735 Manufacturing Support jobs in Singapore

Working hour: 8am-5pm

Location: Woodlands

Responsibilities

• Report weekly and monthly data on production and staffing
• Create presentations for internal meetings
• Support analysis of cycle time, headcount, and factory capacity
• Help with time studies and process improvement projects

PREREQUISITES

• Diploma or ITE in Industrial Engineering or related field (option)
• Comfortable with Excel and PowerPoint (intermediate level)
• Good with numbers and data accuracy
• Able to work independently and manage tasks

We regret that only shortlisted candidates will be notified.

PERSOLKELLY Singapore Pte Ltd

EA License No: 01C4394| DAPHNE CHIAM WERN XIN| Reg No: R

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Job Summary

As a Manufacturing Support 1, you will be working in a team to ensure that the manufacturing line are up and running especially for debagging and packaging process.

Role and Responsibilities:

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

- Handle drums and related equipment.

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

- Document the material / lot number.

- Operate forklift , hand pallet jacks and hand trucks.

- Print and label packaging

- Fabricate boxes / supersack for packaging of finished products.

- Assist in cleaning other areas within the department.

- Complete any other assignment given by the Supervisor.

Job Requirements:

• Possess Forklift License is at advantage but not necessary

• Able to read, speak and understand basic English

• Strong Communication Skills

• Must be able handle bulky items

• Ability to perform duties under specific time requirements

• Ability to adapt to changing duties and responsibilities

• Able to work rotating shift, overtime or weekend (if required )as assigned

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

• The job is require to bend, stoop, and lean over for a period of time

Working pattern:

5 days work week in 3 rotating shifts.

7am-3pm

3pm-11pm

11pm -7am

Job Summary

As a Manufacturing Support 1, you will be working in a team to ensure that the manufacturing line are up and running especially for debagging and packaging process.

Role and Responsibilities:

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

- Handle drums and related equipment.

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

- Document the material / lot number.

- Operate forklift , hand pallet jacks and hand trucks.

- Print and label packaging

- Fabricate boxes / supersack for packaging of finished products.

- Assist in cleaning other areas within the department.

- Complete any other assignment given by the Supervisor.

Job Requirements:

• Possess Forklift License is at advantage but not necessary

• Able to read, speak and understand basic English

• Strong Communication Skills

• Must be able handle bulky items

• Ability to perform duties under specific time requirements

• Ability to adapt to changing duties and responsibilities

• Able to work rotating shift, overtime or weekend (if required )as assigned

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

• The job is require to bend, stoop, and lean over for a period of time

Working pattern:

5 days work week in 3 rotating shifts.

7am-3pm

3pm-11pm

11pm -7am

Job Summary

As a Manufacturing Support 1, you will be working in a team to ensure that the manufacturing line are up and running especially for debagging and packaging process.

Role and Responsibilities:

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

- Handle drums and related equipment.

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

- Document the material / lot number.

- Operate forklift , hand pallet jacks and hand trucks.

- Print and label packaging

- Fabricate boxes / supersack for packaging of finished products.

- Assist in cleaning other areas within the department.

- Complete any other assignment given by the Supervisor.

Job Requirements:

• Possess Forklift License is at advantage but not necessary

• Able to read, speak and understand basic English

• Strong Communication Skills

• Must be able handle bulky items

• Ability to perform duties under specific time requirements

• Ability to adapt to changing duties and responsibilities

• Able to work rotating shift, overtime or weekend (if required )as assigned

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

• The job is require to bend, stoop, and lean over for a period of time

Working pattern:

5 days work week in 3 rotating shifts.

7am-3pm

3pm-11pm

11pm -7am

Responsibilities

• Be responsible for the preparation of buffers and media for drug substance manufacturing according to GMP.
• Participate in and execute production projects, completing production plans on time.
• Complete production records in accordance with GMP requirements.
• Assist in drafting/ upgrading SOPs, URS, PQ, and other documents.
• Perform other tasks as assigned by leadership.

