Associate Specialist, Quality Control
3 weeks ago
R339521 Associate Specialist, Quality Control Shift - 2 Years Contract
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
WHAT YOU WILL DO
Associate Specialist, VSM Laboratory (In-Process Control Lab)
The position of Associate Specialist in Value Stream (VSM) Laboratory will be responsible for ensuring and maintaining high standards of quality and compliance within our organization.
In this role, you will be responsible for all or subset of the key responsibilities below:
- Perform analytical testing of incoming materials, in-process samples, cleaning samples, environmental monitoring samples, utility systems, intermediates and finished drug substances/ products according to approved procedures.
- Participate in analytical method transfer/ validation/ verification, new product introduction and equipment qualification.
- Assist in conducting laboratory investigations and ensure effective implementation of related actions within the agreed timeframe.
- Provide inputs for the development and revision of Analytical Standards, Standard Operating Procedures, Work Instructions and other GMP documents.
- Maintain proper laboratory housekeeping, laboratory inventory and ensure inspection readiness.
- Execute quality and laboratory improvement initiatives and other special projects.
- Perform equipment preventive maintenance and calibration.
- Perform review of laboratory documents such as orphan data check and equipment logs.
- Perform other duties as assigned by their direct manager.
WHAT YOU SHOULD HAVE
Qualifications & Experience
- Bachelor's degree in Science/ Life Science, Pharmaceutical Science, Engineering or proven relevant experience.
- 2 to 3 years of applied professional work experience in the quality laboratory
Personal Qualities
- Leadership skills and ability to influence/collaborate with stakeholders at various levels.
- Customer focus with strong business acumen and continuous improvement mindset.
- Strategic and critical thinking mindset with a collaborative and problem-solving attitude.
- Strong communication and interpersonal skills.
- Ability to work effectively in a team-based environment.
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 no prior work experience in Biopharma industry are welcomed to apply
- Open to two years contract and shift work (12 hours rotating shift (day/night) including Sat/Sun. Shift allowance is provided
WHAT YOU CAN EXPECT
- Limitless opportunities across various areas in Manufacturing; well-structured career path
- A state-of-the-art facility that delivers solution to its customers world-wide
Preventive Maintenance
Quality Control
Housekeeping
Critical Thinking
Business Acumen
GMP
Value Stream
Equipment Qualification
Customer Focus
Regulatory Requirements
Laboratory
VSM
Calibration
Utility Systems
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