Manufacturing Process Specialist - Bioprocessing

MANUFACTURING PROCESS SPECIALIST - BIOPROCESSING - LEIDEN, NETHERLANDS - €42 - €46 PER HOUR - 8 MONTHS

TITLE: Manufacturing Process Specialist Operations Bioprocessing Services We are looking for a motivated enthusiastic process owner (Manufacturing Process Specialist) within Operations Bioprocessing Services Department

The Operations Bioprocessing Services (OBPS) department, as process and system owner, is responsible for the availability of qualified production equipment, qualified production processes and production computer systems. These must comply with EHS & S and cGMP regulations. This concerns the (supporting) production areas Buffer Preparation, Media Preparation and Equipment Preparation, but also Manufacturing Execution Systems and the first-line troubleshooting and support for these departments.

ACTIVITIES AND RESPONSIBILITIES:

For this position we are looking for a motivated (Sr) Manufacturing Process Specialist who will strengthen the OMS department.

The Manufacturing Process Specialist owns production processes within their own area of responsibility, carries out improvement projects and introduces new processes in the factory. The Manufacturing Process Specialist is leading in solving acute complex disruptions in production. As a Manufacturing Process Specialist you work closely as process owner with other process and system owners and Manufacturing Associates (technicians) within the department.

SPECIFIC TASKS:

- Ensuring that the production process is in a validated state and maintained and maintained so that production processes can be optimally carried out.
- Ensure that the processes comply with global, EHSS and compliance standards.
- Implement improvements, ensure sufficient availability of equipment, as well as the accompanying production documentation and training.
- To propose a long-term strategy with regard to ownership
- To be the specialist in deviations and inspections and to be in charge of process improvements and standards
- Supporting production in their daily activities by means of Gemba, training and research in case of deviations
- Advise on improvement proposals that are proposed by the production staff (BI/CI).
- The representative of the department/discipline within multidisciplinary and global projects.
- Acute troubleshooting in case of process disruptions

JOB REQUIREMENTS:

- HBO or WO education in Biotechnology, Biochemistry, Biopharma, Medical Biology, Process Technology (or equivalent training)
- Knowledge of production automation ISA-95 is a plus
- A good balance between conceptual thinking and practical technical insight
- Result - and performance-oriented, flexible, critical, problem-solving and innovative
- Optimal awareness and experience with EHSS and GMP standards
- High quality awareness and service-oriented
- Excellent communication skills, written and oral, in Dutch and English

ADDITIONAL INFORMATION ABOUT THE PROCESS

Johnson & Johnson is an American multinational medical devices, pharmaceutical and consumer packaged goods manufacturer founded in 1886.

This job with Johnson & Johnson is a temporary assignment and is being managed by Kelly Services on behalf of Johnson & Johnson. Successful candidates will be placed at the Johnson & Johnson assignment and managed by Kelly Services

If you match these requirements, please apply in the normal way. Elevate will send you an email, please open, click and action that email and your application will be visible to the hiring organisation directly.