What Qc Analyst Jobs are in Singapore?

Join our team and contribute to quality control and food safety initiatives that ensure the delivery of trusted, high-quality products.

Responsibilities:

• Perform daily QC laboratory testing and quality evaluation in accordance with established standards.
• Conduct microbiological analysis of food samples and environmental monitoring of production sites.
• Record laboratory test results, perform data entry, and prepare reports.
• Support document control activities, including the maintenance of food safety and quality records.
• Perform laboratory equipment validation, verification, and routine maintenance.
• Maintain good housekeeping of the QC laboratory, equipment, and apparatus.
• Manage stock-taking and inventory control of laboratory consumables and testing materials.
• Perform other duties as assigned by the superior.

Requirements:

• Diploma/Degree in Food Science or a related field.
• Minimum 1 year of working experience, preferably in food manufacturing.
• Candidates without relevant experience are welcome to apply.
• Positive and proactive, able to work well with cross-functional teams.
• Good organizational and time management skills.
• Work location: Pandan Loop (West).

About our company

Senses International believe in unleashing the potential of employees by providing them with a dynamic and stimulating work environment where creativity and expertise intersect to create unparallel fragrances.  Senses International have a team of passionate individuals who are dedicated to making a difference in the fragrance industry.  As an employee at Senses International, you will be part of a vibrant and diverse team that values collaboration and innovation. The company encourage employees to explore their creativity and push the boundaries of what is possible in the fragrance industry.
The company also foster a culture of continuous improvement and encourage the employees to take ownership of their career. Join Senses International and unleash your potential in the fragrance industry.  With company’s unique blend of creativity and expertise, the sky’s the limit for your career growth and development.

Job Position:
Junior QC Analyst


Job Description:
As a Junior Quality Control Analyst at Senses International Pte Ltd, you will play a critical role in ensuring that our products meet the highest quality standards. You will be responsible for implementing and maintaining quality control procedures, recording and maintaining quality protocols, and driving continuous improvement in our processes.

Key Responsibilities:

• Perform incoming and outgoing quality control sampling processes and procedures.
• Utilization of quality control equipment, which encompass their calibration and upkeep.
• Ensure all quality-related documents are accurately recorded and kept up to date.
• Provide support during audits and guarantee compliance to industry standards and regulatory requirements.
• Collaborate with cross-functional departments to resolve quality issues and implement corrective actions.
• Perform any other duties assigned by the QC Manager.

Qualifications:

• Diploma in Science or Chemistry related field.
• Experience in QC sampling & QC inspection process will be an added advantage.
• Computer-literate.
• Must be physically fit.
• Good communication and interpersonal skills.
• Ability to work both independently and in a team.

What We Offer:   
A collaborative and dynamic work environment.

Opportunities for professional growth and development.

The chance to make a significant impact on product quality and customer satisfaction.

Salary range: SGD2,200 – SGD2,700

Role Summary

Responsible for independent QA oversight of QC laboratory operations (chemical and microbiology, stability), ensuring compliance with GMP, Data Integrity (ALCOA+), and site quality systems. Contributes to Contamination Control Strategy (CCS) and supports aseptic assurance and inspection readiness.

Key Responsibilities

• Provide QA oversight of QC laboratory activities (chemical, microbiology, stability)
• Ensure compliance with GMP, SOPs, and approved methods
• Oversee microbiology activities including EM, sterility, bioburden, endotoxin
• Support CCS implementation and review EM trends and contamination risks
• Independently review analytical and microbiological data (ALCOA+)
• Support batch release and review CoA
• Participate in deviation, OOS/OOT, EM investigations and CAPA
• Provide oversight for method validation, EM methods, and QC systems
• Review and approve QC-related GMP documentation
• Support regulatory inspections and audits
• Identify recurring issues and support continuous improvement

