Life Science Project Consultant
This project requires a master degree in the pharmaceutical and/or biological manufacturing or scientific field
Do you have a question?
Contact Glorian Coeckelberghs via g.coeckelberghs@strandassociates.be
Job 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?
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Project Management: Project Engineers are responsible for planning, executing, and closing out engineering projects. This includes defining project scopes, objectives, timelines, and budgets.
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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.
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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.
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Risk Assessment: Identifying and mitigating potential risks associated with engineering projects to ensure safety, product quality, and continuity of production.
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Cross-functional Collaboration: Working closely with various teams within the company, including manufacturing, quality assurance, research and development, and maintenance, to achieve project goals.
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Documentation: Maintaining accurate documentation of project progress, changes, and outcomes is essential for compliance and future reference.
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Problem Solving: Handling technical challenges and troubleshooting issues that may arise during project implementation.
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Cost Control: Managing project budgets, controlling costs, and ensuring that projects are completed within financial constraints.
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Continuous Improvement: Identifying opportunities for process optimization and efficiency improvements.
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Health, Safety, and Environmental (HSE) Compliance: Ensuring that all engineering activities align with Pfizer's HSE policies and guidelines.
Criteria
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
Offer
- Attractive 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.