Director (m/f/d) - Quality Assurance at Octapharma
Vienna, , Austria -
Full Time


Start Date

Immediate

Expiry Date

17 Jan, 26

Salary

5598.85

Posted On

19 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Quality Assurance, Clinical Trials, Compliance, Regulations, Clinical Operations, Quality Management, Problem-Solving, Analytical Skills, Communication Skills, Organizational Skills

Industry

Pharmaceutical Manufacturing

Description
Become part of a vital chain and contribute to our common goal of making people’s lives better. Octapharma is a leading biotech pharmaceutical company that combines the strength of a global organisation with the values of a family business. We specialize in the development and manufacture of high-quality pharmaceuticals derived from human blood plasma and human cell lines.    With over 1,600 employees, the Octapharma site in Vienna is the largest production site, and successful research and development location. Join us in shaping our vision of providing new health solutions advancing human life.   Your main tasks and responsibilities    Lead the Clinical Quality Assurance team, define tasks and responsibilities covered by the department, keep oversight on Clinical Quality Assurance tasks and responsibilities Ensure clinical trials are conducted following the respective regulations and guidelines Provide compliance advise to operational units Ensure compliance of clinical documents with regulations and guidelines Support preparation, conduct and follow up of regulatory inspections of clinical studies Act as interface between Octapharma’s Corporate Quality Assurance function and global Clinical R&D   Your expertise and ideal skill set    Completed University degree in natural sciences, preferably medical or biosciences At least 5 years of working experience in the Pharmaceutical or CRO Industry, preferably in Clinical Operations Experience in Quality Management Excellent in English, German is a plus (written and oral) Willingness to travel up to >25% Strong problem-solving and analytical skills Excellent written and verbal communication as well as strong organizational skills   Your department - where you make an impact     We, the Research & Development unit, conduct preclinical and clinical research to develop new products and ensure their safe and effective use. Our ultimate focus in our daily work is to enhance patient health and safety.  Thrive with us   Company restaurant & meal subsidy  Training & further education  Health promotion  Parking spaces and good public transport connections   Company and team events  Enjoy these attractive benefits! You can find all offers here: BenefitsThe minimum gross salary according to the collective agreement (chemical industry) is EUR 5,598.85 based on 38 hours per week (full-time). As we strive to offer a salary that reflects your individual profile and qualifications, there is a willingness to pay above the minimum salary.   It´s in our blood We live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion.   Do you have any questions? Then get in touch with your contact person.  Mrs. Johanna Proksch Octapharma Pharmazeutika Produktionsges.m.b.H.  Oberlaaer Straße 235, 1100 Wien  T: +43 (1) 610 32 4299   You can also reach us Monday to Friday via WhatsApp: +43 (0) 664 885 78 113 Want to find out more about us?   Visit our website Octapharma Career and follow us daily on LinkedIn.    

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities
Lead the Clinical Quality Assurance team and ensure clinical trials are conducted in compliance with regulations. Act as an interface between Octapharma’s Corporate Quality Assurance function and global Clinical R&D.
Loading...