Associate Director, Clinical Quality Assurance Permanent Position

Eisai; Hatfield; Hybrid; GBP 150,000 - 200,000; Full time

Job summary

A leading pharmaceutical company in Hatfield is seeking an Associate Director GCP Quality Assurance to conduct compliance activities and manage cross-functional relationships. This high-visibility role requires significant experience in clinical quality assurance and strong leadership skills. The ideal candidate will possess a Bachelor’s degree (advanced degree preferred) and demonstrated experience in clinical research or data management. Attractive benefits and hybrid working options available.

Benefits

Hybrid working

Car / Car Allowance

Electric charging points

Discretionary Bonus

Free onsite parking

Subsidised onsite restaurant

Learning and development opportunities

Retail discounts

Well-being & mental health awareness programmes

Multi-faith prayer room

Qualifications

• Demonstrated experience in Clinical research/operations/data management or related area.
• Demonstrated experience in Clinical Quality Assurance.
• Experience managing cross-functional relationships.

Responsibilities

• Conduct GCP compliance activities.
• Manage cross-functional relationships with internal and external stakeholders.
• Be the Lead Quality Assurance representative to clinical teams.

Skills

Quality Assurance

FDA Regulations

ISO 9001

Root cause Analysis

Biotechnology

Clinical Trials

Quality Systems

Food Processing

Quality Control

Quality Management

cGMP

HACCP

Education

Bachelor's degree in associated functional discipline

Advanced degree preferred

Job description

The Company

Eisai is a leading research based pharmaceutical organisation with an extensive portfolio across the Oncology Neurology and Pain therapy areas.

Your new role

The Associate Director GCP Quality Assurance works within the Global Clinical Quality Assurance (CQA) team to conduct GCP compliance activities at Eisai. The position will manage cross‑functional relationships with internal and external stakeholders and be the Lead Quality Assurance representative to clinical teams on assigned trials. This is a high visibility position with great impact potential.

What are we looking for

• Educated to Bachelors degree in associated functional discipline advanced degree preferred
• Demonstrated experience in Clinical research / operations / data management or related area.
• Demonstrated experience in Clinical Quality Assurance.

Health Authority inspection management

Health Authority inspection management

What we offer in return

Eisai offers a competitive salary and excellent wider benefits package that includes

• Hybrid working (Depending on role)
• Car / Car Allowance (Depending on role)
• Electric charging points for Electric / Hybrid vehicles
• Discretionary Bonus
• Free onsite parking
• Subsidised onsite restaurant and coffee shop
• Learning and development opportunities
• Retail discounts
• Well‑being & mental health awareness programmes
• Multi‑faith prayer room

What you need to do next

If you are interested in this position please click apply now at the top of this advert. Upon submitting your application you will be asked to complete your profile and upload a copy of your CV along with any additional information to support your application.

Eisai Recruitment Statement

Diverse perspectives and experiences are critical to our success and we welcome applications from all people from all backgrounds with the experience and skills needed to perform this role. We look forward to receiving your application.

Eisai EMEA EDI Commitment Statement

We believe that diverse and inclusive teams promote wellbeing learning and innovation helping Eisai serve our patients their families our employees and society. Our commitment is :

• to embrace and celebrate our differences respecting and valuing each other.
• to include equity diversity and inclusion practices in all that we do so everyone has a full sense of belonging.
• to value individual talent where every employee can be themselves and thrive in an environment of openness trust and integrity

Required Experience

Director

Key Skills

Quality Assurance,FDA Regulations,ISO 9001,Root cause Analysis,Biotechnology,Clinical Trials,Quality Systems,Food Processing,Quality Control,Quality Management,cGMP,HACCP

Employment Type

Full-Time

Experience

years

Vacancy

1