10 Pharmaceutical Companies jobs in Singapore

Interested applicants are invited to apply directly at the NUS Career Portal

Your application will be processed only if you apply via NUS Career Portal

We regret that only shortlisted candidates will be notified.

The successful candidate will work with Dr TIAN Chong on synthesis of mechanically interlocked molecules under a project on Bridging Chemistry and Biology: Synthesis, Structure and Properties of Mechanically Interlocked Peptides (MIPS).

The main responsibilities of the position include:
• Research tasks (90%): to carry out research to design and synthesize rotaxanes via novel active template strategies.
• Laboratory safety/ordering (10%): to aid in ordering and maintaining lab supplies, create and review standard operating procedures and risk assessments, assemble reagents, chemicals and media that are needed for experiments.

• PhD of Science required with major in Organic Chemistry. Candidate with strong background in organic synthesis and excellent record of publication is preferred.

Skills:
1. Have an excellent understanding of chemistry.
2. Have expertise in multi-step synthesis.
3. Communicate well in English in writing and in oral and visual presentations.
4. Show an ability to work supportively in a laboratory environment.

Experience:

• Experience in organic synthesis and spectroscopic techniques for compound characterization.

Interested applicants are invited to apply directly at the NUS Career Portal

Your application will be processed only if you apply via NUS Career Portal

We regret that only shortlisted candidates will be notified.

The successful candidate will work with Dr TIAN Chong on synthesis of mechanically interlocked molecules under a project on Bridging Chemistry and Biology: Synthesis, Structure and Properties of Mechanically Interlocked Peptides (MIPS).

The main responsibilities of the position include:
• Research tasks (90%): to carry out research to design and synthesize rotaxanes via novel active template strategies.
• Laboratory safety/ordering (10%): to aid in ordering and maintaining lab supplies, create and review standard operating procedures and risk assessments, assemble reagents, chemicals and media that are needed for experiments.

• PhD of Science required with major in Organic Chemistry. Candidate with strong background in organic synthesis and excellent record of publication is preferred.

Skills:
1. Have an excellent understanding of chemistry.
2. Have expertise in multi-step synthesis.
3. Communicate well in English in writing and in oral and visual presentations.
4. Show an ability to work supportively in a laboratory environment.

Experience:

• Experience in organic synthesis and spectroscopic techniques for compound characterization.

Join to apply for the Automation Engineer (Pharmaceutical Industry) role at Amaris Consulting

2 days ago Be among the first 25 applicants

Join to apply for the Automation Engineer (Pharmaceutical Industry) role at Amaris Consulting

Who are we?

Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade – this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries. Our solutions focus on four different Business Lines: Information System & Digital, Telecom, Life Sciences and Engineering. We’re focused on building and nurturing a top talent community where all our team members can achieve their full potential. Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success.

At Amaris, we strive to provide our candidates with the best possible recruitment experience. We like to get to know our candidates, challenge them, and be able to give them proper feedback as quickly as possible. Here's what our recruitment process looks like:

Brief Call : Our process typically begins with a brief virtual/phone conversation to get to know you! The objective? Learn about you, understand your motivations, and make sure we have the right job for you!

Interviews (the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). During the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. We will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. Of course, you will also get to know Amaris: our culture, our roots, our teams, and your career opportunities!

Case study : Depending on the position, we may ask you to take a test. This could be a role play, a technical assessment, a problem-solving scenario, etc.

As you know, every person is different and so is every role in a company. That is why we have to adapt accordingly, and the process may differ slightly at times. However, please know that we always put ourselves in the candidate's shoes to ensure they have the best possible experience.

We look forward to meeting you!

Job Description

ABOUT THE JOB

• Support the execution of test protocols to validate the upgraded process control system in compliance with GxP requirements
• Support hardware installation and integration activities for the new system
• Assist in generating and updating documentation for the upgraded system (user manuals, technical specs, test reports)
• Support the implementation of changes, including change control documentation, execution, and verification
• Troubleshoot and resolve technical issues related to software upgrades with minimal disruption to operations
• Collaborate with cross-functional teams and external vendors throughout the system upgrade lifecycle
• Contribute to the continuous improvement of processes and compliance across the automation project
• Ensure alignment with pharmaceutical industry standards and site-specific procedures
  
  
  

• Academic background: Degree in Automation Engineering, Electrical Engineering, Computer Science or related field.
• Experience with automation engineering, process control systems, or software upgrades (2 to 5 years)
• Experience with validation protocols in GMP or regulated environments
• Knowledge of change control management and regulatory documentation practices
• Familiarity with pharmaceutical manufacturing systems and automation architecture
• You demonstrate strong problem-solving skills, excellent collaboration, and adaptability in dynamic environments
  
