Healthcare Jobs jobs

h]CFO[h/]

Slovenia[h/]

[h/]100,000¬ Basic + 20% Performance Bonus[h/]

The role is a golden opportunity to progress through the financial department of a huge global pharmaceutical company.

As the subsidiary of a global pharmaceutical company headquartered in Basel my client is itself a giant in the manufacturing of generic pharmaceuticals.

This role would be looking for an ambitious candidate to join the company in Slovenia. The right candidate will be ambitious and results driven.

Success in this role will result in promotion within 3 years into a bigger role with in the parent company. A good example of a progressive move after this would be to act as CFO for the Russian region with a turnover of $500m.

The role requires a candidate with previous experience in a CFO type role and experience with in Financial SAP.

The company are looking to fill this role as soon as possible.

Senior Toxicologist
Located: Cologne
Our client was founded in 2006 and is specialised on infectious diseases. The company's activities comprises discovery, research and development of novel antiviral and antibacterial agents in the indications HIV, Herpes, Hepatitis B and C, Human Cytomegalovirus and (multi)resistant bacterial infections treated in the hospital.

The company has a highly innovative pipeline addressing specialist markets and severe, potentially life threatening infections with high medical need.

Senior Toxicologist (m/f)
Our client wishes to recruit a toxicologist with industry experience as Animal Toxicology and Safety Manager.
He/she reports to the Head of Preclinical Drug Safety and
coordinates parts of non-clinical Drug Safety Evaluation (DSE) throughout the preclinical and development stages and will be the Company's source of expertise on all matters relating to DSE
manages outsourcing of activities in terms of safety pharmacology and toxicology packages
writes/supervises/monitors DSE studies and reports
tracks reports and prepare data reviews and respond to questions raised by project teams and regulatory authorities
proposes and manages the DSE budget
Skills and Qualifications

• MD / PharmD / DVM or PhD


• at least 4 years in similar responsibilities in toxicology in a pharmaceutical company or CRO


• authority and credibility within the toxicology arena


• innovative and strategic thinking skills - ability to anticipate issues and develop appropriate strategies


• flexibility, proactivity and hands-on approach to thrive in a fast-changing entrepreneurial environment


• interpretation of scientific data, Study Monitoring experience with CRO, development of DSE strategies and writing of regulatory documents (e.g. IMPD, IB, DSUR)


• experience of interacting with regulatory agencies, ideally including track record of successful safety dossier submissions


• anti-infective experience is an advantage but not mandatory


• excellent organisational and communication skills, able to promote interdisciplinary relationships, capable of setting priorities and managing high workload


• strong communication (written and verbal) and presentation skills


• business fluent in English, German skills would be beneficial

We offer an exciting and challenging job in an expanding and innovative company with an excellent R&D portfolio and a highly motivated team exhibiting many years of Big Pharma experience.

Job Title: Senior Quality Specialist [h/]

Salary: Competitive [h/]

Location: Hertfordshire [h/]Our client employ over 75,000 people across over 120 countries. As one of the worlds leading research-focussed healthcare groups they look to continually improve the quality of the work they do to innovate healthcare.
They are currently looking to recruit a Senior Quality Specialist with the purpose to support functions with PV business process development and correspondence. This role includes working on various topics and process improvement teams with the purpose of providing advise on documentation matters.
As a member of the Clinical Quality Assurance department, the Senior Quality Specialist - PV is responsible for:

• Collaborate with Business Process Owners and facilitate the development of cross functional PV Standard Operating Procedures (SOPs)


• Provide guidance on PV SOPs (content, quality, document lifecycle)


• Write and review SOPs


• Develop and deliver PV SOP training


• Participate in initiatives (cross functional teams) applying solid knowledge of processes, procedures and regulations


• Collaborate with Quality Risk Areas groups and other quality functions

Youre someone who wants to influence your own development. Youre looking for a company where you have the opportunity to pursue your interests across functions and geographies, and where a job title is not considered the final definition of who you are, but the starting point.

Qualifications:[b/]

• Bachelor's degree or equivalent in a scientific field


• Experience in a PV area (e.g. safety compliance or safety operations) is essential for this position. Experience in quality or process management is an advantage

Skills and Experience:[b/]

• Sound knowledge and understanding of ICH, FDA and EU PV regulations/guidelines


• Excellent interpersonal skills as well as oral and written communication skills


• Detail but at the same time solution oriented and ability to apply critical thinking


• Ability to simultaneously work on different documents at the same time


• Basic project management skills and ability to work effectively and independently and contribute as a team member.