Quality Control / Quality Assurance Associate at Clinigen

Singapore, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

07 May, 26

Salary

0.0

Posted On

06 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Management, Documentation Processes, Product Releases, Vendor Approvals, Customer Approvals, Validation Activities, Collaboration, Organizational Skills, Time Management, Attention to Detail, Communication Skills, Proactive Attitude, Healthcare Industry Knowledge, Pharmaceutical Industry Knowledge, Food Industry Knowledge, Good Distribution Practice

Industry

Pharmaceutical Manufacturing

Description

Clinigen is at the forefront of delivering critical medicines and support to healthcare professionals and patients. As part of our ongoing commitment to excellence, we are seeking a Quality Control / Quality Assurance Associate to join our esteemed team in Singapore. In this pivotal role, you will be instrumental in upholding our quality management standards as we expand our operations in the Southeast Asia region. Your primary responsibilities will include: Overseeing documentation processes for our Quality Management System (QMS)/electronic QMS (eQMS) Facilitating product releases to ensure compliance with established quality standards Conducting vendor and customer approvals and validations Providing support for secondary packaging processes Assisting with validation activities to maintain operational efficacy Collaborating with warehouse and cleanroom facilities to ensure adherence to quality parameters The ideal candidate will possess the following qualifications and skills: A tertiary qualification in Science, Pharmacy, or a relevant technical discipline, or equivalent professional experience Minimum of 2 years of experience in a quality assurance or quality control role; experience within a warehouse and cleanroom environment in the Healthcare, Pharmaceutical, or Food industries is highly desirable Familiarity with Good Distribution Practice (GDP) and Good Manufacturing Practice (GMP) quality management systems Exceptional communication skills, both verbal and written The ability to cultivate collaborative relationships with cross-functional team members Strong organizational and time management skills, with a focus on detail-oriented execution A commitment to excellence in administrative and documentation practices A proactive attitude, with a willingness to contribute positively to our mission of enhancing patient care In return for your valuable contributions and commitment to our organization, we are pleased to offer you an attractive and comprehensive benefits package that includes: A competitive monthly salary that reflects your experience, skills, and the industry standards, ensuring that you are fairly compensated for your hard work and dedication. A performance bonus designed to reward exceptional performance and achievements, providing you with additional financial incentives as you excel in your role. Generous annual leave of 20 days, allowing you the opportunity to take time off for rest, relaxation, and personal pursuits, promoting a healthy work-life balance. Ongoing professional development opportunities, including training programs, workshops, and access to resources that will help you enhance your skills and advance your career within our organization.

Responsibilities

The Quality Control / Quality Assurance Associate will oversee documentation processes for the Quality Management System and facilitate product releases to ensure compliance with quality standards. Additionally, the role involves conducting vendor and customer approvals, supporting secondary packaging processes, and collaborating with warehouse and cleanroom facilities.