Project and Quality Manager Associate

hace 2 semanas


Barcelona, España Stalicla SA A tiempo completo

STALICLA is an international and fast-growing biopharmaceutical company on a mission to

build a new therapeutic space for patients with disorders of the developing brain.

As the company is rapidly scaling, STALICLA is looking to recruit an agile Project and Quality

Manager Associate to support the next stages of the company’s development.

**Project and Quality Manager Associate**

Permanent Position - Full Time - World Trade Center, Barcelona

**The role**

The Project and Quality Manager Associate will work closely with the other members of the

STALICLA Discovery and Data Science unit to ensure the achievement of milestones

associated to DEPI, a first-in-class precision medicine platform using systems biology,

machine learning & statistical modeling to accelerate drug development for patients with

neurodevelopmental disorders (NDDs). S/he will ensure successful execution of tasks in

relation to the design, implementation and the analysis of computational models and

algorithmic approaches towards the characterization of “actionable” molecular, genetic, and

clinical features in NDDs. S/he will manage various ongoing computational systems biology

and biomedical data analysis projects, ranging from the development of next-generation

sequencing (NGS) and clinical data mining pipelines to identification of molecular & pathway

level characteristics associated with ASD patient subgroups. S/he will also be involved in

with previous experience on NGS analysis (WGS, WES, and/or RNAseq), workflow

development, and cloud computing, or who are open to learning these skills, are preferred.

**Your responsibilities**
- Support project management (PM), including planning, coordinating and monitoring

tasks as well as their proper reporting
- Supervise quality management system (QMS), including the support of its set up &
maintenance
- Ensure the use of good standard practices among developers and data analysts
- Coordinate and review of documentation, code, and data in relation to QMS
- Maintain code and data inventory up to date

**Your profile**
- MSc and/or PhD. in engineering, computational sciences, biotechnology or

equivalent experience in industry

World Trade Center | Moll de Barcelona, s/n, Edif Este | 08039 Barcelona | Spain | + 34 931 682 868
- Minimum 2 years of **project management experience** in academia, pharma or CRO,

with **good knowledge of project management tools**

methodologies, preferably in biomedical domain
- Previous experience in the implementation of a quality management system for

software development is desirable
- Prior experience in the field of systems biology and/or neurodevelopmental

disorders or NGS analyzes is a plus
- Experience in Linux, R and/or Python, CI/CD tools is an asset
- Experience in shell scripting, Git/Gitlab, Makefile, Docker, Nextflow (or equivalent) is

an asset
- Knowledge of good coding, data analysis & reporting standard practices
- Experience with IT management, cluster and/or cloud computing (AWS preferred) is

a plus
- Strong interpersonal, communication, presentation, reporting skills
- Good verbal and written communication skills in English
- A high comfort level working in a high paced start-up environment, where a

pragmatic, resourceful, well organized, and effective approach is required with

limited resources
- A passionate, energetic, and enthusiastic personality that will ensure commitment

to the company and its vision

**More about STALICLA**

Ready to join a science-driven, international, multidisciplinary, passionate, hard-working, and

meritocratic environment?

STALICLA is suited for individuals with a strong interest in Precision Medicine and

Neurodevelopmental Disorders field, as well as the ability to go above and beyond to make

things happen As part of its Corporate Social Responsibility policy, STALICLA promotes

are strongly encouraged to apply.

World Trade Center | Moll de Barcelona, s/n, Edif Este | 08039 Barcelona | Spain | + 34 931 682 868



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