Qualifications

Bachelor degree or above in Microbiology, Chemistry or related field

12+ years Quality experience in GMP environment

Experience in microbiology lab or aseptic support preferred

Technical Competencies

GMP knowledge (NMPA/FDA/EMA)

Analytical and microbiology testing

Environmental Monitoring and CCS

Data Integrity (ALCOA+)

Expectations

• Works independently in QC/Micro QA scope
• Provides sound QA decisions for routine activities
• Identifies risks and escalates complex issues
• Understands microbiological risks and EM trends
• Acts as reliable QA partner to QC

Job Summary

Responsible for overseeing timely and compliant disposition of GMP materials and products, ensuring adherence of critical quality attributes to applicable internal procedures and regulatory requirements.

Responsibilities

• Review and approve GMP manufacturing batch records and related quality documentations.
• Responsible for ensuring all material qualification activities are completed and documented prior to use in GMP manufacturing
• Approve or reject batches based on established specifications, SOPs and regulatory requirements.
• Collaborate with Procurement, QC, Warehouse and Manufacturing to maintain qualified supplier and material status.
• Collaborate with QA and manufacturing teams to resolve discrepancies, deviations, and CAPAs prior to disposition.
• Contribute to the establishment of an effective quality system and ensure its efficient operation across all GMP functions and processes in daily operations.
• Manage quality events, including deviations, change controls, CAPA, and lab investigations etc.
• Support both internal and external audits.
• Carry out additional tasks as assigned by leadership.

Qualifications

• Bachelor's degree or higher in Biologics, Pharmacy, Pharmaceutical Engineering, Bioengineering, or other relevant fields.
• 5-10 years of relevant QA experience (preferably in Lot Disposition) in Biopharma or Pharmaceuticals industry
• Familiar with FDA, EMEA, and PICS GMP requirements.
• Knowledgeable in biological product manufacturing and related quality control requirements.
• Experience with a new site start-up is preferred.
• ADC manufacturing and quality management experience is a plus.
• Proficient in English listening, speaking, reading, and writing.
• Skilled in Microsoft Word, Excel, PowerPoint, etc.
• Strong learning ability.
• Excellent cross-functional communication and collaboration skills.
• Strong logical thinking and conflict management abilities.
• Demonstrates strong ownership.

MiRXES is a Singapore-headquartered molecular diagnostic company with R&D, manufacturing, and clinical lab operations in Singapore, USA, Japan, and China. We specialize in microRNA technologies and the development, manufacturing, and provision of diagnostic test kits and clinical services. Our mission is to enable early disease detection and provide insights for better patient care by harnessing the power of microRNA to augment traditional testing. Our vision is to be the world’s leading developer and provider of accurate, actionable, and affordable microRNA-powered diagnostic tests.

Job Location: Tukang

Job Summary

QC Supervisor will work as part of the Quality team to support the QC of day-to-day operations and maintain detailed records for all the tasks assigned. The individual will inspect the products in different stages of manufacturing process such as incoming raw materials, intermediates, in-process and finished good. The individual will also participate in the investigation of nonconforming products and follow-up with the actions that arises from these inspections.

Roles and Responsibilities:

• Manage team performance, including training, competency assessments and ensuring the technical proficiency of QC staff.
• Supervise QC Specialists and Technicians to ensure smooth execution of routine QC operations.
• Plan and schedule daily QC routine and ad hoc testing.
• Oversee QC lab housekeeping, including cleanliness, equipment maintenance, document archival, and reagent inventory tracking.
• Perform routine QC testing of raw materials, in-process materials and finished goods.
• Evaluate data, draft and/or review QC reports, highlighting deviations from standard operating procedures.
• Perform trend analysis and utilize Statistical Process Control (SPC) tools to identify process anomalies and prevent failures.
• Troubleshoot QC failures and raise nonconformance reports when needed. Investigate nonconformances to determine root causes.
• Support validation and stability studies for lab development and diagnostic products as needed.
• Ensure all laboratory activities and documentation are complaint with ISO13485 and relevant regulatory requirements.
• Draft and update QC work instructions and contribute to the continuous improvement of workflow procedures and processes.
• Apply good documentation practices on all records for better traceability, transparency, and the purpose of auditing.
• Perform any other duties as assigned.

