71 Pharmaceutical Field jobs in Singapore

Skip to content

Procurement Officer – Direct Materials (Pharmaceutical Manufacturing)

Our client is seeking a Procurement Officer – Direct Materials (Pharmaceutical Manufacturing) to join their team!

About Our Client

Our client is a well-established pan-Asian pharmaceutical brand with a rich history spanning decades. Known for their bestselling medicine and strong brand recognition across Asia, they are now expanding their operations in Singapore. With a commitment to innovation, sustainability, and excellence, they are poised for an exciting phase of growth in the pharmaceutical industry.

What you'll be doing?

Manage procurement processes: Oversee end-to-end procurement for direct materials, ensuring timely delivery, cost optimization, and quality compliance.

Develop supplier relationships: Build and maintain strong connections with suppliers, focusing on favorable terms, reliable supply, and cost savings.

Evaluate and select vendors: Assess suppliers based on key performance indicators and continuously monitor their performance.

Negotiate and manage contracts: Prepare and oversee supplier contracts, ensuring favorable terms and regulatory compliance.

Optimize inventory levels: Work closely with the Supply Chain team to balance supply and demand, minimizing production downtime.

Collaborate across teams: Work with Manufacturing, Quality Assurance, R&D, and Supply Chain teams to align procurement activities with operational needs.

Ensure compliance: Maintain regulatory compliance and quality standards for all procured direct materials.

Manage costs and reporting: Oversee procurement budgets, provide regular reports, and identify cost reduction opportunities.

Drive continuous improvement: Participate in initiatives to enhance procurement processes and increase overall efficiency.

Who are they looking for?

Educational background: Degree in Supply Chain Management, Pharmacy, Chemistry, Engineering, or a related field.

Relevant experience: 4-6 years of direct materials procurement experience in the pharmaceutical or related manufacturing industry.

Industry knowledge: Strong understanding of procurement processes, vendor management, and contract negotiation.

Regulatory awareness: Familiarity with pharmaceutical industry regulations, including GMP and quality standards.

Communication skills: Excellent interpersonal and communication abilities to collaborate effectively with teams and suppliers.

Analytical mindset: Strong analytical skills with a focus on cost optimization and efficiency.

Adaptability: Ability to thrive in a fast-paced environment while managing competing priorities.

Why you should consider this opportunity?

Our client offers an attractive remuneration package and other benefits, such as:

Opportunities for training, development, and career advancement

A key role in driving manufacturing success through essential material sourcing

Other Information:

Working Hour: Monday-Friday;9am-6pm

Salary Range: $4,000 - $6,000

How to apply

Ready to join this role? Click Apply now to submit your resume and share your availability and expected salary with us!

We encourage applications from candidates with diverse backgrounds and experiences who are passionate about making an impact in the pharmaceutical industry.

All information received will be kept strictly confidential and will be used only for employment-related purposes.

#SmartHire

Unlock job insights

Salary match Number of applicants Skills match

Your application will include the following questions:

What can I earn as a Procurement Officer

QC Lab Analyst (Pharmaceutical Manufacturing MNC, Chemical engineering)
Primary Objectives of this Job
This position is required to provide services to the Quality Control Laboratories on Sample Management and Inventory Management in the Lab Services team.
Responsibilities
Sample Management
Receipt of Routine and Non-Routine samples and distribute samples to their respective storage locations.
Performs Aliquoting on Process and Non-Protein samples on a daily basis.
Tracking of Sample Receipt on a daily basis at the Lab Services Tracking Boards.
Performs testing on Utilities samples on weekend, when required.
Performs peer review for verification of task and data related to Sample Management.
Inventory Management
Ensures good inventory of critical materials via QC Kanban system to support testing.
Purchase of Laboratory Consumables, Services and Chemicals/Biologics in Requisition System.
Receipt of QC Reference Substances, Controls and Critical Reagents.
General Responsibilities
Assists in the review and writing of SOPs related to Sample and Inventory Management.
Identifies and report any excursion / atypical issues / safety concerns in QC to Supervisor in a timely manner.
Carry out 5S and ensures good housekeeping of Lab Services area.
Support and participates in Operation Excellence initiatives (such as GEMBA and GMP walk).
Responsibility to adhere to any applicable EHS requirements.
Commitment to a fair and respectful relationship to others and behavior in accordance with Code of Conduct.
Any other duties as assigned by Supervisor.
Education and Experience Requirements
Knowledge with Microsoft Office applications.
Willing to work on rotating Day Shift (0730 to 1930 hours).
Experience working in cGMP Manufacturing Laboratory will be an advantage.
Experience in performing Total Organic Carbons (TOC) and Conductivity tests will be added advantage.
Key Skills and Competencies
Min Diploma or Degree in Chemistry, Biochemistry, Biotechnology or equivalent, preferably with more than 1 year of related laboratory experience.
Good Interpersonal, Verbal and Written Communication Skills required.
Ability to work and collaborate within the team.
Strong Planning and Organization Skills.
Must be detail oriented.
Training will be provided, all are welcome to apply.
If you are interested in the position, do kindly drop your most updated resume to
(Attn: QC Lab Analyst - Leon) .
Thank You.
R1551708
Recruit Express Pte Ltd (Healthcare & Lifesciences Division)
#J-18808-Ljbffr

