Assistant Manager – Regulatory Affairs
6 days ago
About your role We have vacancy for Global Regulatory Expert role in Regulatory Affairs team We are looking for Assistant Manager This individual will be based in Mumbai Hyderabad The candidate has the possibility to utilize his her own strengths with the support of the professionals Your key responsibilities Responsible for preparation checking review of pharmaceutical quality part all forms of registration dossiers and variations amendments annual reports renewals as applicable documents according to EU regulatory requirements To identify and classify the changes as per EU regulatory variation guidance To prepare response to regulatory deficiencies letters according to EU regulatory requirements To collaborate with other departments partners To maintain lists documents records Responsible for keeping Orion internal regulatory system up to date and accurate To achieve his her responsibilities within the agreed timescales To actively participate in the development of regulatory skills within the regulatory team by continuous up-dating Other possible tasks appointed by Supervisors What we offer An excellent opportunity to work in an inspiring and important role in the area of Regulatory Affairs Great opportunity to become part of the wholly owned subsidiary of globally operating Orion Group Possibility to utilize your own strengths with the support of the professionals Flexible high-spirit working environment where your skills are appreciated Hybrid Work Policy In a week - 3 days work from office and flexibility to work remotely for two times Good work-life balance Clear transparent processes and responsible supervisors are our benefits to the personnel At Orion your work creates true impact and well-being for our customers patients and society at large Our culture of friendliness respect mutual appreciation and diversity creates a safe working environment where you can strive for excellence We offer a wealth of career paths and development opportunities that support the development of innovative solutions and improving the quality of life Please visit our website to find further information about our values and Orion as an employer Our expectations Essential competences education and way of working At least 8 years work experience in international regulatory affairs from Pharma industry and Confirmed knowledge of EU requirements and ICH guidelines with Specific focus on product life cycle management Experience in Formulations Analytical Development Formulations Development or Pharmaceutical product development activities and eCTD submissions will be an added advantage Fluency in oral and written English Ability to work well independently as well as in a team environment Task oriented with learning attitude and Team work skills Familiarity with Microsoft Office Qualification Bachelors Master degree in Pharmacy or Chemistry from a reputed College University How to apply and additional information Email your CV on please share below details - Required documents CV Resume - Current CTC Expected CTC Notice Period - Application deadline 3 12 2025 About Us Orion Pharma is a globally operating Nordic pharmaceutical company - a builder of well-being for over a hundred years We re home to more than 4 000 Orionees around the world and we re proud to be known as a responsible employer and a great place to work At Orion Pharma people are truly valued and trusted encouraged to grow and supported by a culture where every voice is heard We appreciate each other strive for excellence and build the future Together we develop manufacture and market human and veterinary pharmaceuticals and active pharmaceutical ingredients Our extensive portfolio includes proprietary and generic medicines as well as consumer health products The core therapy areas of our pharmaceutical R D are oncology and pain Proprietary products developed by Orion Pharma are used to treat cancer neurological diseases respiratory diseases and more We offer careers with a clear purpose empowering people to live their lives to the fullest
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