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Automation Specialist Quality Control - 2406182341W

Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.

We are seeking a talented and motivated Automation Specialist (1 year contract) to join our Quality Control team. The Automation Specialist will play a key role in optimizing our quality control processes through the implementation and management of automated systems. This individual will collaborate closely with cross-functional teams to ensure the highest standards of quality are consistently met.

Key responsibilities:

• Implement Automated Quality Control Systems: Deploy automated solutions for quality control processes, including but not limited to automated testing, inspection, and data analysis.

• Technical implementation of new systems within the organization in collaboration with other teams. Lab systems vary from (standalone) analytical equipment to complex global platform projects which connect to LIMS (Laboratory Information Management Systems).

• Implementation of SDMS (Scientific Data Management System) and future new paperless opportunities.

• Integration of Automation Tools: Evaluate, select, and integrate automation tools and technologies that streamline quality control processes and enhance efficiency.

• Lead and execute projects

• Continuous Improvement: Identify areas for process optimization and automation within the quality control workflow. Implement improvements to enhance product quality and reduce time-to-market.

• Quality Assurance: Work closely with Quality Assurance teams to establish and maintain quality standards. Ensure that automated processes adhere to regulatory requirements and industry best practices.

• Documentation and Reporting: Document automation processes, workflows, and procedures. Responsible for documenting administrator procedures, technical installation procedures and maintenance procedures.

• Training and Support: Provide training and support to team members on the use of automated quality control systems. Act as a subject matter expert and mentor to facilitate knowledge transfer.

• Collaboration and Communication: Collaborate with cross-functional teams, including Engineering, Manufacturing, and Product Management, to ensure alignment on quality objectives and priorities. Communicate effectively to drive consensus and achieve shared goals.

Qualifications

• Bachelor's degree in Engineering, Computer Science, or related field.

• Proven experience in automation, quality control, or related fields.

• Proficiency in programming languages such as Python, Java, or C .

• Experience with automation tools

• Experience in project management framework

• Strong analytical and problem-solving skills.

• Excellent communication and interpersonal skills. Pro-active, works independently, takes actions in the absence of specific instructions, and can write protocols/reports, business correspondence and procedures

• Ability to work effectively in a fast-paced, collaborative environment.

Preferred qualifications:

• Master's degree in Engineering, Computer Science, or related field.

• Minimal 2 years of work experience in Pharma with GMP and automation skills

• Laboratory Experience is considered a plus

• Project Leadership experience is a plus

• Experience with continuous integration/continuous deployment (CI/CD) pipelines.

• Experience with (Computer) System Validation in a GxP environment

• Experience with the following software is considered as a plus: Empower, Softmax pro, SDMS, Deskman, LIMS, 32Karat, Trackwise.

• Familiarity with quality management systems (e.g., ISO 9001, Six Sigma).

• Experience in regulated industries such as healthcare, automotive, or aerospace.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Primary Location Europe/Middle East/Africa-Netherlands-South Holland-Leiden

Organization Janssen Biologics (7266)

Job Function Digital Quality

Req ID: 2406182341W