Manufacturing Process Owner

10 Jan 2024

Vacancy expired!

The Process Owner will collaborate with Manufacturing, Quality, and Facilities & Engineering to ensure it continues to meet internal customer, business, and patient needs. The primary aim of the role is to lead key process transformation, design and improvement efforts. The Process Owner will lead a mix of strategic and tactical assignments of various complexities each with an opportunity to achieve measurable results. The incumbent will exhibit knowledge and provide coaching/training to colleagues while leading process and quality initiatives, as necessary.

Responsibilities:

  • Demonstrated ability to understand what is critical about the process.

  • Monitors process performance with data by including both input/process parameters and output measures.

  • Monitor data compiled by process operators and summarize into a dashboard.

  • Ensures the process is documented, and that the documentation is used and updated routinely .

  • Closely collaborates with internal and global functions (Manufacturing, Quality, and Facilities & Engineering) to ensure a control plan is in place.

  • Ensures that any improvements identified through projects are incorporated and maintained in the process.

  • Act as Process SME during internal and/or external Regulatory inspections.

  • Provides necessary training and resources for the process operators to do their jobs well and keep getting better. Resources may include appropriate training, materials, information, and equipment.

  • Foster a culture of continuous improvement through employee selection, training and mentoring while focusing on operational efficiency and the elimination of “non-value added” activities.

  • Provide a positive and equitable working environment emphasizing the CSL Values: Customer Focus, Innovation, Integrity, Collaboration, and Superior Performance.

  • Complies with requirements from CSL Behring’s Safety Program, including Health and Safety mandates and OSHA requirements.

  • Completes any other duties/responsibilities assigned by senior management.

Requirements:

  • Bachelor’s Degree in Mechanical, Chemical or Manufacturing Engineering or equivalent degree may be considered dependent upon experience.

  • 4+ years of relevant experience and a BS

  • 2+ years of relevant experience and a MS.

  • Prior experience in pharmaceutical industry is preferred.

  • Proficient knowledge of Good Manufacturing Practices (GMPs)

  • Audit and Investigation Skills, Report Writing Skills.

  • Strong verbal, technical writing and interpersonal skills are required.

  • Proficiency in Microsoft Office applications.

  • Must possess a strong knowledge of the FDA and cGMP standards as well as regulatory guidance documents.

Our Benefits

We encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL.

About CSL Behring

CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.

We want CSL to reflect the world around us

As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.

Do work that matters at CSL Behring!

  • ID: #23588041
  • State: Illinois Kankakee 60901 Kankakee USA
  • City: Kankakee
  • Salary: TBD
  • Job type: Full Time
  • Showed: 2022-01-10
  • Deadline: 2022-01-25
  • Category: Et cetera