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Engineer Fill Finish - Melbourne

PSC Biotech -
Melbourne VIC

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Job Details

Contract | Fixed term

Qualifications

Engineering
Analysis skills
Education
Bachelor's degree
Negotiation

Full Job Description

Job Information

Date Opened

03/02/2026

Job Type

Consultant

Industry

Pharma

Work Experience

4-5 years

City

Melbourne

State/Province

Victoria

Country

Australia

Job Description

POSITION SUMMARY:

We are looking for a Fill Finish Engineer to join our team on a 12-month contract. The Fill Finish Engineer will play an essential role in supporting the technical transfer of processes and products into GMP manufacturing at PSC Biotech. This position requires a strong understanding of 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:

Partner with GMP manufacturing and Capital project teams as the Fill Finish SME in a greenfield fill & finish process
Oversee automation readiness, ensuring system integration with filling lines and compliance with validation requirements.
Document protocols, engineering tests, and validation reports to ensure compliance with regulatory and client requirements.
Working closely with the Fill Finish team ensure project milestones are achieved and attending reoccurring and adhoc meetings as required
Collect and trend process data for external (client) and internal review
Support MES recipe startup, debugging, and documentation updates to align with process optimization efforts.
Assist with training GMP Manufacturing staff on Client processes
Provide deviation resolution and qualification support by addressing process deviations, troubleshooting startup and PQ issues, and coordinating with the client and vendors to maintain project timelines.Assist Clients in regulatory filing support as a process SME
Support MFG team with hands on cleanroom guidance as necessary
Other duties as assigned

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:

B.S. in Chemical Engineering, Chemistry, Biology, Life Sciences, or related field with 3+ years of experience in fill & finish validation and process engineering -OR- equivalent industry experience.Knowledge/expertise relevant to protein and virus manufacturing in a cGMP environment
Expertise in sterile filtration, washer and tunnel validation, filling and capping operations, and isolator qualification.Experience with automation and process integration, including MES recipe development and debugging. desirable
Experience in a CMO environment or in a similar client-customer based work environment is a plus
On-site presence, as the role requires time on the manufacturing floor and cross-functional collaboration

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