Automation Engineer

1 month ago


Stone Cross East Sussex, United Kingdom Russell Tobin Full time

Automation Engineer – Sandwich (fully onsite) – 23 months contract - £22.13 per hour inside IR35 Umbrella
The Automation Engineer role will play an integral part in supporting automation and validation activities at clinical drug product manufacturing sites and data collection and integration with sites in EU. The successful candidates will progress DPMs digital and automation strategy by implementing data collection, analysis and automation solutions for manufacturing processes. Other responsibilities also include support of compliance related activities, including GMP documentation, validation, training, and quality system.
Automation and Technology Support:
# Daily support of systems that are utilized and managed by Drug Product Manufacturing.
# Learn and practice with the systems to develop a front-end and back-end knowledge base. Collaborate with Digital for system maintenance, upgrades, and audit activities.
# Contribute to the completion of projects, develop plans for own projects and leads small project teams.
# Generate and develop standard work practices for data collaborations with PGS sites.
# Modify moderately complex logic/scripts that require a degree of scientific and/or manufacturing process expertise.
# Support Data strategy initiatives related to Manufacturing Systems including data integration initiatives.
# Demonstrate good planning, organizing, time management and team participation skills.
Manage day to day work to ensure timely completion of activities – drive improvement and performance.
BS degree in Engineering, Computer Science or equivalent discipline with 0-2+ years of engineering, automation or relevant experience required
Demonstrated experience in a pharmaceutical / medical device setting.
Technical Writing Experience
Teamwork spirit, good communication skills and training abilities
Fundamental knowledge of manufacturing operations
Experience in a GMP manufacturing production environment
Experience with GMP Validation Lifecycles (Equipment or Software)
Manufacturing Executions System Experience
Relevant pharmaceutical experience
MS SQL, Python, Redshift or Snowflake
Understanding of programming, and proficiency in at least one language
Frequent travelling to sites (Freiburg, New Bridge and Ascoli etc.) Support of off-shift and weekend manufacturers when necessary.
#


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