We're looking for a Compliance Consultant - Hørsholm
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Hørsholm
Are you our new teammate?
Epista Life Science is a consultancy dedicated to continuously improving regulatory compliance, for our clients and for the entire Life Science industry. Since our founding in 2009, Epista has experienced excellent growth and now numbers over 50 hard-working and fun-loving team members. We’ve got a fantastic company culture and big ambitions for the future. And if you’re the cream of the crop, this is where you come in. We are looking for a new team member.
Job Description:
As an Epista compliance consultant, you’ll be a part of our highly skilled and dedicated team that bridges the gap between Quality Assurance, IT and Line of Business in the Life Science Industry. You’ll be involved in a wide variety of projects, primarily focusing on IT compliance and validation. Much of your time will be spent with our clients, both Danish and international pharma and medical technology companies. You’ll be involved in different project teams with skilled subject matter experts.
Due to the diversity of our projects, you must master many different competencies: technical skills, regulatory knowledge and experience. Depending of your expertise and interest, you’ll work on everything from strategy development to actual compliance, validation and quality work, and also customer’s projects – from identifying, planning, specification and implementation. The Epista team has extensive experience in the various Life Science fields, in addition to technical expertise and project management experience. Together with our new team member, we’ll help Epista’s clients achieve optimal solutions and better results.
Your qualifications:
You have a higher education and a minimum 5 years of experience working with IT compliance, computer system validation, auditing or similar in a regulated industry. It’s an advantage if you have experience in the IT QA/QC field in the pharmaceutical industry and/or consulting experience.
As a person, you are trustworthy and have a high level of situational awareness and flair for communicating with very different personalities. This will ensure you become a credible partner for Epista's clients. You are driven, result oriented and ambitious. You’re also comfortable working independently and are able to structure your own working day.
About Epista:
The key to our success is a focus on long-lasting relationships, both within our own team and with our clients. We have a dynamic and informal atmosphere in the office and we take pride in meeting our clients with respect and professionalism. We believe that the best results are achieved by allowing individuality and skills to interact across the organization. We take work-life balance seriously and respect individuals and their personal lives. Our headquarters is in Hørsholm, and we also have offices in Lund, Sweden and Villingen-Schwenningen, Germany.
Read more about Epista, our vision, values and our concrete services. Then, see what our clients have to say about us.
Get in touch:
If you fit the bill, we want to hear from you! Send your application and CV (or questions about the job) to Thomas Bjerggaard at [email protected].
Kilde: Jobnet.dk
Epista Life Science is a consultancy dedicated to continuously improving regulatory compliance, for our clients and for the entire Life Science industry. Since our founding in 2009, Epista has experienced excellent growth and now numbers over 50 hard-working and fun-loving team members. We’ve got a fantastic company culture and big ambitions for the future. And if you’re the cream of the crop, this is where you come in. We are looking for a new team member.
Job Description:
As an Epista compliance consultant, you’ll be a part of our highly skilled and dedicated team that bridges the gap between Quality Assurance, IT and Line of Business in the Life Science Industry. You’ll be involved in a wide variety of projects, primarily focusing on IT compliance and validation. Much of your time will be spent with our clients, both Danish and international pharma and medical technology companies. You’ll be involved in different project teams with skilled subject matter experts.
Due to the diversity of our projects, you must master many different competencies: technical skills, regulatory knowledge and experience. Depending of your expertise and interest, you’ll work on everything from strategy development to actual compliance, validation and quality work, and also customer’s projects – from identifying, planning, specification and implementation. The Epista team has extensive experience in the various Life Science fields, in addition to technical expertise and project management experience. Together with our new team member, we’ll help Epista’s clients achieve optimal solutions and better results.
Your qualifications:
You have a higher education and a minimum 5 years of experience working with IT compliance, computer system validation, auditing or similar in a regulated industry. It’s an advantage if you have experience in the IT QA/QC field in the pharmaceutical industry and/or consulting experience.
As a person, you are trustworthy and have a high level of situational awareness and flair for communicating with very different personalities. This will ensure you become a credible partner for Epista's clients. You are driven, result oriented and ambitious. You’re also comfortable working independently and are able to structure your own working day.
About Epista:
The key to our success is a focus on long-lasting relationships, both within our own team and with our clients. We have a dynamic and informal atmosphere in the office and we take pride in meeting our clients with respect and professionalism. We believe that the best results are achieved by allowing individuality and skills to interact across the organization. We take work-life balance seriously and respect individuals and their personal lives. Our headquarters is in Hørsholm, and we also have offices in Lund, Sweden and Villingen-Schwenningen, Germany.
Read more about Epista, our vision, values and our concrete services. Then, see what our clients have to say about us.
Get in touch:
If you fit the bill, we want to hear from you! Send your application and CV (or questions about the job) to Thomas Bjerggaard at [email protected].
Kilde: Jobnet.dk
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Hørsholm.
Jobbet er oprettet på vores service den 10.12.2019, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Hørsholm
- Tirsdag den 07. januar 2020
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Statistik over udbudte jobs som øvrige i Hørsholm
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Statistik over udbudte øvrige i Hørsholm over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 11. januar 2025 | 15 |
| 10. januar 2025 | 15 |
| 9. januar 2025 | 16 |
| 8. januar 2025 | 16 |
| 7. januar 2025 | 17 |
| 6. januar 2025 | 19 |
| 5. januar 2025 | 20 |
| 4. januar 2025 | 20 |
| 3. januar 2025 | 20 |
| 2. januar 2025 | 17 |
| 1. januar 2025 | 17 |
| 31. december 2024 | 18 |
| 30. december 2024 | 18 |
| 29. december 2024 | 18 |
| 28. december 2024 | 18 |
| 27. december 2024 | 19 |
| 26. december 2024 | 18 |
| 25. december 2024 | 18 |
| 24. december 2024 | 18 |
| 23. december 2024 | 16 |
| 22. december 2024 | 17 |
| 21. december 2024 | 17 |
| 20. december 2024 | 19 |
| 19. december 2024 | 18 |
| 18. december 2024 | 18 |
| 17. december 2024 | 17 |
| 16. december 2024 | 14 |
| 15. december 2024 | 14 |
| 14. december 2024 | 15 |
| 13. december 2024 | 16 |
| 12. december 2024 | 15 |