Associate Quality Manager (mfd)

Work Flexibility : Hybrid or Onsite

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.

Travel Percentage : 40%

Required Experience :

Manager

Key Skills

Distribution,IT,Access Control System,B2C,Courier Delivery,Broadcast

Employment Type : Full-Time

Experience : years

Vacancy : 1