Recently added jobs Remote working jobs Apprenticeships & Graduates Education & Public Sector jobs Paid by the hour / Shift work

80 Biotechnology / Life Sciences jobs in Greenwich, Amber Valley

Senior Director QA Audit ...

Salary Not Specified

Worldwide Clinical Trials, Inc., The Park, City of Nottingham

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Business Development Mana...

Salary Not Specified

O&m Halyard Emea, The Park, City of Nottingham

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Product Manager Dermatolo...

Salary Not Specified

SUN PHARMA, The Park, City of Nottingham

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Successful jobseekers create high quality email alerts

A great alert means less time searching & more time applying.

Clinical Solutions Design...

Salary Not Specified

Umotif Limited, The Park, City of Nottingham

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Full Stack Software Engin...

Salary Not Specified

Princeton Biopartners, The Park, City of Nottingham

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Key Account Manager, UK -...

Salary Not Specified

HARTMANN, The Park, City of Nottingham

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Research Consultant (Data...

Salary Not Specified

Lotus Flower, Can be based anywhere.

  • Full time
  • Temporary

Apply on company site

Posted 1 day ago, 25 Apr

Executive Engagement Prog...

Salary Not Specified

Twilio, Can be based anywhere.

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Safety Technician, WHST

Salary Not Specified

Amazon.com, Inc, Spital, Chesterfield

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Apprenticeship - Laborato...

Salary not available. View on company website.

LabCorp, The Holmes, City of Derby

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Senior Statistical Progra...

Salary not available. View on company website.

ICON PLC, Can be based anywhere.

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Senior Quality Management...

Salary not available. View on company website.

Worldwide Clinical Trials, Inc., Can be based anywhere.

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Principal Medical Writer

Salary not available. View on company website.

ICON PLC, Can be based anywhere.

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Senior Clinical Research ...

Salary not available. View on company website.

Worldwide Clinical Trials, Inc., Can be based anywhere.

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Senior Security Analyst -...

Salary not available. View on company website.

Worldwide Clinical Trials, Inc., Can be based anywhere.

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Product Manager Fuels

Salary Not Specified

The Lubrizol Corporation, Hazelwood, Derbyshire

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

(Associate) Director, Cli...

Salary Not Specified

Qiagen, Can be based anywhere.

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

LI-AL1

Salary not available. View on company website.

Unisys, Can be based anywhere.

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Sales professional

Salary not available. View on company website.

Amazon.com, Inc, Can be based anywhere.

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr

Principal Biostatistician

Salary not available. View on company website.

ICON PLC, Can be based anywhere.

  • Full time
  • Permanent

Apply on company site

Posted 1 day ago, 25 Apr
Close

Senior Director QA Audit and Inspection Program UK REMOTE

Salary Not Specified

Worldwide Clinical Trials, Inc., The Park, City of Nottingham

  • Remote working
  • Full time
  • Permanent

Posted 1 day ago, 25 Apr

Job ref: d0fac7f4a6204d239683e4982945ca74

Full Job Description

The Sr. Director of QA Audit and Inspection Program is responsible for the Strategic Vision, oversight, planning, execution, reporting and quality management of QA Audit & Inspection Program reporting to the EVP Global Head of Quality.
What you will do
+ Act as the QA Global head for the QA Audits & Inspections reporting directly to the EVP Global Head of Quality
+ Plans, adjusts, manages and optimizes all resources (budgets, staff and technologies) for the advancement of the QA's goals and objectives for the Audit & Inspection Program
+ Oversees, monitors and reports on all internal and external QA audits to ensure timely completion of applicable CAPAs to prevent reoccurrence and to drive process improvements
+ Defines, monitors, tracks and reports Key Quality Indications (KQI) and Quality Tolerance Limits (QTL) for the Audit & Inspection Program
+ Oversees the management, planning, hosting, reporting, documentation and follow up of all GCP Regulatory Inspections and Sponsor audits
+ Serves as the Subject Matter Expert on QA Quality Management Processes for Audits and Inspections

What the Senior Director QA Audits and Inspection Programs does at Worldwide, + Demonstrates excellent organizational leadership competences, inclusive of scheduling and leading team meetings that are effective, efficient and documented
+ Demonstrates excellent project management and decision-making skills
+ Communicates professionally, concisely, clearly and consistently to external and internal customers both verbally and in writing
+ Demonstrates an excellent understanding of clinical research principles and processes for clinical trials
+ Demonstrates ability to work collaboratively with cross functional stakeholders to drive process improvements based on Quality Indicators
+ Demonstrates the ability to implemented risk management strategies
+ Previous experience with leading/participating in FDA BIMO inspections, MHRA GCP inspections, Health Canada GCP inspections, EMA GCP inspections, and other international
+ Regulatory inspections is required
Your experience
+ Excellent understanding of the principles for a GCP Quality Management System
+ Excellent working knowledge of ICH Guidelines, FDA regulations, European Directives, MHRA Statutory Instruments, AIFA CRO Decree
+ Possesses broad experience related to understanding the principles and application of quality and regulatory compliance related to GxP activities, specifically GCP
+ GcLP, GLP, GVP, GPP, Device and GMP knowledge required
+ Previous experience in preparing an organization for GCP Regulatory Inspection and being the primary lead of GCP Inspections for MHRA, Health Canada, EMA, or FDA in the last 2 years.
+ Demonstrated experience for implementing GCP inspection readiness activities and tools in past 2 years.
+ Excellent experience in conducting QA Audits, specifically GCP for each type (Clinical Investigator Audits, Vendor Audits, Internal Process Audits) in last 5 years.
+ Excellent understanding or risk-based approaches to auditing
+ Demonstrated experience for leading Sponsor Audits independently
+ Previous experience in trending and analysis methodologies
+ Understanding of 21 CFR Part 11 regulations and other international guidelines specifically addressing Computer Systems Electronic Record/Electronic Signature (ERES)
+ Excellent understanding of the Drug Development Process
+ Proven experience in developing, managing and complying with annual budgets
+ Ability to speak, read and write English fluently
+ M.S. in a scientific or allied health filed and 7+ years of relevant GCP, GcLP, GLP, GVP and GPP experience
Or
+ Four-year college curriculum with concentration in nursing, biological, physical, health, pharmacy or other related science and 10+ years of relevant GCP, GLP, GVP experience
+ And 8-10 years of strong managerial experience
+ IT literate, experienced with Microsoft based applications, including proficiency in Excel, Word, Trackwise, SharePoint, and PowerPoint.
+ Domestic and international travel required (approximately 25%)

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

Do you like this job?

We can email jobs like this to your inbox

  • Facebook

Copy the direct link to this job

www.jobs24.co.uk/job/senior-director-qa-audit-inspection-program-uk-124987979
Displaying results 1 to 20 of 80 found
Create a high quality job alert