298 Pharmaceutical Manufacturing jobs in Singapore

Job Title:

Job Description:

We are seeking a Quality Engineer with expertise in medical devices and pharmaceuticals to join our team. As a Quality Engineer, you will be responsible for ensuring the quality of our products and services, implementing pharmacovigilance and medical device vigilance according to local and global standards.

You will work closely with our Operations Team to maintain the local Vigilance system and ensure compliance with regulatory requirements. Additionally, you will be responsible for managing quality incidents, reconciliations, and self-assessments, as well as public adverse event reporting and agency reporting.

Key Responsibilities:

Job Overview:

We are seeking a skilled MES and Historian Integration Specialist to join our team on a 12-month contract basis.

The successful candidate will be responsible for enabling contextualized data acquisition, including Alarm and Event and Audit Trail data, through the development and optimization of SQL queries.

Key Responsibilities include:

• Designing and implementing system interfaces between MES and Historian systems
• Collaborating with cross-functional teams to ensure seamless integration
• Reviewing and approving technical specifications for system interfaces
• Supporting test case execution and performance of teat case activities as required

The ideal candidate will have proficient knowledge of both Waterfall and Agile project methodologies.

Deep expertise in deploying and configuring Aspen Historian Suite, including Aspen IP.21, APRM, Event21, CIM-IO, Batch Extractor, and Aspen SQL + is necessary.

Configuring Kepware, including driver setup for protocol transaction and data aggregation, is also required.

Experience working in pharmaceutical manufacturing environments is essential.

Proven experience integrating with a wide range of automation and control systems, including DCS systems such as Emerson DeltaV, SCADA platforms like WinCC and Wonderware, PLCs, benchtop instruments, and other lab/manufacturing equipment, is necessary.

Technical Proficiencies include Database: MySQL, Microsoft SQL Server, Oracle; Data and Industrial Protocols: ODBC, FTP, MQTT, OPC-UA, OPC-DA, Modbus; Scripting and Automation: PowerShell scripting for automation and data handling; and Infrastructure Knowledge: In-depth understanding of networking principles and operating systems (Windows/Linux).

About
The QA Validation Engineer will play a vital role in establishing and maintaining high-quality standards at a growing pharmaceutical manufacturing startup. This position ensures that all manufacturing processes, systems and equipment comply with regulatory standards and quality specification. The incumbent will support continuous improvement initiatives and collaborate with cross-functional teams to build robust quality systems for a successful, compliant manufacturing operation.
We are a distinguished brand with more than sixty years of expertise in the pharmaceutical industry. We aim to broaden our presence by using Singapore as a central hub for expansion into other countries.
Responsibilities
Develop and execute validation protocols for facilities, equipment, utilities, materials, manufacturing process, cleaning and computerized systems.
Document validation activities and results and maintain records for all validation activities.
Analyse validation test data to determine whether systems or processes have met validation criteria.
Author of validation reports
Develop and maintain validation master plan.
Develops re-qualification or re-validation plans to keep the systems in validated states.
Support audits and inspections as a subject matter expert.
Provide impact assessment for any planned change to the site and execute any change actions that result from the assessment.
Work closely with stakeholders to coordinate validation activities.
Collaborate with cross functional teams to address deviations and implement corrective actions and to prepare periodic product review.
Train staff on validation procedures and maintain documentations for audits.
Maintain knowledge of current regulatory intelligence and industry trends.
Qualifications:
Bachelor’s degree in Engineering, Pharmacy, Science or a related field.
Prior work experience as a Validation Engineer or similar role in the pharmaceutical industry or medical device industry.
Proficient with validation software tools.
Experience with audit management, regulatory inspections, and handling regulatory queries on validation matters.
Strong analytical, problem-solving, and organizational skills with a keen attention to detail.
Strong sense of accountability and ownership of responsibilities.
Excellent verbal and written communication skills with the ability to present technical concepts to cross-functional teams and senior leadership.
A commitment to maintaining high standards of quality, safety, and compliance at all times.
What We Offer:
Competitive salary and benefits package.
Opportunities for professional development and advancement.
A dynamic and collaborative work environment.
#J-18808-Ljbffr

