339 Production Lines jobs in Singapore

• Oversee the implementation and maintenance of GMP and HACCP standards.
• Ensure compliance with local food regulations (e.g., SFA and GMP standards).
• Manage internal and external audits (e.g., regulatory bodies, customer audits).
• Review and update QA documentation, SOPs, and records regularly.

• Lead hazard analysis, food safety plans, and critical control point monitoring.
• Manage allergen control, traceability, and recall procedures.

• Supervise the QC team in performing inspections, sampling, and laboratory testing (microbiological, chemical, physical).
• Analyze trends from quality data and implement improvements.
• Approve incoming raw materials, in-process, and finished product quality.

• Train and mentor junior QA/QC staff on quality systems and food safety.
• Conduct regular staff training on hygiene, GMP, and process controls.

• Initiate and lead quality improvement projects (e.g., reducing customer complaints, process optimization).

• Degree/Diploma in Food Science, Food Technology, Microbiology, or related field.
• 5 years of QA/QC experience in the food manufacturing industry.
• Strong knowledge of HACCP and GMP standards.
• Experience with audits, documentation control, and risk assessment.
• Excellent communication, leadership, and problem-solving skills.

Overview

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: 2 Tukang Innovation Grove, JTC MedTech Hub, Singapore

The QC Specialist will work as part of the Quality team, supporting day-to-day QC operations and maintaining accurate and detailed records of all the assigned tasks. This role involves inspecting products at various stages of the manufacturing process, including incoming raw materials, intermediates, in-process materials and finished goods. This person will also participate in investigations of nonconforming products and assist in implementing corrective actions arising from these inspections.

• Perform routine QC testing of incoming raw materials, in-process materials and finished goods.
• Plan and schedule daily routine and ad hoc QC runs assigned by line manager.
• Evaluate data and generate reports, highlighting any deviations from standard operating procedures (SOPs).
• Raise nonconformance for failures observed during QC runs.
• Support troubleshooting and investigation of nonconformance to determine root causes.
• Draft and revise QC work instructions as required.
• Support validation and stability studies for lab development and Diagnostic products, when necessary.
• Perform general laboratory support activities, including housekeeping, equipment maintenance, document archival, and inventory tracking of laboratory reagents, etc.
• Contribute to the continuous improvement of laboratory procedures and processes to ensure compliance with GMP requirements.
• Apply Good Documentation Practices (GDP) to all records to ensure traceability, transparency, and audit readiness.
• The tasks and responsibilities listed are essential to the role, however, reasonable accommodations may be made to support additional responsibilities based on evolving business needs.

• Degree/ Diploma in Biomedical Science, Biotechnology, Molecular Biology, Biochemistry, Life Science related courses or equivalent.
• Knowledge and hands-on experience with qPCR, including operation of qPCR machines will be an advantage.
• Proficient in using standard laboratory equipment such as pipettes, centrifuges, etc.
• Familiar with basic laboratory procedures; experience in assay-based workflows and QC testing is an advantage.
• Able to work independently with minimal supervision, as well as collaboratively with cross-functional teams.
• Excellent organizational and time management skills.
• Demonstrate a high degree of initiative and ownership.
• Possess a positive, proactive and willing-to-learn attitude.
• Strong interpersonal and communication skills.
• Basic computer competency, including proficiency in Microsoft Office applications.
• 2-3 years of relevant experience in quality control, preferably within the medical device manufacturing industry.
• Good understanding of Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP) is preferred.

This position is based in Singapore.

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

The Quality Inspector is responsible for ensuring the quality of incoming materials, in-process components, and finished products through detailed inspection and testing. This role ensures that all products meet quality standards throughout the manufacturing process, from receipt of components to final product delivery

Incoming Quality Control:

• Inspect and verify incoming materials and components for micro assembly and PCBA against specifications and quality standards.

• Ensure proper documentation and traceability of incoming materials.

In-Process Quality Control:

• Monitor and inspect the micro assembly and PCBA assembly process to ensure in process quality control are in compliance according to standards.

• Perform in-process testing to detect defects early and minimize waste or rework.

Outgoing Quality Control:

• Inspect and test finished products before shipment to ensure they meet specifications, functionality, and visual standards.

• Conduct final functional and visual inspections to ensure product readiness.

Defect Identification & Reporting:

• Identify and document quality issues, defects, and deviations from standards during incoming, in-process, and outgoing inspections.

• Work with the production team to resolve issues and implement corrective actions.

Documentation & Compliance:

• Maintain accurate records of inspections, test results, and non-conformance reports.

• Ensure compliance with industry standards (IPC, ISO) and company quality policies.