Requirements

• Diploma or higher qualification in Biological, Chemical, Pharmaceutical Engineering, or other related specialties; candidates with equivalent work experience will also be considered.
• Ability to adapt to a GMP cleanroom environment, including the requirement to wear dust-free clothing, masks, and goggles.
• Possess good communication and comprehension ability.
• Display good working attitude, strong work ethic, and team collaboration
• Be open to accepting temporary work assignments, including overtime on weekends or weekdays, and other roles as required.

Career Development

• Comprehensive in-house training program (E-learning / OJT / Mentorship)
• Dual career development tracks – Professional & Managerial Tracks
• Opportunity for internal job rotation / Cross-BU transfer / Cross-country assignment
• Cross cultural learning
• GMP greenfield start-up experience

Responsibilities

● Be responsible for the preparation of buffers and media for drug substance manufacturing according to GMP.

● Participate in and execute production projects, completing production plans on time.

● Complete production records in accordance with GMP requirements.

● Assist in drafting/ upgrading SOPs, URS, PQ, and other documents.

● Perform other tasks as assigned by leadership.

Requirements

● Diploma or higher qualification in Biological, Chemical, Pharmaceutical Engineering, or other related specialties; candidates with equivalent work experience will also be considered.

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

● Possess good communication and comprehension ability.

● Display good working attitude, strong work ethic, and team collaboration

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

Career Development

● Comprehensive in-house training program (E-learning / OJT / Mentorship)

● Dual career development tracks – Professional & Managerial Tracks

● Opportunity for internal job rotation / Cross-BU transfer / Cross-country assignment

● Cross cultural learning

● GMP greenfield start-up experience

Responsibilities

●    Maintain the SAP system according to the production plan and generate process orders and production batches.

●    Handle material receiving, delivery, returns, consumption, and other SAP operations.

●    Manage product inventory and output and complete the Pass-Through checklist.

●    Assist in reviewing BOM documents, creating material codes, and drafting material-related documents.

●    Manage samples and assist with GMP sample transportation.

●    Handle abnormal materials and vendor complaints.

●    Perform other tasks assigned by leadership.

Requirements

●    Diploma or higher qualification in Biological, Chemical, Pharmaceutical Engineering, or other related specialties; candidates with equivalent work experience will also be considered.

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

●    Possess good communication and comprehension ability.

●    Display good working attitude, strong work ethic, and team collaboration

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

Responsibilities

● Be responsible for updating, reviewing, and archiving relevant documents within the department.

● Draft and update project batch records.

● Handle various departmental operations, including reimbursement, attendance, procurement, finance, and meeting arrangements.

● Oversee GMP training for department staff and related tasks.

● Coordinate departmental audits.

● Manage Lean Management and WBS projects within the department.

● Address EHS-related tasks.

● Oversee production master planning and scheduling.

● Perform other tasks assigned by leadership.

Requirements

● Diploma or higher qualification in Biological, Chemical, Pharmaceutical Engineering, or other related specialties; candidates with equivalent work experience will also be considered.

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

● Possess good communication and comprehension ability.

● Display good working attitude, strong work ethic, and team collaboration

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

Career Development

● Comprehensive in-house training program (E-learning / OJT / Mentorship)

● Dual career development tracks – Professional & Managerial Tracks

● Opportunity for internal job rotation / Cross-BU transfer / Cross-country assignment

● Cross cultural learning

● GMP greenfield start-up experience

Site Name:
Singapore - Tuas

Posted Date:
Sep 8 2025

Help us get ahead of disease together with our Vaccines manufacturing.
Education required
:
BS or higher degree in Chemical Engineering, Mechanical Engineering, Manufacturing Engineering, Biotechnology, or related Life Science.

Other requirements:
Demonstrated skill and knowledge with analytical methods, equipment, process, software, cleaning, and facility/utility validation strategies and policy, protocol and report writing and execution.

