Quality Executive

at  British American Tobacco

Monterrey, N. L., Mexico -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate24 Jan, 2025Not Specified25 Oct, 20242 year(s) or aboveGood communication skillsNoNo
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Description:

WHY JOIN BAT?

We’re one of the few companies named as a Global Top Employer by the Top Employers Institute – certified in offering excellent employee conditions.
Collaboration, inclusion and partnership underpin everything we do here at BAT. We are looking forward to enabling every individual to thrive, regardless of gender, sexual orientation, marital or civil partnership status, gender reassignment, race, religion or belief, colour, nationality, ethnic or national origin, disability, age, skills, experience, education, socio-economic and professional background, veteran status, perspectives and thinking styles. We know that embracing talent from all backgrounds is what makes us stronger and best prepared to meet our business goals.
We see the career breaks as opportunities not obstacles. Through The Global Returners program, we support professionals looking to restart their careers after an extended absence from the workforce (e.g. time out caring for family, parental leave, national service, sabbatical and/or starting an own venture).
Come bring your difference and see what is possible for you at BAT. Learn more about our culture and our award winning employee experience here.
If you require any reasonable adjustments or accommodations to help you perform at your best during the recruitment process, you are encouraged to notify us. We are fully committed to support you by making appropriate arrangements for you to demonstrate your full potential

Responsibilities:

  • Actively create, maintain, and update documentation for all manufacturing processes for compliance with internal/ external teams to ensure process alignment with manufacturing processes.
  • Define strategy and logistics for FDA inspections and readiness, perform mock inspections and ensure training for inspections is developed and delivered.
  • Manage oversight and audit of regulatory processes such as Document Management, Change Control, Consumer Complaints, CAPA and Non-Conformance
  • Assist with the development and deployment of new materials and process improvement for new and modifies products at factory level, through specifications in SAP.
  • Act as key contact point for manufacturing to support trials, new Product implementations and monitoring of performance data in cooperation with the Product Team
  • Ensure the Data integrity based on protocols, regulations, and BAT intern guidelines.
  • Assist with product specification maintenance in accordance with product quality and PIM analysis.
  • Execute, ensure, and improve the activities of the Innovations team through materials standardization plans, savings opportunities, and process efficiency.


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Pharmaceuticals

IT Software - Other

Clinical Pharmacy

Graduate

Industrial engineering process engineering chemist or related field

Proficient

1

Monterrey, N. L., Mexico