MES Engineer (Manufacturing/ Siemens OpCenter /Pharmaceutical)

12-Months Contract

Location: Tuas

Salary up to $6,000 depending on experience

Industry : Pharmaceutical

Responsibilities

• Develop MES Functional Specification documents for Upstream and Downstream processes, along with support equipment workflows
• Recipe development based on Siemens OpCenter
• Development of test protocols for Upstream and Downstream processes, along with process support workflows (equipment cleaning/calibration/etc)
• Execute MES recipe qualification (IQ/UAT)
• Creation of shopfloor supporting documents (SOP/job aids)
• Provide shopfloor support during production exécution.

Requirements:

• Degree in Engineering / Digital / Life Sciences
• Experience in the Life Sciences industry
• Knowledge in MES recipe development and its interfaces with third-party systems such as SAP and DCS – experience in Siemens OpCenter (previously known as Simatic IT)
• Proven ability to work as part of an integrated, networked team, and collaborate across functional, organizational, and location boundaries and be people-first values driven

Lim Pey Chyi (Apple) -

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd

EA Licence: 02C3423

Validation Engineer (Pharmaceutical, Office hours 5 days, Manufacturing)
Overview:
Under general supervision, reviews specifications and determines the critical aspects of facilities, utilities, computer systems and manufacturing equipment with regard to product and process quality, writes qualification protocols for operating systems and records related test results. Prepares final reports that identify the results of protocol testing and the conditions of release.
Essential Job Functions:
Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws.
Writes protocols that challenge the critical parameters related to installation, operation, and performance of the related facility, utilities, computer systems, or equipment.
Assures that protocols are approved through proper channels; writes and revises validation protocols.
Executes validation and qualification protocols per related SOPs and assures that acceptance criterion related to validation and qualification protocols are met.
Analyzes new and existing equipment, recommends equipment modifications as needed for validation optimization.
Assures that all test data is gathered and recorded in accordance with cGMP requirements.
Analyzes data to ascertain if it meets related protocol acceptance criteria; writes deviation reports as required upon failures to meet protocol acceptance criteria.
Writes final reports and assures that they are approved through proper channels.
Performs necessary equipment and system IQ, OQ, and PQ's to assure compliance in all manufacturing and support areas.
Develops and communicates project timelines and status.
Complies with all GMP and safety requirements, SOP's and Company policies and procedures.
Performs related duties as assigned.
Work in a self-directed manner and must be able to work on problems of a complex scope where analysis of data requires an in-depth evaluation of various factors.
Ability to exercise judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results.
Demonstrated understanding and use of statistical methods in experiment design, data analysis, validation, and process monitoring.
Job Skills & Knowledge:
Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
Pharmaceutical principles, practices and applications.
Principles of mathematical and statistical computations.
Interpreting software and ladder logic diagrams and flowcharts.
Interpreting electrical and mechanical blueprints and specifications including HVAC systems and construction plans.
Solving practical problems and considering a variety of concrete variables in situations where only limited standardization exists.
Basic Qualifications:
Min 5 years experience working in a regulated environment.
Working knowledge of Standard Operating Procedures and Protocols/Reports.
Understanding of validation/qualification strategies.
Knowledge of applicable quality regulations and standards.
Quality or quality support experience in a regulated environment (GLP, cGMP, ISO).
3 years quality assurance or quality control experience in cGMP pharmaceutical or drug development organization.
Working knowledge of facility equipment commissioning and qualification.
Working knowledge of process and cleaning validation.
Working knowledge of Computer System Validation.
Quality assurance or quality control experience in a cGMP pharmaceutical setting.
Education: B.S. in an Engineering discipline, or Life Science degree.
Required: 3-5 years quality or quality support experience in a cGMP pharmaceutical setting.
Desired: 4-7 years facility, equipment, and/or cleaning validation experience in a cGMP manufacturing setting.
Sound working knowledge of processing equipment used to manufacture APIs.
Knowledge of clean room standards.
Professional Skills, Qualifications and Experience:
Strong ability to manage multiple priorities, self-starter attitude, good oral and writing skills and the ability to work independently and as a team in an efficient manner.
Ability to utilize Good Documentation Practices during document creation and review.
Working knowledge of current regulatory guidelines and standards.
Ability to apply and incorporate pharmaceutical standards, rules and guidances. (e.g. FDA, EU, ISO, ICH, ISPE, etc.)
Comfortable in a fast-paced environment with the ability to adjust to changing priorities.
Flexible and accountable.
Detailed oriented work standards.
Interested candidates please send a copy of your resume to

Email Subject: Validation Engineer
Leon Leong De Cong
R1551708
Recruit Express Pte Ltd (Healthcare & Lifesciences Division)
EA License: 99C4599
#J-18808-Ljbffr

Our client is a regional pharmaceutical company with strong Asian presence. Due to expansion, it is increasing its headcount in its Singapore office, and is seeking various positions including a Sales Representative to broaden its market in Singapore.

