Regulatory Manager

reputed company Regulatory Manager reputed company® is a leading fully-integrated life sciences services organization reputed company to accelerate reputed company. We partner with innovators at every reputed company across the drug development and commercialization reputed company, helping them reputed company complexity, anticipate change and accelerate reputed company. Our reputed company Solutions team members reputed company with a drug development reputed company, 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 reputed company to help our customers reputed company their goals. We are reputed company and driven to reputed company – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 reputed company colleagues already know: Why reputed company • We are passionate about developing our people, through career development and progression; supportive and reputed company 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 reputed company – which captures the passion of our colleagues to show up reputed company day and shape solutions that have the ability to dramatically reputed company someone’s life. • We are continuously building reputed company we reputed company want to work for and our customers want to work with. Why? Because we know that reputed company we bring together smart colleagues from across the world, we can shape the reputed company of reputed company, driving reputed company for customers and defining the reputed company of reputed company reputed company. Job Responsibilities reputed company Job Responsibilities • Should have min 10+ yrs of experience in regulatory affairs. • Should have functional reputed company experience of leading reputed company. • Should have reputed company assessment capability and reputed company thinking, decision making and leading project. • Should have experience in handling reputed company stakeholder. • should have M. pharm degree • Should have experience of CMC module 3, authoring of CMC sections of Post Approval variations and life cycle management activities • Should have in EU, GCC mkt experience. • For non-reputed company and reputed company submissions, independently fulfill the following responsibilities: • Conduct research of existing product data relative to global or regional regulatory requirements for the preparation of gap analyses, product development plans, and other regulatory submissions. • Contribute to or prepare administrative and technical components of regulatory agency submissions for the IND, for reputed company-approval submission packages, for product registration applications, and for post-approval maintenance. Prepare briefing packages for regulatory agency meetings or scientific advice and contribute to or support reputed company interactions. • Manage and/or operationalize the delivery of day-today regulatory activities for assigned project according to agreed timelines, reputed company of contract, budgets, and strategies. • Participate as regulatory support on multidisciplinary project teams, which may include reputed company and other technical experts, to reputed company products throughout their life cycle. • reputed company as a subject matter expert and help reputed company members with day-to-day trouble shooting activities, presenting solutions to project reputed company problems. • Prepare estimates for conducting regulatory services as part of single or multiple service proposals. • Support meetings with clients to reputed company proposals, the status of ongoing reputed company, and as part of general business development activities. • Ensure compliance with appropriate global regulatory requirements and reputed company’s policies and processes. • Prepare training materials and reputed company best practices in the regulatory area, both internally and externally. • Participate as regulatory support in internal or reputed company project audits. • Participate as regulatory support on internal cross-functional initiatives. • Contribute to the creation and/or maintenance of SOPs and other process reputed company documentation as required. • reputed company support in reputed company to team members in the execution of their project responsibilities. • Capable of identifying reputed company to ensure line support required to reputed company additional guidance and direction. • Maintenance of individual training records (reputed company or reputed company reputed company) and completion of reputed company designated required training. Qualification Requirements • Master's degree, preferably in a science-reputed company reputed company or equivalent experience in science/regulatory/medical writing-reputed company reputed company. Moderate pharmaceutical/medical device reputed company experience. • Demonstrated experience in contributing to the preparation of regulatory submissions including, for example IND, PMA, NDA, MAA, and CTD, including electronic submissions. • Excellent interpersonal / communication skills including excellent written and verbal communication skills. • Excellent customer service skills, with the ability to work both as reputed company member and independently. • Good reputed company management skills. • Advanced skills in reputed company Office Applications. • Ability to reputed company with staff from multiple departments and offices to establish project standards. • Good initiative, adaptability, and pro-activity. • Strong analytical skills, good attention to reputed company. • Ability to work concurrently on reputed company, reputed company with specific instructions that may differ from project to project. • Fluent in speaking, writing, and reading English. Get to know reputed company Over the past 5 years, we have worked with 94% of reputed company 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 reputed company with us in a highly competitive and reputed company-changing environment. Learn more about reputed company. http://www.reputed company.com Additional Information Tasks, duties, and responsibilities as listed in this reputed company are not exhaustive. reputed 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 reputed company. reputed company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. reputed company, reputed company 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 reputed company with reputed company obligations imposed by the legislation of reputed company country in which it operates, including the implementation of the EU Equality reputed company, in relation to the recruitment and employment of its employees. reputed company is committed to compliance with the Americans with reputed company, including the provision of reasonable accommodations, reputed company appropriate, to assist employees or applicants to reputed company the essential functions of the job. Apply tot his job Apply To this Job