Quality Assurance - Manager

at  Sanofi

Budapest, Közép-Magyarország, Hungary -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate10 Jul, 2024Not Specified11 Apr, 20241 year(s) or aboveChemistry,Biology,Medicine,Training,Completion,Life Science,Special Events,Personal DevelopmentNoNo
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Description:

QA Responsible Person Consumer Healthcare (CHC) - Hungary (Budapest) - Sanofi
Key Responsibilities:
The QA Manager – Consumer Healthcare (CHC) will manage the implementation and maintenance of the CHC Hungarian Affiliate Quality System, ensuring compliance with GxP regulatory requirements, Global Quality standards, and national EU legislation.
This role includes overseeing/supervision Good Distribution Practice of medicinal products for human use and Medical Devices.

Key responsibilities include:

  • Implementing and maintaining a quality management system for various health-regulated products.
  • Managing authorized activities, ensuring accuracy and quality of records.
  • Ensuring and maintaining training programs.
  • Coordinating recall operations for various products.
  • Handling customer complaints effectively.
  • Approving suppliers, customers, and subcontracted activities impacting GDP.
  • Conducting regular self-inspections and implementing corrective measures.
  • Deciding on the final disposition of returned, rejected, recalled, or potentially falsified products.
  • Ensuring adherence to national law requirements.
  • Overseeing the management and documentation of the QMS Medical Devices.
  • Managing document management system
  • Proactively participates to achieve Site Quality Risk Assessment, in developing and implementing the Organization Quality Plan
  • Proactively participates under the guidance of Country Quality Head to local implementation of Global policy / guidelines / standards / procedures from Quality Manual

Scope and Role Impact:

  • Cross-functional management within the CHC Hungary Affiliate.
  • Key role in ensuring consistent application of Quality requirements.

Required Skills and Experience:

  • Educational Qualifications: Candidates must hold a diploma, certificate or other evidence of formal qualifications awarded on completion of a university or other higher education course of study in pharmacy, chemistry, medicine, biology, or a related life science.
  • Experience: Candidates should have significant experience in the Good Distribution Practice (GDP) domain within an affiliate setting, demonstrating a thorough understanding of the specific challenges and requirements of this area. More than 1 year experience as in performing the functions of a Responsible Person on a WDA.
  • Knowledge:

o Advanced understanding of GxP, Quality risk analysis and management, Regulatory requirements.

o Familiarity with EU Good Distribution Practices.

  • Technical/Professional:
  • Experience in Quality Systems,
  • Continuous Improvement
  • Life-cycle Management
  • Veeva Quality knowledge will be considered as a plus.
  • Computer literacy
  • Soft Skills:
  • Very good communication skills, negotiation, and problem-solving skills.
  • Ability to act for change, commit to customers
  • This role will be based 100% in Office in Budapest
  • Languages: English - advanced

When joining our team, you will experience:

  • An international work environment, in which you can develop your talent and realize ideas and innovations within a competent team
  • An attractive, market-oriented salary and cafeteria benefits
  • Collective life and accident insurance
  • Yearly medical check-up
  • An individual and well-structured introduction and training of new employees and we will dedicate a Buddy for you to better navigate in your first weeks
  • Your own career path within Sanofi[. Your professional and personal development will be supported purposefully
  • Practice your language skills within our “Language Club”
  • Join a great community & special events (Monthly Board Game Nights, Summer Events, Well-Being Lectures & Sport Clubs)

When joining our team, you will experience:

  • An international work environment, in which you can develop your talent and realize ideas and innovations within a competent team
  • An attractive, market-oriented salary and cafeteria benefits
  • Collective life and accident insurance
  • Yearly medical check-up
  • An individual and well-structured introduction and training of new employees and we will dedicate a Buddy for you to better navigate in your first weeks
  • Your own career path within Sanofi. Your professional and personal development will be supported purposefully
  • Practice your language skills within our “Language Club”
  • Join a great community & special events (Monthly Board Game Nights, Summer Events, Well-Being Lectures & Sport Clubs)

Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability, gender identity or Veteran status.
Watch our https://www.youtube.com/watch?v=SkpDBZ-CJKw&t=67s and check out our Diversity Equity and Inclusion actions at https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness!
#Sanofi #WeNeverSettle
#SanofiCareers
#PursueProgress
#DiscoverExtraordinary
#joinsanofi
#careerswithpurpose

Responsibilities:

Key responsibilities include:

  • Implementing and maintaining a quality management system for various health-regulated products.
  • Managing authorized activities, ensuring accuracy and quality of records.
  • Ensuring and maintaining training programs.
  • Coordinating recall operations for various products.
  • Handling customer complaints effectively.
  • Approving suppliers, customers, and subcontracted activities impacting GDP.
  • Conducting regular self-inspections and implementing corrective measures.
  • Deciding on the final disposition of returned, rejected, recalled, or potentially falsified products.
  • Ensuring adherence to national law requirements.
  • Overseeing the management and documentation of the QMS Medical Devices.
  • Managing document management system
  • Proactively participates to achieve Site Quality Risk Assessment, in developing and implementing the Organization Quality Plan
  • Proactively participates under the guidance of Country Quality Head to local implementation of Global policy / guidelines / standards / procedures from Quality Manua

Scope and Role Impact:

  • Cross-functional management within the CHC Hungary Affiliate.
  • Key role in ensuring consistent application of Quality requirements


REQUIREMENT SUMMARY

Min:1.0Max:6.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Software Testing, Clinical Pharmacy

Trade Certificate

Pharmacy chemistry medicine biology or a related life science

Proficient

1

Budapest, Hungary