GDP Operational Quality Assurance, Senior Specialist (Contract) 23528

placeBoston calendar_month 

Job Description:

The Quality Senior Specialist role will work with the GDP Operational QA Management team to ensure that medicines are distributed in the USA in compliance with GDP and GMP requirements. The Quality Senior Specialist will manage the day-to-day Quality oversight of the Third Party Logistics providers and provide support for key stakeholders within Vertex.

This Position Reports to: Senior Quality Manager, GDP Operational Quality

The ideal candidate will have experience in a GDP environment with a focus on Quality Assurance and Distribution.

Key Accountabilities:

  • Support the oversight of Distribution Partners within the USA, including:
  • - Preparation and maintenance of Quality Agreements
  • Review of deviations, CAPA and changes
  • Maintaining KPIs
  • Analyze, resolve, or assist in solving compliance and customer issues.
  • Escalation of issues
  • Finish Goods Release at 3PL
  • Remain up to date in GDP and logistics developments and emerging regulations to guide the maintenance of the QMS
  • Accountable for New Product Launch activities within the US providing distribution requirements and expectations.
  • Working collaboratively with key internal stakeholders
  • Support Clinical QA Distribution

Key Responsibilities:

  • Maintain QMS within the Vertex Pharmaceuticals Incorporated.
  • Ensure distribution licences (where required) accurately reflect the current organisation, vary licence where necessary
  • Support recalls, mock recalls and any other on-market activity.
  • Serve as QA assessor/approver on Change Controls: resolve gaps, approve change plans, classifications, strategy for GDP/GMP actions.
  • Support the GDP Management Review process; Review and assess the risk of inputs such as metrics, regulatory intelligence, and identified risks and gaps; Recommend mitigation approaches.
  • Participate in expansion activities to ensure that Quality related actions are planned into projects and completed in line with the commitments, e.g. QMS build out, Distribution licences (or equivalent) application, audits, and Quality Agreements.
  • Planning/ Preparation/supporting/hosting for Regulatory inspections
  • Providing front and backroom inspection support
  • Post inspection follow-up with responses and CAPAs (Continuous improvements)
  • Manage/Approve/Assess event investigations “deviations” (including Fast Track deviations)
  • Manage CAPAs and Effectiveness Checks
  • Perform other duties as per GDP guidelines and Vertex policies and procedures
  • Work with Vertex Product Complaints team to ensure that customer complaints are dealt with effectively.
  • Ensure that customers and suppliers are approved
  • Approving any subcontracting activities that may impact GDP.
  • Ensuring that self-inspections are performed at appropriate regular intervals following a prearranged program and necessary corrective measures are put in place.
  • Deciding on the final disposition of returned, rejected, recalled or counterfeit medicines, including the approval of returns to saleable stock.
  • Ensure that any additional requirements imposed on certain products by national law are adhered to.
  • Create/review and approve Standard operating Procedures and other Quality Documents

Minimum qualifications:

Master’s degree and 3-5 years of relevant work experience, or Bachelor’s degree in a scientific or allied health field (or equivalent degree) and 5+ years of relevant work experience, or relevant comparable background.

Preferred Qualifications:

  • Bachelor's in a scientific or allied health field and relevant GDP & GMP work experience, or relevant comparable background.
  • 5+ years’ experience serving in a Quality role.
  • Clear understanding to ensure operations do not compromise the quality of products and can demonstrate compliance with GDP.
  • Influencing skills in areas with no direct reporting authority.
  • Strong interpersonal and communication skills.
  • Auditing skills, appropriate qualifications in auditing an advantage.
  • Fluency in English is required
  • Proficiency in using Microsoft Office applications required (MS Word, MS Excel, MS PowerPoint)

Pay Range:

$55-$65/hr

Requisition Disclaimer:

This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer.
The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law.

In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements

By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex’s Careers Privacy Notice.

Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners

(collectively, “Atrium Alerts”). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties.

Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact Atrium at privacyadministrator@atriumstaff.com.

If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.

No C2C or Third-Party Vendors

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