Key Responsibilities

• Manage the storage and inventory of laboratory samples
• Conduct analytical testing and documentation for APIs, drug substances/products, complaints, packaging materials, and stability samples
• Ensure strict compliance with cGxP standards, including data integrity requirements
• Execute and document stability testing (if not centralized), including storage, testing, and reporting to cGxP standards
• Follow all Health, Safety, and Environment (HSE) guidelines
• Identify and report safety risks or potential incidents, and propose preventive solutions
• Participate in mandatory training and retraining programs
• Support operations during rotating day/night shifts

Role Requirements

Essential Qualifications and Experience

• Prior experience in a laboratory setting within the pharmaceutical industry (QA, production), with exposure to aseptic techniques preferred
• Proficiency in administrative and documentation tasks compliant with GMP and HSE standards
• Demonstrated strengths in:
• Breakthrough analysis and problem-solving
• Resilience and adaptability
• Operational efficiency and continuous learning
• Digital fluency and technical skills

Technical Competencies

• Hands-on knowledge of laboratory instruments and QC testing procedures
• Strong command of GxP, TQM principles, and lab excellence standards
• Ability to maintain QC IPC/DS laboratory equipment and systems in accordance with cGMP compliance
• Competent in executing product testing within timelines and contributing to validation and method transfer protocols
• Skilled in performing routine in-process, release, and stability testing, including documentation review
• Capable of supporting lab investigations and leading root cause analysis
• Detail-oriented in preparing and verifying QC documentation to ensure accuracy, consistency, and regulatory compliance
• Proactively identifies opportunities to optimize testing procedures
• Supports audit readiness and participates in internal audits and inspections by health authorities

Overview

The Quality Inspector is responsible for performing basic inspections and verifications of equipment components and assemblies to ensure compliance with engineering drawings, industry standards, and customer requirements. The role supports the organization’s quality objectives of Zero Defects and Zero Quality Escapes by identifying non-conformities early and ensuring proper documentation.

• Computer literate and familiar with Microsoft Office software at a minimum.
• Record inspection results in inspection checklists, quality reports, or ERP/QMS system.
• Report recurring defects and assist QC Supervisor in root cause investigations.
• Provide feedback on opportunities to improve inspection processes.
• Responsible for inspecting products using established inspection tools and techniques.
• Performs and documents First Article, In-Process, and Final inspections on parts in production to ensure that customer requirements, quality plans and quality standards are met.
• Inspects material and product received from outside sources to ensure compliance with quality standards, quality plans and customer specifications.
• Timely complete all assigned technical and safety trainings.
• Work in the field (outside conditions) providing assistance with the movements of materials for Inspection.
• Clean drilling tools and rig equipment for inspection.
• Take responsibility for the safety of all cleaning machinery and responsibility for environmental control over the working areas.
• Report any unsafe conditions or acts to the Supervisor.
• Ensure that work assignments are performed in accordance with approved plans, schedules and programs.
• Provide technically correct operation of equipment and other fixed assets under responsibility of the department.
• Apply Weatherford, and where appropriate Client Company Quality, Health, Safety & Environment Policy and Management Systems.
• Must understand and comply with all safety rules and company policies of Weatherford.
• Work assignments carried out to the highest quality level.
• Perform various other duties and activities as assigned by supervisor within the physical constraints of the job.

• Min secondary school graduates
• Minimum 3 years of related experience in QC inspection.
• Above average verbal and written communication skills in English.
• Perform dimensional, visual, and basic functional inspections on raw materials, in-process parts, and finished equipment.
• Ability to read and understand basic and advanced blueprints and charts.
• Comfortable working night shifts
• Ability to maintain accurate inspection records to ensure traceability per company procedures.

• API19SS/API Q1/ISO 9001:2015 is a plus.
• High or ITE/ technical education/ Diploma education is a plus
• Oil and Gas Industry is a plus
• Certified ASNT (American Society for non-destructive testing) level -2 at least 2 NDE methods (LPT & VT) is a plus.

• Mid-Senior level

• Full-time

• Quality Assurance

• Oil and Gas

Direct message the job poster from ESCO ASTER PTE LTD

Esco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.

Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017.

Esco Aster is a contract research development and manufacturing organization founded and deeply rooted by scientists enabling fellow scientists to translate their bench work into commercially available products at affordable prices.

Our scientific work is in emerging and frontier biology utilizing cells as a final product or deriving products from cells which often we use cells as the factory to derive our target product.

Our first commercial breakthrough success is Esco Aster is commercially first in class being first in the world to be certified for cultivated/cell-based meat to FSSC 22000 and by a competent food regulatory body.

We are first in the region to operate an end-to-end integrated full cell line creation/immortalization or engineered cell line, cell culture process development, analytical development for stem cells and exosomes with full cGMP Capabilities from Drug Substance and small-scale fill & finish for final Cell Therapy Product.

