CQV/Fill Finish Engineer - Melbourne

PSC Biotech® Corporation; Melbourne; On-site; AUD 90,000 - 130,000; Full time

Job summary

PSC Biotech Corporation is seeking a CQV/Fill Finish Engineer to join our team on a 12-month contract in Melbourne. The role supports CQV activities and fill-finish processes within a GMP manufacturing environment, requiring strong CQV knowledge and collaboration with project teams.

The successful candidate will assist in creating key documentation, track milestones, and provide hands-on support in cleanroom environments, with exposure to isolators, depyrogenation tunnels, and sterile processing

Qualifications

• 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.

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.

Skills

CQV experience

Fill finish

GMP knowledge

Project management

Technical writing

Stakeholder engagement

Cross-functional

Education

Bachelors in Eng or Life Sci

Job description

We are looking for a CQV/Fill Finish Engineer to join our team on a 12-month contract. The 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.

We are looking for a CQV/Fill Finish Engineer to join our team on a 12-month contract. The 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.