364 Manufacturing jobs in Tuas

Debagging :

Handle, cut and dump bags weighing as much as 25kg into blenders /mixers as many 8MT per shift.

Operate forklift and hand pallet Jacks.

Handle drums and related equipment.

Utilize weighing scales and floor scales to properly weigh the required material.

Document the material / lot number.

Assist in cleaning other areas within the department.

Complete any other assignments given by the Supervisor.

Packaging :

Operate forklift and hand trucks.

Handle and pack 25kg bags as many as 8MT per shift.

Print and label packaging onto each 25kg bags.

Fabricate boxes / supersack for packaging of finished products.

Assist in cleaning other areas within the department.

Complete any other assignment given by the Supervisor.

QC/QA Test:

Assist to conduct QC/QA tests including sample preparation.

Requirements:

·    Basic Communication Skills

·    Must be able to lift and carry up to 25kg

·    Ability to perform duties under specific time requirements

·    Ability to adapt to changing duties and responsibilities

·    Able to listen and speak clearly

·    No color blindness, skin allergy

·    Able to work rotating shift, overtime as assigned

·    Able to work on weekend as assigned

·    Ability to work in a dusty, hot and humid environment

·    Ability to bend, stoop, and lean over for a period of time

·    Ability to wear required safety equipment

Responsibilities

·    Cultivate and express antibody intermediates in an industrial-scale cell culture platform using single-use technologies.

●    Perform vial thawing, cell expansion and passage, cell culture, and harvest manufacturing in drug substance facilities in accordance with GMP requirements.

●    Operate equipment and appliances following the guidance of SOPs and relevant documents.

●    Prepare relevant documents, such as production batch records, SOPs, and validation reports.

●    Communicate and resolve any inconsistencies and/or anomalies in production operations.

●    Monitor processes, including real-time review of process parameters and process data/trends.

●    Ensure that the manufacturing operations for drug substances comply with quality and safety regulations.

●    Perform other tasks assigned by leadership.

●    Participate in shift production as required and ensure that shift production meets SOP requirements.

Requirements

●    Diploma or Degree in Biological, Chemical, Pharmaceutical Engineering, or other related specialties with min 3-5 years of relevant working experience

●    Possess thorough scientific reasoning and methodical work habits, with strong execution and planning abilities.

●    Ability to adapt to a GMP cleanroom environment, including the requirement to wear dust-free clothing, masks, and goggles.

●    Possess good communication ability and comprehension ability.

●    Display a good working attitude, strong work ethic, and willingness to follow leadership directives.

●    Be open to accepting temporary work assignments, including overtime on weekends or weekdays, and other roles as required.

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift

Job Description

Responsibilities

• Assemble Single-Use Bio-Processing Containers for critical sterile liquid-handling applications in the biopharmaceutical industry.
• Follow standard work instructions and interpret technical drawings to ensure consistent product quality.
• Maintain strict adherence to ISO 13485:2016, ISO 22301:2019, and current Good Manufacturing Practices (cGMP) documentation standards to ensure regulatory compliance and quality assurance.
• Complete all relevant training before performing any task.
• Timely completion of relevant batch records with adherence to Good Documentation Practice (GDP).
• Participate in Practical Process Improvements (PPI) to improve production efficiency and product quality.
• Adhere to all safety protocols and guidelines to maintain a safe working environment.
• Work collaboratively with team members, including engineers, quality assurance, and maintenance personnel.
• Communicate effectively with supervisors and colleagues to ensure smooth production operations.
• Ensure accurate storage and handling of materials to prevent contamination or damage.
• Perform any other duties as assigned by the Manager.

Requirements

• Minimum 2 years of relevant experience in pharmaceutical manufacturing.
• Minimum GCE 'O' Level/Nitec.
• Physically fit to lift objects up to 20kg when required.

Responsibilities:

• Lead and execute multiple Change Records (Planned events) for the assigned area for creation of new Batch Records and Standard Operation Procedures for Production,
• Support Change Records Assessment and GMP documentation Review.
• Responsible for providing support to the assigned manufacturing operations by developing, coordinating and facilitating small to medium projects to ensure planned, predictable production operations in compliance with GMP regulations.
• Lead and execute Continuous Process Improvements, CAPAs and Change Records in assigned area.
• Provide routine and ad hoc support for planning, coordinating, execution, and performance improvement of key manufacturing processes such as product change over.
• Lead project teams to trouble shoot medium to complex problems and support continuous process improvement. Facilitate root cause analysis (RCA) with input from SMEs, develop and implement change to improve performance.
• Collaborate with multidisciplinary teams to achieve project objectives.
• Assist in experimental design and troubleshooting as needed.

