Overview
QAIT Quality Specialist/View Pharma OR Biotech industry Jobs in New York, New York, USA at LS Solutions
Position: QAIT Quality Specialist (Global View) & (Pharma OR Biotech industry Required)
Location: New York
QAIT Quality Specialist (Global View)
Job Title: QAIT Quality Specialist (Global View)
Contract Duration: 6+ Months
Summary:
The Consultant – QAIT Quality (Consultant) specialist will provide guidance to support IT Quality and Data Integrity programs in the organization. The Consultant will serve as SME by supporting investigations, risk assessments, and IT Operations while verifying that GxP computerized systems operate as expected post-validation. This role requires interactions with personnel at all levels across multiple functional areas to ensure timely completion of Quality Assurance responsibilities.
Job Responsibilities include, but are not limited to:
Engage with both Corporate IT and IOPS IT to ensure IT processes and procedures meet Quality System requirements.
Participate and support the Quality Risk Management (QRM) principles in the formal and informal risk assessment initiatives.
Provide support and guidance with quality system records activities such as change controls, corrective and prevention action plans (CAPAs), risk assessments, data integrity initiatives, deviations, internal and external audits, standard operating procedures (SOPs), work instructions/job aids, policies, etc.
Provide ongoing support to the Quality Auditing function with respect to IT vendors and audits.
Support the development, review, and approval of Quality Assurance Agreements (QAA), along with the Approved Supplier List (ASL) process.
Collaborate with other functional areas to collect information and provide guidance through all stages of the quality management system and improvement projects.
Ensure new systems/processes/procedures are compliant with SOPs, WIs, and data and regulatory guidelines for IT and Software validation process.
Assist in the resolution of inspection management concerns as they relate to software applications, processes, procedures, and data integrity.
Experience:
7+ years of experience in IT, Computer Science, Engineering, or Chemistry in an FDA regulated manufacturing environment.
Thorough understanding of IT CSV and QAIT roles and responsibilities in support of GxP compliance is required.
Experience working in an FDA regulated environment with a strong emphasis on a risk-based approach to validation/qualification.
Strong knowledge of FDA CFRs, Eudralex, and other biotech/pharma industry regulations (pertaining to IT, laboratory systems, automation, and manufacturing).
Strong knowledge of Data Integrity, System Development Life Cycle (SDLC) validation methodology, and Software Quality requirements.
Understanding of root cause analysis and risk management techniques.
Experience with quality management systems including change control, incident management, and deviation management.
Strong Project Management experience leading efforts requiring coordination between cross-functional teams within at least one area of systems validation – e.g., laboratory equipment, facilities, utilities, manufacturing equipment, information systems, etc.
Continuously drive to improve processes for improved performance.
Excellent technical writing and communication skills.
Excellent analytical and problem-solving skills.
Seniority Level: Mid-Senior level
Employment Type: Contract
Job Function: Science, Analyst, and Manufacturing
Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
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Title: QAIT Quality Specialist/View Pharma OR Biotech industry
Company: LS Solutions
Location: New York, New York, USA
Category: Quality Assurance – QA/QC (Data Analyst)
