Mgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

7250 inVentiv Health Clinical Mexico, S.A. de C.V.; Argentina; A distancia; ARS 1.000.000 - 1.800.000; Jornada completa

Descripción de la vacante

Syneos Health is seeking a Mgr/Sr Regulatory CMC Consultant for small molecule projects and Veeva RIM expertise. The role supports global CMC strategies, prepares submissions, and provides regulatory guidance to cross-functional teams across development and commercialization programs.

Successful candidates will have strong knowledge of FDA/EMA/ICH guidelines, cGMP, and a biology- or chemistry-based background.

Formación

• Experience preparing and guiding CMC submissions for regulators (FDA, EMA, etc.).
• Ability to interpret global regulatory requirements and advise cross-functional teams.
• Strong problem solving, planning, and communication skills.

Responsabilidades

• Reviews CMC sections of regulatory submissions and interfaces with agencies.
• Contributes to global CMC strategies for development and commercial products.
• Guides cross-functional teams on regulatory CMC topics and changes.
• Advises on product compliance topics including deviations and GMP investigations.

Conocimientos

Regulatory CMC knowledge

Cross-functional collaboration

Strategic thinking

Regulatory guidelines experience

Educación

Bachelor's degree in Life Sciences/Regulatory Affairs

Herramientas

Veeva RIM

Descripción del empleo

Mgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to building an inclusive culture – where you can authentically be yourself.
• Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
• We are continuously building the company we all want to work for and our customers want to work with.

Job Responsibilities General Position Summary

The Chemistry Manufacturing Controls Manager will supportthe execution of global regulatory CMC strategies for marketed and development products.

This role contributes to the preparation and submission of regulatory CMC documentation for a small molecule.

This role also provides regulatory support and guidance to various cross functional teams to ensure all applicable global regulatory requirements are considered and appropriately incorporated into development and commercial programs.

Key Duties & Responsibilities

• Reviews CMC sections of regulatory submissions, as well as the interactions and responses with regulatory agencies
• Contributes to the development of global regulatory CMC strategies for commercial products
• Works with regulatory colleagues in development of global regulatory CMC strategies and Submissions
• Provides regulatory CMC guidance to cross-functional teams and key stakeholders
• Supports regulatory assessment and guidance on product compliance topics including change controls, deviations, and GMP investigations

Required Education Level & Experience

Strong interpersonal skills to exchange complex information with others and to guide others.

Proficiency in regulatory (FDA, EMA, Health Canada, LATAM, Middle East, and ICH) guidelines.

Experience in the preparation, including writing, of CMC submissions.

Strategic thinking and strong problem solving skills.

Ability to collaborate and communicate in an open, clear, complete, timely and consistent manner.

Strong sense of planning and prioritization, and the ability to work with all levels of management.

Capable of strategic thinking with ability to resolve complex and ambiguous situations.

Sound knowledge of cGMP, FDA, EMA, ICH.

Bachelor's degree, with a preference in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices, or another related life-science field.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.

Learn more about Syneos Health. http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Discover what our Syneos Health colleagues already know: work here matters everywhere. Work alongside the brightest minds in the biopharmaceutical industry taking down walls and removing barriers to speed our customers’ delivery of important therapies to patients. We are strategic thinkers who actively seek different perspectives, whether across offices or across oceans. Because we solve some of the toughest challenges facing the most prestigious healthcare companies today, you'll gain exposure and be supported with comprehensive resources including emerging technologies, data, science and knowledge sharing. The diversification and breadth of Syneos Health creates a multitude of career paths and employment opportunities.

We’re a growing, global company dedicated to advancing our talent past their initial role. Discover what our 29,000 employees already know: work here matters everywhere.

We work hard, and smart, all in the name of getting much-needed therapies to those who need them most.

A career with Syneos Health means your everyday work improves patients’ lives around the world.

Selecting us as an employer secures a career in which you’re guaranteed to: Partner with the most diverse team of experts in the industry. From the top down, our people are inspiring. Everyone has a voice and is encouraged to use it. Work in specialized Syneos Health teams that are therapeutically or functionally aligned for expert collaboration. We assemble clinical teams where everyone, from CRAs to senior management, is skilled in the same therapeutic area or customer teams. With this structure, everyone on your team speaks the same language and can deliver unique insights into the therapeutic environment and patient population. We are partners with purpose. We integrate seamlessly with our customers and do what’s best for their success. Our people provide the brilliant ideas, valuable insights and endless energy that accelerates the impact of life changing therapies worldwide.