About You:

• Bachelor's degree in a relevant life science field (e.g., biology, biotechnology, biochemistry).
• Candidates with Batch Record Creation experience in a GMP environment in biologics or pharmaceutical industry are preferred.
• Strong attention to detail, organizational skills, and the ability to work independently or in a team.
• Excellent communication skills, both written and verbal, in English.
• Adherence to safety protocols and regulatory compliance.

Job Type: Contract

Contract length: 9 months

Pay: $4, $6,500.00 per month

Experience:

• Change Records: 1 year (Preferred)
• Batch Record Creation: 1 year (Preferred)

Job Highlights:

• Basic salary $2,000/-month, gross up to $3K+
• Monday to Friday | 7:45 AM – 5:30 PM
• Opportunity to earn EXTRA with HIGH OT
• Tuas location (transport provided from Jurong East & Pioneer MRT)
• Benefits: Daily meal & transport allowance, medical & dental coverage, and variable bonus up to 4 months

Job Responsibilities:

• Carry out daily production tasks as assigned.
• Check product quality and promptly report any defects to the Supervisor.
• Assist in maintaining cleanliness and housekeeping of the work area.
• Comply with all workplace safety rules and regulations.
• Perform other duties as assigned by the Supervisor.

Requirements:

• Technical qualifications will be an advantage.
• Prior experience in a manufacturing environment will be an advantage.
• A good team player with initiative, drive, and commitment, and able to communicate effectively with team members.
• Must be able to work overtime when required.

If you are keen to explore this opportunity, kindly send a copy of your updated resume to or simply click the button to APPLY NOW We regret that only shortlisted applicants will be notified.

Tan Sze Ching Shannon - R

EA License No: 16C8261

Responsibilities

·    Bioconjugation Reactions and Purification of Antibody Intermediates and Conjugated Drug Substances

·    Perform downstream protein purification manufacturing operations for drug substances under the guidance of SOPs. This includes, but is not limited to, chromatography system operation, conjugation, low pH viral inactivation, nanofiltration, ultrafiltration washing and filtration, and final bulk dispensing.

·    Operate equipment and appliances following SOPs and relevant documents.

·    Prepare relevant documents, such as production batch records, SOPs, and validation reports.

·    Communicate and resolve inconsistencies and/or anomalies in production operations.

·    Monitor processes, including real-time review of process parameters and data/trends.

·    Ensure that drug substance manufacturing operations comply with quality and safety regulations.

·    Perform other tasks assigned by leadership.

·    Participate in shift production as required and ensure that shift production meets SOP requirements.

Requirements

●    Diploma or Degree in Biological, Chemical, Pharmaceutical Engineering, or other related specialties with min 3-5 years of relevant working experience

●    Possess thorough scientific reasoning and methodical work habits, with strong execution and planning abilities.

●    Ability to adapt to a GMP cleanroom environment, including the requirement to wear dust-free clothing, masks, and goggles.

●    Possess good communication ability and comprehension ability.

●    Display a good working attitude, strong work ethic, and willingness to follow leadership directives.

●    Be open to accepting temporary work assignments, including overtime on weekends or weekdays, and other roles as required.

Responsibilities:

• Involve in hands-on execution of the plant operations and assist Manufacturing Associates in trouble-shooting
• Monitor and analyze processing parameters for atypical trends and improvement opportunities
• Perform solution and equipment preparation
• Stage components for autoclaving and washing
• Support in-process testing of production samples, prior experience with analytical instrument will be a plus point
• Actively support continuous improvement initiatives
• Support Safety audits
• Adhere to any applicable EHS and regulatory requirements
• Ability to follow written procedures, recognize and report malfunctions
• Ability to evaluate documentation/data according to company and regulatory guidelines
• Ability to interact with inspectors (internal and external)
• Ability to interpret and apply Good Manufacturing Practice (GMP) knowledge
• Basic statistical mathematical skills
• Ability to organize work and handle multiple priorities and meet deadlines
• Ability to understand, apply and evaluate basic chemistry, biology and physical principles
• Understanding of analytical methods

Basic Qualifications:

• Diploma in Science or Engineering

Preferred Qualifications:

