Sr Mgr, Validation
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Job Location:
Heredia - Costa Rica
Monthly Salary:
Not Disclosed
Posted on:
4 days ago
Vacancies:
1 Vacancy
Job Summary
Manage the operational strategy of the validations area ensuring that the plants equipment processes and systems remain properly qualified and validated according to Allergan standards regulations and procedures as well as actively supporting business growth and continuous improvement.
KEY RESPONSIBILITIES:
- Identify best practices in resource management to ensure low turnover maximization of resources and appropriate results that guide the operational success of the company.
- Negotiate with client areas and external representatives on priorities and tasks regarding validation and associated studies safeguarding the main interests of the company.
- Coordinate with different areas regarding plant validation needs for equipment and processes.
- Identify the competencies of area resources to assign tasks to the personnel in charge ensuring results and providing appropriate follow-up.
- Facilitate task completion by providing administrative support focused training and specialized courses.
- Identify improvement opportunities and ensure the professional and personal growth of assigned resources.
- Participate in the development and implementation of new products and processes.
- Identify and actively implement process improvements.
- Ensure compliance with regulatory standards.
- Prepare and manage the assigned budget for the area.
- Participate in evaluating changes to validated processes.
Other duties:
- Ensure compliance with corporate and legal EHS requirements and global policies (integrity/ethics adverse events etc.) by adherence to applicable policies and internal procedures.
- All other functions inherent to the position and those assigned by your immediate supervisor.
- Ensure the motivation of team members by ensuring timely formal and informal reinforcement and recognition of behaviors that promote Allergans culture.
Qualifications :
Education and Experience:
- Masters Bachelors or Licentiate degree in Industrial Electrical Electronic Electromechanical Engineering Biotechnology Chemistry or related field.
- At least five years experience in quality areas including staff supervision.
- Experience in medical devices industry and validations
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Full-time
Key Skills
- Python
- SOC
- Debugging
- C/C++
- FDA Regulations
- Minitab
- Technical Writing
- GAMP
- OS Kernels
- Perl
- cGMP
- Manufacturing
About Company
AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more
