Job Description

Job Description

POSITIONSUMMARY:

The Fill Finish Engineer will play an essentialrole 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.

DUTIESANDRESPONSIBILITIES:

  • 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

    • DEMONSTRATEDCOMPETENCIES:

  • 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

    REQUIREDEDUCATIONANDWORKEXPERIENCE:

  • 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.
  • 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

    • Apply for this Position

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