Lead Engineer - Analytical Equipment Validation

Reposted 2 Days Ago
Be an Early Applicant
Portsmouth, NH
In-Office
Senior level
Pharmaceutical
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization.
The Role
The Lead Engineer will oversee computer systems validation activities, ensure compliance with regulatory guidelines, and mentor junior team members.
Summary Generated by Built In

 

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:  https://www.lonza.com/careers/benefits.

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.

Top Skills

21 Cfr Part 11
Computer Systems Validation
Data Integrity
Gamp
Ich Q7A
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The Company
HQ: Basel
0 Employees
Year Founded: 1897

What We Do

At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization. Our community of 16,000 talented employees work across a global network of more than 30 sites to deliver for our customers across the pharma, biotech and nutrition markets.

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