Covance Head of Quality, SEA & ANZ - Good Clinical Practice (GCP) in Singapore, Singapore
Are you ready to explore an exciting opportunity to provide strategic and operational leadership for our Quality Assurance team in the Asia Pacific region? You will work in partnership with global senior leaders to drive excellence in clinical research and lead a team of highly skilled auditors to develop and execute audit programs for the region. If you are a high performer looking for your next challenge let's talk.
Covance in Asia Pacific has an outstanding reputation for quality. You will join an exceptionally talented team of industry leading professionals that together will assure all systems, processes and their outcomes comply with standards that meet applicable international and national regulations and guidelines, and fulfil client and Covance requirements.
To do well in this job you will:
Be responsible for the execution of the Quality Assurance regional audit program and the oversight/direction of regional auditors, assuring alignment with global quality strategies, optimal utilization of audit resources, and of reporting of results/outcomes, ensuring adequacy of corrective and preventive actions (CAPA) to address issues, trending of audit findings and supporting continual quality improvement.
Be required to work with all levels of internal regional functional management (up to and including Executive Leaders), to drive the culture of quality.
Assure all systems, processes and their outcomes comply with standards that meet applicable international and national regulations and guidelines, and fulfil client and Covance requirements.
Tempted in moving your career to a growing organisation? If so, please apply today!
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
University/college degree, BA/BS (life science preferred) or equivalent experience Preferred
Masters or other advanced degree (e.g. postgraduate qualification in Quality Assurance) or equivalent experience
Resource management skills and ability to inspire effective teamwork and motivate staff
Excellent technical knowledge, understanding an experience applying ICH/FDA / Good Clinical Practices
Strong analytical skills
Excellent oral, written and presentation skills
Excellent planning and organizational skills
Proven interpersonal skills
Demonstrated ability to handle multiple competing priorities
Ability to function as a member of a global clinical team
Proven ability to understand, analyse and communicate the impact of global regulatory issues affecting the drug development process
4 years’ experience in Clinical Quality Assurance, preferably with GCP experience
7 years’ experience in other professional roles within pharmaceutical/CRO environment. Other required work-related experiences
Thorough knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs
Knowledge of the drug development process from the perspective of a contract research organization
Job Number 2018-18699
Job Category Quality Assurance
Position Type Full-Time
Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.