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Lead Engineer - Analytical Equipment Validation

Portsmouth, NH, US • Posted 15 hours ago • Updated 2 hours ago

Full Time

On-site

Fitment

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Job Details

Skills

Analytical Skill
FOCUS
Test Scripts
Technical Drafting
GMP
Agile
Insurance
Data Integrity
QMS
Change Control
Corrective And Preventive Action
Auditing
Documentation
Mentorship
Computer Science
Software Engineering
GAMP
Computerized System Validation
Communication
Management
Accountability
Collaboration
Innovation
Law
Life Sciences

Summary

Lead Engineer - Analytical Equipment Validation

Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.

The focus of the Computer Systems Validation (CSV)Lead Engineer role is to identify or create industry best practices and implement these within the framework of existing GAMP regulations. Responsibilities of the CSV Lead Engineer will include risk assessing systems, reviewing change requests and test scripts, drafting protocols and initiating and reviewing GMP documentation revisions as well as ownership of department procedures. The position provides guidance to junior team members.

What you will get

An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Medical, dental and vision insurance.

Our full list of global benefits can be found here: ;/b>

What you will do

Lead collaboration between internal teams and CSV to prioritize and complete activities on time
Maintain knowledge of Lonza policies, 21 CFR Part 11, Data Integrity, ICH Q7A, and GAMP principles
Perform QMS processes (Change Control, Deviation, CAPA) and validation maintenance of computerized systems
Participate in audits and inspections as a Subject Matter Expert
Own, revise and maintain CSV SOPs
Support qualification activities and documentation for CSV validation in line with regulatory guidelines
Mentor and train junior team members

What we are looking for

Bachelor's Degree is required (preferably in Computer Science/Software Engineering)
5-10 years' of Computer Systems Validation experience
Experience with 21 CFR Part 11 and ISPE GAMP guidelines as they relate to Computer Systems Validation
Strong written and oral communication skills
Strong organizational and time management skills

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Dice Id: SYCAMR
Position Id: 6a2defc3b926e442fb7be326a8353884
Posted 15 hours ago

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