Total 14 job vacancies by Corestaff Pte. Ltd.

About the role
As a Pharmacist (QA), you will play a vital role in ensuring the quality and safety of healthcare products within the company's supply chain operations in the Pioneer West Region. This is a full-time position that offers the opportunity to make a significant impact on the delivery of critical healthcare services.

What you'll be doing

• Developing and implementing quality assurance protocols for the procurement, storage, and distribution of pharmaceutical and medical products
• Conducting routine inspections and audits to monitor compliance with relevant regulations and standards
• Investigating and resolving any quality-related issues or complaints
• Collaborating with cross-functional teams to optimise supply chain processes and ensure the timely delivery of products
• Providing expert guidance and training to warehouse and logistics personnel on best practices for handling and storing healthcare products
• Maintaining comprehensive documentation and reporting on quality control activities
• Staying up-to-date with industry regulations, guidelines, and emerging best practices in pharmaceutical quality assurance

What we're looking for

• Registered Pharmacist with a valid practicing certificate
• Minimum 2 years of experience in a quality assurance or regulatory role within the pharmaceutical or healthcare supply chain industry
• Strong understanding of Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), and other relevant quality standards and regulations
• Proficient in data analysis, report writing, and project management
• Excellent problem-solving, decision-making, and critical thinking skills
• Ability to work collaboratively in a team environment and communicate effectively with stakeholders at all levels
• Highly organized, detail-oriented, and committed to maintaining the highest standards of quality and compliance

About the Company:

Our client is a leading provider of integrated healthcare solutions in Singapore, dedicated to enhancing the delivery of healthcare services. The company combines innovative technologies with expert logistics and consulting services to streamline healthcare operations. Committed to efficiency and collaboration, the company works with institutions and government agencies to tailor solutions that meet the evolving needs of the healthcare sector. Join their dynamic team and make a meaningful impact in healthcare!

How to Apply:

Interested candidates, please submit your updated resume by using Apply button

*We regret to inform that only shortlisted candidates will be informed.*

Sarah Sevilla

Registration Number: R22107553

EA License No: 18C9027

About the Company:

Our client is a leading provider of integrated healthcare solutions in Singapore, dedicated to enhancing the delivery of healthcare services. The company combines innovative technologies with expert logistics and consulting services to streamline healthcare operations. Committed to efficiency and collaboration, the company works with institutions and government agencies to tailor solutions that meet the evolving needs of the healthcare sector. Join their dynamic team and make a meaningful impact in healthcare!

Job Summary:

The Pharmacist - QA plays a key role in maintaining product quality by supporting quality control activities and assisting in the implementation of Quality Plans. The role will involve working with cross-functional teams to ensure compliance with regulatory standards and support the Quality Management System (QMS). This position is ideal for candidates who are detail-oriented, with a passion for ensuring the highest quality standards in pharmaceutical products.

Key Responsibilities:

Customer Relationship Support

• Assist in responding to customer inquiries and addressing product quality concerns.
• Collaborate with internal teams to recommend basic improvements to product services.

Continuous Improvement and Technology Utilization

• Support the implementation of continuous improvement initiatives within the QA process.
• Assist in using data analytics to monitor quality trends and identify areas for improvement.

Quality Assurance and Operations

• Execute established quality procedures and support Supplier Quality activities.
• Assist in monitoring quality activities such as complaints and non-conformities.
• Help generate and prepare reports to meet key performance indicators (KPIs).
• Participate in internal audits and support the implementation of process improvements.

Training and Development Support

• Assist in the coordination of team training on quality-related topics.
• Participate in training on QMS and basic regulatory requirements.
• Support the analysis of training outcomes to identify gaps.

Job Requirements:

• Bachelor’s degree / Diploma in Pharmacy or a related field.
• Experience in pharmacy practice, quality assurance, or regulatory compliance.
• Strong analytical skills and proficiency in data analysis tools.
• Excellent communication and interpersonal skills.
• Ability to work with cross-functional teams and manage multiple priorities.

