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1,840

Qa jobs in Singapore

Change Control Specialist (Pharma/Biotech)

NUSANTARA PRIME CONSULTING PTE. LTD.

Singapore
On-site
SGD 60,000 - 80,000
30+ days ago
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Head of Quality Assurance & GMP Compliance

Takeda Pharmaceuticals

Singapore
On-site
SGD 120,000 - 160,000
30+ days ago

Senior QA Engineer — CI/CD & Test Automation Leader

Doodle Labs LLC

Singapore
On-site
SGD 70,000 - 100,000
30+ days ago

CX Operations - Senior Complaints Trainer

P2P

Singapore
On-site
SGD 107,000
30+ days ago

Quality Assurance - Japanese Speaking

JAC RECRUITMENT PTE. LTD.

Singapore
On-site
SGD 36,000 - 68,000
30+ days ago
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Service Delivery Manager

ST ENGINEERING E-SERVICES PTE. LTD.

Singapore
On-site
SGD 42,000 - 60,000
30+ days ago

Executive, Training & Quality Assurance (Contact Centre)

INCOME INSURANCE LIMITED

Singapore
On-site
SGD 45,000 - 70,000
30+ days ago

QA Logistics Executive (East/MAX $5200)

Forte Employment Services Pte Ltd

Singapore
On-site
SGD 36,000 - 60,000
30+ days ago
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Facilities Management Supervisor

GKN Automotive

Singapore
On-site
SGD 60,000 - 85,000
30+ days ago

Contract Asst QA/ QC Engineer (Infrastructure) - 2 shift #HHL

RECRUIT EXPRESS PTE LTD

Singapore
On-site
SGD 60,000 - 80,000
30+ days ago

1 year Contract Quality Assurance Specialist (Medical Devices/ Up to $5000) #HGN

RECRUIT EXPRESS PTE LTD

Singapore
On-site
SGD 60,000 - 80,000
30+ days ago

Quality Assurance Engineer - Japanese Speaking

JAC Recruitment Pte Ltd

Singapore
On-site
SGD 40,000 - 65,000
30+ days ago

PromptCloud - Associate Technical Program Manager

PromptCloud

Singapore
Hybrid
SGD 1,200,000 - 2,000,000
30+ days ago

Machine Maintenance Technician

GE Aerospace

Singapore
On-site
SGD 40,000 - 60,000
30+ days ago

QA EXECUTIVE

FEI FAH MEDICAL MANUFACTURING PTE LTD

Singapore
On-site
SGD 35,000 - 50,000
30+ days ago

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Change Control Specialist (Pharma/Biotech)
NUSANTARA PRIME CONSULTING PTE. LTD.
Singapore
On-site
SGD 60,000 - 80,000
Full time
30+ days ago

Job summary

A leading consulting firm in Singapore is seeking a qualified individual to manage change control processes within a biopharmaceutical manufacturing environment. The successful candidate will coordinate with cross-functional teams to ensure compliance and timely execution of changes. This role requires a Bachelor's degree in a relevant field and at least 3 years of experience in a GMP-regulated setting.

Qualifications

  • 3+ years of experience in a GMP-regulated biopharmaceutical or pharmaceutical manufacturing environment.
  • Demonstrated experience with change control systems and processes.
  • Understanding of ICH Q10, FDA, EMA, and other regulatory expectations related to change management.

Responsibilities

  • Serve as the primary manufacturing representative for initiating, assessing, and implementing change controls.
  • Collaborate with cross-functional teams to assess the impact of proposed changes.
  • Draft and review change control documentation.

Skills

Organizational skills
Attention to detail
Effective communication
Collaboration skills
Technical documentation writing

Education

Bachelor’s degree in Biotechnology, Chemical Engineering, Life Sciences

Tools

Electronic Quality Management Systems (TrackWise, Veeva)
Job description

Responsibilities:

  • Raise change control from end to end
  • Serve as the primary manufacturing representative for initiating, assessing, and implementing change controls impacting production processes, equipment, materials, and procedures.
  • Collaborate with cross-functional teams (QA, QC, Validation, Engineering, Supply Chain) to assess the impact of proposed changes.
  • Draft and review change control documentation, including impact assessments, implementation plans, risk assessments, and supporting evidence.
  • Ensure timely execution and closure of change controls in compliance with regulatory and company timelines.
  • Support investigation and documentation of deviations or discrepancies arising from changes.
  • Coordinate with QA to ensure proper documentation, approval, and traceability of changes.
  • Maintain change control metrics and dashboards to track progress and compliance.

Key Skills and Competencies:

  • Strong organizational and documentation skills.
  • Attention to detail and a methodical approach to process evaluation.
  • Ability to manage multiple change controls concurrently under strict deadlines.
  • Effective communication and collaboration skills across cross-functional teams.
  • Proficiency in writing technical documentation and change justifications.

About You:

  • Proficient computer skills.
  • Bachelor’s degree in Biotechnology, Chemical Engineering, Life Sciences, or related discipline.
  • 3+ years of experience in a GMP-regulated biopharmaceutical or pharmaceutical manufacturing environment.
  • Demonstrated experience with change control systems and processes.
  • Familiarity with electronic quality management systems (e.g., TrackWise, Veeva etc).
  • Understanding of ICH Q10, FDA, EMA, and other regulatory expectations related to change management.
  • Strong verbal and written communication skills.
  • Meticulous and attention to detail.
  • Positive and proactive attitude towards work.
  • Ability to work effectively within a collaborative team environment.
  • Motivated, keen to learn, hardworking and a good team player.
  • Able to drive projects and meet the required deadline.
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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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