Job Description & Requirements
Our Quality group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe.
What will you do
- Responsible for planning, scheduling and performing calibration, maintenance and qualification of laboratory equipment.
- Responsible for maintaining laboratory chemicals and consumables inventories and disposals.
- Responsible for archival/retrieval of retention samples.
- Ensure laboratory equipment calibration, maintenance and qualification within timely manner and in compliance to standard operating procedures with necessary laboratory safety precautions.
- Liaise and coordinate with external service providers in carrying out calibration, maintenance and qualification of laboratory equipment and tools.
- Liaise with external vendors to ensure chemicals and consumables supply continuity.
- Support laboratory investigation on laboratory equipment failure, Out of Tolerance and Out of Specification
- Be the subject matter expert of laboratory maintenance and participate as auditee in site internal audit/external audit.
- Coordinate with laboratory team to ensure equipment availability for calibration, maintenance and troubleshooting work.
- Manage archival/retrieval of record for laboratory calibration, maintenance and qualification related documents.
- Understand customer needs and identifies solutions to non-standard requests by interpreting existing procedures, processes and practices.
- Ensure work and behave in accordance with EHS procedures and guidelines.
- Maintains positive working relationships among employees and fosters an environment where employee engagement, empowerment, teamwork and accountability are the cultural norm.
- Participate in continuous improvement initiative as part of the production system culture in Singapore.
- Participate in EHS, Business Compliance, cGMP and all other compliance-related matters, where applicable.
- Uses formal data based analytical tools (such as Lean Six Sigma process) to identify and implement operating improvement opportunities to eliminate waste, improving accuracy, compliance and productivity.
- Any other duties as assigned by the Senior Manager/Director.
What you must have
To be successful in this role, you will have:
QUALIFICATION:
Bachelor Degree in Science/ Life Science, Pharmacy, Pharmaceutical Science or Engineering or proven relevant experience.
EXPERIENCE:
This is a career conversion programme under Workforce Singapore (WSG) and candidates must meet the following criteria:
- Singaporeans/Singapore PRs only
- PMETs/Mid-Careerist with no prior work experience in Biopharma industry are welcomed to apply
- Open to two years contract
- Minimum 2 years of relevant experience in GMP manufacturing environment, preferably laboratory operations.
QUALIFICATION:
Bachelor Degree in Science/ Life Science, Pharmacy, Pharmaceutical Science or Engineering or proven relevant experience.
Expertise, Professional and Functional Competencies
· A continued improvement mindset.
· Good knowledge and understanding of GMP
· To be familiar with simple statistic to apply statistical analysis and process control techniques.
· Experience in MS-office applications.
· Proficient in English.
Other Personal Attributes:
· Good organization and time management skills.
· Able to work independently.
· Meticulous with high integrity.
· Good interpersonal and communication skills, with ability to work in cross-functional teams.
· Continuous improvement mindset.
· Positive attitude and self-motivated.
