Hiring.Camp

Project & Validation Engineer

GSK

·

Today

Location
Jurong, Singapore
Workplace
Onsite
Type
Full-time
Department
Engineering
Experience
4+ years
Closing date
Today
Source
Workday

Description

Job Purpose

Manage capital projects; scope and design, source and procure equipment and instrumentation, manage activities across all project phases. Support GMP qualification activities for new technology and continuous improvement projects.


Key Responsibilities


Capital Projects

  • Manage capital project- work with stakeholders to scope out project, manage activities across all project phases and ensure on-time completion
  • Responsible for sourcing and procuring of equipment and instrumentation required for the project
  • Ensure contractors’ work on site is carried out safely and to a high level of quality
  • Ensure project deliverables satisfies GSK Quality Management System (QMS) standards and Engineering Standard (GES) requirements
  • As a SME, work with Automation Engineer to design and implement system automation 
  • Work closely with site utilities experts to implement, monitor energy usage/ efficiency of new air cooled chiller system
  • Train FM Engineers and Plant Technicians on maintaining/operating new equipment
  • undefined

Commissioning and Qualification

  • Support process engineering team in commissioning and qualification activities for new technology/capability and improvement projects
  • Develop, execute, and review validation protocols and related documentation
  • Lead the resolution of validation events and escalate concerns in a timely manner

 

Key Requirement

  • Minimum degree in relevant engineering field with at least 4 years of relevant engineering experience.
  • Highly knowledgeable and competent in their field of work.
  • Demonstrate excellent GMP behaviour and safe practices.
  • Strong knowledge in pharmaceutical trouble-shooting experience.
  • Strong leadership in team management.
  • Good analytical skill in investigation.
  • Lead complex issues investigation and detailed troubleshooting.


Skills

Asset Life Cycle Management, Data Integrity, Digital Fluency, GxP Regulations, Lean Management, Manufacturing Technologies, Pharmaceutical Manufacturing, Problem Solving, Risk Awareness, Standards Compliance

 

 

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.

We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact [email protected]. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.

Important notice to Employment businesses/ Agencies

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.

Skills

GMPComplianceProcurement

Similar Jobs

30

Linguistic Validation Project Manager- Language Solutions

Iqvia·Taguig City, Philippines

2d ago

F135 ECU HPC Validation Project Engineer (Onsite)

RTX·US-CT-EAST HARTFORD-CWSTF ~ 400 Main St ~ BLDG CWSTF, US·Onsite

2w ago

PLM & Validation Project Engineer (normes de test)

ALTEN·Rabat, Rabat-Salé-Kénitra·Hybrid

1mo ago

Validation Project Lead / Documentation Audit Lead

FST Technical Services·Durham, NC

2mo ago

Sr. Validation Project Manager (Life Sciences)

Barrywehmiller·Santa Ana, CA USA

7mo ago

Senior Validation Project Manager

Cagents·Princeton, New Jersey +1·Onsite

1y+ ago

Project and Validation Chief (Onsite)

RTX·US-CT-EAST HARTFORD-ETC ~ 400 Main St ~ BLDG ETC, US·Onsite

4d ago

Linguistic Validation Junior Project Manager

Iqvia·Dalian, Liaoning +2

2w ago

Project Manager Validation Services

Sartorius·Bangalore, India·Onsite

4mo ago

Validation Engineer - Project Farma

Newperkinelmer·Customer Site - IN, US

4mo ago

Validation - Lead Engineer - Project Farma

Newperkinelmer·US Remote - CA, US·Remote

1w ago

Project Manager, Research & Validation Studies

Sleep.ai·Carlsbad, CA

3w ago

Sr. Project Engineer, System Validation

Magna·ROOM 706 & 707, E03 BUILDING

3w ago

Validation - Engineer II - Project Farma

Newperkinelmer·Customer Site - CO, US

3mo ago

Sr. Validation Engineer (cGMP) - Project Farma

Newperkinelmer·Customer Site - NC, US +1

3mo ago

Validation Engineers & Leads (cGMP) - Project Farma

Newperkinelmer·US Remote - NC, US +3·Remote

1w ago

Validation - Engineer I/II - Project Farma

Newperkinelmer·Customer Site - IN, US +5

1w ago

2026 EGM Ethernet Validation Engineer for SDV project in Braking System

Robert Bosch·Coimbatore, India

3w ago

Senior Manager / Associate Director, CMC Project Management - Process Development & Validation

Artiva Biotherapeutics·San Diego, California

3mo ago

C&Q Validation Manager / Senior Manager - Project Farma

Newperkinelmer·Customer Site - NC, US +2

3mo ago

Validation - Engineer I / II - Project Farma

Newperkinelmer·Customer Site - DC, US +5

3mo ago

Validation - Engineer I / II - Project Farma

Newperkinelmer·Customer Site - CA, US +6

3mo ago

Validation - Manager / Senior Manager - Project Farma

Newperkinelmer·Customer Site - DC, US +5

3mo ago

Validation - Manager / Senior Manager - Project Farma

Newperkinelmer·Customer Site - CA, US +6

3mo ago

Project Engineer 2 - Production Equipment Validation

Abbott·United Kingdom > Witney : Production Facility

3mo ago

Engineering Project Team Leader - Electric Drive Validation

Cat·Mossville, Illinois

3mo ago

Validation - Engineer III / Lead Engineer - Project Farma

Newperkinelmer·Customer Site - CA, US +6

3mo ago

Validation - Engineer III / Lead Engineer - Project Farma

Newperkinelmer·Customer Site - DC, US +5

3mo ago

Senior Validation or Validation SME for new filling line project (Osaka Plant)

Takeda is an industry·JPN - Osaka - Osaka Plant, Japan

8mo ago

Technical Project Manager II (Client-facing RNA/ DNA Mfg., Method Development/ Validation)

Danaher·USA - Fargo - Aldevron - B1, US +1·Onsite

2mo ago