The work we do creates a remarkable and lasting impact on our world. We offer you an opportunity to be part of this exciting journey to own your career and firsthand exposure to new emerging modalities supporting translational sciences.

Join us as we redefine BioSolutions for One World and One Health for the current and future generations to come.

One World Biosolutions for One Health.

Who we’re looking for

• Ability to understand protocols, technical reports and technology transfer documents.
• Ability to understand standard operating procedures and other related documents.
• Able to commit to weekend work when needed, off in lieu will be given for work on public holidays.
• Repetitive motions due to certain laboratory techniques.
• Good Understanding of Aseptic Techniques.
• Work performed in a clean room environment wearing PPE.
• Ability to define problems, collect data, establish facts and draw conclusions.
• Ability to focus regardless of circumstances and stress induced pressure.
• Ability to take proactive approach.
• Meticulous and systematic.
• Commitment to continuous learning and staying updated with industry best practices.
• Have a strong focus on safety, quality and timeliness.
• Have strong critical thinking skills.

Job Responsibilities

Sample and QC Process Management:

• Ensure all QC sample management, testing, including process validation, cleaning, raw materials, stability samples, water samples, etc., are planned and executed on time.
• Prioritize and plan all testing activities to support processing schedules.
• Plan QC testing on a FIFO basis to eliminate backlog and meet internal QC KPIs.
• Plan work assignments for all QC analysts based on the production plan.
• Support future setup of central QC lab for all BioSolutions within Esco Aster.

Leadership and Team Management:

• Lead the implementation of the Laboratory Information Management System (LIMS).
• Lead Quality Control SOP implementation.
• Collaborate with the Analytical Development Team and manage QC Analytical, Microbiology Team to manage the revision and/or change control of QC documents as needed.
• Ensure new Analysts and Specialists are trained appropriately.
• Supervise, develop, engage, and motivate a young and driven team of QC Team Members.
• Manage the routine operations of the QC lab, ensuring business delivery at the right quality, cost, and speed.
• Able to build and lead across functional department consisting of different QC functions and supervisors / deputies / subject matter.

Operational Oversight:

• Oversee several sub-teams such as sample management, reference management, regulatory management, and QC instrument and equipment management.
• Lead the team to comply with internal requirements in all aspects through end-to-end quality control system oversight.
• Ensure all activities in the QC team are performed in compliance with cGMP, data integrity, and EHS requirements.
• Keep up to date with the latest trends in Quality Controls Tools.

Training and Development:

• Oversee the training, evaluation, and management of staff in the QC lab, including coaching, developing, and supporting them to reach their full potential.

Regulatory Compliance:

• Manage GMP audits from regulatory authorities and clients, respond to audit reports, and create CAPAs as applicable.
• Support analytical method transfer activities.
• Author and review OOS/OOT and Deviation investigations for approval, maintaining investigation records in accordance with company policies.
• Participate in Quality Risk Assessment Programs.
• Provide input and expertise on QC testing and practices for all departments.
• Serve as the QC representative for all customer and agency audits and support the audit of all 3rd party contract facilities.
• Oversee the management of Sample and Controlled Substance inventories.
• Provide technical support and advice on QC matters to other areas within the site: Production, Procurement, Supply Chain, Warehouse, and Process Developments.
• Work with Analytical Sciences and Technology (ASAT) to internal or external tech transfer from developed protocols from Analytical Development to Quality control including overseeing method verification, qualification, and validation activities.

Compliance Management:

• Participate in self-inspection and support client audits.
• Manage compliance tasks to ensure the Quality Control department is current and compliant.
• Maintain purchase orders, cost centers, and budgets for the QC department.
• Manage implementation and adherence to all applicable SHE and cGMP regulations.
• Support and oversee 3rd party test labs and ensure test labs are qualified per our QMS.
• Perform calibration and maintenance of QC laboratory equipment working with our CMMS and as per Iso 17025 standards and relevant GLP standards.
• Support/ oversee QC laboratory equipment/system qualification.

The job function listed is not exhaustive and shall also include any responsibilities as assigned by the Supervisor and Management from time to time to support GMP activities.

