990 Pharmaceutical Compliance jobs in Singapore

• Location: Bugis/CBD

• Working hours: 08:30 to 17:30 (Monday to Friday)

• AWS + Commissions

Job responsibilities:

• Represent the company to promote the assigned pharmaceutical products to Medical Practitioners and Allied Health Professionals in clinics and hospitals
• Have a good understanding in the relevant therapeutic areas concerning the products, i.e. anti-infectives and psychiatry.
• To list company products to Private and Restructured Hospitals’ formularies, clinics, etc
• Maintain up to date knowledge of the products, branding strategy, positioning, customers and competitors in the relevant therapeutic areas
• Execute territorial management through sales reports analysis and market intelligence
• Execute and coordinate sales and marketing strategies to achieve targets set by the company
• Provide accurate weekly sales forecast to achieve top-line sales targets
• Responsible for detailing and sharing scientific materials with Healthcare Professionals (HCPs) and Key Opinion Leaders (KOL)
• Maintain and build positive relationships with existing customers and proactively seek new accounts to secure in Singapore
• Build a strong network by engaging with existing and new KOLs
• Provide planning of schedules and appointments to ensure coverage of visits to targeted doctors at appropriate frequency
• Ensure strict compliance to Company Code of Conduct and internal SOPs/Policies for the promotional of pharmaceutical products and interaction with HCPs
• Handle customer complaints, product technical complaints, adverse events and medical enquiries quickly and professionally in accordance with company procedures

Job requirements:

• Degree in pharmacy, business, marketing, communications, or life science is 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
• Preferably Private and Restructured Hospitals sales experience for this position
• Class 3 driving license
• Strong ethics and compliance mindset
• Self-motivated and proactive
• Demonstrates strong selling, presentation and negotiating skills
• Excellent communication skills & interpersonal skills
• Dynamic, sales-driven with strong presentation skills
• Ability to work well in teams

Interested applicants, please send your resume to Charlene (R22105303) at with the email subject header "Product Specialist (Pharmaceutical industry) ".

We regret that only shortlisted candidates will be notified. Other applications will be updated in our database for future job opportunities.

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Pasona Singapore Pte Ltd

EA License No:90C4069

(Lau Rui Lin, Charlene, EA Registration No: R22105303)

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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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CIP Engineer – Biotech/Pharmaceutical Industry

Get AI-powered advice on this job and more exclusive features.

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

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Consulting and Engineering

• Industries

  Pharmaceutical Manufacturing

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We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

We are seeking a seasoned CQV Engineer with extensive experience in the pharmaceutical and cGMP industry. The ideal candidate will possess strong leadership skills, technical expertise, and excellent communication abilities.

• Lead and participate in Engineering, Procurement, Construction, Validation for GMP facilities.
• Prepare, execute, and review IQ, OQ, PQ validation protocols for equipment, facilities, and utilities.
• Conduct root cause analysis and lead quality investigations (deviations, CAPA, change control).
• Manage validation schedules and resource alignment.
• Support manufacturing process setup and technical activities.
• Perform FAT/SAT activities and temperature mapping.

• 8+ years CQV experience in pharma/cGMP.
• Strong understanding of cGMP, USP, EMA, ICH, 21 CFR, GAMP5, ISPE, PDA, ASME BPE.
• Proven problem-solving and project coordination skills.
• Excellent communication abilities.
• Bachelor of Science in Chemical/Biological Engineering or related field.

• USP
• CAPA
• Construction
• Risk Assessment
• GMP
• Root Cause Analysis
• Procurement
• Python
• Change Control
• ASME
• Project Coordination
• Regulatory Requirements
• Manufacturing
• Commissioning
• Trackwise
• Mapping

CIP Engineer – Biotech/Pharmaceutical Industry
Get AI-powered advice on this job and more exclusive features.
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.
If you’re passionate about CIP/SIP system design and optimization in the biopharmaceutical industry, we’d love to hear from you! ?
Seniority level
Seniority level Entry level
Employment type
Employment type Full-time
Job function
Job function Consulting and Engineering
Industries Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Hyde Engineering + Consulting by 2x
Get notified about new Engineer jobs in
Singapore .
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr

Job Responsibilities

• Conduct screening and due diligence review on prospects and referral partners before onboarding
• Conduct ongoing monitoring on existing clients
• Responsible for the implementation and enhancement of the Compliance framework within the company
• Conduct post transaction review to ensure adherence to balanced scorecard requirements, regulation and internal policies
• Track the CPD training hours of the licensed representatives and maintain the record keeping
• Prepare and maintain the compliance reports for management and regulatory reporting
• Assess the Outsourced Service Providers and administer the Outsourcing Register of Outsourced Service Providers
• Handle compliance related queries from staff

Job Requirements and Qualifications

• Bachelor's degree, preferably in Business related fields
• Minimum 3 years of compliance experience in the financial services or insurance industry
• Meticulous, good analytical and problem solving skills
• Familiar with Financial Advisers Act (FAA), Insurance Act, MAS Notices/Guidelines or Balanced Scorecard (BSC) framework is an added advantage

HOW TO APPLY:

Interested applicants, please click on "Apply Now". We regret only shortlisted candidates will be notified.

