CSV Analyst 12 Month FTC

Reposted 25 Days Ago
Be an Early Applicant
Hengoed, Caerphilly, Wales, GBR
In-Office
Mid level
Pharmaceutical
The Role
Support and maintain IT Quality and Computer System Validation (CSV) processes and documentation to meet GxP and regulatory requirements. Provide CSV subject matter expertise across projects, review changes, support testing and risk-based validation approaches, assist audits, and drive continuous improvement of validation policies, procedures and training.
Summary Generated by Built In

Want a 3D Career? Join Norgine.

At Norgine, our colleagues Dare themselves to be different and try new things, Drive to achieve their goals and beyond, and Develop themselves and their community.

We call it the 3D career at Norgine and it offers you a fully-rounded experience with no limits.

Bring everything about yourself that you’re proud of, whether that’s your passion for making a difference, focus on others’ well-being, or intellectual curiosity to unleash in a fast-paced environment and supportive community.

In return, get a sense of belonging, a long-term career with ongoing development and upskilling, and a company that cares about people’s wellness as much as you do.

Because at Norgine, we transform lives with innovative healthcare solutions.

We have an exciting opportunity for a CSV Analyst 12 Months - FTC to join Norgine.

Core Responsibilities:

This role is responsible for ensuring that Norgine IT Quality Management System, Validation documentation and all related processes, procedures and systems meet the requirements of all applicable regulations. This means not only working with other team members and consultants to identify any such weaknesses but also being instrumental in closing any such gaps identified. This may involve both directing others regarding what is needed and also making such changes themselves.

If you want a multi-dimensional 3D career in a leading healthcare organisation, join us.


Requirements
  • Assist the CSV/Lead Process Analyst in continued improvement and delivery of the Global IT validation strategy and approach taking into account the relevant GxP requirements (e.g. EU Annex 11, FDA 21 CFR Part 11, Part 820, etc.) and also other relevant regulatory requirements
  • Support the continuous improvement of appropriate procedures to be used in validating computerized systems:
  • Develop, review and approve CSV policies, procedures, plans and protocols, and champion their adoption.
  • Support project teams in defining the appropriate level of validation required based on a risk assessment
  • Support project teams in the creation of the agreed validation pack of documents to support the validated state
  • Support the business functions in the periodic review of systems to assess the current validated state
  • Acts as a quality contact and primary Subject Matter Expert (SME) for Computer System Validation (CSV) and Risk Management
  • Review proposed changes to validated computerized systems and identify the validation requirements necessary to maintain the system’s validation status after execution of the change.
  • Support project teams in the assessment of proposed new computerized systems or software for GxP impact and where GxP impact is identified provide guidance on the risk based validation approach for the system, working with key stakeholders to achieve business goals.
  • Support formal testing of computerized systems ensuring that test plans, test scripts and test results comply with the regulatory requirements based on system risk.
  • Ensure that the Local Validation Master Plan is maintained and is aligned to corporate policies as they relate to computer systems validation
  • Assists in all forms of audit and responds to audit observations and corrective actions as they pertain to computer systems validation
  • Interacts professionally with company management, internal departments and other areas of the business to effectively implement and maintain Quality Systems as they relate to CSV
  • Identifies and implements improvement opportunities with the CSV/Lead process Analyst for established Quality Systems, processes, procedures, and training to support IT CSV activities
  • Maintain up to date knowledge of evolving regulatory requirements, availability of current/new techniques, and literature regarding compliant computer operations, and act as an information resource for the team and wider business.
  • Such other activities as may be necessary from time to time

Education and experience

  • Bachelor’s degree preferred
  • Experience in a validation and qualification of complex computer systems
  • Thorough knowledge of cGMP regulations related to CSV
  • Good written and oral communication skills
  • Competent user of Microsoft Office

Technical Skills

  • Familiarity with multiple system types such as ERP and BI, LIMS, HRIS etc.
  • Good understanding of business requirements, high-level solutions and infrastructure components, combined with CSV system experience.
  • Wide experience of the various regulatory requirements relating to Eudralex Annexe 11, FDA CFR21 Part 11, etc..
  • Experience of the data integrity implications of the regulated environment

Team Skills

  • Confident communicator, able to network effectively in a diverse business community.
  • Proactive, professional approach, undertakes tasks and responds to business requests in a positive and constructive manner.
  • Keeps industry and organization knowledge current in order to provide up to date solutions and be best placed to advise on future capabilities.