  
  

• Global Diversity: Be part of an international team of 110+ nationalities, celebrating diverse perspectives and collaboration.
• Trust and Growth: With 70% of our leaders starting at entry-level, we’re committed to nurturing talent and empowering you to reach new heights.
• Continuous Learning: Unlock your full potential with our internal Academy and over 250 training modules designed for your professional growth.
• Vibrant Culture: Enjoy a workplace where energy, fun, and camaraderie come together through afterworks, networking events, and more.
• Meaningful Impact: Join us in making a difference through our CSR initiatives, including the WeCare Together program, and be part of something bigger.
  
  
  

• Seniority level Entry level

• Employment type Full-time

• Job function Engineering and Information Technology
• Industries IT Services and IT Consulting

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Johor Baharu, Johore, Malaysia 6 days ago

Ang Mo Kio, North East Community Development Council, Singapore 1 week ago

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Safety Officer supports the EHS (Environment, Health & Safety) team in ensuring compliance with workplace safety and health regulations within a GMP-regulated pharmaceutical facility . This role involves assisting in inspections, documentation, training coordination, and basic safety monitoring.

• Assist in conducting safety inspections across production, lab, and warehouse areas.
• Support the review and preparation of risk assessments and safe work procedures .
• Monitor PPE compliance , safety signage, and basic emergency equipment checks.
• Help maintain safety records, including incident reports , training logs , and audit follow-ups .
• Participate in toolbox talks , safety briefings, and basic EHS training sessions .
• Assist in chemical inventory checks and waste management tracking .
• Coordinate with contractors and vendors to ensure compliance with site safety rules.
• Support the EHS team during internal audits and regulatory inspections (e.g., HSA, MOM).
• Learn and follow Good Manufacturing Practices (GMP) and safety protocols .

Requirements:

1. Diploma in Workplace Safety & Health , Life Sciences , Engineering , or a related field.
2. WSQ Basic or Advanced Certificate in Workplace Safety and Health (WSH) preferred.
3. 0–2 years of experience in a similar role, preferably in pharmaceutical , biotech , or manufacturing industries.
4. Familiarity with basic safety regulations and GMP principles is an advantage.
5. Good communication and observation skills.
6. Eagerness to learn and grow within a structured safety environment.
7. This position is open to fresh graduates. Candidates must be available to join immediately.

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We’re Hiring: CIP Engineer – Biotech/Pharmaceutical Industry (Singapore Citizens Only) ?

Join our team to design, develop, and optimize Clean-In-Place (CIP) and Sterilize-In-Place (SIP) systems in a GMP-regulated environment.

• Key Responsibilities:
• Support the design and optimization of CIP/SIP systems for biotech drug substance facilities, including new installations and remediation projects.
• Assist in developing User Requirement Specifications (URS), Functional Requirement Specifications (FRS), and Design Risk Assessments (DRA) for CIP/SIP systems.
• Conduct hydraulic calculations and design CIP/SIP circuits, ensuring proper flow rates, pressures, and cleaning effectiveness.
• Generate Mass Balance calculations, Process Flow Diagrams (PFDs), and Piping & Instrumentation Diagrams (P&IDs) for CIP/SIP systems.
• Support the development of CIP/SIP sequence matrix charts, ensuring effective cycle design and automation.
• Work on CIP skid design/layout, collaborating with clients, vendors, and design engineers.
• Qualifications & Experience:
• Bachelor’s degree in Chemical Engineering, Biochemical Engineering, Biotechnology, or a related field.
• Experience in biopharmaceutical facility design, troubleshooting, start-up, and commissioning.
• Familiarity with process control strategies, automation, and clean utility systems.
• Proficiency in AutoCAD, Visio, Revit, Schedule Pro, and other process design software (Desirable).
• We are looking for professionals who are Singapore Citizens.
  
  
  

• Seniority level Entry level

• Employment type Full-time

• Job function Consulting and Engineering
• Industries Pharmaceutical Manufacturing

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Job no: 498802
Department: Food, Chemical and Biotechnology
Contract type: Contract
Apply now

As a University of Applied Learning, SIT works closely with industry in our research pursuits. Our research staff will have the opportunity to be equipped with applied research skill sets that are relevant to industry demands while working on research projects in SIT.

The primary responsibility of this role is to deliver on a Pharmaceutical Innovation Programme Singapore research project where you will be part of a collaborative team exploring innovative ways of understanding extrusion processing for pharmaceutical drug materials and products using rheological measurements.

