WHAT YOU WILL DO
JOB PURPOSE:
• Perform manufacturing operations per production schedule in compliance with cGMP and achieve the operational objectives.
• Meet Site's safety, health and environmental (SHE) performance objectives through compliance with site SHE rules.
• Actively contribute to resolving problems/ opportunities in their work module.
MAIN RESPONSBILITIES:
1. Manufacturing Excellence
Routine Operation:
• Responsible for completing all assigned pharm operations, ensuring accurate documentation completion on modules.
• Meet performance metrics of the assigned operations.
• Provides timely and accurate information to visual boards.
• Responsible for maintaining good facility housekeeping.
• Effectively communicates during shift handover.
Non-Routine Operation I Campaign turnaround Activities:
• Performs equipment cleaning/maintenance/calibration and equipment setup and support equipment cleaning for all operations like Dispensing/ Charging/ Blending, Granulation, Compression, Film Coating.
• Responsible to support IQ/OQ/PQ when assigned.
Quality Event Investigation:
• Provide detailed information for all events and atypical to assist in notification /investigation.
• Responsible to escalate pharm Operations issues to appropriate level when required.
• Support in data collection to assist investigations.
2. Quality/ SHE Stewardship
• Ensures manufacturing related activity is completed according to established procedures and all associated documentation is completed to a high standard.
• Ensures compliance to all Safety and cGMP requirements.
• Actively report Environmental Events, Unsafe condition or Near Miss in day-to-day work to contribute to achieve a Safe Workplace
3. People Excellence
•Exhibit a positive attitude and provide constructive feedback & solutions to issues /opportunities in the workplace.
•Responsible to participate in improvement projects and actively generate ideas.
•Develops and updates on career path with manager, which is aligned with Performance Management Process.
•Ensures both operational knowledge and technical skills are maintained and compliant against individual training requirements.
•Use Tier process and other opportunities to engage positively with others to improve both communication and teamwork skills.
· Maintain good attendance and plan leave effectively to support production activities.
Qualification:
• A Diploma or Technical School graduate with background in operations and maintenance in pharmaceutical environment.
• Must be willing to work in 12 hours rotating shift (day/night).
• Minimum two years of working experience.
• Strong background in operation of chemical systems including hands on experience.
• Understand safety procedures/practices.
• Familiarized with cGMP working environment.
• Has a good writing and communication skill.
This is a career conversion programme under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:
- Singaporeans/Singapore PRs only
- PMETs/Mid-Careerist with more than 2 years working experience in manufacturing industries preferred
- Open to two years contract
- 12 hours rotating shift (day/night) including Sat/Sun. Shift allowance will be provided
WHAT YOU CAN EXPECT
- Limitless opportunities across various areas in Pharmaceutical Manufacturing.
- A state-of-the-art facility that delivers solution to its customers world-wide
- Highly engaging team that aims to innovate the future
