Manager, Commercial Quality

Posted 8 Hours Ago
Be an Early Applicant
Hiring Remotely in London, England, GBR
In-Office or Remote
Senior level
Biotech • Pharmaceutical
The Role
Lead Commercial Quality across the Ergomed group, providing GxP subject-matter expertise for proposals, RFIs, bid defence, and client engagements; develop commercial quality materials, maintain cost grids, oversee metrics/reporting, and mentor quality staff while supporting project quality, deviations, CAPAs, audits, and training coordination.
Summary Generated by Built In
Company Description

We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. 

PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and becoming one of the global leaders in its fields. We cover all therapy areas including medical devices. 

We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved. 

Come and join us in this exciting journey to make a positive impact in patient’s lives.  

Job Description

Role and Responsibilities

The Manager, Commercial Quality, is responsible for leading and overseeing across the Ergomed Group Quality operations with responsibility for the management, upkeep and delivery of Quality Cost Grids, Quality as a Service information and supporting Request for Information (RFI) and Bid Defence activities. 

The Manager, Commercial Quality, works closely with the Associate Director, Client Quality Management to ensure alignment with established frameworks, standards, and expectations. 

As needed mentors and develops Quality staff within the function to ensure their competence and confidence in developing skills to become subject matter experts. 

Leadership and Compliance:

  • Lead and guide Commercial Quality activities across the Ergomed group, ensuring compliance with global GxP regulations and standards.
  • Act as the Subject Matter Expert for GxP Commercial Quality, providing input into Ergomed procedures, policy, and training as required.

Business Development and Client Engagement:

  • Act as the central point for commercial quality activities
  • Drive quality input into client proposals, Requests for Information, presentations, and bid defence activities across the Ergomed group.
  • Actively participate in the Business Development process as a subject matter expert, providing strategic and tactical input at bid defence meetings.
  • Interact with Business Development in identifying new business opportunities, developing budgets and proposals, and preparing for and presenting at client meetings and teleconferences.
  • When required, represent the company by attending client meetings, speaking engagements, and publishing scientific or industry-related articles in industry journals.

Commercial Materials and Quality Management:

  • Develop commercial materials to support Quality as a Service activities, maintaining high-quality, consistent deliverables.
  • Maintain Quality commercial slide decks used to develop collateral for commercial quality needs.
  • Manage the maintenance of Quality cost grids

Metrics and Reporting:

  • Oversee the preparation and analysis of Commercial Quality-related metrics, providing periodic reports to management.

Team Leadership and Development:

  • As required, lead, educate, mentor, and develop quality group employees to support Commercial Quality activities, ensuring their competence and confidence in developing skills to become subject matter experts.
  • Foster a collaborative, high‑performing quality culture across global teams and regions.
  • Provide coaching and professional development opportunities to enhance staff capability and succession planning.

Client Quality Management: 

  • May manage project quality and compliance activities, including deviations, CAPAs, training coordination, document management, and support for audit/inspection related activities. 

Qualifications

Education, Qualifications, and Professional Memberships:

  • Degree in Life Sciences, Pharmacy, Nursing, or a related healthcare field.

Experience:

Essential 

  • Proven experience in client-facing and stakeholder management roles, with the ability to effectively engage, communicate, and collaborate with internal and external stakeholders.
  • Experience in preparing presentations, capability decks, and client-facing materials.
  • Able to demonstrate a sound knowledge of pharmacovigilance and clinical knowledge in order to carry out related duties to a competent level 

Desirable

  • Experience in preparing and contributing to bids, proposals, and RFP/RFI responses within the Life Sciences and Healthcare domain 
  • Exposure to project management, governance, and operational excellence initiatives. 
  • Experience supporting quality management activities, including deviations, CAPAs, audits, inspections, or process improvement initiatives. 
  • Experience coordinating cross-functional teams in a global or matrix environment. 

Special Skills:

  • Proficiency in Microsoft Office Suite (PowerPoint, Excel, Word) and collaboration tools. 

Language Skills:

English - fluent (spoken, written) 

Additional Information

We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.  

To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us. 

We offer: 

  • Training and career development opportunities internally

  • Strong emphasis on personal and professional growth 

  • Friendly, supportive working environment 

  • Opportunity to work with colleagues based all over the world, with English as the company language 

Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!  

  • Quality 
  • Integrity & Trust  
  • Drive & Passion  
  • Agility & Responsiveness  
  • Belonging 
  • Collaborative Partnerships  

We look forward to welcoming your application. 

#LI-remote

Skills Required

  • Degree in Life Sciences, Pharmacy, Nursing, or related healthcare field
  • Proven client-facing and stakeholder management experience
  • Experience preparing presentations, capability decks, and client-facing materials
  • Sound knowledge of pharmacovigilance and clinical concepts
  • Proficiency in Microsoft Office Suite (PowerPoint, Excel, Word) and collaboration tools
  • English fluency (spoken and written)
  • Experience preparing/contributing to bids, proposals, and RFP/RFI responses
  • Exposure to project management, governance, and operational excellence initiatives
  • Experience supporting quality management activities (deviations, CAPAs, audits, inspections, process improvement)
  • Experience coordinating cross-functional teams in a global or matrix environment
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The Company
HQ: London
535 Employees
Year Founded: 1997

What We Do

Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology. • 1,400+ highly qualified professionals • Global full-service CRO • 25+ years of experience • Therapeutic specialization in oncology • Strong expertise in rare disease trials • Robust clinical safety system • Choice of leading drug safety databases Our key services include: • Clinical Research Services • Pharmacovigilance • Medical Information • Regulatory • Medical Writing • Site Management • Study Physician Support • Biostatistics • Patient Study Support

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