Overview
The QA Validation Engineer will play a vital role in establishing and maintaining high-quality standards at a growing pharmaceutical manufacturing startup. This position ensures that all manufacturing processes, systems and equipment comply with regulatory standards and quality specification. The incumbent will support continuous improvement initiatives and collaborate with cross-functional teams to build robust quality systems for a successful, compliant manufacturing operation. We are a distinguished brand with more than sixty years of expertise in the pharmaceutical industry. We aim to broaden our presence by using Singapore as a central hub for expansion into other countries.
Responsibilities
Develop and execute validation protocols for facilities, equipment, utilities, materials, manufacturing process, cleaning and computerized systems.
Document validation activities and results and maintain records for all validation activities.
Analyse validation test data to determine whether systems or processes have met validation criteria.
Author validation reports.
Develop and maintain validation master plan.
Develop re-qualification or re-validation plans to keep the systems in validated states.
Support audits and inspections as a subject matter expert.
Provide impact assessment for any planned change to the site and execute any change actions that result from the assessment.
Work closely with stakeholders to coordinate validation activities.
Collaborate with cross functional teams to address deviations and implement corrective actions and to prepare periodic product review.
Train staff on validation procedures and maintain documentation for audits.
Maintain knowledge of current regulatory intelligence and industry trends.
Qualifications
Bachelor’s degree in Engineering, Pharmacy, Science or a related field.
Prior work experience as a Validation Engineer or similar role in the pharmaceutical industry or medical device industry.
Proficient with validation software tools.
Experience with audit management, regulatory inspections, and handling regulatory queries on validation matters.
Strong analytical, problem-solving, and organizational skills with a keen attention to detail.
Strong sense of accountability and ownership of responsibilities.
Excellent verbal and written communication skills with the ability to present technical concepts to cross-functional teams and senior leadership.
A commitment to maintaining high standards of quality, safety, and compliance at all times.
Required Skills
Proficient with validation software tools.
Strong analytical, problem-solving, and organizational skills.
Excellent verbal and written communication skills.
Preferred Skills
Experience with audit management and regulatory inspections.
Prior work experience in the pharmaceutical or medical device industry.
Pay range and compensation package
Competitive salary and benefits package.
Equal Opportunity Statement
We are committed to diversity and inclusivity in our hiring practices.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Quality Assurance
Pharmaceutical Manufacturing
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr

Responsibilities

• Implement and maintain all quality and food safety control processes in compliance with company standards, HACCP, ISO, local statutory requirements, and Halal standards.
• Oversee and implement QC & QA procedures across production.
• Conduct inspections on raw materials, in-process, and finished goods.
• Schedule and keep track of product testing activities.
• Maintain and calibrate QC tools and equipment to ensure accuracy.
• Handle audits, documentation, and corrective actions.
• Collaborate with production teams to uphold consistent product quality.
  Perform ad-hoc duties as assigned by management.

Requirements

• Diploma in Food Science, Food Technology, or related field.
• Minimum 2–3 years of working experience in a QA/QC-related field within the food industry.
• Positive work attitude and strong self-initiative.
• Good knowledge of GMP, HACCP, MUIS Halal, ISO 22000, FSSC 22000, and related standards.

Key Responsibilities:

• Perform Incoming Quality Control activities to ensure only qualified materials delivered.
• Support all daily activities assigned by supervisor.

• Support on IT solution development for productivity improvement.

• To auto update the information between 'QVL and Sampling Frequency List Fields, Data Setting Maintenance> system and 'Sampling Grade', 'Sampling time' & 'Conformance Test'.

• To notify the IQC by email when a new RT is created by warehouse personnel.
• To notify SQM should any material inactive for >2 years via email.
• Auto email to supplier for requesting the sample.

Qualifications:

• Candidates pursuing diploma or Degree are welcome
• Strong attention to detail and organizational skills.
• Familiarity with Microsoft office (e.g., Microsoft Word, MS Excel, MS PowerPoint, PDF editors).

Job Description:

The Quality Control (QC) Supervisor for Mechanical will support Site Management Team in monitoring quality and compliance throughout the construction of a Power Plant project located in Jurong Island. Reporting to the QA Manager and working closely with the Mechanical Manager, the QC Supervisor for Mechanical is responsible for overseeing the mechanical execution works performed by the EPC contractors, ensuring strict adherence to contractual quality requirements, engineering specifications, applicable codes, and international best practices.

