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Global Quality Specialist Job
Eingestellt von Yoh
Gesuchte Skills: Support, Client
Projektbeschreibung
Top Skills Should You Possess:
- Quality Assurance
What You'll Be Doing:
- Liaise with Suppliers to ensure successful delivery of projects/supplies
- Make decisions and advise the Supplier Management Team regarding quality and pharmaceutical technology issues within their area of expertise.
- Responsible for Quality Assurance Supplier Management including but not limited to: Annual Assessments; Quality Assurance Agreements; trending and reporting of data; assessing, reviewing and improving quality systems at Suppliers; attendance at Quality and Business Review Meetings.
- Maintains a high level of understanding of relevant production processes and quality systems.
- Performs the QA review and/or approval of the following cGMP documentation for their Suppliers:
- Change Requests
- Annual/Product Quality Reviews (API and F benchmarks internal and external QA practices to identify innovative efficient and effective practices
- Collaborates in data analysis and report creation on quality metrics and key performance indicators
- Develops and maintains effective business relationships with Suppliers
- Specific to the support and management of GES Quality Management System, may be responsible for one or more of the following:
- Manages quality data and records in relevant quality management support systems, as required.
- Assist in the production of, or contribution to, quality documentation
- Develops and maintains a high level of understanding of technical production processes and quality systems being utilized within PCO Supplier Management teams
- Accountable for QA decision-making; works directly with the Supplier Management leader and other team members to deliver objectives
- Ensures compliance with all GMP Compliance and Regulatory requirements by providing proper coaching, mentoring and consultation to the Supplier Management Team
- Provide functional direction as required.
What You Need to Bring to the Table:
- Three to five (3-5) years of global quality assurance experience
- Pharmaceutical industry experience
OPPORTUNITY IS CALLING, APPLY NOW!
RECRUITER: Hannah Cihlar
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V. If you are an individual with a disability and you require an accommodation in the application process, please email.
J2W: CLINICAL
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Ref:
SFSF: LS
Projektdetails
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Einsatzort:
Wilmington, Vereinigte Staaten
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
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Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Sonstiges