How to Apply:

Interested candidates, please submit your updated resume by using Apply button

*We regret to inform that only shortlisted candidates will be informed.*

Sarah Sevilla

Registration Number: R22107553

EA License No: 18C9027

About the Company:

Our client is a leading provider of integrated healthcare solutions in Singapore, dedicated to enhancing the delivery of healthcare services. The company combines innovative technologies with expert logistics and consulting services to streamline healthcare operations. Committed to efficiency and collaboration, the company works with institutions and government agencies to tailor solutions that meet the evolving needs of the healthcare sector. Join their dynamic team and make a meaningful impact in healthcare!

Job Summary:

The QA Executive / Pharmacist plays a key role in maintaining product quality by supporting quality control activities and assisting in the implementation of Quality Plans. The role will involve working with cross-functional teams to ensure compliance with regulatory standards and support the Quality Management System (QMS). This position is ideal for candidates who are detail-oriented, with a passion for ensuring the highest quality standards in pharmaceutical products.

Key Responsibilities:

Customer Relationship Support

• Assist in responding to customer inquiries and addressing product quality concerns.
• Collaborate with internal teams to recommend basic improvements to product services.

Continuous Improvement and Technology Utilization

• Support the implementation of continuous improvement initiatives within the QA process.
• Assist in using data analytics to monitor quality trends and identify areas for improvement.

Quality Assurance and Operations

• Execute established quality procedures and support Supplier Quality activities.
• Assist in monitoring quality activities such as complaints and non-conformities.
• Help generate and prepare reports to meet key performance indicators (KPIs).
• Participate in internal audits and support the implementation of process improvements.

Training and Development Support

• Assist in the coordination of team training on quality-related topics.
• Participate in training on QMS and basic regulatory requirements.
• Support the analysis of training outcomes to identify gaps.

Job Requirements:

• Bachelor’s degree / Diploma in Pharmacy or a related field.
• Experience in pharmacy practice, quality assurance, or regulatory compliance.
• Strong analytical skills and proficiency in data analysis tools.
• Excellent communication and interpersonal skills.
• Ability to work with cross-functional teams and manage multiple priorities.

How to Apply:

Interested candidates, please submit your updated resume by using Apply button

*We regret to inform that only shortlisted candidates will be informed.*

Sarah Sevilla

Registration Number: R22107553

EA License No: 18C9027

About the Company:

Our client is a leading provider of integrated healthcare solutions in Singapore, dedicated to enhancing the delivery of healthcare services. The company combines innovative technologies with expert logistics and consulting services to streamline healthcare operations. Committed to efficiency and collaboration, the company works with institutions and government agencies to tailor solutions that meet the evolving needs of the healthcare sector. Join their dynamic team and make a meaningful impact in healthcare!

Job Summary:

The Senior Pharmacist ensures quality control throughout the production process by inspecting products, implementing customized Quality Plans, and addressing customer complaints. This role requires expertise in regulatory affairs and compliance to align the Quality Management System (QMS) with industry standards. The Senior Pharmacist will drive continuous improvement initiatives, develop documentation and training, and effectively communicate with stakeholders.

Key Responsibilities:

Customer Relationship Management

• Maintain strong customer relationships, addressing inquiries and resolving product issues.
• Collaborate with teams to recommend enhancements to product services.

Continuous Improvement and Technology Advancement

• Drive research for product development to maximize customer value.
• Promote technology adoption and utilize data analytics to identify trends.
• Implement lean practices and monitor quality process gaps.

Quality Assurance and Operations

• Oversee quality plan frameworks and ensure QA alignment with various teams.
• Execute approved quality procedures and manage Supplier Quality.
• Customize Quality Plans for individual clients.
• Monitor quality activities including complaints and non-conformities, and generate reports to meet KPIs.
• Conduct audits and recommend process improvements.

Team Leadership and Development

• Lead training initiatives to improve team performance and retention.
• Develop and deliver training on Quality Management Systems (QMS) and regulatory requirements.
• Analyze training outcomes to address gaps and foster a culture of professional growth.

Job Requirements:

• Bachelor’s degree in Pharmacy or a related field.
• Experience in pharmacy practice, quality assurance, or regulatory compliance.
• Strong analytical skills and proficiency in data analysis tools.
• Excellent communication and interpersonal skills.
• Ability to lead cross-functional teams and manage multiple priorities.

