Job Description

Description

Salary: up to $4600

Duration: 1 year contract

Working Days & Hours: Monday to Friday Office Hours

Location: Paya Lebar

: 1 . Contract/External Manufacturer Quality Oversight

• Quality oversight of contract manufacturers including: OOS/NCR/Deviation and CAPA, Change Control and routine stability testing monitoring. On time and in compliance to GMP and applicable standards.

2.
Release of Products

• No recalls or Critical product quality issue on product in the market due to batch release oversight.
• Release timeframe within target timeframe.

3.
Change Control

• Actioning individual change controls.
• Oversight and management of change control process.
• Change Controls and tasks to be actioned within the defined target dates and in compliance to GMP and SOPs.

4. Artwork review

• Artwork review according to requirements.

5.
Deviations, NCR & CAPA

• Actioning individual deviations, NCR & CAPA.
• Oversight and management of process.
• Deviations to be completed in compliance with GMP and SOPs and in alignment with timeframes of business needs.
• No recalls or Critical product quality issue on products in the market due to due diligence oversight.

6.
Customer Complaints

• Work with internal departments and 3rd party suppliers to maintain oversight of the complaints process to ensure complaints are managed according to compliance requirements.
• Complaints resolved within required timeframes as defined in SOPs and according to the compliance requirements of regulations and SOPs.
• Timely reporting of complaints.

7.
Document Management

• Update of SOPs/WIs/FGS as per position responsibility.
• All documents under responsibility to be maintained and updated within the required due dates and in compliance with regulations and SOPs.

8.
Internal and External Auditing

• Follow up of any NCR/CAPA identified.
• Ensure audits are conducted within the defined timeframes and in compliance to regulations and SOPs where applicable.
• Facilitate process to ensure that audit findings are resolved and closed out within the agreed timeframes where applicable.

9.
Training and Development

• Individual training.
• Individual training to be completed on time in full before due date.

10. Other responsibility and project that are assigned as per business requirement

• On time basis and as per assignment

Job Requirements: Min Degree in Life Sciences/Engineering or similar w min 3 yrs of relevant QA experience in Pharmaceutical industry

Interested candidates, please submit your resume to: allylok@recruitexpress.com.sg

Ally Audrey Lok Xin Woon

Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R21102307

allylok@recruitexpress.com.sg

Industry

Healthcare / Pharmaceutical / Life Science / Medical Device

Specialization

Healthcare - Pharmaceutical / Life Science / Medical Device / Clinical Research / Regulatory Affairs

Location

East

Employment Type

Contract / Temp

Salary

S$2,601 - S$4,000 / mth
S$4,001 - S$6,000 / mth

If you meet the requirements of this role, please email a detailed resume in Word document to Audrey Lok Xin Woon (Ally).
CEI Registration No.: R21102307
Email: allylok@recruitexpress.com.sg
Tel: 67363280
*All information will be treated with strictest confidence. We regret that only short-listed applicants will be notified.

Recruit Express