Senior Pharmaceutical Commissioning Qualification Validation Engineer in Melbourne

Senior Pharmaceutical Commissioning Qualification Validation Engineer in Melbourne

Melbourne Full-Time 130000 - 180000 $ / year (est.) On-site
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At a Glance

  • Tasks: Join our team to develop documentation for pharmaceutical commissioning and validation.
  • Company: CAI, a 100% employee-owned company in the life sciences sector.
  • Benefits: Highly competitive salary, continuing education, and opportunities on cutting-edge projects.
  • Other info: Diverse and inclusive workplace with excellent career growth opportunities.
  • Why this job: Be a key player in bringing lifesaving therapies to market, including COVID-19 solutions.
  • Qualifications: 5-12 years in FDA regulated industries; strong problem-solving and teamwork skills required.

The predicted salary is between 130000 - 180000 $ per year.

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 COVID-19 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.
  • 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.

Senior Pharmaceutical Commissioning Qualification Validation Engineer in Melbourne employer: CAI

CAI is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration in the advanced therapeutics sector. Located in Sydney, employees benefit from a vibrant city life while engaging in meaningful projects that drive personal and professional growth. With a strong emphasis on training and development, CAI empowers its team members to excel in their roles and contribute to impactful outcomes in GxP compliance.

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Contact Details:

CAI Recruitment Team

We think you need these skills to ace Senior Pharmaceutical Commissioning Qualification Validation Engineer in Melbourne

Commissioning
Qualification
Validation
Protocol Writing
Field Verification
Project Management
cGMP Leadership