Qc Administrator - Burnaby, Canada - Evonik

Evonik
Evonik
Verified Company
Burnaby, Canada

1 month ago

Sophia Lee

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Sophia Lee

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Description

EVONIK Vancouver Laboratories (VAN), the operating drug delivery service site of Evonik Canada Inc., is a Contract Development and Manufacturing Organization (CDMO) that provides CMC services to biotechnology and pharmaceutical companies engaged in the development and manufacture of complex delivery-based drug formulations.

EVONIK has a successful track record of helping Customers move their programs forward. Evonik's Vancouver business operations is a development partner to the world's pharmaceutical companies for parenteral lipid nanoparticle drug products.

As an enabling contract development manufacturing organization (CDMO) partner, we offer drug formulation design, process development, scale-up, and clinical production.


EVONIK's range of services extends from initial formulation prototype identification, manufacturing process development & scale-up, analytical method development & validation to support raw material, in-process, release and stability testing, all the way through to sterile product manufacturing under GMP for Phase I-II clinical trials.

Products include the LIPEX line of Extruders, which are designed to enable small-scale to commercial scale manufacturing of liposomal drug products.

With over 25 years of experience and having transacted business in about 50 different countries,

WHY EVONIK?


Evonik offers excellent benefits such as competitive compensation, benefit & pension plans, vacation and time off, and many wellness resources.

And there is to a Comprehensive Health Promotion program and Regional and Global resources for ongoing training and development.

Best of all, you will work within a great team of professionals in an engaging workforce who value trust and openness.

Are you looking to join a dynamic company with an exciting and expanding future in the pharmaceutical industry? Then Evonik is the next step in your career.

Grow with us

Click here to learn more from our Vancouver Laboratories employees:
WHY VANCOUVER?

Vancouver has something for everyone British Columbia is beautiful and exciting. From the people, to the mountains, to the sprawling coastline, everywhere you look. Nestled on the warm Pacific Coast with the Rockies blocking cold arctic winds. Vancouver has the good fortune of being spared the typically chilly winters associated with Canada.

Vancouver is often called 'two cities in one' because people are equally prone to enjoy the bustling nightlife and experiencing a plethora of activities in the surrounding nature.

Imagine enjoying a day-long trek through our world-renowned rain forests, then heading into the city for a night out. Vancouver truly is as beautiful as people say and more.

What we offer

You will work on exciting and challenging topics together with a team in an ultra-modern, innovative and creative environment. Intensive on-the-job training with expert colleagues guarantees you will quickly become familiar with your duties and perform them independently. Performance related pay and the opportunity for personal and professional development are of course part of the package. Since 2009 Evonik Industries AG has been certified as a family-friendly company by the German Hertie Foundation.

Click on the link to learn more about Evonik from our employees:

RESPONSIBILITIES

  • Lead a team of QC personnel to proactively collaborate with stakeholders of various functional groups to prioritize the work for QC to meet the business needs to achieve the bestinclass operation for a Contract Development and Manufacturing Organization (CDMO)
  • Be the change agent to proactively influence and motivate the QC organization to optimize the planning and operational activities
  • Act as a QC representative to provide operational input for all clients' projects which includes attending routine operational and project meetings; provide QC operational input and participate in the review of Statement of Works (SOW) for Client's projects; provide QC progress updates to Project Management and the site operational team
  • Lead the team to assure all samples delivered to QC are received and accurately documented/ login to the QC system, stored in the defined locations of the required storage condition, and shipped for external testing in a timely manner
  • Assure all data and records are accurate, documented and maintained effectively and in compliance with Good Documentation Practice (GDP) and data integrity requirements
  • Assure all required training are completed and up to date before performing the tasks
  • Where applicable, support the development and update/ revision of applicable SOPs and QC documents in compliance with effective site policies and procedures
  • When required, lead and/or participate in nonconformance investigation, Change Control, CAPA and Complaint processes
  • Participate in Quality Risk Management to support GMP operations
  • Proactively participate in the preparation of internal and external audits

REQUIREMENTS:


  • BSc.
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