QA Validation Engineer

COALESCE MANAGEMENT CONSULTING PTE. LIMITED; Singapore; On-site; USD 50,000 - 90,000; Full time

Job summary

An established industry player is seeking a QA Validation Engineer to join their dynamic team. This role involves supporting projects with effective testing services, ensuring compliance with safety policies, and collaborating with major pharmaceutical companies. Candidates should have a strong background in life sciences and experience in GMP environments. This position offers a unique opportunity for professional growth and development in a fast-paced setting. Join a community that values excellence and teamwork, and make a significant impact in the Life Science and Technology sectors.

Benefits

Annual Leave Benefits

Full Health Coverage

Training and Development Allowance

Qualifications

• 4+ years of experience in GMP environments preferred.
• Strong interpersonal skills and ability to work collaboratively.

Responsibilities

• Support validation of new equipment and draft validation protocols.
• Ensure safety policies are implemented during site activities.
• Assist in deviation investigations and documentation.

Skills

GMP Compliance

Communication Skills

Problem Solving

Multitasking

Education

Bachelor's degree in Life Sciences

Job description

Position: QA Validation Engineer

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.

Job Description:

We are currently expanding our team and are looking for a QA Validation Engineer on site with a client. In summary, you will be supporting projects 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:

• Support in the validation of new equipment / replacement of equipment project for Technology transfer.
• Support the drafting, execution, reviewal of 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
• Support deviation investigations, ensuring proper closure, and recording of work documentation.

Requirements:

• Bachelor's degree in a relevant life science field (e.g., biology, biotechnology, biochemistry). ·
• Min. 4 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.