Covance Senior Manager QA Process Lead (Individual Contributor) in Indianapolis, Indiana
The Senior Manager QA Process Lead position is an individual contributor that has responsibility for oversight and delivery of the Internal Process Compliance function activities. This position and department will be aligned as partners to the functional areas of the Clinical Development and Commercialization Services (CDCS) business to ensure appropriate quality/compliance oversight and solution partnering. Driving compliance excellence within the organization through execution of key activities, improvement methodologies and governance forums. Of importance are the requirements to lead, strategize, partner and influence across various functions and locations.
Provides regulatory compliance and quality assurance advice, guidance and support to internal CDCS teams and functions and collaborating with other internal stakeholders (e.g; Legal) for proactive interactions and quality management.
This position can be remote-based.
A minimum of a Bachelor’s Degree in Life Sciences preferred (or equivalent Life Science experience)
Experience may be substituted for education.
10 years in regulatory environment (experience in GXP roles)
Experience & regulatory expertise of industry quality systems/standards
Ability to interpret applicable regulations/standards
Ability to analyse and interpret data in order to lead process improvement initiatives
Ability to communicate and negotiate with internal stakeholders effectively
Ability to distill critical information
Ability to effectively lead project teams to implement change
Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.
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