15 Pharmaceutical Companies jobs in Singapore

We are seeking a skilled Manufacturing & Laboratory Technician to join our team in the pharmaceutical industry. As a key member of our staff, you will be responsible for performing various tasks related to laboratory quality control, equipment management, and facility maintenance.

The ideal candidate should possess excellent analytical skills, strong attention to detail, and the ability to work effectively in a fast-paced environment. Additionally, proficiency in basic office software applications and fluency in English are essential.

• Minimum NITEC or Diploma Holders
• Background in Pharmaceutical, Life and Food Sciences, Process Manufacturing, Engineering or equivalent welcome
• Strong teamwork spirit with enthusiasm for learning new skills and collaboration
• Diligent in documentation with commitment to maintaining workplace cleanliness and safety

As a valued member of our team, you can expect:

• Competitive salary and benefits package
• Opportunities for career growth and professional development
• A supportive and collaborative work environment

Additional responsibilities may include:

• Laboratory QC Microbiological Testing, Environmental Monitoring
• Samples Receipt and Management
• Equipment and Facility Management & Cleaning
• Method Validation and Qualification, In-Process Control
• Documentation and Compliance, Quality Assurance Support, Investigations and Deviations

Successful candidates will undergo an interview to discuss their interest and suitability for the role. Shortlisted applicants will be contacted shortly after the interview process.

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 Brandon I Morinaka on Production and characterization of new natural products under a project on Genome Mining For Peptide Natural Products And Biosynthetic Enzymes.

The main responsibilities of the position include:
• Production of new peptide natural products in E. coli.
• Characterization of new natural products using spectroscopic techniques.
• Biological evaluation of new natural products for antimicrobial activity.

• Qualifications / Discipline: BSc in pharmacy, chemistry, biology or field related to research.
• Skills: Biochemistry, molecular biology, analytical chemistry
• Experience: Previous research experience in natural products chemistry and biosynthesis.

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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Join to apply for the Research Fellow / Engineer (Pharmaceutical Innovation Programme Singapore (PIPS)) - AZN4 role at Singapore Institute of Technology

1 week ago Be among the first 25 applicants

Join to apply for the Research Fellow / Engineer (Pharmaceutical Innovation Programme Singapore (PIPS)) - AZN4 role at Singapore Institute of Technology

Job Description

Research Fellow / Engineer (Pharmaceutical Innovation Programme Singapore (PIPS)) - AZN4

Job Description

Research Fellow / Engineer (Pharmaceutical Innovation Programme Singapore (PIPS)) - AZN4

Posting Start Date: 21/07/2025

Schemes of Service: Research

Division: Food, Chemical and Biotechnology

Employment Type: Fixed Term

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.
• Any other adhoc duties assigned.
  
  

• 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.

• Seniority level Not Applicable

• Employment type Full-time

• Job function Research, Analyst, and Information Technology
• Industries Higher Education

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Queenstown, Central Singapore Community Development Council, Singapore 1 month ago

Queenstown, Central Singapore Community Development Council, Singapore 3 months ago

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Job Responsibilities:

· Conduct analytical method transfer, validation, verification, and equivalency studies in compliance with SOPs, ALCOA principles, and data integrity standards.

· Perform analytical testing in accordance with GMP and GLP requirements, ensuring accuracy and efficiency.

· Lead or participate in 5S and housekeeping initiatives, maintaining adherence to safety procedures.

· Assess product impact due to changes or updates in compendial monographs.

· Support regulatory submissions and respond to queries related to post-transfer activities.

· Write and review SOPs, OJT materials, protocols, reports, test procedures, and position papers.

· Investigate laboratory incidents, identify root causes, and implement appropriate CAPAs.

· Provide hands-on training to colleagues on instruments and analytical methods.

· Review and approve laboratory test results.

· Manage QTS actions and handle GMP-impacting change controls.

· Coordinate with donating sites to facilitate smooth method transfers.

· Conduct training on new laboratory methods for QC team members.

· Contribute to continuous improvement initiatives within QC or cross-functional teams.

· Actively participate in Tier meetings by updating performance metrics, highlighting issues, and supporting solution development.

· Perform cleaning method development and validation.

· Ensure documentation complies with GDP practices and is accurately maintained.

· Execute method verification per site or pharmacopeial standards on schedule.

· Keep training records current and properly filed to reflect testing qualifications.

· Adhoc tasks and projects as assigned

Job Requirements

· Minimum Diploma in a related discipline

· Minimum 2 years of relevant quality check experience

· Experience within the Pharmaceutical industry would be an added advantage

· Able to start immediately or within short notice

Interested candidates, kindly email your detailed resumes in MS word format to

Attention to Joseph Koh Wei Jie (R1873431)

Shortlisted candidates will be notified

EA Registration Number: R1873431

Data provided is for recruitment purposes only

Business Registration Number: 200611680D. License Number: 10C5117

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.

We are seeking a Product Specialist to join our team, responsible for promoting pharmaceutical products to medical professionals in clinics and hospitals. The ideal candidate will have a strong understanding of therapeutic areas, including anti-infectives and psychiatry.

