Job Title: Validation QE II and SR QE(Validation)
Location: San Diego, CA, USA
Duration: 12 Months
Description:
100% onsite 5 days a week
Job Summary Validation QE II and SR QE(Validation) :
As directed by the Quality Engineering Leader, the Quality Engineer II is accountable validation execution
for manufacturing equipment and support in process validation or verification studies. Successful
performance requires close work with quality management, operations, suppliers and/or BD associates
to assure compliance with all BD quality policies, procedures, and practices.
Must demonstrate a working understanding of the ISO 13485 Quality Systems Regulations on Class I/II/II
products. Preferred core experience in Quality Assurance, Quality Control, Validation (IQ,OQ,PQ) and
Nonconformance management for regulated devices (i.e.: Good Manufacturing Practices, ISO, FDA).
Proven ability to develop solutions to a variety of problems of moderate scope and complexity, using
policies and procedures for guidance.
Job Responsibilities: (Primary Duties, Roles, and/or Authorities)
Experience performing equipment and process validation studies such as writing and/or reviewing protocol, report, data analysis and deviations for new, existing and site relocation activities.
Have a working knowledge of medical device or biological equipment maintenance from Quality standpoint such as Preventive Maintenance, Calibration and Out Of Tolerance activity support to the site and equipment owners.
Author and execute installation, operational, and performance qualifications for analytical and manufacturing equipment.
Execute validation and qualification of GMP equipment and functions throughout the manufacturing facility.
Review and update FMEA or Risk documents as needed for validation activity for the site
Perform additional duties to ensure business continuity during the relocation of the manufacturing processes into new area. Duties include but not limited to execution of QA inspection to support dual operations, review and approval of documents such as batch records to support finished product release.
Education and Experience:
BS Biological Sciences, Chemistry, Bio-tech engineering, Bio-engineering or related field
Minimum of 3-5 years of experience for QE II and 5-7 years for Sr. QE in Medical Device, Biotech or
Pharma Industry.
Knowledge and Skills:
Strong verbal and written communication skills; ability to write technical documents. Knowledge of
quality system methodologies
Statistical Analysis basic knowledge e.g Minitab or Excel
Strong knowledge of Process Validation and equipment validation
Strong understanding and knowledge on ISO 9001, ISO 14971 and/or ISO 13485 (Design Control, Supplier Management and Risk Management)
Hands on experience using Six Sigma methodology
SAP knowledge
Equipment management system such as BMRAM knowledge preferred
The ability to work in teams and independently with minimal supervision to obtain results as required.
Must be self-motivated/directed, organized, detail oriented and have ability to multi-task projects.
Physical Demands: (if applicable)
General physical requirements: ability to work in controlled environmental
Ability to work with laboratory grade equipment such as refrigerators, freezers, centrifuges, etc during validation work.
Work Environment: (if applicable)
Onsite model
Ability to be present in manufacturing area as needed
