Valeant Pharmaceuticals

Senior Quality Engineer

US-FL-Clearwater
Job ID
9506
Category
Quality
Pos. Type
Full Time

Overview

Valeant Pharmaceuticals International, Inc. is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization’s potential and what we hope it will become.

 

Provide support for Surgical development projects from project inception through successful Technology Transfer/Scale-Up at the manufacturing facility.   Additionally, the role will support marketed product changes and updates (MOB). The role includes working with multidisciplinary teams to insure medical device development activities are planned and executed in compliance with Design Control Requirements and Bausch + Lomb/Valeant procedures.   Provide Quality Assurance support to sites as needed.

 

Currently there are no direct or indirect reports associated with this position.

 

Responsibilities

Represent Design Quality on multi-disciplinary new product development and MOB teams.  Duties will include:

                          

  • Ensure project plans adequately address design, validation and Quality departmental requirements and standards.  Work with functional departments to ensure tasks are executed compliantly.  Management and documentation of Design Control activities through post launch review (approximately 1 year post launch).
  • Documentation of Risk Management requirements per ISO 14971.
  • Review/approve GMP documents (e.g. production records, analytical method validation, engineering/validation protocols/reports, specification updates (DCO’s, QCR’s)
  • Facilitate GMP production readiness and launch activities, including technology transfer and validation.
  • Support Quality System development and improvement with respect to GMP systems and development team compliance to ISO and FDA regulations.
  • Support post launch design changes and product updates as required.

 

Qualifications

  • Bachelor’s Degree (BS) in engineering or scientific discipline (Chemistry, Biology, Microbiology).
  • Five years experience in Medical Device and/or Pharmaceutical Industry in Quality, R&D, Engineering or Laboratory environment. Specific experience desired is as follows:
  • Three years developing and implementing product requirements in compliance with US federal and international regulatory standards relating to medical devices.
  • One year utilizing corrective and preventive action (CAPA) system that is in compliance with US federal and international regulatory standards relating to medical devices.
  • One year Complaint management, complaint review and corrective action.
  • One year Utilization of root cause analysis tools, including fault tree analysis, 5 Whys, Is/Is Not,
  • One year risk analysis experience.

Be Aware of Recruiting Fraud

Valeant is an EEO/AA employer M/F/D/V.

 

Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.

 

To learn more please read Valeant’s Job Offer Fraud Statement.

 

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