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Please Contact: To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Priyanka Mahant at email address Priyanka.mahant can be reached on # .
We have Contract role Validation Engineer for our client at San Diego, CA. Please let me know if you or any of your friends would be interested in this position.
Position Details:
Validation Engineer - San Diego, CA
Location : San Diego, CA 92121 (On-site)
Project Duration: 06 Months of contract
Shift : 8:00 AM - 5:00 PM (Mon-Fri)
Payrate : $37.00/hour on W2
Job Summary:
Please Contact: To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Priyanka Mahant at email address Priyanka.mahant can be reached on # .
We have Contract role Validation Engineer for our client at San Diego, CA. Please let me know if you or any of your friends would be interested in this position.
Position Details:
Validation Engineer - San Diego, CA
Location : San Diego, CA 92121 (On-site)
Project Duration: 06 Months of contract
Shift : 8:00 AM - 5:00 PM (Mon-Fri)
Payrate : $37.00/hour on W2
Job Summary:
- Abbott Rapid Diagnostics (formerly Alere) is part of Abbott s Diagnostics family of businesses, bringing together exceptional teams of experts and industry-leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions. At Abbott, diverse ideas, perspectives, and expertise allow us to create life-changing solutions that help people live healthier lives. In 150 countries and with businesses spanning nutrition, diagnostics, medical devices, and branded generic pharmaceuticals, Abbott offers you enormous opportunities to explore your interests and help you achieve your career and personal goals.
- Abbott is looking for an outstanding Validation Engineer-Contractor who will effectively lead quality related validation activities to support the Quality Management System. The end goal is to deliver consistent and high-quality validation and supporting documentation for design and development organization. This role requires strong technical, communication, interpersonal and organizational skills, and a solid understanding of the application of FDA, ISO 13485, ISO 14971 standards and company strategies.
- This opportunity is available with Infectious Disease Developed Markets (IDDM) Business unit within Abbott, at our location in Towne Centre San Diego, CA.
- This job description will be reviewed periodically and is subject to change by management.
- Write procedures, investigations, protocols, deviations, CAPA s, reports, change controls, etc. to support ARDx Towne Centre site departments.
- Perform and document investigations related to validation activities and performs risk assessments of equipment, processes and systems to determine the scope of validation efforts.
- Generates validation documentation as required (URS, FRS, DRS, FAT, DQ, engineering studies, IOQ, PQ, PV) for cleaning, shipping, sterilization, facilities,
- utilities, systems, equipment qualification/requalification, computer system validation, spreadsheets, test method validation and process validation.
- Writes and/or revises IQ, OQ, PQ related documents, including any or all of the following: SOP s, validation master plans, guidelines and execution plans, automation test plans and technical documents.
- Responsible for writing Standard Operating Procedures related to Validations and responsible for training Quality Assurance and R&D personal in the validation processes.
- Performs on site or support work, including but not limited to:
- Validation protocol executions for FAT/SAT/IQ/OQ/PQ/PV.
- Equipment Qualification test execution.
- Investigations and deviations.
- Provides gap analysis, risk management, risk assessment, risk analysis and validation strategy.
- Data integrity assessments and review of client data
- Executes protocols and resolves deviations/discrepancies, analyzes data and writes reports.
- Performing and supervising thermal mapping of temperature-controlled units, Laboratories, warehouses, etc.
- Ensures that validations are documented using Good Documentation Practices and are in compliance to FDA, ISO 13485, and Abbott Policies and Procedures.
- Evaluate impact on legacy qualifications/validations and determines the scope of re-validation.
- Support the continuous improvement to the Quality Management System, with a specialty focus on validation processes.
- Responsible for maintaining a Site Master Validation Plan and ensuring that critical Performance Qualification and/or Process Validations are performed per established schedule.
- Identify and propose remediation for existing and potential validation issues; provide technical expertise and provide solutions to maintain compliance.
- Assist with internal and external audits.
- Manages validation metrics.
- Manages change control for validation deliverables in the electronic documentation management system.
- Participate in multiple, concurrent projects.
- Develops timelines and tracks project status on assigned projects.
- Keeps stakeholders informed on the status of important projects.
- Performs other duties as assigned by Management.
- Bachelors degree (B.S.) in a Science related field (Engineering, Biology, Chemistry or equivalent)
- 5+ years of related work experience in a medical device industry with strong technical competency in performing equipment qualification (IQ/OQ/PQ), facility/lab qualification, process validations and excel spreadsheet validations.
- Proficient understanding of Design Control, Good Documentation Practices (GDP), and current Good Manufacturing Practices (cGMP)
- Significant experience with application of the FDA regulations and recognized standards (e.g., FDA 21 CFR 820.30, FDA 21 CFR 820.70, FDA 21 CFR Part 11, ISO 13485, ISO 14971, cybersecurity)
- Experience in validation of In Vitro Diagnostic Lab equipment (e.g., Real- Time PCR System, Freezers, Refrigerators, Environmental Chambers, Incubators) and Thermal Mapping, Computerized System Validation.
- Experience supporting ISO 13485 inspections and FDA inspections.
- Experience in a multi-site development environment.
- Experience in compliance management within a rapid-growth, dynamic organization.
- Statistical or Lean Six Sigma background
- Working experience with GAMP5 and FDA s Computer Software Assurance initiatives
- Working experience with Agile, Maximo and View Linc.
- Good working knowledge of Excel and MS Word software
- Working knowledge of quality techniques such as root cause analysis, 5 why s, and Ishikawa diagrams.
- Excellent problem solving and decision-making skills.
- Self-starting, detail oriented, and ability to focus on task at hand
- Initiative to work towards goals with minimal supervision
- Ability to work independently with multiple departments to resolve Validation issues
- Must be able to work effectively in a fast paced, cross-functional team-oriented environment
- Well-developed English written and verbal communication skills
About the company
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