Desired Skills and Competencies:

• Diploma/Bachelor/ Master of Science/ Engineering or equivalent in Biotechnology, Biochemical, Biochemistry, Analytical Chemistry, Molecular Biology/ Life Science related courses.
• Have qPCR knowledge and experience in using qPCR machine.
• Familiar with the basic laboratory procedures. Relevant experience with laboratory testing, and QC of assays-based workflow will be an advantage.
• Able to work independently with minimal supervision and with others within and outside his/her function.
• Excellent organizational and time management skills.
• High degree of initiative and ownership.
• Possess a positive and willing-to-learn attitude.
• Good logical thinking and reasoning ability.
• Good Documentation Practices and ability to write protocols and procedures
• People management experience including training, development and mentoring/coaching of technical staff would be an added advantage.
• 4-5 years of relevant experience in quality control and preferably in medical device manufacturing industry.
• GMP and/or ISO 13485 experience would be an added advantage.

This position is based in Singapore.

We appreciate your interest in the above-mentioned position, however, only shortlisted candidates will be contacted.

Job Scope:

• Responsible for coordinating QC and QA work in the team
• Responsible for the completion of key orders and trouble shooting
• Responsible for statistics and analysis of production data, and assist the supervisor to optimize and improve the  production process or technology
• Participate in or be responsible for the management of multiple promotion projects and promote the achievement of project objectives
• Responsible for the formulation and update of SOP, summarize and solidify work experience and train up junior employees
• Assist the supervisor to complete quality monitoring and safety inspection, and timely complete problem rectification
• Complete other tasks assigned by the supervisor

Key Requirements: 

• Bachelor’s degree or above in cell biology, molecular biology, biomedicine and other related majors
• Familiar with the experimental operation of SDS-PAGE, Western blot, LC-MS, HPLC and other protein detection, 
• Good trouble shooting and project management skills
• Good communication skills (verbal and written)
• Good collaboration skills

#GS

GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.

GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.

Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform. 

Are you a detail-driven science graduate looking to build a meaningful career in quality assurance? Here's your chance to join a reputable multinational chemical company on Jurong Island — where your analytical skills will directly impact product quality, safety, and operational excellence.

Role Details

• Remuneration Package: Up to $4,000 + Monthly Allowances $1,000 (Experienced Candidates)

• Annual Bonus: AWS + Company Variable and Performance Bonus

• Location: Jurong Island (company transport provided to/from Jurong Island)

• Employment Type: Permanent, Full-Time

• Shift: 12-Hour Rotating Shifts

• Career Growth: Structured development within a global MNC

Key Responsibilities:

As a QC Analyst , you'll be at the heart of laboratory operations — ensuring every product that leaves the facility meets the highest quality and safety benchmarks.

• Conduct routine and non-routine QC analysis on raw materials, in-process samples, and finished products

• Interpret QC results and make sound, independent decisions to support process control

• Collaborate with cross-functional teams to uphold compliance with quality standards

• Take full ownership of the QC laboratory outside of regular hours

• Lead short-term projects including non-routine analysis and customer complaint investigations

• Maintain calibration records and ensure all lab equipment is in optimal condition

• Communicate results accurately and promptly to relevant departments

• Mentor and guide new team members

Key Requirements:

• Degree in Chemistry or a related discipline

• Minimum 2 years of QC experience within laboratory environment

• Familiarity with quality management systems and laboratory techniques

• Strong analytical mindset with sharp attention to detail

• Comfortable working independently in a fast-paced, shift-based environment

• Good verbal and written communication skills

Ready to Take the Next Step?

Submit your CV in MS Word format to

We regret that only shortlisted candidates will be notified.

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