Language requirement:
Written and spoken fluency in English

Expected
Start date:
ASAP.

Application deadline:
We will close this vacancy when we have enough applications, so please apply as soon as you can so your application can be considered.

Looking to gain valuable real world work experience and help
positively impact the health of billions of people
?
Apply for a GSK Traineeship today
The Career Conversion Programme (CCP) (Train-and-Place with Commitment to Hire) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals is a talent development programme aimed at building the next generation of skilled manpower for Singapore's Biopharmaceuticals manufacturing industry in anticipation of hiring demand.

The training programme consists of 15 months of local attachment with GSK. Due to the nature of the programme, we can only consider Singapore Citizens and Singapore Permanent Residents. For more information, please visit Career Conversion Programmes (CCP) for Individuals.

A certificate will be given to successful trainees upon completion of the programme.

What will you do?
The Manufacturing Science & Technology (MSAT) Manufacturing Support team is an agile and fast responsive team that contributes to the MSAT department mission by driving commercial manufacturing processes improvements and providing technical expertise in various process disciplines. It also provides technical support to enable Value Streams to deliver their operational objectives optimally and in compliance with cGMP requirements.

Areas of support includes deviation investigations, process and Equipment troubleshooting, CAPA management, Change management of equipment, process and/or in-coming materials, QMS gap analysis and risk assessment of technical topics. Lead continuous improvement projects and process optimization.

MSAT Manufacturing Support Engineer is responsible for validating/qualifying the systems used to develop and/or manufacture products within manufacturing facility. They will ensure systems are running according to necessary specifications and operate within regulations to ensure data integrity and the production of quality products. MSAT Manufacturing Support Engineer directly implement, execute, and support validation strategy in use at the GSK Tuas Site ensuring it is harmonized with local, regulatory, and GSK standards. They manage, schedule, coordinate and execute assigned qualification or validation activities to ensure timely completion of the Validation Plan in coordination with the User, Technical Services, Quality Control, Quality Assurance and Regulatory departments. They support maintenance of all process equipment and critical systems at GSK Tuas site in a validated state.

Direct contact to other MPUs for knowledge sharing. Assist MSAT Product Stewardship and MSAT Technology Transfer teams in managing operational projects

What will you learn?

• Manufacturing Operations such as manage technical deviations and CAPAs, manage investigations and troubleshooting of process and equipment issues.
• Continuous improvements
• Audit preparation and management
• Project management
• Validations
• Environment, safety, health and wellness

What are we looking for?

• At least 3 years' experience in Engineering, pharmaceutical industry or equivalent education preferred.
• Familiar with global regulations validation/qualification requirements.
• Good troubleshooting skill
• Knowledge in equipment used in vaccines manufacturing processes.
• Experience with quality and process improvement methodologies and tools (Lean, six Sigma, value stream mapping, FMEAs, DMAIC) is desired. Experience with product/process development and project management is a plus.
• Lean Sigma/ Green Belt certification is a plus.
• Highly effective communication, facilitation, negotiation, and teamwork skills are required.
• Excellent interpersonal, written, and verbal communication skills.
• Adaptable to fast-paced, dynamic work environment with shifting demand.
• Continuous improvement mindset.

What do we offer you?

• Understand and experience the GSK Culture
• Work with a diversified team of professionals
• Implement technical knowledge and skills that you have acquired at school
• Apply and develop soft skills such as interpersonal, communications and negotiation skills
• Transport to and from site to MRT stations in centralised locations all across Singapore (only for manufacturing sites)

Let's do this
You'll find hints, tips and guidance on our recruitment process on our website –

Learn more about the application process | GSK

You can learn more about GSK and our careers here

Apply now
Need help with your application?
Please email us at

and let us know how we can help you.
**Why GSK?

Uniting science, technology and talent to get ahead of disease together.**
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

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GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.