How to Apply:

Interested candidates, please submit your updated resume by using Apply Now button

*We regret to inform that only shortlisted candidates will be informed.*

Sarah Sevilla

Registration Number: R22107553

EA License No: 18C9027

About the Company:
Our client is a global technology company and a market leader that develops and provides leading-edge solutions in surface mount technology, equipment and materials for the semiconductor assembly and packaging industries.

Responsibilities:

• Onboard new suppliers according to company's standards
• Ensure top suppliers are regularly audited (Schedule) & most importantly, corrective actions are followed through/closed.
• Develop & implement quality prevention processes internally/externally (at suppliers).
• Manage review and approve First article inspection submitted by suppliers for new products and changing requirements on approved parts.
• Develop & implement quality prevention processes internally/externally (at suppliers).
• Maintain & analyse supplier service levels & performance data and communicate performance measures internally and to suppliers.
• Identify Global Suppliers to work with and drive the supplier development & performance processes and continuous improvement of any quality topics.
• Create (SAP) & maintain reporting of non-conformance, using databases, Excel spreadsheets and graphical recording of data.
• Structure and chair monthly supplier performance / scorecard meetings.
• Job required hands on inspection capability

Requirements:

• Bachelor/Master’s Degree in Mechatronics Engineering
• Background in quality assurance or supplier quality (minimum 5 years) in a capital equipment or manufacturing environment.
• CMM knowledge is a must, preferably Zeiss CMM.
• Must have detailed understanding of an ERP system, ideally SAP.
• Must be able to read drawings and specification.
• Able to demonstrate a good understanding of quality requirements corrective & preventative action.
• Possess leadership skill; Able to lead supplier for continuous improvement
• IPC Certified specialist, Lead Auditor, Six Sigma Methodology, Statistical analysis, Understanding of 3D measurement equipment principles.
• Knowledge of manufacturing process such as Motor, Cables, Casting, machining, sheet metal and module assembly.
• Preferably knowledge with Industry 4.0 practices and implementations

How to Apply:

Interested candidates, please submit your updated resume in MSWORD format by using Apply Now button

**We regret to inform that only shortlisted candidates will be informed.**

Sarah Sevilla

Registration Number: R22107553

EA License No: 18C9027

About the Company:
The nature of business of our client is Construction and Civil Engineering company supporting the Oil & Gas and Chemical Processing Industry. They have decades of experience supporting large MNCs operating in Singapore, both on the mainland and offshore islands, in Civil Engineering Construction, and Maintenance projects.

Responsibilities:

• Act as the main QAQC adviser on project site for subcontractors, crafts people, and operatives
• Overseeing quality control and health and safety matters on site
• Review requirements, specifications, and technical design documents to ensure compliance in the inspection test plan (ITP), method statement, and installation
• Create detailed, comprehensive, and well-structured ITP to meet client needs
• Maintain, formulate, and follow through quality assurance system and follow through the audit requirements
• Formulate and implement a quality assurance program for the worksite including but not limited to training, assessment, and implementation to ensure quality works on site
• Estimate, prioritize, plan, and coordinate testing activities
• Liaise with consultant and internal teams to identify process system and site requirements and quality execution
• Day-to-day management of the site, including supervising and monitoring the site supervisory crew, labor force and the work of any subcontractors
• Investigate the causes of non-conforming cases and train users to implement solutions
• Preparing reports as required

Requirements:

• Possess at least a bachelor’s degree related to Civil Engineering and/or QA/QC knowledge
• Prior experience related to civil engineering in Oil and Petrochemical industry is necessary
• Good knowledge of Civil Engineering industries’ quality control/assurance

How to Apply:

Interested candidates, please submit your updated resume by using Apply Now button

**We regret to inform that only shortlisted candidates will be informed.**

Sarah Sevilla

Registration Number: R22107553

EA License No: 18C9027

The company is a high-tech manufacturer of contact lens solutions, sterile pharmaceutical solutions, first-aid eye and wound irrigations as well as eye comfort drops.

