System User, Optical Inspection

Johnson & Johnson•Wilson, NC

13h•Onsite

About The Position

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. As a part of this new team, this role will work in close cooperation with other parenteral DP sites in the J&J network and lead and implement the recruitment ramp-up plan within the project timelines and budget.

Requirements

Bachelor's or higher degree in Life Sciences, Pharmacy, or Engineering is required; a Master's or higher degree is preferred
A minimum 8 years of experience in the pharmaceutical industry, including people leadership, is required.
A minimum 3 years of experience in Optical Inspection (manual and automated visual inspection, test kits, and operator qualification) of parenteral filled products
Knowledge of Good Manufacturing Practice (GMP) regulations and a proven track record of successfully implementing and maintaining cGMP compliance is required
Strong knowledge of applying digital and robotics technologies, with a commitment to staying updated with emerging tools and platforms
Strong creative thinking skills and a track record of developing innovative solutions for complex challenges
Excellent interpersonal skills, with the ability to work collaboratively in diverse, global teams.
Adept at analyzing complex issues and formulating effective solutions in a constantly evolving environment.
Willingness and ability to adapt to shifting job requirements and work environments.
Capacity to handle stress and challenges effectively, promoting a healthy work-life balance.
An approach that recognizes opportunities and is willing to take calculated risks, and encourages entrepreneurial thinking

Nice To Haves

Lean/Six Sigma certifications

Responsibilities

Participation in all safety related reviews (HAZOP, machine safety, ergonomic safety)
Review and approval of all User Requirement Specifications. (URS’s)
Review the deliverables from concept refresh, basis-and detailed engineering (e.g.: PFD’s , P&ID’s, process descriptions, functional design specifications, equipment specifications)
Writing and/or review of Process Support Operational documentation (Master Batch Records, SOP’s, WI’s)
Actively support all commissioning and qualification batches
Preparation and execution review & approval of validation related qualification documents and the resourcing of execution of associated tasks (water batch, engineering batch, aseptic process simulation, validation batches)
The identification of required spare parts in accordance with the approved spare part list for the support systems and liaise with relevant parties for their procurement.
Generation and execution of the above-mentioned activities within budget and current schedule
Monitoring and ensuring all user requirements are met
Signed URS
Timely answered requests from information forms
A list of in-process test equipment
Operational documentation for all process support equipment
Creating training plan for operators