For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
Are you a skilled and experienced regulatory affairs professional looking for your next challenge? Do you have a passion for ensuring compliance with regulatory requirements for pharmaceutical products? If so, we have an exciting opportunity for you!
Our company is currently seeking a Pharmaceutical Regulatory Affairs Contractor to join our team in Switzerland. In this role, you will be responsible for managing regulatory submissions and ensuring compliance with local and international regulatory requirements.
To be successful in this role, you should have a minimum of 5 years of experience in pharmaceutical regulatory affairs, with a strong understanding of Swiss and EU regulatory requirements. You should also have excellent communication and project management skills, with the ability to work independently and as part of a team.
Responsibilities:
Manage regulatory submissions for pharmaceutical products
Ensure compliance with local and international regulatory requirements
Provide regulatory support to cross-functional teams
Develop and maintain regulatory strategies
Liaise with regulatory authorities and external partners
Qualifications:
Minimum of 5 years of experience in pharmaceutical regulatory affairs
Strong understanding of Swiss and EU regulatory requirements
Excellent communication and project management skills
Ability to work independently and as part of a team
Bachelor's or Master's degree in a relevant field
If you meet the above qualifications and are looking for an exciting new opportunity in the pharmaceutical industry, we encourage you to apply for this position.
Please submit your CV and cover letter to Charlie.harris@propharma.com.
We look forward to hearing from you!
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving the pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio... Read More
