|
Timestamp
|
| |
1786512260
|
|
Fetch Consultant ID
|
| |
51
|
|
Unique ID
|
| |
81e27
|
|
Running No
|
| |
10139
|
|
Method
|
| |
Solo
|
|
Edit
|
| |
No
|
|
Frontend
|
| |
True
|
|
Role
|
| |
Consultant
|
|
Requestor View
|
| |
No
|
|
Status
|
| |
Closed
|
| Who's Hiring? |
|
Consultant In Charge
|
| |
Kimberly Wong
|
|
Company Profile
|
| |
Astrazeneca Singapore Pte Ltd
|
|
UEN
|
| |
199002462M
|
|
Client Manager
|
| |
Mohamed Osman – C – Valid
|
|
Designation
|
| |
Global CAPEX Procurement
|
|
Type of Placement
|
| |
Contract (KF)
|
|
Urgency
|
| |
High
|
|
Mode of Communication
|
| |
Email
|
|
Visibility
|
| |
Unpublish
|
|
Job Posting Date
|
| |
12/08/2026
|
|
Posting Validity (Days)
|
| |
90
|
| Job Posting Details |
|
Enable AI
|
| |
No
|
| Basic Details |
|
Job Title
|
| |
C&Q Compliance Support
|
|
Job Type
|
| |
Contract
|
|
SSOC
|
| |
Chemical engineer (excluding petroleum and petrochemical)
|
|
Number of Headcount Required
|
| |
1
|
|
Expected Date to Join
|
| |
01/09/2026
|
|
Work Hours Per Week
|
| |
40
|
|
Period
|
| |
Months
|
|
No.
|
| |
12
|
|
Salary Type
|
| |
Range
|
|
Hide Salary
|
| |
No
|
|
Negotiable
|
| |
Yes
|
|
Currency
|
| |
SGD
|
|
Min
|
| |
6,000
|
|
Max
|
| |
8,500
|
|
Period
|
| |
Monthly
|
|
Add Allowance
|
| |
No
|
| Entitlements |
|
Work from home
|
| |
No
|
|
Primary Work Location
|
| |
Singapore 339510
Singapore
Map It
|
|
Classifications of Location
|
| |
Tuas
|
|
Country
|
| |
Afghanistan
|
| Job-Specific Details |
|
Level of Competency
|
| |
Mid-level Position
|
|
Years of Relevant Experience
|
| |
5
|
|
Classification
|
| |
Technical
|
|
Sector
|
| |
Manufacturing
|
|
Project Experience
|
| |
- Pharmaceutical Manufacturing
|
|
Specialization
|
| |
|
|
Professional Characteristics
|
| |
- Detail-oriented
- Compliance-focused
- Strong Communication & Coordination Skills
|
|
Primary Responsibilities
|
| |
- Support the C&Q Manager and Compliance Lead in executing the project C&Q programme
- Develop implementation plans and strategies in line with C&Q plans, global guidelines and SOPs
- Coordinate with EPCM, third-party suppliers, end users and QA
- Ensure C&Q activities are executed in accordance with approved plans
- Guide preparation and review of C&Q documentation
- Support C&Q scheduling and change control activities
- Lead meetings related to commissioning topics
- Support digital C&Q platforms and compliance activities
- Ensure quality and GMP standards are maintained throughout C&Q execution
|
| Competencies |
|
Minimum Qualifications
|
| |
Bachelor's Degree or equivalent
|
|
Specify the Field of Study
|
| |
Yes
|
|
Field of Study
|
| |
- Chemical Engineering
- Engineering
|
|
Language Spoken
|
| |
|
|
Language Written
|
| |
|
|
Key Skills
|
| |
|
|
Are the Key Skills selections good enough?
|
| |
Yes
|
| Summary of Key Requirements |
|
Summary of Key Requirements
|
| |
- Bachelor’s Degree in Chemical, Mechanical, Process Engineering or related discipline
- Relevant experience in C&Q / CQV / validation within a pharmaceutical, biotech or GMP environment
- Familiarity with risk-based validation methodologies
- Experience with cGMP
- Experience with digital execution platforms such as Kneat, Veeva or ValGenesis is advantageous
- Strong documentation, coordination and stakeholder management skills
- Able to work within strict project deadlines
- Good written and spoken English
|
|
Featured
|
| |
No
|
|
On Hold
|
| |
No
|
