AdressThe opportunity
The Senior Consultant - Compliance and Quality Assurance will be key in supporting a variety of Life science clients across various phases of development and commericalisation within Pharmaceutical and Biological industry. Within these projects, the successful candidate will be responsible for strategic development; project leadership; acting as the SME and providing key support to a range of clients in QA. This role will allow the successful applicant the chance to work on some of the most fascinating projects the market has to offer with the opportunity to fast-track your development across various therapeutic disciplines. In addition, ProPharma also has the opportunity to offer remote working; a competitive remuneration package and a positive work-life balance.
Essential Functions Include:
- The Senior Consultant Compliance, Quality Assurance (CQA) position is primarily responsible for being a key Subject matter expert in assigned areas of Quality Assurance and regulatory/GxP.
- They will be responsible for providing Independent consultation with clients and project leadership to a range of challenging and fascinating projects across the CQA space.
- Lead and manage project work on client's WDA projects, such as acting as an RP, GxP auditing, developing Quality Management Systems (QMS) etc.
- Ensure the successful execution of key projects and ensure profitability
- Keep pace with the regulatory and technological changes in the CQA field
- Be a critical team member who contributes to the implementation and successful execution of risk-based and phase appropriate GxP projects.
- Act as the SME within the commercial process with clients as required and identify scope and effort required to successfully address client needs.
- Actively promote CQA services within the industry across various platforms
- Promote continual improvement regarding customer satisfaction with emphasis on CQA consulting services.
- Provide CQA specific training to clients and associates within other business units.
- Provide support to clients and all functional units of ProPharma as GxP issues such as deviations and non-conformances arise.
- Provides consultation for the implementation of proper CAPA to resolve deviations and non-conformances. Also, is responsible for ensuring compliance of company operations to quality principles and participation in the development of quality systems through SOP writing and training.
- Directly engages with employees at all levels to educate on compliance and Quality Assurance to drive continuous improvement.
- Actively perform the function as Responsible Person for clients and Qualified Person if trained in the area
- Other duties as assigned
Experience required
- Ideally educated to at least a BSc level in Pharmacy or another appropriate discipline
- Must hold 10 years or more experience within Quality Assurance within GXP settings
- 2-3 years or more experience working as a Responsible Person is required
- Qualified Person status/accreditation would be highly desirable
- Ideally skilled in development and marketed products
- Thorough understanding of the Regulatory landscape within the industry
- Fluency in English and ideally Sweden
- Demonstrated project management skills with the ability to prioritise workload and meet deadlines.
- Excellent collaboration and stakeholder skills
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