COMPETENCIES

SHAPING / LEADING / IMPACTING / CONTRIBUTING

Communication

  • Reinforces Norgine's culture and values through appropriate communication styles and methods, taking into account language and cultural differences.
  • Able to confidently and effectively communicate with smaller groups or individuals.
  • Asks relevant questions to clarify understanding and determine appropriate action to be taken.
  • Listens to information and interprets impact on immediate area.

Change

  • Embraces change and sees it as an opportunity and deals with it constructively.
  • Displays adaptability and flexibility in accepting change.
  • Agrees and implements processes to enable change within area of responsibility.
  • Seeks value-adding improvements to processes and services, even if it means challenging the status quo.

Leadership

  • Understands Norgine's vision and values and considers actions accordingly.
  • Leads by example in setting high personal performance standards.
  • Has a positive influence within area of responsibility.
  • Makes clear day to day decisions individually or collaboratively within area of responsibility, ensuring those affected understand decisions taken.

People & Relationship Management

  • Develops positive working relationships with colleagues within area of responsibility and across associated functional areas.
  • Readily shares knowledge, skills and experience to improve others' outputs.
  • Recognises diversity and reinforces that discrimination, bullying and harassment is unacceptable.
  • Deals with conflict situations and seeks to reduce negative impact.

Delivery (Results & Service)

  • Shows a high level of awareness of the impact of actions on business results.
  • Shows awareness of risks to business goals and understands contingency plans in place.
  • Maintains high customer service standards and keeps customer informed.
  • Recognises and understands the importance of "how" as well as "what" is achieved.

Personal Effectiveness

  • Proactive with a focused and structured approach to work - although willing to change direction if required.
  • Prioritises and manages time to achieve tasks.
  • Displays resilience when under pressure.
  • Possesses self awareness and is able to modify behaviour in different situations in order to be more effective.

Benefits

Our benefits may vary per location. Please liaise with the Norgine TA representative to obtain more information.

Sound good? Find out more about the career you’ll have with Norgine, then apply here.

#LI-PP1

Skills Required

  • Experience in validation and qualification of complex computer systems
  • Thorough knowledge of cGMP regulations related to CSV
  • Familiarity with ERP, BI, LIMS, HRIS and other system types
  • Experience with regulatory requirements (Eudralex Annex 11, FDA 21 CFR Part 11, ISO etc.)
  • Experience of data integrity implications in regulated environments
  • Good written and oral communication skills
  • Competent user of Microsoft Office
  • Bachelor's degree
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The Company
HQ: Amsterdam
980 Employees

What We Do

Norgine is a leading European specialist pharmaceutical company that has been bringing transformative medicines to patients for over a century. Our commitment to transforming people’s lives drives everything we do and our European experience, fully integrated infrastructure and exceptional partnership approach enables us to quickly apply creative solutions to bring life-changing medicines to patients that they may not otherwise be able to access. Norgine is proud to have helped 24 million patients around the world in 2021 and generated €505 million in net product sales, a growth of 10% over 2020. Norgine has a direct presence in 16 European countries, as well as Australia and New Zealand. We also have a strong global network of partnerships in non-Norgine markets. We are a flexible and fully integrated pharmaceutical business, with manufacturing (Hengoed, Wales and Dreux, France), third party supply networks and significant product development capabilities, in addition to our sales and marketing infrastructure. This enables us to acquire, develop and commercialise specialist and innovative products that make a real difference to the lives of patients around the world. In 2012, Norgine established Norgine Ventures, a complementary business which supports innovative healthcare companies through the provision of debt-like financing in Europe and the US. For more information, please visit www.norgineventures.com.

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