• NTC/ITC/Diploma in Chemical, Pharmaceutical, Life Sciences or Bio-processing related disciplines
• Possess minimum 0 - 2 years of relevant experience in the biotechnology, pharmaceutical or petrochemical industry. Fresh graduates will be considered.
• Proficiency in reading and writing English
• Demonstrate commitment to cGMP, EHS compliance aspects of clean-room plant operation, prior experience and demonstration of cGMP knowledge is a plus
• Knowledge of plant and unit operations (autoclave, parts washers, process equipment), good problem solving skills
• Excellent self-motivated team player with hands-on attitude and good communication skills
• Experience with Emerson DeltaV, LIMS, TrackWise
• Ability to understand, apply and evaluate basic chemistry, biology and physical principles
• Ability and willingness to work any shift in support of operations that may include 24/7
• Mechanical ability/expertise

Kindly note that only shortlisted candidates will be contacted.

By sending us your personal data and curriculum vitae (CV), you are deemed to consent to PERSOLKELLY Singapore Pte Ltd and its affiliates collecting, using and disclosing my personal data for the purposes set out in the Privacy Policy which is available at I also acknowledge that I have read, understood, and agree to the said Privacy Policy.

PERSOLKELLY Singapore Pte Ltd
• RCB No E EA License No. 01C4394
• EA Registration No. R Ling Kai Jin)

Job duties and responsibilities:

• Monitor and inspect production areas according to ISO 22000 and customer requirements, feedback to relevant departments on any rectification required.
• Maintain and update documentations, records for ISO 22000 and act as a Food Safety Team Member.
• Perform outgoing goods inspection.
• Conduct physical, microbiological analysis for finished food products and environmental monitoring of facility and personnel.
• Work with R&D chef for shelf-life testing and conduct trend analysis when required.
• Coordinate with third-party laboratory on sample submission where required.
• Highlight any abnormalities detected during analysis, review and investigate as required.
• Prepare Certificate of Analysis where required.
• Upkeep of laboratory consumables and cleanliness.
• Responsible for verification of cleaning chemical concentration.
• Conduct customer complaint investigation and prepare corrective action report where required.
• Coordinate and provide support in all internal, external, and regulatory audits.
• Act as Qualified Personnel (QP) for food export processes and liaise with relevant regulatory authorities (e.g. SFA, HPB).
• Perform assigned tasks and work to achieve company goals and department objectives.
• Any ad-hoc duties as assigned by the management.

Job Requirements:

• Degree / Diploma in Food Science, Food Technology, Food Microbiology or similar discipline.
• Minimum 2 years of experience in a Quality Assurance role / Microbiological Laboratory preferably from the food industry.
• Knowledge in ISO 22000 Food Management System, GMP, GLP and ICP.
• Positive working attitude, analytical, willingness to learn, team player, initiative and effective interpersonal skills.
• Multilingual will have an added advantage.
• Proficient with Microsoft Office

Why Join Us?

At Gan Teck Kar, we are dedicated to providing high-quality, safe, and delicious products. As a member of our team, you'll work with like-minded professionals in a supportive environment that values innovation, collaboration, and growth. We offer competitive compensation, benefits, and opportunities for career advancement within our organization.

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Job Description

When you're part of the team at Thermo Fisher Scientific, you'll do important work. And you'll have the opportunity for continual growth and learning in a culture that empowers your development. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give equal opportunity to our people on the resources and chances to create significant contributions to the world.

Discover Impactful Work

• Manufacturing engineer is responsible for product and manufacturing operation process throughout product life cycle. Maintain and ensure systems and procedures are in compliance with ISO and Regulatory requirements.
• Support New Product Introduction (NPI) and product transfers from R&D and other manufacturing sites. Plan and ensure smooth start up of new product transfers to production.
• Provide Product second level failure analysis, cost reduction through value engineering activity. Set up and maintain Bill of materials (BOM) and drawings in SAP, and manage changes through OCPLM.
• Provide Sustaining Engineering support such as improving manufacturing First Pass Yield (FPY), support manufacturing process improvement and evaluating alternate parts for End of Life (EOL) replacement.
• Provide Engineering support to functional tester development and sustaining at contract manufacturer site.

Education / Experience

• Degree in Engineering (Electrical or equivalent) with more than 3 years working experience, preferably in manufacturing environment.
• Experience in life science/ medical devices in the engineering function.

Knowledge, Skills, Abilities

• Good troubleshooting skill in PCBA and instrument level
• Test programming knowledge/experience (e.g. LabVIEW/TestStand, VC++, C#) will be added advantage
• Good knowledge on engineering change process (e.g. OCPLM CR/CO process)
• Have good communication, analytical capability, and good spoken and written English skill

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation