Supervisor II, Quality Assurance (2nd Shift)

Hispanic Alliance for Career Enhancement; Cataluña; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company in Spain is seeking a Quality Assurance Supervisor II to oversee the Quality Assurance team in manufacturing operations. Responsibilities include ensuring GMP compliance, leading process improvements, and providing Quality support on the manufacturing floor. The ideal candidate will have a degree in sciences or engineering, 2+ years of manufacturing experience, and a strong understanding of FDA regulations. This role requires a commitment to high performance and mentorship of the team.

Servicios

Paid time off (vacation, holidays, sick)

Medical/dental/vision insurance

401(k) plan

Formación

• 2+ years of experience in a manufacturing production environment.
• Experience in regulated pharmaceutical industry is preferred.
• Thorough knowledge of Quality Assurance operations including safety and FDA regulations.

Responsabilidades

• Lead a high performing team and ensure quality compliance.
• Provide Quality support on the manufacturing shop floor.
• Review and release batch records and manage training needs.

Conocimientos

Effective problem-solving

Decision-making

Teamwork

Negotiation

Conflict resolution

Educación

Bachelor's degree in sciences or engineering

Descripción del empleo

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 at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

Purpose

The Quality Assurance Supervisor II is responsible for the organization, administration, and supervision of Quality Assurance employees within the manufacturing operations. Responsible for properly overseeing the day-to-day operations by prioritizing shop floor presence. This includes delivering high levels of customer service, ensuring quality of product and services, complying with all regulatory requirements, achieving desired financial performance including cost reductions, and building a culture of high performance for the team. Ensures that appropriate controls are developed and maintained for new, intermediate and finished products. Responsible for GMP compliance, manufacturing quality, product control and release, system execution and quality planning for the manufacturing areas that it supports. The Quality Assurance Supervisor II is expected to work independently and serve as a mentor to other supervisors.

Responsibilities

• Responsible for leading a high performing team and prioritizing presence with the team.
• Leads a team in the Quality function and is responsible for hiring, setting performance expectations, driving team engagement, providing continuous and on-time performance feedback, developing staff, assisting team in problem-solving, and handling employee matters. Ensures that the department has the appropriate talent and level of performance to meet business objectives. Monitors administration of training, identifies training needs, and development of team.
• Provide Quality support on the manufacturing shop floor.
• Responsible for supporting Operations efforts in meeting established production schedule.
• Partner with Operations employees to document exception documents, including re-inspection, and resolve other outstanding plant quality/compliance issues.
• Propose changes, updates, author, and implement departmental procedures consistent with objectives of simplification and process efficiencies/improvements which ensure ongoing compliance.
• Investigate QC hold, quarantine and reject for materials not meeting standards, ensure the initiation of exception documentation and oversee the implementation of any corrective action.
• Responsible for the review and approval of Procedures and Change Requests.
• Assist/serve/provide feedback on continuous improvement initiatives/teams.
• Reviews and releases batch records. May serve as a backup when the Quality Manager is unavailable. Performs other tasks/projects as assigned.

Significant Work Activities

• Frequent to continuous computer usage (greater or equal to 50% of the workday) is required.

Qualifications

• Bachelor's degree in sciences or engineering or equivalent experience.
• 2+ years of experience in a manufacturing production environment.
• Experience in regulated pharmaceutical industry is preferred.
• Thorough knowledge of Quality Assurance operations including safety, application of FDA and GMP regulations.
• Direct manufacturing and regulatory interface experience is preferred.
• Effective problem-solving, decision-making, teamwork, influence, negotiation, and conflict resolution skills required.
• Ability to work cross-functionally and coordinate work both within the department and with other departments.
• Ability to identify, communicate, and follow through to completion and assist in the development of necessary corrective action plans to resolve problems with supervision.
• Demonstrated strong leadership skills and ability to foster an inclusive environment.

The selected candidate must be available to work on an extended second shift and weekends.

Additional Information

• The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
• This job is eligible to participate in our short-term incentive programs.
• This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company’s sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

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.

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