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EA License No: 19C9950

EA Personnel: Gao YueWen

EA Personnel Reg No: R23118964

The primary focus of this role is to ensure that all transactions align with customer profiles. You will be responsible for conducting periodic and ad-hoc AML reviews, including post-STR checks. Additionally, you will perform enhanced due diligence for high-risk clients, verify SOWs, identify and plug KYC gaps, highlight red flags or documentation issues, and assist with administrative tasks as needed.

• Conduct regular and ad-hoc AML reviews, including post-STR checks
• Perform enhanced due diligence on high-risk clients, including SOW verification
• Identify and address KYC gaps, highlighting potential risks or documentation issues
• Evaluate transaction data to ensure alignment with customer profiles
• Support administrative tasks and projects as required

• Degree in Banking, Finance, Accountancy, or Business
• Excellent stakeholder engagement skills
• Self-motivated team player with a strong work ethic

About FirstCom Academy

At FirstCom Academy, we equip individuals and businesses with the digital skills needed to thrive in today's fast-evolving landscape. As a leader in adult education, we're committed to ensuring the highest standards of course delivery, assessments, and learner outcomes.

Job Overview

We are seeking a detail-oriented and meticulous Internal Compliance Officer to join our team. This role is pivotal in upholding the integrity, compliance, and quality of learner assessments, tests, and other related documents across all courses. You will be responsible for reviewing completed assessments to ensure proper marking, trainer adherence to assessment guidelines, and overall academic quality assurance.

Key Responsibilities

* Conduct regular audits of learner assessments, test papers, and other related documents to ensure they meet internal standards and regulatory compliance (e.g. SSG, WSQ frameworks).

* Verify that trainers have marked assessments accurately and consistently according to official marking schemes and rubrics.

* Identify discrepancies, incomplete marking, or procedural lapses in the evaluation process.

* Prepare audit reports summarizing findings, non-compliance areas, and suggested corrective actions.

* Collaborate with trainers and curriculum developers to clarify assessment standards and improve consistency.

* Provide feedback and recommend improvements to enhance assessment processes and documentation practices.

* Track and follow up on corrective actions to ensure resolution and compliance.

* Ensure assessment documents are properly archived and audit-ready at all times.

* Participate in internal meetings and contribute to continuous improvement initiatives.

Requirements

* Diploma or Degree in Education, Business Administration, Quality Assurance, or a related field.

* Fresh graduates are welcome to apply – training will be provided.

* Meticulous with a keen eye for detail and a strong sense of responsibility.

* Strong written and verbal communication skills.

* Comfortable working with documentation, checklists, and spreadsheets (e.g. Excel, Google Sheets).

* Able to work independently and manage tasks in a structured and timely manner.

* A willingness to learn about academic compliance standards and contribute to process improvements.

* Bonus: Familiarity with adult education, WSQ frameworks, or assessment documentation is a plus.

Why Join Us?

* Be part of a growing and dynamic team that's passionate about education.

* Contribute to shaping the quality and credibility of digital education in Singapore.

* Attractive remuneration package and career progression opportunities.

* Friendly and vibrant working environment.

• 3 to 8 years of experience in a compliance or regulatory role within a bank, payment services provider, or licensed financial entity.
• Strong communication and negotiation skills in English; multilingual abilities are a plus.
• A proactive and adaptable attitude in a fast-paced work environment.
• Keen interest in the fintech industry, e-commerce platforms, and cross-border payments.
• A sharp and strategic compliance mindset, capable of handling compliance reporting, anti-money laundering (AML) issues, and KYC requirements.
• Demonstrated agility in tackling challenges and problem-solving.

• Stay current with relevant payment license regulations, notices, and enforcement actions in Singapore.
• Advise management and internal stakeholders on compliance with applicable laws and regulations.
• Implement and maintain an effective compliance program in line with requirements from the Monetary Authority of Singapore (MAS) and other relevant authorities.
• Serve as the Money Laundering Reporting Officer (MLRO), managing AML/CFT-related escalations, analyses, reporting, and ensuring adherence to legal obligations.
• Develop and review internal compliance policies, procedures, and support system enhancement projects.
• Conduct periodic and ad-hoc risk assessments across various compliance risk areas.
• Create and oversee action plans in response to audit findings or compliance violations.
• Regularly review internal procedures and documentation to identify and mitigate risks.
• Support or lead responses to regulatory matters including filings, reporting, consultations, and inspections by MAS or other regulators.
• Ensure staff are up to date on compliance policies and regulatory changes through regular training.
• Collaborate with regional and global compliance teams.

• In-depth exposure to the fintech and e-commerce ecosystem, including partnerships with global e-sellers.
• Opportunities to learn from experienced professionals and mentors.
• Direct involvement in shaping strategic compliance initiatives and regulatory relationships.
• Career development in a high-growth environment with regional and international exposure.