• Proactively pursue fresh sales prospects.
• Undertake market research to pinpoint potential sales avenues and assess customer requirements.
• Partner with the Chinese procurement team to enhance outcomes.
• Gather necessary customer payments and guarantee the prompt resolution of any payment concerns.
• Engage in negotiations and finalize agreements while addressing complaints or objections effectively.

Requirements:

• Highly motivated and target driven with a proven track record in sales
• Excellent selling, negotiation, and communication skills
• Prioritizing, time management and organizational skills
• Ability to create and deliver presentations tailored to the audience needs
• Relationship management skills and openness to feedback

Interested candidates are invited to send in your resume stating your past work experience, reasons for each leave, past and expected remuneration.

We regret to inform that only shortlisted candidates will be notified.

By submitting an application to us, you will be deemed to have agreed for us to collect, use and disclose your personal data which you have submitted to your prospective employers, for the purpose of job search, and/or other services which you have consent us to perform on your behalf.

Attn: R24123795 Woo Gu Ming
Cultivar Asia Pte Ltd (EA License: 19C8782)

Our client is a regional pharmaceutical company with strong Asian presence. Due to expansion, it is increasing its headcount in its Singapore office, and is seeking various positions including a Sales Representative to broaden its market in Singapore.

• Proactively pursue fresh sales prospects.
• Undertake market research to pinpoint potential sales avenues and assess customer requirements.
• Partner with the Chinese procurement team to enhance outcomes.
• Gather necessary customer payments and guarantee the prompt resolution of any payment concerns.
• Engage in negotiations and finalize agreements while addressing complaints or objections effectively.

Requirements:

• Highly motivated and target driven with a proven track record in sales
• Excellent selling, negotiation, and communication skills
• Prioritizing, time management and organizational skills
• Ability to create and deliver presentations tailored to the audience needs
• Relationship management skills and openness to feedback

Interested candidates are invited to send in your resume stating your past work experience, reasons for each leave, past and expected remuneration.

We regret to inform that only shortlisted candidates will be notified.

By submitting an application to us, you will be deemed to have agreed for us to collect, use and disclose your personal data which you have submitted to your prospective employers, for the purpose of job search, and/or other services which you have consent us to perform on your behalf.

Attn: R24123795 Woo Gu Ming
Cultivar Asia Pte Ltd (EA License: 19C8782)

Our client is a regional pharmaceutical company with strong Asian presence. Due to expansion, it is increasing its headcount in its Singapore office, and is seeking various positions including a Sales Representative to broaden its market in Singapore.
Proactively pursue fresh sales prospects.
Undertake market research to pinpoint potential sales avenues and assess customer requirements.
Partner with the Chinese procurement team to enhance outcomes.
Gather necessary customer payments and guarantee the prompt resolution of any payment concerns.
Engage in negotiations and finalize agreements while addressing complaints or objections effectively.
Requirements:
Highly motivated and target driven with a proven track record in sales
Excellent selling, negotiation, and communication skills
Prioritizing, time management and organizational skills
Ability to create and deliver presentations tailored to the audience needs
Relationship management skills and openness to feedback
Interested candidates are invited to send in your resume stating your past work experience, reasons for each leave, past and expected remuneration.
We regret to inform that only shortlisted candidates will be notified.
By submitting an application to us, you will be deemed to have agreed for us to collect, use and disclose your personal data which you have submitted to your prospective employers, for the purpose of job search, and/or other services which you have consent us to perform on your behalf.
Attn: R24123795 Woo Gu Ming
Cultivar Asia Pte Ltd (EA License: 19C8782)
#J-18808-Ljbffr

About the job

Looking to launch your career at the cutting edge of healthcare? Join Sanofi for a chance to develop with mentoring and guidance from inspirational leaders while helping to make an impact on the lives of countless people worldwide. As a Sales and Marketing intern, you will be assisting hands-on experience in selling and marketing in the pharmaceutical space.  After completing the training, the Intern will be assigned a project to work on with a Sales / Marketing Executive to ensure learnings are executed eventually.

Main responsibilities:

Key responsibilities and Tasks

• Call on hospitals, physicians and/or pharmacies
• Support the National Sales & Marketing team in following up and building long-term relationships with Healthcare Professionals
• Will have the opportunity to learnabout analysing data on the specific disease landscape through omni-channel engagements
• Deliver insights for strategic brand planning
• Other key operational duties as assigned

About you

Experiences/Competencies Required

• Currently pursuing a bachelor’s degree, ideally in communications, business, political science, or any related field.
• Strong command in written English and verbal communication skills, with a keen eye for details.
• A proactive and creative mindset, with a willingness to learn and possesses strong project management skills.
• Exhibit organizational and interpersonal skills, with the ability to collaborate effectively within a team.
• Flexible and adaptable to change, self-initiated and driven.
• Innovative, accountable, collaborative, and challenges the status quo.
• Good to have: Previous leadership and/or writing experience in school or student varsity activities. Skilled in Canva.

Why choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team.
• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.