Quality Assurance Sr. Specialist (Contract) 905

Vertex Pharmaceuticals LLC; Boston (MA); Hybrid; USD 90,000 - 96,000; Full time

Job summary

Vertex Pharmaceuticals LLC in Boston, MA seeks a Senior Specialist to apply QA and regulatory compliance principles across development programs. The role ensures timely delivery of QA activities, supports drug substance and product disposition, and collaborates with CMC Regulatory, GDP Finish Goods, and R&D Quality to drive compliant program progression.

Ideal candidates have working knowledge of GMP from early phase to commercial, strong written and verbal communication, and prior QA

Qualifications

• Bachelor’s degree in a scientific or allied health field
• 3 years of relevant work experience

Responsibilities

• Supports quality oversight for root-cause analysis and product impact assessments for investigations.
• Supports change control assessments, implementation, and closure.
• Identifies and facilitates continuous improvement efforts.
• Drafts and revises Quality Agreements between CMOs/Suppliers and Vertex.
• Represents Vertex Quality on cross-functional teams; supports batch disposition review.
• Performs review of executed batch documentation and release data.
• Supports GMP document review, including certificate of analysis.

Skills

Root Cause Analysis

CAPA

GxP Knowledge

Quality Systems

Cross-functional Collaboration

Change Control

Regulatory Compliance

Investigations

Problem Solving

Communication Skills

Education

Bachelor's degree in science or allied health

Job description

Job Description

The Senior Specialist is recognized as having a functional knowledge in the principles and applicationofqualityassuranceandregulatorycompliance.TheSenior Specialist ensurestimelydeliveryof activities to support developmental programs.

The Senior Specialist supports or executes a wide range of straightforward quality activities and supports new/existing project initiatives. This role is responsible for the execution of Quality systems to support production and product advancement as well as the performance of product disposition of clinical products which includes drug substance, drug product intermediate (spray dried dispersion), bulk drug product, and finished goods.

The Senior Specialist will demonstrate strong collaboration with key cross functional colleagues from Pharmaceutical Sciences, CMC Regulatory, GDP Finish Goods, Supply Chain and R&D Quality to compliantly advance programs through the product lifecycle. The Senior Specialist work with CMC and Quality partners to ensure that compliance and business requirements are optimized. The Senior Specialist will align with internal Quality functions, Vendor Management, Inspection Readiness and Audit /Inspection Management, to support all quality related activities associated with the programs.

**The ideal candidate will possess a working knowledge of early phase to commercial GMP drug substance and drug product manufacturing regulations and good written and verbal communication skills. Prior Quality experience supporting multiple projects and teams involved in drug development activities. **

Key Responsibilities:

• Supports quality oversight for root-cause analysis and product impact assessment for investigations as a result associated with deviations, OOS, and OOT investigations ensuring appropriate CAPA actions are identified.
• Supports change control assessments, implementation, and closure.
• Identifies and facilitates continuous improvement efforts.
• Supports drafting and revising Quality Agreements between CMOs/Suppliers and Vertex, as needed.
• Helps represents Vertex Quality on cross-functional working teams, applying strong communication and collaboration skills.
• Support continuous improvement projects.
• Performs the review of executed batch documentation from external and/or internal manufacturing and testing (executed batch records, release data, in-process controls, testing and stability data)
  • Use knowledge of functional area to inform decisions and support the success of batch disposition for drug substance, drug product intermediate, drug product and finished goods.
  • Supports GMP document review, including certificate of analysis,

PREFERRED QUALIFICATIONS:

• Experience supporting multiple projects/teams within stated objectives and timelines.
• Experience supporting cross-functional team members and collaborate effectively.
• Good communication skills (written and verbal) and the ability to exchange potentially complex information.
• Able to integrates activities with other groups, departments and project teams as needed.
• Demonstrated ability to support evaluation of quality matters and solve straightforward problems using technical experience and judgement based on precedent.
• Ability to work in a fast-paced environment and meet quality, accuracy, and timeliness objectives.
• Expanded conceptual knowledge of cGMP's in a pharmaceutical setting.
• Proficient in leading event investigations, Root Cause Analysis (RCA), and CAPA.
• Operational QA experience in analytical or manufacturing setting with experience in small molecule Experience with biologics, devices, gene therapy a plus.
• Practical GxP knowledge and understanding across lifecycle of the product including the application of:
• GMP regulations and application to
• Root Cause Analysis methodology and tools.
• Analytical techniques and data review
• Ability to evaluate routine quality matters and make decisions utilizing risk-based
• Ability to communicate cross-functionally to a wide variety of
• Relationship management/conflict management

MINIMUM QUALIFICATIONS:

Bachelor’s degree in a scientific or allied health field (or equivalent degree) and 3 years of relevant work experience, or equivalent combination of education and experience.

Pay Range

$65-$70/hr