Associate Quality Manager (mfd)

Join Our Team as an Associate Quality Manager!

As leader of a dedicated Quality Operations team for our new manufacturing site in Waghäusel provide direction
in quality assurance within operations and other business functions with a focus on
preventative measures and continuous improvement of products and processes.
Has responsibility for delivering the compliance and business objectives of the
function with primary responsibility to drive engagement and lead the quality team
while ensuring compliance to Stryker Corporate and site specific requirements Quality
System Regulations and standards.

What Youll Do:

Will work within the Quality Operations structure in a management capacity has
responsibility for quality related activities which includes but not limited to the
following:
Leads integration of the existing AMB QMS into the Stryker QMS from a base business perspective.

Leads Quality Engineering Team to provide support and technical guidance
/ direction to the operational and functional areas on site fostering an
environment of proactive and continuous improvement approach to Quality.
Supports and aligns with the site commitment to ensure the organisations
conformance to producing products meeting or exceeding customer
requirements and the relevant regulatory standards.
Fosters a positive employee relations environment by promoting open
communication engagement and development of team members.
Promotes a culture of inclusiveness trust flexibility and teamwork.
Create a highly talented team by sourcing hiring and placing individuals in
positions that play to their strengths and future potential
Drive an environment of compliance within Stryker by working with all
function managers and their support staff to define expected quality
standards and the roles/responsibilities in the maintenance of these
standards.
Participates in ensuring the site(s) maintains continued certification to all
regulatory bodies. Plays a lead role in all internal and external audit
programmes such as Corporate notified body & FDA audits.
Ensures effective control of product/process deviations for all released
product and for the implementation of effective corrective action when nonconformances arise. Assesses product & patient risk.
Supports the planning pipeline of quality improvement activities including
initiatives to increase product quality NCR & CAPA resolution reduce cost
decrease in-efficiencies and improve risk management
Oversight and responsibility to ensure site maintains adherence to Quality
KPIs performance indicators and takes timely action to address adverse
trends and deviations. Continuously monitors and partakes in global forums
to assess opportunities for improvement.
Assist in developing and supports local and global strategies for the Quality
Operations function.

What Youll Need:

Degree in Engineering Science discipline or equivalent. Business
Management or MBA is an advantage.
Minimum of 6 years experience in a Medical Pharmaceutical BioMedical/Pharma Automotive or regulated manufacturing environment.