EngineeringManufacturing Science and Technology (MS&T)ValidationSite EngineeringDigital Plant
Education, Experience, and Qualifications:
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 experienceKnowledge 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, TrackWise, Veeva Vault and electronic or paper based batch records desirable.Excellent Technical writing and oral communication skills are required.Background in problem solvingKnowledge of Data integrity principlesProven attention to detailsComfortable working in an FDA regulated environment.
Contractor must be able to come onsite Monday through Friday - 1st shift