São José da Laje, Alagoas, Brazil · On-site
We are currently looking for a Principal Scientist Tech Ops (CMC Science) to join our global team in Bern. In this position you will be responsible for supporting and executing Chemistry, Manufacturing, and Controls (CMC…
Skills: CMC Strategy, Drug Substance Development, Drug Product Development, Analytical Method Validation, Process Characterization
São José da Laje, Alagoas, Brazil · Remote Solely
About the role We are looking for a Senior SDET (Software Development Engineer in Test) to improve software quality across the engineering organization through automation, testing platforms, quality standards and enginee…
Skills: Python, Playwright, MySQL, Mongo DB, AWS
São José da Laje, Alagoas, Brazil · Remote OK
About the company At Nuitée, we are building the API backbone for the global travel industry. Founded in 2017, Nuitée is on a mission to transform a fragmented travel ecosystem with simple, scalable, and API-first infras…
Skills: Go, Backend Engineering, API Design, Distributed Systems, Product Development
São José da Laje, Alagoas, Brazil · Remote OK
About the company At Nuitée, we are building the API backbone for the global travel industry. Founded in 2017, Nuitée is on a mission to transform a fragmented travel ecosystem with simple, scalable, and API-first infras…
Skills: Data Engineering, Data Science, Business Intelligence, Data Modeling, Cloud Data Platforms
São José da Laje, Alagoas, Brazil · Remote OK
About the company At Nuitée, we are building the API backbone for the global travel industry. Founded in 2017, Nuitée is on a mission to transform a fragmented travel ecosystem with simple, scalable, and API-first infras…
Skills: Golang, Backend Development, API Design, Distributed Systems, Cloud Infrastructure
São José da Laje, Alagoas, Brazil · Remote Solely
About the role As an Android Engineer at Sporty you’ll be responsible for applying the latest and greatest technologies and frameworks to ensure a smooth user experience for a massive user base. Our Stack Languages: Java…
Skills: Java, Kotlin, MVVM, Retrofit, Okhttp
São José da Laje, Alagoas, Brazil · On-site
About the company At Nuitée, we are building the API backbone for the global travel industry. Founded in 2017, Nuitée is on a mission to transform a fragmented travel ecosystem with simple, scalable, and API-first infras…
Skills: Go, Backend Development, API Design, Infrastructure, Stakeholder Management
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Responsible for executing Chemistry, Manufacturing, and Controls (CMC) strategies for pharmaceutical and biologic products from clinical development to early commercialization. This includes managing external partners, driving technical deliverables, and authoring regulatory submissions for global authorities.
Requires a PhD or MSc in Chemistry, Pharmaceutical Sciences, or a related scientific discipline with 8-10 years of experience in biotech or pharma development. Candidates must have demonstrated expertise in CMC development, regulatory guidelines (ICH, GMP), and managing external manufacturing partners.
We are currently looking for a Principal Scientist Tech Ops (CMC Science) to join our global team in Bern. In this position you will be responsible for supporting and executing Chemistry, Manufacturing, and Controls (CMC) strategies for pharmaceutical and/or biologic products across clinical development and early commercialization. This role ensures that drug substance and drug product development activities meet regulatory, quality, and business objectives.
This role works cross-functionally to drive CMC deliverables, manage external partners, and support global regulatory submissions.
Contribute to the development and implementation of phase-appropriate CMC strategies
Support CMC activities for assigned programs from early development through late-stage clinical development
Identify risks and develop mitigation strategies to ensure timelines and quality standards are met
Support drug substance and drug product development activities
Support analytical method development, validation, and specification setting
Support process characterization, validation, and lifecycle management
Manage relationships with CDMOs and manufacturing partners
Support technology transfer and scale-up activities
Ensure compliance with GMP requirements
Author, review, and contribute to CMC sections of regulatory submissions (IND, CTA, NDA, BLA)
Support interactions with global regulatory authorities, including the U.S. Food and Drug Administration and the European Medicines Agency
Address regulatory questions and inspection readiness activities
Partner with Regulatory Affairs, Quality, Supply Chain, and Technical Operations teams
Provide technical expertise to management team
Support budget planning and timeline management for CMC activities
PhD, MSc, or equivalent degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, Biochemistry, or related scientific discipline.
Typically 8-10 years of experience in pharmaceutical or biotechnology development.
Demonstrated experience in CMC development and regulatory submissions.
Experience managing external manufacturing partners preferred
Strong scientific and technical expertise in CMC disciplines
Knowledge of global regulatory guidelines (ICH, GMP)
Project leadership and stakeholder management
Risk assessment and problem-solving skills
Excellent communication and organizational skills
Are you interested? We are looking forward to receiving your online application
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/.
For more information on CSL benefits visit How CSL Supports Your Well-being | 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
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 a leading global biopharma company with a dynamic portfolio of lifesaving medicines, including those that treat haemophilia and immune deficiencies, vaccines to prevent influenza, and therapies in iron deficiency, dialysis and nephrology. Since our start in 1916, we have been driven by our promise to save lives using the latest technologies. Today, CSL – including our businesses, CSL Behring, CSL Seqirus, and CSL Vifor – provides lifesaving products to patients in more than 100 countries and employs 29,000+ people. Our unique combination of commercial strength, R&D focus and operational excellence enables us to identify, develop and deliver innovations so our patients can live life to the fullest. See our community guidelines: https://bit.ly/3Bs17Ra
Offices: 655 Elizabeth St, Melbourne, Victoria 3000, AU · 1020 1st Ave, King of Prussia, PA 19406, US
There are currently 27 open engineering positions in São José da Laje, Brazil listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include CSL, Nuitée, Remote, Alpaca, Arize AI, among others. Browse the listings above to see every active employer.
Yes — 17 of the 27 open engineering positions offer remote or hybrid work (16 remote, 1 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
