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PerkinElmer

For 85 years, we have pushed the boundaries of science with a clear purpose – to help our customers achieve theirs.

Senior Automation Engineer – cGMP

QA Automation EngineerQA Automation EngineerFull TimeRemoteSeniorTeam 5,001-10,000Since 1938H1B SponsorCompany SiteLinkedIn

Location

Alabama + 4 moreAll locations: Alabama | Florida | Illinois | North Carolina | Missouri

Posted

6 days ago

Salary

0

Seniority

Senior

Bachelor Degree5 yrs expExperience acceptedEnglish

Job Description

Senior Automation Engineer – cGMP

PerkinElmer

• Provides technical guidance for assigned project team members • Creates an approachable, inclusive team environment • Encourages active participation in project team discussions • Engages with leadership to provide continuous improvements suggestions to the DT&A and overall PF Strategy • Leads medium sized projects or scope of work for large projects • Builds a strong collaborative relationship with clients • Supports scope definition, change management, and client communications • Builds a strong relationship with other 3rd party vendors or system integrators • Identifies opportunities to expand work for PF • Broadens knowledge of the overall Digital Transformation and Automation pillars • Develops project execution and Configuration Strategy • Resolves moderately complex operational and people-related challenges • Encourages teams to explore new methods, tools, and industry developments • Identifies execution risks and takes corrective action proactively • Reviews deliverables for quality and compliance before client submission • Balances schedule, quality, and client priorities in decision-making • Manages team utilization and workload forecasting to meet billability goals • Ensures quality assurance, risk management and compliance across all aspects of DT&A

Job Requirements

  • Bachelor's Degree (and/or Masters) in Life Sciences, Engineering, Regulatory or related discipline OR a combination of equivalent experience in quality assurance, cGMP facility start-up, regulatory assurance, relevant military and/or professional services.
  • 5-15+ years of experience in Automation and Digital Systems environment in the GMP life sciences (biotech, pharma, ATMP).
  • Expert-level experience with one or more aspects of Process Control, MES and Digital Systems platforms.
  • Willingness to travel as required for client project assignments.
  • Strong communicator and influencer across engineering, quality, IT/OT, and manufacturing.
  • Structured thinker with advanced troubleshooting and problem solving skills.
  • Skilled at managing multiple priorities in a high pressure, regulated environment.
  • Demonstrated leadership and mentorship abilities.

Benefits

  • Professional development opportunities
  • Mentorship and knowledge sharing

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