H&P Search & Interim AB is a company with substantial experience in recruitment (Search) as well as placing consultants (Interim). Our focus is 100 percent on Life Sciences in the Nordic region: pharmaceuticals, biotechnology, medical technology, and related industries. We have a broad network of contacts and a keen awareness of changes in the market. Our employees themselves have medical, natural science and economic backgrounds, as well as great experience in leadership at all levels. H&P Search & Interim are specialists in recruitment (Search) and placing consultants (Interim) at all levels and areas within a company. We help clients to find the right co-workers and consultants within, e.g. sales and marketing; market access; medical, clinical, quality assurance and regulatory affairs; logistics and distribution. For further information, please see www.hpsearch.se
H&P Search & Interim is now recruiting staff within Regulatory Affairs with different levels of experience and specific capabilities for future assignments as a consultant or employee in the Pharmaceutical and/or MedTech industries.
About H&P Search & Interim
We are a recruitment and staffing company, specializing within the Life Science domain and receive assignments from customers with operations throughout the Nordic region. Our areas of expertise apply within the context of pharmaceuticals, OTC, biotechnology and medical technology, which also represent the basis of our large and wide network of contacts that we draw from. We work to help our customers find the right skillsets for both temporary and permanent necessities, while providing our employees with stimulating tasks and development opportunities, to satisfy their career interests.
The recruitment consultants at H&P Search & Interim have medical, scientific and financial backgrounds as well as extensive experience as leaders and managers within these areas. Altogether, our experience amounts to over 125 years within the Life Science industry.
Examples of tasks that could be included in different assignments
The customers need may of course vary related to the organisation (manufacturing, R&D, local marketing company, distributor etc). Here are some examples:
- Responsible for the fulfillment of regulatory CMC requirements, for new Marketing Authorization Applications and Post Approval Activities
- Development and implementation of regulatory CMC strategies for new Marketing Authorization Applications and Post Approval Activities.
- Assessing, approving, progressing and ensuring timely implementation of change controls
- You may also coordinate assembly of submission-ready documents to support lifecycle submissions
- You will keep business wide electronic systems up to date in order to be consistent with regulatory submissions and commitments
- You may also support externalization projects and the transferring of CMC documentation to external partners
What we can offer you
You certainly have the opportunity for personal development through various roles, responsibilities and projects with our customers. We offer market-based compensation and benefits as well as collective bargaining agreements and relevant insurance, wellness allowance and company car if the work so requires. As a consultant with H&P Search & Interim, you will be part of a consulting team within Life Science and thus have the opportunity to broaden your own network and exchange experiences with colleagues in a similar situation. A couple of times a year, consultancy training will be held for you, allowing to strengthen your skills and your ability to compete within the industry. In addition to training, we commit to regular communication and monthly meetings to ensure that you thrive and develop in your workplace.
You have a university degree in Pharmaceutical or Science such as civil engineering, biomedicine, chemistry, biology or equivalent. You have good knowledge of both Swedish and English language and can express yourself well both orally and in writing. Previous experience in Regulatory Affairs within the pharmaceutical industry and/or the MedTech industry is needed. Furthermore, you should have experience of regulatory guidelines and legislation within the CMC area. You are a structured person but still flexible allowing change to potentially take place at short notice. To fit the role, you should possess the ability and enjoy working independently as well as cross-functional as part of teams with many different duties.
You are welcome to submit your application. Interviews and selection processes take place on an ongoing basis as we have a continuous need for competent consultants/employees.
How to apply
If this sounds interesting, please contact
- Torbjörn Ströberg, Torbjorn.Stroberg@hpsearch.se, +46 (0)70 377 87 74 or
- Catharina Bergold, firstname.lastname@example.org, +46 (0)70 2179879
Welcome with your application!