• Represent the company to promote assigned pharmaceutical products to medical practitioners and allied health professionals
• Develop in-depth knowledge of relevant therapeutic areas concerning products
• List company products to private and restructured hospitals formularies
• Maintain up-to-date knowledge of products, branding strategy, positioning, customers, and competitors
• Execute territorial management through sales reports analysis and market intelligence
• Coordinate sales and marketing strategies to achieve set targets
• Provide accurate weekly sales forecasts to achieve top-line sales targets
• Detail and share scientific materials with healthcare professionals and key opinion leaders

• Degree in pharmacy, business, marketing, communications, or life science highly preferred
• Minimum 2 years of experience in the pharmaceutical industry
• Preferably more than 2 years of sales experience in infectious disease and psychiatry settings
• Class 3 driving license required

By joining our team, you will gain valuable experience in the pharmaceutical industry, develop your skills in sales, marketing, and communication, and work in a dynamic environment with opportunities for growth and development.

Project Senior Sales Engineer

• Mon-Fri 8.30AM to 5.30PM
• Tuas
• Basic up to $8,500 + Variable Incentive ( Sales Commission from Project Sales's Value ) + Variable Bonus
• No AWS, transport claim per km if have own car, with medical benefits and min 14 days to 21 days max

( Must Fulfill All 5 Requirements )

• Diploma or Bachelor’s degree in mechanical engineering or related field
• Minimum 5 - 10 years of related industry experience in project sales with a strong track record (able to bring in 5 - 10 million sales per year)
• Highly prefer someone with project sales experience in pharmaceutical and/or wastewater treatment industry.
• Hunter sales role in generating sales leads and bring in new project & clients for company. (Farmer role is not suitable)
• Strong technical skills in engineering design, analysis, and testing.

Job Scopes:

• Follow up with site walk and client enquiry for the new job or project and work together with project engineer and manager for the quotation and tender submission, ensuring purchase order is secured.
• Coordinating with engineering, construction and liaise with the client on detail engineering requirements.
• Prepare quotation, budget plan and submission to have approval from project engineer or manager.
• Prepare method of statement, lifting plan and work schedule to provide safety personnel to prepare risk assessment.
• Prepare MTO and raise MR for all materials required for the project.
• Responsible for equipment installation, structure installation, piping erection operations and pipe support installation in accordance with schedule, procedures, specifications, priorities and availability of construction drawings.
• Handling all the technical queries and investigating all the work related problems, including the drawing of field sketches when necessary.
• Review of Project specification, ISO drawings and P&ID.
• Responsible for counter checking by ISO drawings, P&ID and GA drawings for the correct location, orientation, alignment and plumpness.
• Carrying out final P&ID check of installed piping systems in the module. Preparation of “AS BUILT” drawings.
• Responsible for carrying out mechanical clearance, conducting hydro and pneumatic tests, fulfilling commissioning and Pre-Commissioning requirements for the project.
• Responsible for line checking after hydro testing or pneumatic testing to complete the post punch list prior to sign-off the test packages before signing the completion of piping / mechanical.
• Ensure that all punch list items are resolved; client handover is satisfactorily concluded and that there is no prolongation of project.
• Take prompt corrective and preventive action to remove any quality issue, any unsafe elements and unhealthy conditions at site.
• Sales Cycle Management: Conduct the full sales cycle, including lead generation, follow-up, service delivery, and transaction closure.

WhatsApp: +65 9642 0989 (Han)

Email:

Chaw Chiaw Han, Reg No：R22106723

The Supreme HR Advisory Pte Ltd, EA No：14c7279

• Mon-Fri 8.30AM to 5.30PM
• Tuas
• Basic up to $8,500 + Variable Incentive ( Sales Commission from Project Sales's Value ) + Variable Bonus

( Must Fulfill All 5 Requirements )

• Diploma or Bachelor’s degree in mechanical engineering or related field
• Minimum 5 - 10 years of related industry experience in project sales with a strong track record (able to bring in 5 - 10 million sales per year)
• Highly prefer someone with project sales experience in pharmaceutical and/or wastewater treatment industry.
• With strong customer connection and able to generate sales leads for company.
• Strong technical skills in engineering design, analysis, and testing.

Job Scopes:

• Follow up with site walk and client enquiry for the new job or project and work together with project engineer and manager for the quotation and tender submission, ensuring purchase order is secured.
• Coordinating with engineering, construction and liaise with the client on detail engineering requirements.
• Prepare quotation, budget plan and submission to have approval from project engineer or manager.
• Prepare method of statement, lifting plan and work schedule to provide safety personnel to prepare risk assessment.
• Prepare MTO and raise MR for all materials required for the project.
• Responsible for equipment installation, structure installation, piping erection operations and pipe support installation in accordance with schedule, procedures, specifications, priorities and availability of construction drawings.
• Handling all the technical queries and investigating all the work related problems, including the drawing of field sketches when necessary.
• Review of Project specification, ISO drawings and P&ID.
• Responsible for counter checking by ISO drawings, P&ID and GA drawings for the correct location, orientation, alignment and plumpness.
• Carrying out final P&ID check of installed piping systems in the module. Preparation of “AS BUILT” drawings.
• Responsible for carrying out mechanical clearance, conducting hydro and pneumatic tests, fulfilling commissioning and Pre-Commissioning requirements for the project.
• Responsible for line checking after hydro testing or pneumatic testing to complete the post punch list prior to sign-off the test packages before signing the completion of piping / mechanical.
• Ensure that all punch list items are resolved; client handover is satisfactorily concluded and that there is no prolongation of project.
• Take prompt corrective and preventive action to remove any quality issue, any unsafe elements and unhealthy conditions at site.
• Sales Cycle Management: Conduct the full sales cycle, including lead generation, follow-up, service delivery, and transaction closure.

Chin See Min Reg No. : R22107450

The Supreme HR Advisory Pte Ltd EA No. : 14C7279