Requirements

• Bachelor’s degree in life sciences with minimum of 5 years of experience in Quality Control within highly regulated cGMP pharmaceutical industry. Experience is Biologics and ATMPs (i.e. Cell and Gene) is an added advantage.
• Candidates with experience in ATMPs (Cell & Gene) manufacturing are highly preferred but not mandatory.
• Familiar and keeping up to date with current GMP and applicable GxP regulations and standards; experience with regulatory requirements such as Singapore/HSA, US/FDA, EU/EMEA, etc.
• Good understanding of GMP requirements in release testing (Potency, Identity, Content, Impurities, Microbiological safety assays).
• Experience in HPLC, Flow Cytometry, ELISA, dPCR/PCR, Assays and method qualification.
• Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).
• Strong analytical skills and the ability to interpret data to drive decisions and improvements.
• Able to work independently, self- starter, self-motivated and task oriented.
• Good communication skills and leadership skills to effectively collaborate with cross-functional teams.
• A thorough understanding of the principles and management of cGMP compliance, and a strong quality mindset.
• Must be able to work in a team as well as independently.
• Proven leadership and team management skills.
• Excellent communication and organizational skills.
• Experience with LIMS and other laboratory management systems.
• Experience in Laboratory Equipment Qualification is an added advantage.
• Will be able to commit 5 working days per week in a fixed pattern.
• Apply now by submitting a Cover Letter and CV to

Apply now by submitting a Cover Letter and CV to

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Raichur, Baramulla, Kozhikode, Vishakhapatnam, Pala, Ooty, Panchkula, Patna, Dibrugarh

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Quality Control (QC) Specialist is to promote and integrate quality into every aspect of our BioReIiance biologics safety testing business in Singapore. Duties of the role include the support of QC operations (environmental monitoring and release of critical raw materials), data integrity and systems administration to ensure that laboratory testing operations are in full compliance with sound scientific practice, GxP and Standard Operating Procedures (SOPs). As a QC Specialist, you will ensure quarantine materials are received and released for use as per appropriate quality procedures. The ability to develop and maintain effective working relationships with operational, support services and quality assurance personnel will be critical for success in this role.

• Graduate degree in life sciences or microbiology or higher related degree
• Minimum of 2-3 years of experience
• Demonstrable scientific expertise in microbiology related works
• Previous experience working in a Quality Control materials release environment
• Previous Pharmaceutical experience would be ideal; however, other industry backgrounds would be considered
• You will have previous work experience within a GLP / GMP regulated environment would be highly desirable
• You are strongly focused on quality and safety, with strong planning and organisational skills
• You have good communication and interpersonal skills and are highly self-motivated, with strong initiative and drive

We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

• Seniority level: Associate
• Employment type: Full-time
• Job function: Quality Assurance and Science

Get AI-powered advice on this job and more exclusive features.

Ventós is a distributor of aroma chemicals and essential oils for flavors and fragrances industries all over the world. Young, dynamic, highly-specialized professionals make up our team of technicians, accountants, sales, purchases, logistics and production.

With more than 3.500 products permanently available in stock we can offer a just-in-time response to our customers needs. We have established commercial agreements with important producers of raw materials, which give Ventós a leading position as agents or distributors of their products.

We are looking to strengthen our team in Singapore by adding a Quality Control Specialist.

Responsibilities:

• Ensure the quality control of raw materials and finished products through routine analytical testing (GC, GC-MS, physical properties, etc.), in compliance with internal specifications and international standards.
• Conduct thorough inspection and testing of incoming materials, in-process production, and finished goods to ensure compliance with established quality standards and specifications.
• Develop and maintain detailed QC documentation, including inspection reports, test records, non-conformance logs, and trend analysis.
• Prepare and maintain technical documentation (CoAs, TDS, SDS, IFRA certificates, allergen declarations, etc.) for internal use and for customer requests.
• Collaborate with production and R&D teams to ensure regulatory compliance of products across different markets (EU, US, Asia, etc.).
• Monitor and implement updates to relevant legislation and international regulatory frameworks (REACH, CLP, IFRA, FDA, etc.).
• Assist with internal and external audits, ensuring all records are up to date and accessible.
• Support the Regulatory Affairs Manager in preparing product dossiers and registration files when required.
• Coordinate with suppliers to collect technical and regulatory documentation of raw materials.
• Participate in continuous improvement projects to optimize quality and compliance processes.
• Maintain accurate and organized records in compliance with ISO and GMP standards.

Profile:

• Bachelor’s degree in Chemistry, Pharmacy, Chemical Engineering, or a related scientific field. Additional training in Regulatory Affairs or Quality Management is a plus.
• Minimum of 2–3 years of experience in a similar role within the chemical, fragrance, cosmetics, or food industry.
• Solid understanding of international regulatory frameworks (REACH, CLP, IFRA, GHS, etc.).
• Familiarity with analytical techniques such as GC and GC-MS is highly desirable.
• Excellent organizational and multitasking abilities, with strong attention to detail.
• Fluent in English; additional languages (especially Spanish) are an advantage.
• Proficient in Microsoft Office and experience working with ERP systems (Navision highly valued).

Additional Information:

• Working hours: From 8am to 5pm with 1 hour for lunch
• Employment Type: Permanent contract with 3-month probation period

Would you like to join our team? Send us your application!

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Quality Assurance
• Industries Chemical Manufacturing and Wholesale Chemical and Allied Products

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