Key Responsibilities:

• Conduct site inspections, audits, and tests to verify that mechanical installations and repairs adhere to design technical specifications, codes, and quality standards
• Ensure all mechanical work complies with relevant industry codes, project specifications, company policies, and contractual obligations
• Oversee critical mechanical activities including material inspection, installation, welding, Non-Destructive Testing (NDT), pressure testing, and final alignment and pre-commissioning checks
• Maintain detailed, accurate, and auditable records of all inspection activities, equipment history, non-conformance reports, and quality documentation
• Identify, document and track quality documentation
• Identify, document, and track quality defects
• Ensure all quality control activities are performed in full compliance with company Health, Safety, and Environment (HSE) policies and local regulatory requirements
• Support and facilitate quality-related meetings with contractors, engineers, and inspectors to resolve issues and drive continuous improvement
• Review and comment contractor-submitted Inspection & Test Plans (ITPs), method statements, and quality documentation prior to execution
• Ensure all mechanical systems are installed, tested, and documented in accordance with punch list and commissioning readiness requirements

Requirements:

• Minimum 10 years' field experience, with relevant inspector's qualification/certification in mechanical works preferably in Oil & Gas, Shipyard or Power Plant industries
• Strong knowledge of mechanical systems, equipment and construction practices
• Familiarity with international standard, especially ASME code, and inspection methods
• Ability to plan, schedule and allocate work to ensure efficient operations and minimal downtime
• Effective communication in good coordination with other departments
• Proficiency in managing project quality plans, inspection and test plans (ITPs) and reports
• Ability to identify and resolve technical issues effectively

• 5 Days Work
• Annual Leave
• Performance Bonus
• Career development opportunities

Responsibilities:

• Conduct quality audits and inspections on incoming and outgoing products to ensure compliance with company standards.
• Carry out QC processes such as product checks, reworks, repairs, and defect documentation.
• Maintain accurate records of QC data, supplier invoices, and stock handling procedures.
• Support continuous improvement initiatives in production and quality processes.
• Perform other quality-related and ad-hoc duties as assigned.

Requirements:

• Minimum Nitec qualification with at least 1 year of quality control experience (retail jewellery or manufacturing preferred).
• Strong attention to detail with basic knowledge of production processes and MS Office.
• Good communication skills, able to multi-task, and quick to learn.

Please submit your updated resume in MS Word format via the "Apply Now" button.

We regret that only shortlisted candidates will be notified.

StaffKing Pte Ltd (20C0358) | Stanley Chin (R

The Quality Control Team Leader is responsible for leading and executing quality control activities, ensuring that Pall products meet internal specifications, customer expectations, and regulatory standards. This role requires strong leadership, technical expertise in analytical testing, and a commitment to maintaining a safe and compliant laboratory environment.

This position is part of the Quality Control Department reporting to the Senior Quality Manager and will be located in Benoi Sector, Singapore.

In this role, you will have the opportunity to:

• Lead the QC team in performing inspections and analytical testing of raw materials, SFG and FG products.
• Develop and maintain QC protocols, SOPs, and documentation aligned with Pall Filtration standards and applicable regulations. Ensure compliance with ISO, GMP, and other relevant quality and regulatory frameworks.
• Monitor and report on quality metrics, including defect rates, test results, and process capability. Conduct root cause analysis and implement corrective and preventive actions (CAPA) for quality issues.
• Collaborate with cross-functional teams including Manufacturing, Engineering, R&D, and Quality Assurance to resolve quality-related issues.
• Support internal, customer, and regulatory audits, ensuring readiness and compliance. Drive continuous improvement initiatives focused on product quality, process efficiency, and team capability.
• Ensure safety and risk assessment (RA) protocols are implemented and followed in the QC laboratory, including chemical handling, equipment usage, and emergency preparedness.
• Maintain calibration and validation of QC equipment and ensure proper documentation.

The essential requirements of the job include

• Bachelor's degree in chemistry, Chemical Engineering, or a related discipline.
• Minimum 5 years of experience in quality control or assurance, ideally within filter manufacturing or similar sectors.
• Proven ability to lead QC teams and oversee laboratory operations efficiently.
• Deep understanding of filtration technologies, materials science, and chemical manufacturing processes.
• Well-versed in ISO standards, GMP, and other relevant regulatory frameworks.
• Skilled in advanced test methods including ICP-MS, GC-MS, NVR, LPC, and TOC.
• Strong analytical thinking, problem-solving capabilities, and effective communication skills.

It would be a plus if you also possess previous experience in:

• PhD or Master's Degree in Chemistry or a related scientific discipline.
• Experience in chemical or filter manufacturing, membrane technologies, or advanced material testing. Proficiency in ICP-MS, GC-MS, NVR, LPC, and TOC test methods.
• Experience with statistical process control (SPC), risk assessment, and laboratory information management systems (LIMS).

Pall Corporation, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what's next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit