BIOPHARMACEUTICAL - Senior Filling/Finish CQV

MMR Consulting

• $120K — $145K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Engineering (preferably Mechanical)
  • 8+ years experience in GxP environments for pharmaceutical packaging operations
  • Prior experience in the pharmaceutical/biotech industry with cGMP knowledge
  • Demonstrated leadership skills for multi-stakeholder projects
  • Ability to manage multiple projects in a fast-paced setting
  • Must be able to lift up to 50 pounds
  • Flexibility for occasional travel and off-hours work

Responsibilities

  • Lead design and operations of pharmaceutical product packaging
  • Collaborate to create User Requirements Specifications (URS)
  • Work with vendors to develop Design and Functional Specifications (FS)
  • Evaluate packaging operations for troubleshooting and improvement
  • Drive innovations in packaging technologies
  • Conduct reliability and optimization studies for equipment
  • Document and execute FAT/SAT/Commissioning of systems
  • Coordinate cross-functional meetings to track project progress

Benefits

  • Relocation packages are available
  • Travel packages may also be provided
  • Opportunity to work in a growing team
  • Engagement in innovative packaging technologies
  • Potential for leadership development opportunities
  • Work in a dynamic and fast-paced environment
Full Job Description
Previous Pharmaceutical/Biotech experience is mandatory for this role.

Relocation packages or travel packages are available for this role

This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers involved in the design, commissioning & qualification, start-up and project management of various processes, systems, and facilities. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers.

This role is for to work on the filling and packaging operations within a sterile / aseptic pharmaceutical manufacturing environment. Tasks may include all or in part, design / re-design, installation, start-up / commissioning, qualification as well as operation support for analysis, trouble shooting and / or process improvements of the filling / packaging equipment systems. The ideal candidate should possess technical as well as leadership skills to independently perform or manage resources and activities related to the filling and packaging operations.

The work will require working out of client's facilities, which are in Portland, Oregon.

Responsibilities
  • Lead or participate in design or operations of packaging pharmaceutical products into their final forms and containers by fill / finish and packaging like, vials, syringes and other delivery systems.
  • Work with production and packaging groups to create User Requirements Specifications (URS) for ongoing operations or new projects
  • Collaborate with vendors for packaging machinery, equipment systems, automation controls, materials and consumables, to create Design Specifications (DS) and Functional Specifications (FS) to implement solutions for reducing contamination risks & process failures
  • Assess current packaging operations for troubleshooting, efficiencies and continuous improvement opportunities
  • Spearhead innovations in packaging technologies to support existing client needs
  • Perform reliability studies on packaging equipment
  • Perform optimization studies for the optimal use of packaging equipment systems for use in campaigns
  • Support documentation and/or execution of FAT / SAT / Commissioning, Qualification of packaging systems
  • Coordinate meetings with cross-functional departments to drive project progress, facilitate decisions, provide updates to higher management
  • Other duties as assigned by client, and / or MMR, based on workload and project requirements.
  • Work may require occasional support over shutdowns or extended hours, specifically during installation and commissioning / validation phases


Qualifications
  • College / Bachelors' Degree or Diploma in Engineering discipline, preferable Mechanical
  • 8+ years in GxP environment typically for design or operation of pharmaceutical packaging operations, including sterile / aseptic manufacturing
  • Previous experience in the pharmaceutical / biotech industry, with knowledge of requirements for a cGMP operations
  • Possess leadership skills and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexity
  • Ability to handle multiple projects and work in a fast-paced environment.
  • Ability to lift 50 pounds
  • Travel and / or off-hours work may be required on occasion


As part of our recruitment process, we may use technology-assisted tools, including AI-enabled systems, to support application review and candidate evaluation. Hiring decisions are made with human oversight and consideration.

Similar Jobs

More Jobs at MMR Consulting

More Pharmaceuticals & Biotech Jobs

Find similar BIOPHARMACEUTICAL - Senior Filling/Finish CQV jobs: