Quality Specialist, Medical Information- remote opportunities

de la Mare Creative
united kingdom
2 weeks ago
Applications closed

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Quality Specialist, Medical Information- remote opportunities

Join to apply for theQuality Specialist, Medical Information- remote opportunitiesrole atde la Mare Creative.

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.

ProPharma is looking for a professional experienced in quality to join our business; this is a remote role across UK/CEE joining a small friendly team. The ideal candidate will be a professional currently working in a quality role within a highly regulated industry. This role would suit a professional with personnel and call centre quality experience.

Duties Include

  • Generate and prepare reports to communicate the outcomes of quality activities.
  • Analyze and investigate deviation and quality events to identify areas for improvement in the quality system.
  • Review, approve and communicate root cause and corrective action to stakeholders.
  • Ensure data integrity and accuracy.
  • Prepare reports on the results of quality inspections.
  • Collection, management, and analysis of data related to CAPAs, deviations, and quality KPI's.
  • Evaluate outcomes of quality inspections and propose corrective measures.
  • Support the Quality Manager during external client reports.
  • Perform effectiveness checks on deviations and quality events to determine the efficiency of CAPA's.
  • Support and facilitate eQMS activities (document management, QA review and approvals, change control assessments, etc).

Ideal Candidate Requirements

  • Electronic Management Systems experience.
  • Deviation and CAPA handling experience.
  • An interest in change management and data analysis.
  • Working knowledge with Salesforce.

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.

Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Manufacturing

Industries

Manufacturing

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