299 Pharmaceutical Industry jobs in Singapore

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 Entry level

• Employment type Full-time

• 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.

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

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.

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

1 day ago Be among the first 25 applicants

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

• Oversee the implementation and maintenance of GMP and HACCP standards.
• Ensure compliance with local food regulations (e.g., SFA and GMP standards).
• Manage internal and external audits (e.g., regulatory bodies, customer audits).
• Review and update QA documentation, SOPs, and records regularly.
• Food Safety & Risk Management
• Lead hazard analysis, food safety plans, and critical control point monitoring.
• Manage allergen control, traceability, and recall procedures.
• Quality Control Oversight
• Supervise the QC team in performing inspections, sampling, and laboratory testing (microbiological, chemical, physical).
• Analyze trends from quality data and implement improvements.
• Approve incoming raw materials, in-process, and finished product quality.
• Train and mentor junior QA/QC staff on quality systems and food safety.
• Conduct regular staff training on hygiene, GMP, and process controls.
• Initiate and lead quality improvement projects (e.g., reducing customer complaints, process optimization).
  
  

• Quality Assurance & Compliance
• Oversee the implementation and maintenance of GMP and HACCP standards.
• Ensure compliance with local food regulations (e.g., SFA and GMP standards).
• Manage internal and external audits (e.g., regulatory bodies, customer audits).
• Review and update QA documentation, SOPs, and records regularly.
• Food Safety & Risk Management
• Lead hazard analysis, food safety plans, and critical control point monitoring.
• Manage allergen control, traceability, and recall procedures.
• Quality Control Oversight
• Supervise the QC team in performing inspections, sampling, and laboratory testing (microbiological, chemical, physical).
• Analyze trends from quality data and implement improvements.
• Approve incoming raw materials, in-process, and finished product quality.
• Team Leadership & Training
• Train and mentor junior QA/QC staff on quality systems and food safety.
• Conduct regular staff training on hygiene, GMP, and process controls.
• Continuous Improvement
• Initiate and lead quality improvement projects (e.g., reducing customer complaints, process optimization).
  
  

• Degree/Diploma in Food Science, Food Technology, Microbiology, or related field.
• 5 years of QA/QC experience in the food manufacturing industry.
• Strong knowledge of HACCP and GMP standards.
• Experience with audits, documentation control, and risk assessment.
• Excellent communication, leadership, and problem-solving skills.

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Quality Assurance
• Industries Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Poli Medical Company Pte Ltd by 2x

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

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

1 day ago Be among the first 25 applicants

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

• Oversee the implementation and maintenance of GMP and HACCP standards.
• Ensure compliance with local food regulations (e.g., SFA and GMP standards).
• Manage internal and external audits (e.g., regulatory bodies, customer audits).
• Review and update QA documentation, SOPs, and records regularly.
• Food Safety & Risk Management
• Lead hazard analysis, food safety plans, and critical control point monitoring.
• Manage allergen control, traceability, and recall procedures.
• Quality Control Oversight
• Supervise the QC team in performing inspections, sampling, and laboratory testing (microbiological, chemical, physical).
• Analyze trends from quality data and implement improvements.
• Approve incoming raw materials, in-process, and finished product quality.
• Train and mentor junior QA/QC staff on quality systems and food safety.
• Conduct regular staff training on hygiene, GMP, and process controls.
• Initiate and lead quality improvement projects (e.g., reducing customer complaints, process optimization).
  

• Quality Assurance & Compliance
• Oversee the implementation and maintenance of GMP and HACCP standards.
• Ensure compliance with local food regulations (e.g., SFA and GMP standards).
• Manage internal and external audits (e.g., regulatory bodies, customer audits).
• Review and update QA documentation, SOPs, and records regularly.
• Food Safety & Risk Management
• Lead hazard analysis, food safety plans, and critical control point monitoring.
• Manage allergen control, traceability, and recall procedures.
• Quality Control Oversight
• Supervise the QC team in performing inspections, sampling, and laboratory testing (microbiological, chemical, physical).
• Analyze trends from quality data and implement improvements.
• Approve incoming raw materials, in-process, and finished product quality.
• Team Leadership & Training
• Train and mentor junior QA/QC staff on quality systems and food safety.
• Conduct regular staff training on hygiene, GMP, and process controls.
• Continuous Improvement
• Initiate and lead quality improvement projects (e.g., reducing customer complaints, process optimization).
  

• Degree/Diploma in Food Science, Food Technology, Microbiology, or related field.
• 5 years of QA/QC experience in the food manufacturing industry.
• Strong knowledge of HACCP and GMP standards.
• Experience with audits, documentation control, and risk assessment.
• Excellent communication, leadership, and problem-solving skills.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Poli Medical Company Pte Ltd by 2x

Sign in to set job alerts for “Quality Assurance Specialist” roles.

