Job Details

ID #45578596
State California
City Southsanfrancisco
Job type Contract
Salary USD $60 - $90 60 - 90
Source DGN Technologies
Showed 2022-09-10
Date 2022-09-01
Deadline 2022-10-31
Category Et cetera
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BSA/Sr BSA - Compliance Specialist

California, Southsanfrancisco, 94080 Southsanfrancisco USA

Vacancy expired!

Job Title: Business Systems AnalystEmployment Type: Contract 6 months

Location: South San Francisco, CA (hybrid)

Candidate will be required to work onsite in South San Francisco 2-3 days per week

Top Skills:1) Strong Business Systems Analyst and communication skills2) Expert-level knowledge of GDPR, CCPA, HIPAA, SaMD, 21 CFR part 11, Article 11 etc3) Ability to manage the compliance documentation processes and systems with limited supervision

The Position:Are you a strong Business Systems Analyst with demonstrated experience on multiple projects who is looking for a creative, challenging and fun work environment and an opportunity to expand your skills? Then PHC is looking for you!

Your specific responsibilities will include:Concurrently manage multiple projects of diverse scope across functional areasManage and deliver projects using agile and waterfall methodologiesManage project budgets, scheduling, planning and contractor resource assignment and track vendor and consultant performance including billing against budget and contractCollaborate with Product Managers, Architects, Engineers, Developers, and User Experience Designers on scope, solutions, constraints, and risks.Manage compliance documentation processes and systems for PHC and business partnersCharacterize for compliance purposes as-built and vendor provided business solutions that may involve automated systems and/or modifications to business processes.Provide expertise in documenting the deployment of systems and/or processes.Perform a key role – as part of a project team in delivery of solutions that are cost effective, sustainable, and meet business requirements.Be accountable for documentation, which may include, but is not limited to:System Risk AssessmentsData Classification ReportsUser RequirementsValidation PlansValidation ReportsValidation RegistriesRequirements Traceability MatricesTest PlansTest ReportsFunctional and/or technical specificationsData and process flow diagramsTraining documentation and/or work instructionsOther Computer System Validation documents and related systemsDepending on the application configure system settings and/or options.Provide consultation to customers regarding enhancement/improvement of current solutions and implementation of new solutions – both systems and processes.Facilitate and/or support customers in UAT planning and execution.Participate in and advise roadmap discussions; be a key member of vendor assessment teams.Drive resolution of business or systems issues.Be a trusted partner for the Global Privacy Office, IT Security, and Business Quality teamsMaintain an expert-level knowledge of the dynamic health authority governance; inclusive of GDPR, CCPA, HIPAA, SaMD, 21 CFR part 11, Article 11.

Experience Profile:BA or BS in life science, informatics, business, or equivalent. MA or MS and post-graduate coursework are desirable.At least 10 years of related experience, domain knowledge of the pharmaceutical industry and manufacturing/quality assurance processes and systems, computer systems validation, GxP, FDA 21 CFR part 11, HIPAA, SaMD & ISO 13485, Data PrivacyExperience and understanding of application development methodology - including Agile and Waterfall approaches, functional requirements, process modeling and re-engineering, use case development, user acceptance testing, organizational change management, and large-scale system implementations.Excellent written and verbal communication skills; able to quickly produce clearly written, well-organized documentation; excellent presentation and meeting facilitation skills.Proven skills in relationship building, customer-focus, decision-making, and problem solving.Demonstrated ability to quickly learn the business in unfamiliar areas.Experience with and understanding of any of the following areas a plus:Pharmaceutical/Biotech Good Clinical Practice (Google Cloud Platform) environmentBusiness processes around financial controls and portfolio management of large scale engineering capital projectsComputer systems validation

Vacancy expired!

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