Responsibilities:

• Inspects incoming raw materials for compliance with current standards.
• Conducts periodic test analysis on products undergoing stability studies.
• Inspects incoming packaging materials for compliance with current standards.
• Performs microbiological testing and environmental monitoring according to SOPs.
• Prepares test solutions, compounds, or reagents for laboratory use.
• Assists Chemist, Lab Supervisor, and Micro Supervisor in maintaining company quality manuals related to operating procedures.
• Assists in GMP audits, validation, qualification, and change control.
• Assist in maintaining QC-related files.

Requirements:

• Min Diploma in Chemistry, Chemical Process Technology, Pharm, Biotechnology, Quality Assurance or any other science-related
• Entry level are welcome, training provided
• Open to shift work

How to Apply:

Interested candidates, please submit your updated resume by using Apply Now button

**We regret to inform that only shortlisted candidates will be informed.**

Tan Zhi Ning

Registration Number: R23116771

EA License No: 18C9027

The company is a high-tech manufacturer of contact lens solutions, sterile pharmaceutical solutions, first-aid eye and wound irrigations as well as eye comfort drops.

Responsibilities:

• Inspects incoming raw materials for compliance with current standards.
• Conducts periodic test analysis on products undergoing stability studies.
• Inspects incoming packaging materials for compliance with current standards.
• Performs microbiological testing and environmental monitoring according to SOPs.
• Prepares test solutions, compounds, or reagents for laboratory use.
• Assists Chemist, Lab Supervisor, and Micro Supervisor in maintaining company quality manuals related to operating procedures.
• Assists in GMP audits, validation, qualification, and change control.
• Assist in maintaining QC-related files.

Requirements:

• Min Diploma in Chemistry, Chemical Process Technology, Pharm, Biotechnology, Quality Assurance or any other science-related
• Entry level are welcome, training provided
• Open to shift work

How to Apply:

Interested candidates, please submit your updated resume by using Apply Now button

**We regret to inform that only shortlisted candidates will be informed.**

Tan Zhi Ning

Registration Number: R23116771

EA License No: 18C9027

The company is a high-tech manufacturer of contact lens solutions, sterile pharmaceutical solutions, first-aid eye and wound irrigations as well as eye comfort drops.

Responsibilities:

• Inspects incoming raw materials for compliance with current standards.
• Conducts periodic test analysis on products undergoing stability studies.
• Inspects incoming packaging materials for compliance with current standards.
• Performs microbiological testing and environmental monitoring according to SOPs.
• Prepares test solutions, compounds, or reagents for laboratory use.
• Assists Chemist, Lab Supervisor, and Micro Supervisor in maintaining company quality manuals related to operating procedures.
• Assists in GMP audits, validation, qualification, and change control.
• Assist in maintaining QC-related files.

Requirements:

• Min Diploma in Chemistry, Chemical Process Technology, Pharm, Biotechnology, Quality Assurance or any other science-related
• Entry level are welcome, training provided
• Open to shift work

How to Apply:

Interested candidates, please submit your updated resume by using Apply Now button

**We regret to inform that only shortlisted candidates will be informed.**

Tan Zhi Ning

Registration Number: R23116771

EA License No: 18C9027

About the Company:
Our client is one of the leading pharmaceutical ophthalmic solutions manufacturers in the world, dedicated in providing sterile pharmaceutical ophthalmologic solutions, from prevention to delivery of care at every touchpoint, advancing wellness in hospitals, clinics and home-care sectors.

Position Overview:
The Senior R&D Chemist is responsible for designing and developing products to meet quality standards and regulatory requirements (cGMP, 21 CFR Part 211, EU MDD/MDR, ISO 13485). He/she coordinates and conducts testing in compliance with SOPs, ISO standards, and global market regulations for physical, chemical, and microbiological aspects.

Responsibilities:

• Lead and oversee a team of chemists in R&D, Technology Transfer, and Projects.
• Develop and implement technical testing methods to meet regulatory requirements for medical devices and pharmaceutical products globally.
• Design testing methodologies for new materials and products and ensure compliance.
• Drive technology transfer initiatives and projects from lab to production scale.
• Identify chemicals to enhance product shelf-life and performance.
• Guide the QC team in good laboratory practices and accurate result interpretation.
• Develop and transfer new chemicals, ensuring thorough equipment and method validation.
• Update SOPs to align with evolving standards and regulatory requirements.
• Support external audits and inspections by certification bodies.
• Practice Good Laboratory Practices, Good Documentation Practices, and 5S.
• Drive innovation and automation in testing processes for efficiency.
• Any other tasks or projects that are being assigned by the immediate supervisor or Head of Department, as and when required.