Key Responsibilities

In this role, you will characterize mixtures of pharmaceutical excipients and drug materials to develop methodologies for screening hot-melt extrusion formulations and selecting optimal operating conditions using rheology, with the objective of producing amorphous-solid-dispersions. You will validate the developed processing space and operating conditions for extruded pharmaceutical formulations using a lab-scale extruder. In collaboration with researchers at the Singapore-MIT Alliance for Research and Technology (SMART), you will characterize the physical properties and performance of intermediate pharmaceutical drug products. The created methods will be transferred to the industrial partner to enhance their product development process using rheological characterization.

More specific responsibilities include:

• Participate in and manage the research project with Principal Investigator (PI), and the research team members to ensure all project deliverables are met.
• Undertake characterization of pharmaceutical active ingredients, polymeric excipients, and plasticizers for producing amorphous-solid-dispersions.
• Perform lab-scale hot-melt extrusion of pharmaceutical materials to validate predicted processing conditions and product outcomes.
• Collaborate with broader pharmaceutical research team at SMART.
• Design, execute, and interpret experiments independently.
• Author papers in high-quality journals in areas that are related to the research.
• Prepare and deliver reports and presentations for industrial partners
• Carry out Risk Assessment, and ensure compliance with Work, Safety and Health Regulations.
• Coordinate procurement and liaise with vendors/suppliers.
• Work independently, as well as within a team.

Job Requirements

• Have deep hands-on experience with at least one of the areas of polymer rheology, extrusion processing, pharmaceutical engineering with small molecules.
• Relevant competence in the areas of wet lab work, analytical instrumentation, material science and formulation
• Have an advanced degree in chemical engineering, mechanical engineering, materials science and engineering, or a related field.
• Knowledge of any of the following will be advantageous: rheology, physical characterisation, crystallisation, polymer melts, extrusion, material physics.
• Able to build and maintain strong working relationships with people within and external to the university.
• Self-directed learner who believes in continuous learning and development.
• Proficient in communicating via technical writing and presentations.
• Possess strong analytical and critical thinking skills.
• Show strong initiative and take ownership of work.

Apply now
Advertised: 11 Nov 2024 Singapore Standard Time
Applications close: 30 Jun 2025 Singapore Standard Time

Organisation/Company SINGAPORE INSTITUTE OF TECHNOLOGY (SIT) Research Field Engineering Chemistry Engineering Researcher Profile First Stage Researcher (R1) Country Singapore Application Deadline 31 Dec 2025 - 00:00 (UTC) Type of Contract Other Job Status Full-time Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Is the Job related to staff position within a Research Infrastructure? No

As a University of Applied Learning, SIT works closely with industry in our research pursuits. Our research staff will have the opportunity to be equipped with applied research skill sets that are relevant to industry demands while working on research projects in SIT.

The primary responsibility of this role is to deliver on a Pharmaceutical Innovation Programme Singapore research project where you will be part of a collaborative team exploring innovative ways of understanding extrusion processing for pharmaceutical drug materials and products using rheological measurements.

Key Responsibilities

In this role, you will characterize mixtures of pharmaceutical excipients and drug materials to develop methodologies for screening hot-melt extrusion formulations and selecting optimal operating conditions using rheology, with the objective of producing amorphous-solid-dispersions. You will validate the developed processing space and operating conditions for extruded pharmaceutical formulations using a lab-scale extruder. In collaboration with researchers at the Singapore-MIT Alliance for Research and Technology (SMART), you will characterize the physical properties and performance of intermediate pharmaceutical drug products. The created methods will be transferred to the industrial partner to enhance their product development process using rheological characterization.

More specific responsibilities include:

• Participate in and manage the research project with Principal Investigator (PI), and the research team members to ensure all project deliverables are met.
• Undertake characterization of pharmaceutical active ingredients, polymeric excipients, and plasticizers for producing amorphous-solid-dispersions.
• Perform lab-scale hot-melt extrusion of pharmaceutical materials to validate predicted processing conditions and product outcomes.
• Collaborate with broader pharmaceutical research team at SMART.
• Design, execute, and interpret experiments independently.
• Author papers in high-quality journals in areas that are related to the research.
• Prepare and deliver reports and presentations for industrial partners
• Carry out Risk Assessment, and ensure compliance with Work, Safety and Health Regulations.
• Coordinate procurement and liaise with vendors/suppliers.
• Work independently, as well as within a team.

