Director of Biopharmaceutical Quality
Company: Dover Corporation
Location: Saint Paul
Posted on: January 15, 2021
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Job Description:
Job Title: Director of BiopharmaceuticalQuality Department:
QualityLocation: Roseville, MNReports to: Vice President of
QualityJob Status: ExemptDate Completed/Updated: November 2020Job
Summary: This role is responsible for the overall product quality
of all CPC biopharmaceutical (Bio) products. The Bio Customer
Quality team will report directly to this role to allow a direct
connection to all incoming product quality issues. This role will
then work within the Quality department and with the other Quality
functional leaders to prioritize and align Bio work. Additionally,
this role will collaborate with other cross-functional leaders and
groups to ensure the Bio Quality teams are receiving the necessary
support. Key performance indicators (KPIs) for this role include:
Bio defective parts per million (DPPM), Bio part function complaint
rate and severity, and Bio customer Net Promotor Scores in quality
areas.Essential Job Responsibilities:Provide strategic level
thought leadership and execution to Quality---s vision, strategy
and annual operational plans.Lead & manage the Customer Quality
team to achieve goals.Collaborate with all Quality leaders to align
and prioritize Quality resources supporting Bio.Collaborates &
influences cross functional leaders and groups to achieve Bio
quality goals.Develop programs, policies and initiatives that
generate significant improvement in meeting customer
requirements.Develop business relationships with external
organizations and service providers that assist Quality goal
achievement.Represent Quality on the Bio Leadership Team.Establish
and/ or improve Quality metrics.Lead or sponsor cross functional
teams supporting customer impacting issues.Establishes effective
and appropriate business relationships with key customers.Keeps
current in the field with external or internal education and
training.Be a Quality advocate internally and externally.Adheres to
all safety regulations.Demonstrates CPC core values.Performs other
job duties as assigned to meet business needs. Essential
Supervisory Responsibilities: Supervises employees in the Quality
department. Carries out supervisory responsibilities in accordance
with the organization's policies and applicable laws, including
interviewing, hiring, and training employees; planning, assigning,
and directing work; appraising performance; rewarding and
disciplining employees; addressing complaints and resolving
problems.Coaches team members for career growth and performance
optimization. Required Job Qualifications:Bachelor---s degree in
engineering or related technical/ life science field. A minimum of
ten (10) years of progressively responsible positions in Quality.A
minimum of seven (7) years of demonstrated success in managing/
leading direct reports and achieving results through others.A
minimum of three (3) years in the medical device, biopharmaceutical
or other highly regulated industries.Understanding of up to date
Quality theories, methods and approaches.Passion for improvement
and drive for change to meet customer requirements.Exceptional
analytical skill - ability to manage complex data including
finance.Strong working knowledge ISO9001 and ISO13485.Proven
ability to lead, influence and motivate both direct reports and
other individual contributors and leaders.Excellent communication
(verbal and writing) skills. Preferred Job Qualifications:MBA or
technical MS/ PhD degreeStrong statistics and/ or product
reliability knowledge ASQ participation and certification(s)Six
Sigma, or similar, certificationsTravel Requirement (assuming no
Covid restrictions): Yes, up to 10% Yes, InternationalYes, domestic
Physical Demands:The physical demands are representative of those
that must be met by an employee to successfully perform the
essential functions of this job. Reasonable accommodations may be
made to enable individuals with disabilities to perform the
essential functions.The employee must frequently lift and/or move
up to 10 pounds. Specific vision abilities required by this job
include close vision. While performing the duties of this job, the
employee is regularly required to sit; use hands and fingers and
talk or hear. The employee is frequently required to reach with
hands and arms. The employee is occasionally required to stand,
walk and/or stoop.Work Environment:The work environment
characteristics described here are representative of those an
employee encounters while performing the essential functions of
this job. Reasonable accommodations may be made to enable
individuals with disabilities to perform the essential
functions.The noise level in the work environment is usually
moderate.This job description is not designed to contain a
comprehensive list of tasks, responsibilities or duties.
CPCreserves the right to amend to meet legal, business and
organizational requirements as necessary.
Keywords: Dover Corporation, St. Paul , Director of Biopharmaceutical Quality, Executive , Saint Paul, Minnesota
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