Manufacturing Analyst (Project)

Allergan; São Paulo; Presencial; BRL 30.000 - 60.000; Tempo integral

Resumo da oferta

An established industry player is seeking a Manufacturing Analyst to join their Core Operations team. This role involves providing technical support for manufacturing processes, troubleshooting issues, and optimizing operations. Candidates should possess a Bachelor's degree in science and have a minimum of 2 years of relevant experience. With a commitment to work-life balance and career development, this position offers a unique opportunity to contribute to innovative solutions in the healthcare sector. Join a team dedicated to transforming lives and making a significant impact in the industry.

Qualificações

• Bachelor's degree in science or related field preferred.
• Minimum of 2 years' experience in a similar role required.

Responsabilidades

• Provide technical support to manufacturing and chemistry-related issues.
• Develop process control recipes for NPIs and optimize existing processes.

Conhecimentos

Technical Support

Troubleshooting

Process Optimization

Data Integrity

Interpersonal Communication

Formação académica

Bachelor's degree in Science

Ferramentas

SAP

S4HANA

Descrição da oferta de emprego

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onX,Facebook,Instagram,YouTube,LinkedInandTik Tok.

Job Description

We believe the paths we take to achieving our breakthroughs matter. At AbbVie, everyone of our 50,000* employees is a part of shaping those paths—and defining our way forward.

We are now recruiting experiencedManufacturing Analyst to join our Core 1 Operations team in AbbVie Westport, Co Mayo.

In the role, you will be performing focused work to provide technical support to the business specifically on the 607 project. You will also support day-day operations activities within the operations function.Other aspects of this role are QMS, compiling and review of project documentation (e.g., SOPs, methods, Master records, Batch Records, Reports). The candidate will also be coordinating with several departments to holistically develop technical and leadership skills.

If great benefits, a defined career path, and work-life balance are important in your next career move, then read on to find out more:

Key activities:

• Provide technical support to all manufacturing and chemistry related issues. Tasks include, daily trouble shooting, optimization, cost reduction, training and coaching of manufacturing personnel
• Support of process front runs / use tests for both NPI and commercial processes.
• When required support commercial operation activities
• Development of process control recipes for NPIs and optimization of existing commercial process recipes
• Ensure all batch records components are present and that all corrections identified during initial review and by Product Release Team are addressed in a timely and compliant manner.
• Use and maintenance of data within key systems such as SAP, S4HANA.
• Participate in non-conformance and exception investigations as necessary.
• Work with QA Teams to align and promote awareness on data integrity and good documentation practices.
• Facilitate and coordinate with project teams to enhance, improve and streamline batch records.
• Provide on-the-floor technical support to the Production Team Leaders for process/equipment optimization and troubleshooting
• Provide assistance when required at Regulatory Inspections.
• Trending and c-ordination of customer complaints investigations.
• Work close with department on corrective actions arising from Environmental excursions.
• Comply with AbbVie policies and procedures and regulatory agency regulations.

Qualifications

Education and preferred experience:

• Bachelor’s degree in science, or a related field is preferred and/or a minimum of 2 years’ experience in a similar role.
• Detailed knowledge of CGMP and aseptic practices, data integrity requirements and GDP is required for this role.
• Strong organizational skills and attention to detail are essential for this role.
• Good interpersonal relations/communications skills

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, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html