Validation Engineer #ez

HAYS SPECIALIST RECRUITMENT PTE. LTD.; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

A global life sciences consultancy seeks to hire a Validation Engineer to work on various projects in a biotech environment. This role involves writing and executing validation protocols, collaborating with clients on compliance, and mentoring junior staff. It's an exciting opportunity with competitive remuneration within a dynamic team.

Qualifications

• Degree or Diploma qualification; B.S preferred.
• Knowledge of GMP facilities and cGMP requirements.
• Minimum of one year of GMP experience.

Responsibilities

• Completing work assignments specified by Validation Project Manager.
• Writing and executing Validation Protocols (IQ, OQ, PQs).
• Generating Validation Summary Reports and SOPs.

Skills

Attention to detail

Teamwork

Education

B.S in Chemical Engineering

B.S in Mechanical Engineering

B.S in Electrical Engineering

Life Sciences degree

Job description

Your new company

Client is a global life sciences consultancy looking to hire Validation Engineers.

Your new role

· Completing work assignments as specified by the Validation Project Manager

· Providing timely updates to the Validation Project Manager

· Adhering to the proper site safety practices; wearing adequate safety equipment when required

· Completing timesheets and expense reports in a timely manner

· Working in a biotech/pharmaceutical environment as a consultant/contractor for various clients

· Working closely with client's employees on various projects and various GMP facilities to help client with validation issues

· Learning new ideas, techniques and systems

· Commuting to clients' manufacturing for validation projects

· Keep client’s proprietary information confidential

· Writing Validation Protocols such as IQ, OQ and PQs

· Executing Validation Protocols such as IQ, OQ and PQs

· Calibrating Thermocouples for Temperature Mapping Studies

· Calculating and interpreting of collected data from validation studies

· Generating Validation Summary Reports and Standard Operating Procedures(SOPs)

· Create Validation Risk Assessments

· Mentoring junior staff and interns

What you'll need to succeed

· Degree or Diploma qualification; B.S in Chemical, Mechanical, or Electrical Engineering (preferred) or Life Sciences degree

· Knowledge of GMP facilities and cGMP requirements

· A minimum of one year of GMP experience in a biotech or sterile pharmaceutical manufacturing environment, or the equivalent. Incumbent with more years of experience may be considered for a senior role

· High energy and attention to detail

· A demonstrated ability to work well in a team environment

What you'll get in return
This is an exciting opportunity to join an MNC. You will be part of a dynamic team and you will be remunerated at market competitive rates.

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Ernie at Hays on [phone] or email [e-mail] for a confidential discussion.

Referrals are welcome.

Registration ID No. R1329386 | EA License number: 07C3924 | Company Registration No. 200609504D