Requirements:

• Bachelor's, Master's, or PhD in Chemistry with at least 8 years of hands-on R&D experience in the pharmaceutical / medical device sector.
• Strong understanding in regulatory standards that include GLP, GDP, cGMP, 21 CFR Part 211, EU MDD/MDR, and ISO 13485.
• Proficient in Product Development, with experience in producing cost-effective and robust technologies.
• Strong leadership skills with a track record of problem-solving and team collaboration.
• Excellent communication skills and ability to work effectively within diverse teams.

How to Apply:

Interested candidates, please submit your updated resume by using Apply Now button

*We regret to inform that only shortlisted candidates will be informed.*

Sarah Sevilla

Registration Number: R22107553

EA License No: 18C9027

About the Company:

For the last 100 years, our client has been a front leader company in providing engines, generators, and UPS products that have powered homes, hospitals, lawn mowers, stadiums and everything in-between.

Job Summary:
Responsible for managing and providing technical support to product quality. This includes reviewing and improving work processes and systems, participating in quality audits, and working with manufacturing plants on quality and operational matters. This role also requires providing guidance to the QA technician on daily inspection.

Responsibilities:

• Ensures operational process operating and meeting process / product requirement / specification.
• Performs Finish Goods Audit on company's products with reference to engineering drawings.
• Performs dimensional, functional, or other tests using specified measuring and test equipment.
• Files and maintains inspection records.
• Reviews incoming quality inspection metrology including first article inspection and prepares a plan to minimize inspections.
• Verifies and ensures closure of all suppliers’ issues including corrective and preventive actions.
• Maintains all the documentations are updated and comply with ISO 9001: 2015 standards.
• Participates in quality improvement programs.
• Responsible for calibrations of inspection and production tooling and equipment.
• Assist in ISO 9001: 2015 (internal and external) and Supplier audits.

Requirements:

• Minimum a Diploma/Degree in Quality/Manufacturing/Mechanical/Electrical Engineering.
• No experience candidate is welcomed to apply.
• Experience working in an ISO 9001 Quality System will be an advantage.
• Good knowledge in MS Office platforms software.
• Proficient in the use of mechanical inspection equipment including calipers, micrometer, torque tester, and other mechanical equipment.

How to Apply:

Interested candidates, please submit your updated resume by using Apply Now button

*We regret to inform that only shortlisted candidates will be informed.*

Sarah Sevilla

Registration Number: R22107553

EA License No: 18C9027

Job Summary: Production / Quality Executive

Are you passionate about revolutionizing the production landscape in the healthcare industry? We are seeking a dynamic Executive who will play a pivotal role in enhancing operational efficiency and ensuring the highest quality standards for the medical products. As a technical guide in the manufacturing facilities, you'll have the opportunity to drive innovation, develop Standard Operating Procedures (SOPs), and make impactful technical adjustments to optimize production processes.

About the Company:

The company envisions to bring value to healthcare institutions, general industry, and governmental agencies by improving healthcare supply chain processes. The company strives to transform Singapore's current multi layered healthcare supply chain into a seamless end-to-end integrated system.

Key Responsibilities:

1) Materials Management Expertise:

• Provide technical advice on optimal materials management SOPs to boost efficiency and minimize loss.
• Advise on industry best practices for environmentally responsible disposal.

2) Equipment and Facility Maintenance:

• Approve production lines post-clearance and cleaning.
• Investigate abnormalities in collaboration with the Quality department.

3) Pharmaceutical and Nutritional Product Production:

• Develop SOPs for equipment calibration in collaboration with Quality and Validation departments.
• Identify technical adjustments to enhance operational efficiency.
• Manage troubleshooting of equipment defects, faults, and breakdowns.

4) Production Workflows Improvement:

• Produce technical solutions to address constraints, inefficiencies, or deviations in production processes.
• Assess the technical feasibility of enhancing production workflows, equipment, and systems.
• Verify correct installation and programming of new and improved manufacturing equipment and systems.

