Sterilization Quality Technician II - Shift A - Coyol

at  Boston Scientific Corporation

Cross River, Cross River, Nigeria -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate28 Nov, 2024Not Specified30 Aug, 20243 year(s) or aboveTechnology,Maintenance,It,Microsoft Office,Shipping,B1,Mes,Availability,Sap,Operations,ManufacturingNoNo
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Description:

MINIMUM QUALIFICATIONS:

  • High School bachelor’s degree (minimum requirement).
  • Technical level requirement: Quality, production or 50% related field.
  • At least 3 years of experience in similar positions.
  • English Level (60-70%) B1

DESIRABLE REQUIREMENTS:

  • Microsoft Office basic knowledge
  • Knowledge in MES and SAP.
  • Good communications skills
  • Proactive
  • Atention to detail
  • Collaborative
  • Valid passport
  • Valid American Visa
  • Availability to travel
    Requisition ID: 589214
    As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.
    So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!
    Job Segment: QA, Quality Assurance, Shipping and Receiving, Facilities, Maintenance, Quality, Technology, Operations, Manufacturin

Responsabilities:

  • Perform the review and approval of all BSC sterilization batch records to assure that all processing parameters have been met according to Boston Scientifics Specifications. Assist in the maintenance of Boston Scientific policies and procedures as they pertain to sterilization and batch approval.
  • Perform the review and approval of operating logs and charts (preconditioning, aeration, SCBI incubation, BI storage & shipping and receiving).
  • Identify quality issues and interface with plant representatives. Executes the disposition of nonconforming loads through approved nonconformance reports.
  • Identify best quality practices and areas for improvement and participate in continual improvement projects across facility.
  • Contributes to maintaining a safe and clean working environment by performing routine area housekeeping and reporting any unsafe conditions.
  • Initiate non-conforming reports and corrective action requests (if applicable) for all cycle non-conformances.
  • Perform other duties as required. Perform tasks not listed in this job description per guidance from Quality Assurance Manager or Corporate management

Responsibilities:

To perform quality assurance activities to assure all BSC processing requirements are met prior to QA approval for all products processed at BSC Coyol. Assists the Quality Assurance Manager to assure that BSC requirements are met according to documented and communicated policies and procedures. Supports BSC Coyol quality initiatives and commitment to improving the quality of patient care and all things Boston Scientific.

Responsabilities:

  • Perform the review and approval of all BSC sterilization batch records to assure that all processing parameters have been met according to Boston Scientifics Specifications. Assist in the maintenance of Boston Scientific policies and procedures as they pertain to sterilization and batch approval.
  • Perform the review and approval of operating logs and charts (preconditioning, aeration, SCBI incubation, BI storage & shipping and receiving).
  • Identify quality issues and interface with plant representatives. Executes the disposition of nonconforming loads through approved nonconformance reports.
  • Identify best quality practices and areas for improvement and participate in continual improvement projects across facility.
  • Contributes to maintaining a safe and clean working environment by performing routine area housekeeping and reporting any unsafe conditions.
  • Initiate non-conforming reports and corrective action requests (if applicable) for all cycle non-conformances.
  • Perform other duties as required. Perform tasks not listed in this job description per guidance from Quality Assurance Manager or Corporate management.


REQUIREMENT SUMMARY

Min:3.0Max:8.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Diploma

Proficient

1

Cross River, Nigeria