Associate Specialist, Quality Assurance (WDA)

Associate II, Quality Assurance Associate

Assistant Vice President, Quality Assurance Specialist

Assistant Vice President, Quality Assurance Specialist

Assistant Vice President, Quality Assurance Specialist

Assistant Vice President, Quality Assurance Specialist

Assistant Manager, Training and Quality Assurance

Manufacturing Quality Assurance (MQA) - Train & Place Program

TikTok LIVE - Content Quality Assurance Specialist (English Speaking)

Quality Assurance & Risk Oversight Specialist

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

Anti-Money Laundering Operations Quality Assurance - MariBank

TikTok LIVE - Content Quality Assurance Specialist (Bahasa Indonesia Speaking)

Healthcare Quality Assurance Associate Manager

Assistant Manager, Quality Assurance (Tobacco - Batam Placement)

Healthcare Quality Assurance Associate Manager

Assistant Manager, Compliance (Quality Assurance Data Analyst)

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

• Oversee the implementation and maintenance of GMP and HACCP standards.
• Ensure compliance with local food regulations (e.g., SFA and GMP standards).
• Manage internal and external audits (e.g., regulatory bodies, customer audits).
• Review and update QA documentation, SOPs, and records regularly.

• Lead hazard analysis, food safety plans, and critical control point monitoring.
• Manage allergen control, traceability, and recall procedures.

• Supervise the QC team in performing inspections, sampling, and laboratory testing (microbiological, chemical, physical).
• Analyze trends from quality data and implement improvements.
• Approve incoming raw materials, in-process, and finished product quality.

• Train and mentor junior QA/QC staff on quality systems and food safety.
• Conduct regular staff training on hygiene, GMP, and process controls.

• Initiate and lead quality improvement projects (e.g., reducing customer complaints, process optimization).

• Degree/Diploma in Food Science, Food Technology, Microbiology, or related field.
• 5 years of QA/QC experience in the food manufacturing industry.
• Strong knowledge of HACCP and GMP standards.
• Experience with audits, documentation control, and risk assessment.
• Excellent communication, leadership, and problem-solving skills.

• Oversee the implementation and maintenance of GMP and HACCP standards.
• Ensure compliance with local food regulations (e.g., SFA and GMP standards).
• Manage internal and external audits (e.g., regulatory bodies, customer audits).
• Review and update QA documentation, SOPs, and records regularly.

• Lead hazard analysis, food safety plans, and critical control point monitoring.
• Manage allergen control, traceability, and recall procedures.

• Supervise the QC team in performing inspections, sampling, and laboratory testing (microbiological, chemical, physical).
• Analyze trends from quality data and implement improvements.
• Approve incoming raw materials, in-process, and finished product quality.

• Train and mentor junior QA/QC staff on quality systems and food safety.
• Conduct regular staff training on hygiene, GMP, and process controls.

• Initiate and lead quality improvement projects (e.g., reducing customer complaints, process optimization).

• Degree/Diploma in Food Science, Food Technology, Microbiology, or related field.
• 5 years of QA/QC experience in the food manufacturing industry.
• Strong knowledge of HACCP and GMP standards.
• Experience with audits, documentation control, and risk assessment.
• Excellent communication, leadership, and problem-solving skills.

Responsibilities:

• Online Quality Checking (Metal Detector, Cooker, Pasteurizer, Steamer)
• Online Finished Product Testing
• Monthly Verification of CCP (Critical Control Point)
• Online Verification Sampling for Microbial Analysis
• Internal Calibration of Weighing Scales
• Verification on goods return
• Handle Customers’ Complaint
• Conduct routine physical, chemical, sensory and other analyses accordingly.
• Take appropriate decisions for rework of material based on historical trend and in consultation with seniors
• Raise non-conformation for quality deviations of Raw Material/Finished Goods and follow up with proper closure of corrective and preventive action
• Initiate actions to investigate customer complaint in consultation with relevant team members
• Collect comprehensive evidence/crucial data, provide sound reasoning and propose possible root cause for customer complaints and internal rejection
• Maintain up-to-date quality control programs, policies, process workflows, procedures and work instructions

REQUIREMENTS:

• Diploma / Degree in Food Science preferred
• At least 2 years of relevant experience will be considered for Senior position
• Experienced and passionate in Continuous Improvement
• Exceptional problem-solving skills
• Good Knowledge of Quality Management Systems (HACCP, BRC, ISO 22000)
• Good Communication, Organizational and Analytical Skills
• Strong ability to work well in a team and independently
• Excellent IT skills, particularly in MS Excel, PowerPoint, Word, Access
• Ability to work with multiple priorities in a fast-paced environment is required.
• 5 Days Work Week + 1 Saturday
• Undertake any other ad-hoc projects/ tasks assigned
• Job Scope, Work Day and Work Hours subject to changes depending on work requirement
• Fresh grads are welcome
• Salary package commensurate with experience