Senior Pharmaceutical Commissioning Qualification Validation Engineer

CAI; Melbourne; On-site; AUD 130,000 - 180,000; Full time

Benefits offered by this job

Highly Competitive Salary

Continuing education

Opportunities to work on cutting-edge projects

Job summary

A leading engineering consulting firm in Melbourne is seeking a Senior Pharmaceutical Commissioning Qualification Validation Engineer. Responsibilities include developing documentation for commissioning and qualification processes and managing project execution. The ideal candidate should have a relevant degree and experience in FDA regulated environments. Competitive salary and opportunities for professional training are offered.

Qualifications

• Experience in commissioning and qualification activities.
• Strong knowledge of project technical issues.
• Ability to work independently and build project teams.

Responsibilities

• Develop documentation for Commissioning, Qualification, and Validation.
• Manage the execution lifecycle from SLIA generation to OQ completion.
• Coordinate and direct small teams in document development.

Skills

Technical problem-solving

Attention to detail

Project management

Education

BS or MS in relevant science or engineering field

5 - 12 years of experience in FDA regulated industry

Tools

Microsoft Word

Microsoft Excel

Job description

Senior Pharmaceutical Commissioning Qualification Validation Engineer

Senior Pharmaceutical Commissioning Qualification Validation Engineer

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CAI is looking for individuals with a range of experience in the areas of commissioning, qualification, and validation to join our team in Australia. Experience in the pharmaceutical, medical device or biotechnology industries is required.

About CAI

CAI is a 100% employee-owned company established in 1996, it has grown year over year to nearly 700 people worldwide. We provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other mission critical industries.

Are You Ready?

Our approach is simple; we put the client’s interests first, we do not stop until it is right, and we will do whatever it takes to get there.

As owners of CAI, we are committed to living our Foundational Principles, both professionally and personally:

We act with integrity

We serve each other

We serve society

We work for our future.

With employee ownership, one person’s success is everyone’s success; we work diligently to accomplish team goals. We place Team Before Self, demonstrate Respect for Others, and possess a can-do attitude. That is how we have grown exponentially.

CAI agents (employees) will be exposed to cutting edge technologies in the advanced medicine space. You will have an opportunity to work with recognized subject matter experts allowing YOU to be a key player in bringing lifesaving therapies to market, including COVID19 Vaccines and therapies. As part of our company culture, we invest in YOUR future, and commit to hands on certifications as well as professional training. Our collaborative culture ensures that our customers benefit from exemplary work across our entire range of professional services.

Requirements Include

Position Description:

We are now seeking a Senior CQV Engineer to join our growing operations in Australia. The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and execution, field verification, and development of summary reports at the client site.

The role of a Senior CQV Engineer in CAI is to:

Develop documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment.

Responsible for protocol writing and execution (field verification), and development of summary reports at client sites. Other responsibilities include planning / coordinating work and directing small teams in document development and / or execution.

Position Requirements

BS or MS in a relevant science or engineering field, or equivalent years of hands-on experience

5 – 12 years’ experience performing commissioning and / or qualification activities in an FDA regulated industry. Ideally, you will already have experience in facilities and equipment startup, walk downs & troubleshooting, utilities (WFI, RO, HVAC), building automation or other pharmaceutical manufacturing processes and equipment, FAT/SAT, URS, design review, P&IDs, IQ/OQ/PQs, generation & execution, etc.

Provide cGMP leadership and guidance for the integration and delivery of CQV services for our Life Sciences clients.

Excellent technical problem-solving and troubleshooting skills, with solid knowledge of typical project technical issues

High attention to detail

Ability to multi-task and take initiative to accomplish assigned tasks accurately by established deadlines

Ability to work independently, while quickly building and nurturing a project team

Managing the C&Q documentation and execution lifecycle from SLIA generation through to OQ completion.

Support onsite and offsite activities, such as: FATs, SATs, IOQ and PQ Executions and System Walkdowns

Experience in planning / directing C&Q activities

Proficient in life science manufacturing processes in areas such as biotech, aseptic processing, aseptic fill/finish, OSD, Gene Therapy or equivalent experience.

Familiarity with Baseline Guide 5 (Second Edition) a plus

Other Requirements

Expertise in Microsoft Word and Excel

Excellent oral and written English are required.

Able to travel domestically if required

Able to work in Australia without sponsorship

In return for your skills and knowledge, CAI offers a wide range of benefits including:

Highly Competitive Salary

Continuing education (internal and external)

Opportunities to work on cutting edge projects in a highly evolving field

We are an equal opportunity employer; we are proud to employ veterans and promote diversity and inclusion in our workplace. Diversity is a strength for our global company. We pledge that CAI will be operated in a way that is fair and equitable to all – our employees, our customers, and the broader society.

This job description is not all inclusive and you may be asked to do other duties. CAI will also consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of the Fair Chance Act (FCA) / Fair Chance Ordinance (FCO).

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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