Job Requirements

• Have deep hands-on experience with at least one of the areas of polymer rheology, extrusion processing, pharmaceutical engineering with small molecules.
• Relevant competence in the areas of wet lab work, analytical instrumentation, material science and formulation
• Have an advanced degree in chemical engineering, mechanical engineering, materials science and engineering, or a related field.
• Knowledge of any of the following will be advantageous: rheology, physical characterisation, crystallisation, polymer melts, extrusion, material physics.
• Able to build and maintain strong working relationships with people within and external to the university.
• Self-directed learner who believes in continuous learning and development.
• Proficient in communicating via technical writing and presentations.
• Possess strong analytical and critical thinking skills.
• Show strong initiative and take ownership of work.

Job no: 498802
Department: Food, Chemical and Biotechnology
Contract type: Contract
Apply now

As a University of Applied Learning, SIT works closely with industry in our research pursuits. Our research staff will have the opportunity to be equipped with applied research skill sets that are relevant to industry demands while working on research projects in SIT.

The primary responsibility of this role is to deliver on a Pharmaceutical Innovation Programme Singapore research project where you will be part of a collaborative team exploring innovative ways of understanding extrusion processing for pharmaceutical drug materials and products using rheological measurements.

Key Responsibilities

In this role, you will characterize mixtures of pharmaceutical excipients and drug materials to develop methodologies for screening hot-melt extrusion formulations and selecting optimal operating conditions using rheology, with the objective of producing amorphous-solid-dispersions. You will validate the developed processing space and operating conditions for extruded pharmaceutical formulations using a lab-scale extruder. In collaboration with researchers at the Singapore-MIT Alliance for Research and Technology (SMART), you will characterize the physical properties and performance of intermediate pharmaceutical drug products. The created methods will be transferred to the industrial partner to enhance their product development process using rheological characterization.

More specific responsibilities include:

• Participate in and manage the research project with Principal Investigator (PI), and the research team members to ensure all project deliverables are met.
• Undertake characterization of pharmaceutical active ingredients, polymeric excipients, and plasticizers for producing amorphous-solid-dispersions.
• Perform lab-scale hot-melt extrusion of pharmaceutical materials to validate predicted processing conditions and product outcomes.
• Collaborate with broader pharmaceutical research team at SMART.
• Design, execute, and interpret experiments independently.
• Author papers in high-quality journals in areas that are related to the research.
• Prepare and deliver reports and presentations for industrial partners
• Carry out Risk Assessment, and ensure compliance with Work, Safety and Health Regulations.
• Coordinate procurement and liaise with vendors/suppliers.
• Work independently, as well as within a team.

Job Requirements

• Have deep hands-on experience with at least one of the areas of polymer rheology, extrusion processing, pharmaceutical engineering with small molecules.
• Relevant competence in the areas of wet lab work, analytical instrumentation, material science and formulation
• Have an advanced degree in chemical engineering, mechanical engineering, materials science and engineering, or a related field.
• Knowledge of any of the following will be advantageous: rheology, physical characterisation, crystallisation, polymer melts, extrusion, material physics.
• Able to build and maintain strong working relationships with people within and external to the university.
• Self-directed learner who believes in continuous learning and development.
• Proficient in communicating via technical writing and presentations.
• Possess strong analytical and critical thinking skills.
• Show strong initiative and take ownership of work.

Apply now
Advertised: 09 Dec 2024 Singapore Standard Time
Applications close: 30 Jun 2025 Singapore Standard Time

SingHealth is establishing the SingHealth Drug and Diagnostic Development Engine (SinD3E) unit. This role offers the opportunity to contribute to healthcare innovation in Singapore through the translation of research into practical applications. As Deputy Director, you will establish and lead this unit, working with a team of domain experts specialising in:

• Medicinal Chemistry

• Assay Development

• Computational Chemistry for therapeutic technologies

• Assay Prototype Development

• Analytical Performance Characterisation

• Diagnostic Product Development Strategy

Key Responsibilities:

• Establish and lead the SinD3E unit

• Drive the development of therapeutic and diagnostic technologies

• Work closely with staff and consultants to advance the commercialisation of SingHealth technologies

• Organise and present at educational forums on drug and diagnostic development

• Support the SingHealth Intellectual Property Team in assessing invention disclosures

Job Requirements:

• PhD in Life, Biomedical or Chemical Science, with at least 14 years of experience leading multi-disciplinary teams in the biotech/pharmaceutical industry or relevant academic research settings

• MBA qualification is preferred

• In-depth understanding of therapeutic and diagnostic development processes

• Strong communication and organisational abilities

• Proactive approach to problem-solving

• Demonstrated leadership capabilities in managing uncertainty

We regret that only shortlisted candidates will be contacted.