[Clinical Trials/ Pharma] Quality Assurance Specialist UP$3.8K #HJA

RECRUIT EXPRESS PTE LTD; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A quality-focused organization in Singapore is seeking a qualified individual for a role involving the management of materials and quality control. The ideal candidate possesses a Degree or Diploma in Pharmaceutical or Science disciplines and has over 3 years of relevant experience. Responsibilities include managing product inspections, overseeing documentation systems, and participating in quality improvement initiatives. Interested candidates should submit their resumes via the provided contact email.

Qualifications

• Degree / Diploma in Pharmaceutical or Science disciplines required.
• 3+ years’ work experience in Medical / Pharmaceutical-related organizations.

Responsibilities

• Manage and ensure appropriate storage of products/materials.
• Support product inspection activities for conformance.
• Participate in quality improvement initiatives.

Skills

Documentation management

Quality control

SOP development

Education

Degree / Diploma in Pharmaceutical or Science disciplines

Job description

SPECIFIC DUTIES, ACTIVITIES AND RESPONSIBILITIES

Materials Management

• Manage and ensure that products/materials are stored appropriately at designated locations, and that lot status is correctly assigned in the inventory system.

• Support incoming products/materials inspection activities to ensure conformance to requirements, including preparation of inspection reports.
• Authorize the release of incoming products/materials from the inventory system.
• Execute new material qualifications (eg, label component), including preparation of inspection reports.

Operational Activities

• Support 100% inspection activities for potential product issues where applicable.
• Authorize approval of the label print setup process to facilitate label printing activities.
• Participate in secondary packaging in-process inspection activities to ensure the process conforms to the requirements.

Training Programs

• Ensure timely completion of Compliance-Wire assigned SOP training prior to the related work activities execution.

Documentation

• Participate in SOPs development and updates to support the system.
• Manage the site documentation system to ensure effective retrieval and archival of documentation.

System

• Track the quality system performance indicators and establish the trend analysis.
• Participate in quality improvement initiatives assigned by the management team.

Other Activities

• Participate in discussion and resolution of potential quality concerns arise in daily operational related activities.
• Report potential inconsistent work practices and non-compliance process activities.
• Participate in review and approval of equipment calibration reports for acceptance.
• Support the non-routine tasks assigned by the management team.

Education and Experience:

• Degree / Diploma preferably in Pharmaceutical or Science disciplines.
• 3+ years’ work experience in Medical / Pharmaceutical-related organizations.

TELE me at @yijingggggg or WA me at https://wa.me/[phone] NOW!

Interested candidates, please submit your resume to [e-mail]

Alison Chen

CEI Reg No: R25126657

Recruit Express Pte Ltd (EA Licence No.: 99C4599)