QC Validation Engineer

Coalesce Management Consulting Pte. Limited; Singapore; On-site; SGD 65,000 - 85,000; Full time

Job summary

A leading consulting firm in Singapore is looking for a QC Validation Engineer to support Quality Control Laboratories. This role involves qualification and validation of equipment, drafting protocols, and ensuring compliance with safety policies. Candidates should have a Bachelor's degree in life sciences and at least 5 years of GMP experience. The company offers health coverage, annual leave, and development allowances.

Benefits

Exposure to major Pharmaceutical Companies

Annual leave benefits

Full Health coverage and benefits

Training and Development allowance

Qualifications

• Min. 5 years of relevant working experience in GMP environments is preferred.
• Great team player with the ability to develop close working relationships.

Responsibilities

• Assist in the qualification / validation of new equipment.
• Collaborate with multi functions to ensure smooth execution activities.
• Draft qualification / validation protocols and reports.

Skills

Excellent communication skills

Ability to multitask

Strong interpersonal skills

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 [e-mail].

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.