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Jubilant HollisterStier Spokane: Associate/Sr. Associate, Qa Validation – Day Shift

Jubilant HollisterStier Spokane

This is a Full-time position in Spokane, WA posted September 11, 2021.

Jubilant HollisterStier LLC provides a complete range of services to support the pharmaceutical and biopharmaceutical industries.

The Allergy business is a worldwide leader in the manufacture of allergenic extracts, targeted primarily at treating allergies and asthma.

Jubilant HollisterStier is also a nationally recognized contract manufacturer of sterile injectable vials, and lyophilized products.

Jubilant HollisterStier is owned by Jubilant Life Sciences.The Associate/Sr.

Associate, QA Validation will provide technical expertise via review and approval of documents including but not limited to Protocols, Acceptance Reports, SOPs and Specifications.

The QA Validation Associate will provide project and client support as a quality representative.

Essential responsibilities include but are not limited to:Work with the production, engineering, maintenance, IT, and technical services departments to assure that all required prerequisite documentation is appropriately developed to support process, cleaning, facilities, aseptic, and filling/packaging activities.Track and provide technical direction for new and continued validation of processes and equipment to ensure compliance with internal policies and procedures, current industry standards, cGMPs and current regulatory requirements.Review product transfer protocols and reports, assess impact to product quality and determine appropriate actions.Create, and write required SOPs pertaining to documentation and QA Validation.Review and approve validation protocols, acceptance reports, SOPs and specifications.Recognize compliance issues that may occur and provide QA SME support for change control and system improvement.Qualifications:Bachelors of Science Degree in a scientific discipline or 5 years of experience in lieu of degree required for a Specialist.

Bachelors of Science degree or 10 years’ experience in lieu of a degree required for a Sr.

Associate.Must have 5 years of related experience for a Sr.

Associate.Minimum of 2 years qualification/validation experience.Must have 3 years pharmaceutical experience.FDA Regulated Industry required.Proficiency in Microsoft Word, Excel and PowerPoint required.This position requires an in-depth understanding of cGMP’s, European regulatory requirements, relevant USP chapters, and scientific principles associated with manufacture of sterile products, testing required on those products, and relationship of quality principles with manufacturing and testingPhysical Requirements: Ability to lift 20 lbs and prolong sitting.Jubilant HollisterStier is a great place to grow!If you’re up for a rewarding challenge, we invite you to take the first step and apply today!https://www.Jubilantcareers.Jubl.ComJubilant HollisterStier is an EEO/AA Employer.All qualified applicants will receive consideration for employment without regard to their protected veteran status and will not be discriminated against on the basis of disability.If you require assistance applying for a position, please contact our HR Department

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