Quality Compliance Specialist
We are Reckitt
Our R&D Team
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
About the role
We're in search of a proactive Supplier Quality Assistance to join the Reckitt team, where innovation and science converge to make a real-world impact. You'll contribute to the growth of our trusted product portfolio, ensuring the highest standards of quality. Your expertise will drive activities from concept to execution, fostering an environment of continuous improvement. If you thrive in a dynamic atmosphere and are looking for a role where your actions directly contribute to the company's success, we would love to see your application.
Location of the role: Mexico City, Tlalpan.
Your responsibilities
- Degree in Chemistry, Biology, Engineering, or another relevant science.
- Familiarity with R & D processes and working within a GMP environment.
- Conduct Risk Assessments.
- Strong project management experiences with demonstrable problem-solving skills.
- Independent and self-starting with the resilience needed to thrive in a fast-paced environment.
- Ability to lead and motivate others, showing strong interpersonal competence and team commitment.
- Commercially aware, with the ability to propose improvements and challenge the status quo for better results.
- Adaptable and collaborative nature, prepared to take accountability for a broad range of activities.
The experience we're looking for
- Bachelor’s degree in Chemistry, Biology, Engineering, or a related scientific field.
- Knowledge of R&D processes and experience working in a GMP-regulated environment.
- Prior experience in the pharmaceutical or food industry, including conducting audits.
- Understanding of production processes.
- Familiarity with regulatory standards such as Cofepris, Anvisa, and FDA requirements.
- Experience performing audits in both Spanish and English.
- Advanced proficiency in English.
- Strong project management background with proven problem‑solving abilities.
- Self‑motivated and able to work independently, demonstrating resilience in fast‑paced settings.
- Capable of leading and inspiring teams, with strong interpersonal skills and a collaborative mindset.
- Commercially aware, with the ability to identify opportunities for improvement and challenge existing practices to enhance outcomes.
- Flexible and team‑oriented, with a willingness to take responsibility for a wide range of tasks.
The skills for success
- Strong commercial acumen with the ability to build strategic business partnerships.
- Proven collaborator skilled in fostering cross‑functional alignment and long‑term partnerships.
- Capable of constructively challenging established practices to drive innovation and continuous improvement.
- Demonstrates accountability and ownership of outcomes.
- Highly adaptable, with the ability to adjust to evolving priorities and organizational needs.
- Effective contributor to R&D initiatives and knowledgeable in product lifecycle management.
What we offer
Equality
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