Randstad GxP Quality Support Lead in boston, Massachusetts
GxP Quality Support Lead
location:Boston, MA (remote)
salary:$59.93 - $68.95 per hour
date posted:Wednesday, April 7, 2021
GxP Quality Support Lead
Come join our team where we are innovators, leaders, and collaborators. And at the heart of everything we do is an intense desire to pursue the toughest challenges and truly change the world for people living with rare and devastating diseases.We are incredibly proud that our work has been recognized globally through some of the industry's highest honor.
location: Boston, Massachusetts
job type: Contract
salary: $59.93 - 68.95 per hour
work hours: 8am to 5pm
This position will be a member of the GxP Rapid Response team initiatives for Central Quality System and Compliance. The Quality Support Lead will also serve as a cross-functional member for key initiatives in Central Quality Systems and Compliance.
The Quality Support Lead is responsible for maintaining and improving Quality System processes to ensure. Quality initiatives are completed and delivered on time. Quality Support Lead requires excellent communication skills and someone self-motivated and a self-starter to drive for implementation and Quality issues. The Quality Support Lead must possess strong verbal and written communication skills and sound organization skills applicable to planning, reporting, and archiving/knowledge transfers
Job Duties & Responsibilities
Work with Subject Matter Experts supporting process compliance/ improvements to Quality Management System Elements such as CAPAs, Deviation, Change Control, Supplier Quality Management, Audit, Inspection, and Notification to Management Be an individual contributor supporting the implementation of Quality process initiatives Serve as active partner across Alexion GxP groups, providing support and consultation to our Quality Business Partners and Business customers Perform other related duties and special projects as required or requested. Support Quality programs in accordance with Health Authority regulations.
4 to 8 years of experience in biopharmaceutical/pharmaceutical or related industry with strong background
Hands-on experience in working in agile or fast paced teams
Experience participating in cross-functional projects
Proficiency with Microsoft Office Suite (Outlook, Excel, Word, Smarts sheets and box etc.)
strong interpersonal communication skills
Demonstrated passion and skills for problem solving
High attentiveness to detail
Proven ability to quickly learn new information and communicate requirements to the appropriate individuals.
Advanced quality certification strongly desired (i.e., Six Sigma Green Belt, Certified Lean Expert, etc.)
Bachelor's degree in chemistry, life sciences, or related field with strong background
Experience level: Experienced
Minimum 5 years of experience
Education: Bachelors (required)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
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