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CMC-D Creator |
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Ever feel burnt out by bureaucracy? Us too. That’s why we’re changing the way we work— for higher productivity, faster innovation, and better results. We call it Dynamic Shared Ownership (DSO). Learn more about what DSO will mean for you in your new role here: https://www.bayer.com/en/strategy/strategy
MAIN PURPOSE
Authoring of CMCD (Module 3 and QoS) documents (TRDs) for Bayer’s Consumer Health new and existing product pipeline in both New Product Development (NPD) and Post Approval Change (LCM)
YOUR TASKS AND RESPONSIBILITIES
- Under the guidance of senior team members, assist in the authoring of TRDs for NPDs.
- Under the guidance of senior team members, author TRDs for renewals and annual reports for existing products (LCM).
- Documentation admin in Veeva Vault and equivalent, for all TRDs for LCMs.
- Support category continuous improvement initiatives.
- Support relevant functional processes.
WHO YOU ARE
- Bachelor's degree in a relevant scientific field (e.g., Chemistry, Biochemistry, Biotechnology), or international equivalent, ideally with +1 years of prior hands-on experience in a technical role within the pharmaceutical, food or related industry (Analytical Development, Formulation Development, Manufacturing, Module 3).
- Master’s degree or higher, in a relevant scientific field (e.g., Chemistry, Biochemistry, Biotechnology), or international equivalent.
- Basic understanding of relevant product development processes.
- Knowledge/understanding of ICH. Knowledge of other quality systems guidelines is a plus.
- Knowledge/understanding of USP, Ph.Eur. and other relevant Pharmacopoeias
- Knowledge/understanding of LATAM/Central America Regulatory guidelines and Health authorities expectations (e.g.coefepris anvisa).
- Understanding of cGMP, principles of Quality Assurance and equivalent.
- Analytical and problem-solving abilities, with ability to prioritize and manage multiple projects simultaneously.
- Communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and stakeholders.
- Proficiency in English and Spanish, both written and spoken. Portuguese is a plus.
- Detail-oriented with the ability to maintain accurate documentation and records.
- Ability to work independently and as part of a team in a fast-paced global environment.
At Bayer we believe in diversity, equity and inclusion. We aim to create an environment in which everybody can feel authentic, respected and equally valued. Every day we strive to reflect our values through our people unique capabilities, self-experiences, and aspirations. We, intentionally seek diversity, to enable our people bring their fullest potential out and encourage others to likewise do so. Our company wins, when we leverage our capabilities to lead the cultural transformation in our business, positively impacting the society.
Candidates who meet the requirements based on the job profile will be considered for employment regardless of physical disability, race, color, religion, sex, age, sexual orientation, gender identity and will not be at a disadvantage if unemployed.
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| Application Period: | 01/28/2026 - 02/10/2026 | Reference Code: | 861355 | |
| Division: | Enabling Functions | Location: | Costa Rica : Heredia : Heredia | |
| Functional Area: | Quality | Work Time: | Full Time | |
| Employment Type: | Regular | |||
| Contact Us | ||||
| Address | ||||
| Heredia, Costa Rica |
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Job Segment:
Pharmaceutical, QA, Quality Assurance, Product Development, Science, Technology, Quality, Research
