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QC Validation Engineer

Coalesce Management Consulting Pte. Limited

Singapore

On-site

SGD 80,000 - 100,000

Full time

Today
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Job summary

A management consulting firm in Singapore is seeking a QC Validation Engineer to support Quality Control Laboratories with effective testing services, ensuring compliance with policies and safety standards. This role involves overseeing equipment qualifications and collaborating with various functions to maintain operational efficiency. The ideal candidate must have a Bachelor's degree in a life science field and at least 5 years in GMP environments. This position offers annual leave benefits and full health coverage.

Benefits

Exposure to major Pharmaceutical Companies
Annual leave benefits
Full Health coverage and benefits
Training and Development allowance

Qualifications

  • Minimum 5 years of relevant working experience in GMP environments preferred.
  • Effective and timely testing services in Quality Control Laboratories.
  • Strong problem-solving skills for issues identified.

Responsibilities

  • Assist in qualification / validation of new equipment.
  • Draft qualification / validation protocols and reports.
  • Ensure implementation of safety policies during site activities.
  • Support technical changes and duties as required.

Skills

Excellent communication skills
Ability to multitask
Strong interpersonal skills
Team player

Education

Bachelor's degree in a relevant life science field
Job description

At Coalesce Management Consulting, we are a community of people with a strong passion for excellence. We deliver bespoke project solutions within the Life Science and Technology sectors through our community of high-calibre industry specialists.

Position: QC Validation Engineer

Job Description:

We are currently expanding our team and are looking for a QC Validation Engineer on site with a client. In summary, you will be supporting Quality Control Laboratories with independent, effective and timely testing services and able to ensure that tasks are performed according to requirements with review/verification of results and problem solving for issues identified.

Key Responsibilities:

  • Assist in the qualification / validation of new equipment / replacement of equipment project.
  • Collaborate with multi functions to arrange, plan and ensure smooth running of the execution activities.
  • Draft qualification / validation protocols / reports, execute qualification / validation of equipment in accordance with relevant policies, standards, procedures and guidelines timely
  • Ensuring the implementation of safety policies during all site activities including pre-planning, review of safe work plans, preparation of site work documentation and monitoring of safe work methods during execution;
  • Draft and manage qualification / validation exceptions, deviation and/or investigations encountered during acceptance test execution representing as Qualification / Validation SME.
  • Support other technical changes and duties as required.

Requirements:

  • Bachelor's degree in a relevant life science field (e.g., biology, biotechnology, biochemistry). ·
  • Min. 5 years of relevant working experience in GMP environments is preferred.
  • Excellent communication skills, both written and verbal, in English.
  • Ability to multitask and work in a fast paced environment with competing priorities.
  • Great team player. Strong interpersonal and communication skills and ability to develop close working relationships and work collaboratively with internal and external contacts at all levels

What’s In It for You?

  • Exposure to the major Pharmaceutical Companies in the industry.
  • Annual leave benefits.
  • Full Health coverage and benefits.
  • Training and Development allowance.

What's Next?

If you are interested in applying for this position, please send an email to allison.aquino@cmcexpertisedelivered.com.

Coalesce Management Consulting operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation, or any other factors with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role.

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