Enable job alerts via email!

Healthcare Quality & Regulatory Specialist - Global Logistics Client

Flintex Consulting Pte Ltd

Singapore

On-site

SGD 65,000 - 85,000

Full time

7 days ago
Be an early applicant

Job summary

A healthcare compliance consulting firm in Singapore is seeking a qualified professional to drive compliance and quality programs in Healthcare Transportation and Facilities. The ideal candidate must hold a pharmacist license and have 3-5 years of relevant experience in the pharmaceutical or healthcare industry, focusing on quality assurance and regulatory affairs. This position offers competitive benefits including a 13th Month Salary and bonuses.

Benefits

13th Month Salary
Incentives (2-3 months)
Joining and Retention Bonus

Qualifications

  • Hold local pharmacist license.
  • 3-5 years of experience in pharmaceutical or healthcare industry in a quality-related role.
  • Experience ensuring compliance with cGMP, GCP, GDP.

Responsibilities

  • Drive compliance and quality programs for Healthcare Transportation and Facilities.
  • Implement compliance and quality programs.
  • Lead and support internal and certification audits.

Skills

Quality assurance
Regulatory affairs
Customer relationship management
Root cause analysis

Education

Bachelor's degree in Pharmacy

Job description

Benefits: 13th Month Salary + Incentives (2-3months), + Joining and Retention Bonus

This role is responsible to drive compliance and quality programs for Healthcare Transportation & Facilities and supporting the Healthcare Quality Management System to ensure processes and systems are compliant with regional and local regulations and customer requirements.

Quality Policies & Procedures:

Determine, implement & promote policies and procedures for Company’s Network and facilities (hubs & stations) to ensure compliance to standards such as GDP, GCP and others

Quality Assessment & Standards:

Write & review SOPs and Work Instructions for transportation & fulfilment solutions pertaining to the healthcare industry

Compliance & Quality Program Management:

Implement compliance and quality programs to support local Quality teams to ensure they are kept up-to-date and prepared.

CAPA Process Management:

Lead in process creation and review of documentation on the implementation and responses to corrective and preventive actions (CAPAs) and monitor action progress until closure.

Healthcare Quality Management System:

Develop, implement & support the system and processes, develop corresponding training programs, and acts as Super User for eQMS system.

Internal Audit Programs:

Provide inputs to support the design & implementation of robust internal audit processes to ensure readiness of various functions & processes when meeting regulatory agencies & customer audits

Certification Audits:

Lead and support various certification audits with relevant regulatory agencies and certification providers for the depot.

Operations & Customer Audit Programs:

Lead regular audit programs / random checks to achieve successful audit outcomes and proper post audit follow up actions.

Healthcare Customer Liaison:

Liaise with customers to understand quality requirements / issues / underlying concerns to advise on the way forward, provide advice based on interpretations as applicable to 3PL and support in issue resolution via conducting root cause analysis (depot).

Healthcare Quality Feedback:

Liaise, consolidate feedback from different functions to update and prepare final copy for Quality Questionnaires, Agreements and RFQ Proposals for customers.

Validation Programs:

Lead and support validation of transportation lanes and critical equipment like cold chain facilities, and packaging systems

Requirements :

  • Hold local pharmacist license

  • Have 3-5 years of relevant experience in pharmaceutical or healthcare industry in a quality related role

  • Have competencies in quality assurance / regulatory affairs, customer relationship management and root cause analysis

  • Have working experience ensuring compliance in accordance to Goods Manufacturing Practise cGMP,)/, Good Clinical Practises cGCP, Goods Distribution Practice (GDP) for Medical Devices and other local certifications in a warehouse and transportation business.

  • IATA CEIV will be desired but not necessary.

  • Familiar with drugs control and secondary labelling system

  • Experience in conducting external and internal audits

  • Must hold at least Bachelor’s degree in Pharmacy from a reputable local institute.

Working hours:

  • Mon to Fri 9am-6pm

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.