Requirements:

• Degree/Diploma in Pharmaceutical Sciences , Manufactory equivalent certifications.
• 1-3 years of relevant working experience.
• Working knowledge of GMP or GDP in the healthcare industry.
• Proficient in MS Office Applications / Microsoft Power Platform Applications.
• Excellent communication and interpersonal skills.

How to Apply:

Interested candidates, please submit your updated resume by using Apply Now button

*We regret to inform that only shortlisted candidates will be informed.*

Sarah Sevilla

Registration Number: R22107553

EA License No: 18C9027

About the Company:

For the last 100 years, our client has been a front leader company in providing engines, generators, and UPS products that have powered homes, hospitals, lawn mowers, stadiums and everything in-between.

Responsibilities:

• Ensures operational process operating and meeting process / product requirement / specification.
• Implements and maintains effective quality system processes in line with ISO9001.
• Responsible for calibrations of inspection and production tooling and equipment.
• Closely monitors the performance of key quality indicators (Quality objectives) and initiates, deploys, and implements plans or measures to meet the goal set.
• Leads team to review and analyze daily processes and issues for improvements.
• Analyzes process weakness, manages customer feedback, and enhance quality performance by working with respective department on quality improvement plan.
• Ensures all documents (Quality management system, Control Plan, audits, and inspection checklist) are updated regularly.

Requirements:

• Minimum a Diploma/Degree in Quality/Manufacturing/Mechanical/Electrical Engineering.
• At least 5 years’ relevant experience in a similar position.
• Experience working in an ISO 9001 Quality System.
• Good knowledge in AutoCAD, SAP, ISO auditing, statistical tools, and MS Office platforms software.
• Proficient in the use of mechanical inspection equipment including calipers, micrometer, torque tester, and other mechanical equipment.

How to Apply:

Interested candidates, please submit your updated resume by using Apply Now button

*We regret to inform that only shortlisted candidates will be informed.*

Sarah Sevilla

Registration Number: R22107553

EA License No: 18C9027

Job Summary: Production Executive

Are you passionate about revolutionizing the production landscape in the healthcare industry? We are seeking a dynamic Production Executive who will play a pivotal role in enhancing operational efficiency and ensuring the highest quality standards for the medical products. As a technical guide in the manufacturing facilities, you'll have the opportunity to drive innovation, develop Standard Operating Procedures (SOPs), and make impactful technical adjustments to optimize production processes.

About the Company:

The company envisions to bring value to healthcare institutions, general industry, and governmental agencies by improving healthcare supply chain processes. The company strives to transform Singapore's current multi layered healthcare supply chain into a seamless end-to-end integrated system.

Key Responsibilities:

1) Materials Management Expertise:

• Provide technical advice on optimal materials management SOPs to boost efficiency and minimize loss.
• Advise on industry best practices for environmentally responsible disposal.

2) Equipment and Facility Maintenance:

• Approve production lines post-clearance and cleaning.
• Investigate abnormalities in collaboration with the Quality department.

3) Pharmaceutical and Nutritional Product Production:

• Develop SOPs for equipment calibration in collaboration with Quality and Validation departments.
• Identify technical adjustments to enhance operational efficiency.
• Manage troubleshooting of equipment defects, faults, and breakdowns.

4) Production Workflows Improvement:

• Produce technical solutions to address constraints, inefficiencies, or deviations in production processes.
• Assess the technical feasibility of enhancing production workflows, equipment, and systems.
• Verify correct installation and programming of new and improved manufacturing equipment and systems.

Requirements:

• Degree/Diploma in Pharmaceutical Sciences , Manufacor equivalent certifications.
• 1-3 years of relevant working experience.
• Working knowledge of GMP or GDP in the healthcare industry.
• Proficient in MS Office Applications / Microsoft Power Platform Applications.
• Excellent communication and interpersonal skills.

How to Apply:

Interested candidates, please submit your updated resume by using Apply Now button

*We regret to inform that only shortlisted candidates will be informed.*

Sarah Sevilla

Registration Number: R22107553

EA License No: 18C9027