Validation Area Specialist - FFEx - Warehouse/Intralogistics
Validation Area Specialist - FFEx - Warehouse/Intralogistics
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1 Vacancy
Job Description
About the Department
You will be joining Fill & Finish Expansions (FFEx) which is responsible for all major expansion activities within aseptic production solid dosage forms finished products fill & finish warehousing and QC across all production areas in Product Supply. The area is anchored in Product Supply Quality & IT which globally employ approx. 20000 of Novo Nordisks 50000 employees.
FFEx is a newly established and growing area with the responsibility to design plan and build all new aseptic filling capacity across Novo Nordisk to serve the needs of millions of patients. We do it by rethinking our production facilities with the use of modern technology as we are setting the standards for the aseptic production of the future. Facilities designed today which we will still be proud of 20 years from now. FF Expansions has a global approach where you will be working with multiple sites and cultures across the world.
What we offer you:
Leading pay and annual performance bonus for all positions
All employees enjoy generous paid time off including 14 paid holidays
Health Insurance Dental Insurance Vision Insurance effective day one
Guaranteed 8% 401K contribution plus individual company match option
Family Focused Benefits including 12 weeks paid parental & 6 weeks paid family medical leave
Free access to Novo Nordisk-marketed pharmaceutical products
Tuition Assistance
Life & Disability Insurance
Employee Referral Awards
At Novo Nordisk you will find opportunities resources and mentorship to help grow and build your career. Are you ready to realize your potential Join Team Novo Nordisk and help us make what matters.
The Position
Primary responsibility is to provide/lead validation services required for the successful delivery of highly automated warehouse processes and projects locally called Intralogistics integrate Automated Storage and Retrieval Systems (ASRS) high density warehouses automated conveyors Automated Guided Vehicles(AGVS)/Automated Mobile Robots(AMRs) and more to fully automate material handling flows across the FFEx site from inbound delivery storage delivery/retrieval to/from production and final outbound delivery. Multiple layers of complex IT/OT automation include Supervisory Control and Data Acquisition (SCADA) Warehouse Control Systems (WCS) and SAP platforms will be integrated to the equipment to create a material handling flow process in the site supply chain with minimal human intervention.
Relationships
Senior Project Manager Site Capacity & Upfit.
Essential Functions
- Provide validation & technical support through the preparation execution data analysis & report writing for IV OV & PV protocols
- Ownership of Change Requests (CRs) related to project validation responsibilities
- Perform compliance & technical reviews/approvals of protocols & protocol data
- Author project quality masterplans (PQMPs) validation plans (VPLs) & other key validation documentation
- Author & execute assigned IV OV & PV protocols for direct impact systems/processes per approved timeframes. Requires no guidance & direction to complete these goals & needs no coaching on technical competencies for goal obtainment. Serves as a source of expertise in the group for validating new systems
- Ensure compliance of validation protocols executed are aligned with local corporate & regulatory regulations
- Lead validation failure investigations & non-conformities utilizing root cause analysis techniques
- Create & modify existing validation procedures & configuration item lists (CILs) as required
- Write/Review specifications procedures & other required supporting documents to maintain the validated state of equipment & processes
- Participate in FAT SAT commissioning efforts for equipment automation systems & processes & successfully transition into the ownership role for validation efforts related to the equipment
- Identify process improvements before equipment systems or processes are placed under change control during validation
- Budget oversight as needed
- Other accountabilities as assigned
Qualifications
- Bachelors degree in engineering Computer Science or applicable technical degree or proven equivalent relevant work experience required
- Masters Degree preferred
- Minimum of seven (7) years validation or quality related discipline experience in pharmaceutical environment required
- Experience with robotics automation and SAP preferred
- Experienced with regulatory requirements & industry standards for pharmaceutical &/or medical device manufacture such as 21 CFR Part 11 GAMP5 ISO electronic records retention configuration items list FDA & ICH guidance documents required
- Demonstrated experience using root-cause analysis techniques to solve problems preferred
- Ability to read write & understand complicated product documentation preferred
- Demonstrated leadership & project management skills: two-way communication skills with customers (internal/external) project team & management; interpersonal & team building skills; achievement of project timelines & customer requirements preferred
- Ability to write technical documentation based on equipment manuals preferred
- Experience in pharmaceutical manufacturing preferred. Knowledgeable in GMP concepts preferred
- Knowledge of standard operating procedures with attention to high-level concepts preferred
- Ability to manage multiple tasks/deadlines & prioritize properly based on process needs preferred
- Demonstrated strong skills in change management within NN preferred
Physical Requirements
May move equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. May be required to be on your feet for up to a 12-hour shift. May required corrected vision to 20/20 or 20/25 based on role. May require color vision based on role. May require the ability to work in loud noise environments with hearing protections.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees the patients we serve and communities we operate in. Together were life changing.
Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race ethnicity color religion sex gender identity sexual orientation national origin disability protected veteran status or any other characteristic protected by local state or federal laws rules or regulations.
If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply please call us at 1-. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.
Required Experience:
Unclear Seniority
Employment Type
Contract
