Regulatory Affairs Manager
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Job Location:
Monthly Salary:
Posted on:
3 hours ago
Vacancies:
1 Vacancy
Job Summary
As a Regulatory Affairs Manager you will take on a highimpact role with global scope influencing regulatory decisions market access and risk management across regions as well as directly shaping Syntegons regulatory posture worldwide.
- Lead the development and execution of regulatory strategies to ensure Syntegon remains fully compliant with applicable national and international laws standards and guidelines.
- This includes compliance with current regulations and the proactive anticipation of forthcoming regulatory changes ensuring Syntegon stays at the forefront of compliance and market access.
- Map and analyze global target markets and translate findings into implications as well as concrete regulatory requirements timelines and implementation plans.
- Establish and govern regulatory processes and organizational structures standardizing procedures and tools across regions to ensure consistent auditable and efficient regulatory operations.
- Support regulatory aspects of due diligence activities for transactions and partnerships assessing product- market- and supplier-related regulatory risks including social and human-rights aspects in the supply chain.
- Interact with various stakeholder groups such as the Legal department external agencies and regulatory authorities to verify compliance and implement corrective actions.
Qualifications :
- At least 5 years of relevant experience in regulatory affairs ideally with experience in regulatory compliance or management reporting.
- Educational background in a relevant field such as Engineering Law or Sustainability or an equivalent qualification; additional relevant certifications are a plus.
- Able to work effectively across different organizational levels with strong stakeholder management skills.
- Strong ability to anticipate trends and synthesize crossfunctional insights into strategic actions.
- Excellent critical thinking skills and a structured systematic approach to tasks complete your profile.
Additional Information :
Kindly note that this position can be filled not only in Terrassa but also at any Syntegon location across Europe.
For Syntegon and its subsidiaries diversity is a key concern. We explicitly welcome an environment where all employees regardless of gender age origin religion sexual orientation gender identity or special needs are treated equally. If this job posting uses only the male form it is for readability purposes and refers to individuals of all genders.
Remote Work :
No
Employment Type :
Full-time
Key Skills
- Proofreading
- Adobe Acrobat
- FDA Regulations
- Manufacturing & Controls
- Biotechnology
- Clinical Trials
- Research & Development
- GLP
- cGMP
- Product Development
- Chemistry
- Writing Skills
About Company
Gemeinsam mit 6.300 Kolleg:innen weltweit sind wir der strategische Partner der Pharma- und Lebensmittelindustrie für Prozess- und Verpackungstechnik. Mit reibungslosen Prozessen, innovativen Technologien und nachhaltigen Lösungen helfen wir unseren Kunden, ihre Ziele zu erreichen. Wi ... View more
