2x Scientist - Technical Operations at CSL

São José da Laje, Alagoas, Brazil -

Full Time

Start Date

Immediate

Expiry Date

30 Jun, 26

Salary

0.0

Posted On

01 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Biochemistry, Biotechnology, Chemical Engineering, Protein Purification, Chromatography, Ultrafiltration, Statistical Analysis, Experimental Design, Quality by Design, Data Analysis, Technical Report Writing, Presentation Skills, Electronic Lab Notebooks, Deviation Management, Scientific Literature, Microsoft Office

Industry

Pharmaceutical Manufacturing

Description

2x Scientist - Technical Operations Location: Bern, Switzerland We are seeking a scientifically driven professional to design, plan, execute, and document laboratory studies that support bioprocess development and lifecycle management. In this role, you will investigate and assess process and product deviations at manufacturing scale, identify and evaluate opportunities for process optimization, and support the implementation of process improvements and alternative materials. You will apply strong experimental design principles, perform rigorous data analysis, and communicate clear, well‑supported technical conclusions. This position operates within a regulated GxP environment and plays a key role in enabling robust, science‑based decision‑making. Main Responsibilities & Accountabilities Design, plan, and execute scientifically sound experimental studies to support deviation investigations, process optimization, and evaluation of alternative materials. Perform literature searches on relevant scientific topics, summarize findings, and present conclusions to cross-functional teams. Develop experimental study designs including definition of readouts, experimental setup, material requirements, sample numbers, analytes, and statistical evaluation methods. Apply Quality by Design (QbD) principles and tools (e.g., pFMEA, CQA, CPP) to experimental design and data interpretation. Prepare materials, equipment, and protocols for laboratory studies using scale-down models and single unit operations. Conduct laboratory-scale protein purification and processing experiments, including chromatography, ultrafiltration/diafiltration, precipitation, and filtration. Collect, label, distribute, and document samples; ensure accurate data capture and traceability in electronic lab notebooks (ELN). Analyze experimental data using appropriate statistical methods and communicate results in the form of technical reports and presentations. Collaborate closely with technical leads, internal stakeholders, and cross-site teams to support project objectives. Operate in compliance with applicable regulatory, safety, and data integrity requirements. Job Specifications & Requirements Bachelor’s or postgraduate degree in a relevant scientific discipline (e.g., biochemistry, biotechnology, chemical engineering, or related field), and/or extensive relevant professional experience. Minimum of 3 years of laboratory experience with training in a relevant technical discipline. Demonstrated experience in protein purification techniques, including chromatography, ultrafiltration/diafiltration, depth filtration, and protein precipitation. Strong knowledge of protein formulation and stability in solution. Proficiency in experimental design and statistical analysis (e.g., Design of Experiments, applied statistics) using relevant software tools. Experience with deviation management systems (e.g., Veeva Vault or similar) and retrieval of key deviation information. Familiarity with scientific literature databases (e.g., PubMed) and reference management tools. Experience working with electronic lab notebooks (ELN) and within biohazard laboratory environments. Strong skills in scientific data analysis, technical report writing, and presentation of results. Proficient in Microsoft Office applications (Word, PowerPoint, Excel). We look forward to receiving your application dossier, including your CV, cover letter, diplomas, and relevant work certificates. Please combine all documents into a single PDF file before submitting. About CSL Behring CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/. Our Benefits For more information on CSL benefits visit How CSL Supports Your Well-being | CSL. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement. CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please click here. CSL Global Privacy Notice for Job Applicants and Candidates

Responsibilities

Design, plan, and execute laboratory studies to support bioprocess development and lifecycle management. Investigate process deviations and optimize processes while ensuring compliance with regulatory requirements.