CQV/Fill Finish Engineer - Melbourne

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Melbourne, Victoria, AUS
In-Office
Mid level
Biotech
The Role
Supports commissioning, qualification, and validation of pharmaceutical fill-finish facilities, utilities, and equipment in GMP manufacturing environments. Responsibilities include controlled documentation, equipment qualification, risk analyses, design reviews, FAT/SAT, IQ/OQ/PQ execution, filling-line integration, MES recipe startup and debugging, project tracking, and stakeholder coordination. The role requires hands-on cleanroom experience with vial filling and aseptic processing systems, plus strong technical writing and project management skills.
Summary Generated by Built In

POSITION SUMMARY:

 

We are looking for a CQV/Fill Finish Engineer to join our team on a 12-month contractThe CQV/Fill Finish Engineer will play an essential role in supporting the CQV activities and fill finish processes in a GMP manufacturing environment. This position requires a strong understanding of CQV and fill & finish processes and the ability to collaborate effectively with project teams. The ideal candidate will be responsible for assisting in the creation of key documentation, ensuring project milestones are tracked, and providing hands-on support in cleanroom environments. 

 

DUTIES AND RESPONSIBILITIES:

  • Commission, qualify, and validate facilities, utilities, and/or equipment in assigned projects.  
  • Assists in authors, revises, reviews, and completes controlled documents for CQV projects.
  • Assists to review and qualify equipment for commissioning, qualification, and validation activities. 
  • Supports to write and review GMP and GDP documents and technical specifications. 
  • Collaborate with multiple departments on assigned project activities and deliverables. 
  • Assist to initiate and coordinate risk analyses, design reviews, execute FAT/SAT, IQ, OQ, and PQ.
  • Ensure system integration with filling lines and compliance with validation requirements.
  • Support MES recipe startup, debugging, and documentation updates to align with process optimization efforts.
  • Collaborate with client teams, vendors, contractors, and cross-functional stakeholders to deliver project objectives. 
  • Manage project activities, timelines, and status reporting while ensuring compliance with cGMP and data integrity requirements. 

DEMONSTRATED COMPETENCIES:

  • Business Development - Identify and target potential clients. Work in a team environment; develop and execute a plan, in alignment with company vision, mission and strategic plans to engage potential customers.
  • Relationship Building – Works with and across formal and informal professional and social networks to build long-term partnerships and connections in the life science industry and Internal team.
  • Negotiation Skills – Active listening, needs assessment, and presents visions to build a consensus.
  • Analytical Skills – Identifies, researches, and demonstrates logical reasoning to communicate critical information.
  • Rational Persuasion – Presents key factors, influencing factors, and strategic goals to assist stakeholders in identifying solutions.
  • Interpersonal Awareness – Ability to be aware of how actions, ideas, and communication can/does affect people and their outcomes.
  • Agility – Meets objectives by responding to competing and changing priorities and multiple tasks under inflexible timelines.


Requirements

REQUIRED EDUCATION AND WORK EXPERIENCE:

  • Bachelor's Degree in Engineering or Life Sciences.
  • Minimum 3 years of CQV and Fill Finish experience within GMP-regulated environments. 
  • Hands-on experience with vial filling equipment and processes.
  • Strong understanding of cGMP requirements, data integrity, and validation lifecycle principles.
  • Excellent technical writing, communication, project management, and stakeholder engagement skills.
  • Exposure to ancillary Fill Finish systems including isolators, depyrogenation tunnels, sterile filtration systems, and related aseptic processing equipment.
  • Ability to manage multiple project priorities while working directly with client and site teams.


Skills Required

  • Bachelor's degree in Engineering or Life Sciences
  • Minimum 3 years of CQV and fill-finish experience in GMP-regulated environments
  • Hands-on experience with vial filling equipment and processes
  • Strong understanding of cGMP requirements, data integrity, and validation lifecycle principles
  • Excellent technical writing, communication, project management, and stakeholder engagement skills
  • Exposure to isolators, depyrogenation tunnels, sterile filtration systems, and related aseptic processing equipment
  • Ability to manage multiple project priorities while working directly with client and site teams
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The Company
HQ: Pomona, CA
445 Employees
Year Founded: 1996

What We Do

Founded in 1996, PSC Biotech Corporation was created with the vision of providing life science companies unmatched support. To date, PSC Biotech Corporation now serves 1000 clients in more than 35 countries worldwide through professional services consulting, cloud-based software solutions, pharmaceuticals contract manufacturing, life science investment consulting, and metrology services. PSC Biotech Corporation has six unique divisions within the parent company – each representing one of our areas of expertise: PSC Biotech, PSC Software, BioTechnique™, PSC Partners, PSC Metrology and PSC Investments. Additionally, PSC Asia and PSC Biotech Ltd represent PSC Biotech Corporation in Asia and Europe, respectively. Together, these divisions enable us to meet the ever-changing needs of our clients with a commitment to excellence and superior quality.

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