Get 360Pharma
Director Product Quality Management
Get 360Pharma, Sauk Trail Beach, Wisconsin, United States
About the vacancy
Engineering Quality (Engineering) General Quality Quality Quality Assurance Compliance Validation IT AI & Machine Learning Enterprise Applications & Systems Regulatory Affairs Pharmacovigilance Staff Project Management Director Bachelor’s Degree (HBO, WO) Permanent Full time 101,000 to 174,800 2340 Beerse, Belgium
About Your Next Job As Director Product Quality Management
The Director Product Quality Management Complaint Investigation Manager position will report to the Senior Director of PQM Strategy Deployment & Excellence and is responsible for investigation, documentation and resolution/closure of Product & Signal Complaint Investigations, Nonconformances and/or CAPAs identified through PQV established processes.
About Your Skills and Experience General Skills
Problem solver, who has excellent written and verbal communication skills.
Excellent independent time management skills, with a proven ability to plan and track deliverables and timelines.
Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business.
Highly committed to quality, flexibility and persistence.
Good conflict handling/negotiation skills, who’s able to create win-win situations with internal and external partners.
Knowledge of corporate structure and culture.
We would love to hear from YOU if you have the following essential requirements:
Requires a BA/BS in Science/Engineering. Master’s degree in life science study or equivalent experience is preferrable,
Minimum of 7 years’ experience previous Pharmaceutical Industry experience is required, with at least 7 years of GXP experience within clinical research and development and/or quality assurance.
Up-to-date knowledge and in-depth understanding of relevant pharmaceutical legislation, legislation related to cGMP regulations (Eudralex, ICH, Ph.Eur., USP, etc) at global, regional and national levels.
Strong analytical thinking, decision-making and leadership skills.
Excellent verbal and written communication skills to negotiate and communicate with customers and partners.
Able to apply appropriate risk assessment strategies to manage business & compliance priorities and translate them into actionable items and an action plan.
Proficient in Microsoft Office applications.
Where Molecules Meet Opportunities Hybrid Work
You are eligible to work in EU We only accept applicants who are eligible to work in the EU
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 https://www.jnj.com
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About Your Next Job As Director Product Quality Management
The Director Product Quality Management Complaint Investigation Manager position will report to the Senior Director of PQM Strategy Deployment & Excellence and is responsible for investigation, documentation and resolution/closure of Product & Signal Complaint Investigations, Nonconformances and/or CAPAs identified through PQV established processes.
About Your Skills and Experience General Skills
Problem solver, who has excellent written and verbal communication skills.
Excellent independent time management skills, with a proven ability to plan and track deliverables and timelines.
Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business.
Highly committed to quality, flexibility and persistence.
Good conflict handling/negotiation skills, who’s able to create win-win situations with internal and external partners.
Knowledge of corporate structure and culture.
We would love to hear from YOU if you have the following essential requirements:
Requires a BA/BS in Science/Engineering. Master’s degree in life science study or equivalent experience is preferrable,
Minimum of 7 years’ experience previous Pharmaceutical Industry experience is required, with at least 7 years of GXP experience within clinical research and development and/or quality assurance.
Up-to-date knowledge and in-depth understanding of relevant pharmaceutical legislation, legislation related to cGMP regulations (Eudralex, ICH, Ph.Eur., USP, etc) at global, regional and national levels.
Strong analytical thinking, decision-making and leadership skills.
Excellent verbal and written communication skills to negotiate and communicate with customers and partners.
Able to apply appropriate risk assessment strategies to manage business & compliance priorities and translate them into actionable items and an action plan.
Proficient in Microsoft Office applications.
Where Molecules Meet Opportunities Hybrid Work
You are eligible to work in EU We only accept applicants who are eligible to work in the EU
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 https://www.jnj.com
#J-18808-Ljbffr