Life Science Project Consultant

il y a 3 semaines

Puurs, Belgique Strand Temps plein

Puurs

Pharma & Life Sciences

**Organization description**: We are looking for several profiles:

- Complaint Specialists
- Project Engineers (QC/QA/RA/Lab/MCT/...)
- Lab operations Project Engineer (Chemical/Microbio)

What's a Project Engineer?
- **Project Management**: Project Engineers are responsible for planning, executing, and closing out engineering projects. This includes defining project scopes, objectives, timelines, and budgets.
- **Equipment and Facility Upgrades**: They may be involved in upgrading or expanding manufacturing facilities, improving production processes, or installing new equipment. This can involve coordinating with various departments and external contractors.
- **Compliance**: Ensuring that all engineering projects adhere to regulatory requirements and quality standards is crucial. The pharmaceutical industry is highly regulated, and compliance is of utmost importance.
- **Risk Assessment**: Identifying and mitigating potential risks associated with engineering projects to ensure safety, product quality, and continuity of production.
- **Cross-functional Collaboration**: Working closely with various teams within the company, including manufacturing, quality assurance, research and development, and maintenance, to achieve project goals.
- **Documentation**: Maintaining accurate documentation of project progress, changes, and outcomes is essential for compliance and future reference.
- **Problem Solving**: Handling technical challenges and troubleshooting issues that may arise during project implementation.
- **Cost Control**: Managing project budgets, controlling costs, and ensuring that projects are completed within financial constraints.
- **Continuous Improvement**: Identifying opportunities for process optimization and efficiency improvements.
- **Health, Safety, and Environmental (HSE) Compliance**: Ensuring that all engineering activities align with Pfizer's HSE policies and guidelines.

**Our offer**: This project requires a master degree in the pharmaceutical and/or biological manufacturing or scientific field.
Following, although not limiting, educations are acceptable: Bio Engineer, Pharmacist, Master in Biology, Biochemistry, Biotechnology, Engineering,...
No experience needed but preferred two or more years of relevant experience in pharmaceutical, GMP environment or combination product or medical device industry.
- Strong written communication skills: for technical reports
- Analytical skills (data analysis)
- Persuasiveness: you can bring different parties together to arrive at the best possible solution
- Good time management and prioritizations skills
- Team player
- Proven problem solving abilities
- Talen (Languages): fluent in Dutch and English

**We ask**:

- **A**ttractive salary** in line with the market and your experience;
- Salary package with very competitive **extra-legal benefits**;
- **Optimum work-life balance** thanks to 12 ADV days, sliding hours and homeworking possibilities;
- **Join a community of over 100 consultants in quality and regulatory affairs, with many social events organized throughout the year;**:

- **Training and workshops to develop/share your skills.

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