Job description
Associate Process Improvement Specialist
Are you looking to make your next career move? CellCarta, a Contract Research Organization, is hiring an Associate Process Improvement Specialist to join our dynamic team. As an Associate Process Improvement Specialist , you will have the opportunity to use your expertise and skills to ensure that our services meet the highest industry standards. Come work with a team of talented individuals who are committed to making a positive impact on human health and well-being. Apply today and take the first step towards an exciting new career with CellCarta!
Summary
The Associate Process Improvement role involves analyzing processes and implementing changes to improve overall performance in the business area, in support of the Process Improvement Manager.
Responsibilities
More specifically, you will participate in the following:
- Collaborate with stakeholders of the process for which improvement is requested, to gain a full understanding of the process in question;
- Complete a critical review of the process flow and data;
- Build and implement strategies to improve operational efficiency and effectiveness;
- Provide training on newly introduced process improvements;
- Perform required maintenance and sustainment activities for implemented improvements;
- Adhere to applicable standards and regulations such as ISO 13485, ISO 15189, CAP/CLIA, GxP, 21 CFR Part 820, and IVDR, as appropriate;
- Oversee improvement timelines with the support of the Manager;
- Identify and escalate issues/risks in a timely and proactive manner;
- Other duties may be assigned as necessary to support business needs.
Education
- Bachelor’s degree in a scientific discipline (e.g., Biology, Chemistry, Biochemistry, Biomedical Engineering) or Computer Programming. A Master’s degree is a plus;
- Project Management Professional (PMP) certification preferred;
- LEAN/Six Sigma belt preferred.
Main Requirements
- Proven experience with process improvement methodologies (e.g., LEAN, Six Sigma, Agile) as well as the development and deployment of programming and efficiency tools;
- Strong interest in analyzing processes and problem-solving abilities;
- Efficient communication skills;
- Eagerness to learn and adapt to new challenges;
- Proficiency in data analysis and reporting tools;
- Mastery of Office 365 suite, including advanced formulas, VBA macros, Power Pivot, Power BI, and Power Automate.
Working Conditions
- Based in Wilrijk, Antwerp (Belgium);
- Hybrid schedule with 2-3 days onsite.
Benefits
- A competitive salary and benefits package;
- A dynamic and rapidly changing global environment that allows for personal growth;
- Training and personal development in a variety of technical and interpersonal areas;
- Career opportunities as the company grows quickly;
- A forward-thinking company that is fit for the future;
- An excellent team to work with.
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China.
Joining CellCarta means working with dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world!
Join us as we make an impact on patient therapy!
The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, “CellCarta”). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta.
CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact [email protected].
