QC Business Process Specialist

Sanofi; Waterford; Sur place; EUR 42 000 - 54 000; Plein temps

Résumé du poste

Sanofi Waterford is seeking a QC Business Process Specialist to join a state-of-the-art biopharmaceutical campus. The role focuses on ensuring QC compliance, driving quality metrics and leading continuous improvement initiatives in a fast-paced environment.

You will support audits, training, and cross-functional collaboration to maintain high quality standards and ensure timely closure of change controls, deviations, CAPAs and QEs.

Qualifications

• Bachelor's Degree in Science/ Engineering or equivalent.
• Minimum of 2 years’ experience in a similar or related role.
• Extensive knowledge of cGMP and GDP in a regulated environment.
• Working knowledge of quality systems in a regulated environment.
• Understand relevant quality/compliance regulations.

Responsabilités

• Raising and management and on time closure of all Quality System processes including assigned Change Controls, Deviations, CAPAs, ILIs & QEs.
• Driving of all Quality Metrics for the department.
• Forward review of Quality Metrics to ensure no over-dues.
• Procedure effectiveness and simplification and actively contribute to continuous improvement initiative.
• Ensure effective co-ordination and support for external and internal audits for the department.
• Perform critical / constructive review of procedures and practices. Identify and lead projects to make step change improvements to the department’s Quality.
• Conduct duties in a safe manner and report all safety issues or concerns.
• Support leadership team in achieving goals / tasks.
• Actively contribute to continuous improvement initiatives utilizing lean methodologies where appropriate.
• Liaise with Quality Assurance Representative to support and improve RFT in the area and Always Audit Ready.
• Ensure all required training is completed on time.
• Maintain training in critical test activities as required in the laboratory (will be defined by head of QC).
• Complete all duties as per relevant SOPs and global procedures.
• Ensure compliance to cGMP at all times.

Connaissances

Attention to detail

Interpersonal skills

Communication skills

Initiative

Formation

Bachelor's Degree in Science/ Engineering or equivalent

Description du poste

QC Business Process Specialist

• Location: Waterford
• Contract: 23-Month FTC

About the job

At Sanofi, we’re committed to providing the next-gen healthcare that patients and customers need.

For more than 20 years, our Waterford team has continued to grow and diversify to serve patients around the world. Today, a team of almost 800 works together at a state-of-the-art biopharmaceutical and medical device campus. Recognized through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of opportunities to grow your career at one location. As well as attractive benefits, the team enjoy access to an onsite gym and medical Center that underpin a strong commitment to health and wellbeing.

To ensure the compliance in the QC Chemistry department at Sanofi are effectively maintained and enhanced.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main responsibilities:

• Raising and management and on time closure of all Quality System processes including assigned Change Controls, Deviations, CAPAs, ILIs & QEs.
• Driving of all Quality Metrics for the department.
• Forward review of Quality Metrics to ensure no over-dues.
• Procedure effectiveness and simplification and actively contribute to continuous improvement initiative.
• Ensure effective co-ordination and support for external and internal audits for the department.
• Perform critical / constructive review of procedures and practices. Identify and lead projects to make step change improvements to the department’s Quality.
• Conduct duties in a safe manner and report all safety issues or concerns.
• Support leadership team in achieving goals / tasks.
• Actively contribute to continuous improvement initiatives utilizing lean methodologies where appropriate.
• Liaise with Quality Assurance Representative to support and improve RFT in the area and Always Audit Ready.
• Ensure all required training is completed on time.
• Maintain training in critical test activities as required in the laboratory (will be defined by head of QC).
• Complete all duties as per relevant SOPs and global procedures.
• Ensure compliance to cGMP at all times.

About you

• Bachelor's Degree in Science/ Engineering or equivalent.
• Minimum of 2 years’ experience in a similar or related role.
• Extensive knowledge of cGMP and GDP in a regulated environment.

• Working knowledge of quality systems in a regulated environment.
• Understand relevant quality/compliance regulations.

Skills and Competencies:

• Excellent accuracy and attention to detail.
• Excellent interpersonal skills.
• Excellent Communication skills.
• Initiative – be able to work in a self-directed manner to see issues through to completion.

Pursue Progress Discover Extraordinary

Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue Progress. And let’s discover Extraordinary together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!