About the Role

We are seeking
Process Engineers
to support ongoing process development and manufacturing scale‑up activities within a
GMP‑regulated environment
. This role will play a key part in ensuring production readiness by supporting the startup of new manufacturing equipment,
optimising
existing processes, and enabling a smooth transition to commercial operations.

The successful candidates will bring
hands‑on experience
in equipment and process startup, with exposure to
aseptic and automated systems
within
medical
device
, biotechnology, or pharmaceutical
environments.

This position is available as:

• 
  One 12‑month contract

• 
  One 6‑month contract

Both roles offer the opportunity to work on critical manufacturing and process development initiatives in a regulated setting.

Key Responsibilities

• 
  Lead and support
  process development activities
  for new and existing manufacturing processes.

• 
  Execute and document
  startup, commissioning, and
  optimi
  s
  ation
  of manufacturing lines and equipment for GMP use.

• 
  Collaborate with cross-functional teams to ensure processes are compliant with
  GMP standards
  and meet operational needs.

• 
  Assist
  with
  tech transfer
  activities, including drafting and reviewing process documentation and procedures.

• 
  Support the development and implementation of
  automation processes
  within aseptic or controlled production environments.

• 
  Troubleshoot process issues and contribute to continuous improvement initiatives.

• 
  Work closely with site engineering, operations, and quality teams to ensure delivery of project milestones.

• 
  Provide input into process risk assessments, validation activities, and equipment readiness.

Requirements

Required Qualifications & Experience

• 
  Bachelor’s degree in Engineering
  (Chemical, Mechanical, Biomedical, Process Engineering, or related discipline).

• 
  2 +
  years experience
  in
  medical
  device
  ,
  biotech
  ,
  pharmaceutical,
  or similar regulated GMP industries.

• 
  Proven experience in
  process development
  within a GMP manufacturing environment.

• 
  Demonstrated experience
  starting up or bringing online manufacturing equipment or processes
  for GMP operations.

• 
  Strong understanding of GMP, quality systems, and regulated industry expectations.

• 
  Experience in
  aseptic processing
  and/or development of
  automated manufacturing lines
  .

• 
  Excellent problem-solving skills and ability to work independently in a fast-paced environment.

Preferred Experiance

• 
  Previous
  tech transfer
  experience within a GMP setting.

• 
  Experience with
  highly automated
  or semi-automated manufacturing lines.

• 
  Exposure to
  scaling up
  early-stage manufacturing processes.