Senior Quality Analyst (2nd & 3rd shift)

AbbVie; Barceloneta (PR); On-site; USD 80,500 - 156,500; Full time

Benefits offered by this job

401(k)

Medical insurance

Dental insurance

Vision insurance

PTO

Job summary

AbbVie seeks a Senior Quality Analyst to support routine operations, ensure quality goals are met, and back up the QA Manager on 2nd and 3rd shifts in a biotechnology environment.

This role participates in cross-functional teams, aligns with regulatory requirements, and contributes to continuous improvement within the AbbVie Quality System.

Qualifications

• Bachelor's degree in biotech, chemistry or engineering.
• Master's degree preferred.
• 4 years in pharma/biotech in similar role.
• Knowledge of GMP and safety regulations.
• Excellent English and Spanish communication.

Responsibilities

• Support routine operations to meet quality goals and comply with AbbVie policies.
• Ensure plant event investigations are timely and well documented.
• Perform product impact analyses and place QA holds when needed.
• Participate in Validation Review Board and approve SOPs and risk documents.
• Provide calibration approvals and maintain compliant records.
• Collaborate with other Quality areas and plant departments.
• Support internal and external audits.
• Assist with new product introductions and risk assessments.

Skills

Quality assurance

Regulatory compliance

Statistical analysis

Quality investigations

Bilingual English/Spanish

Education

Bachelor's in Biotechnology/Engineering

Master's in Science preferred

Job description

Senior Quality Analyst (2nd & 3rd shift)

• Full-time
• Salary Min: 80500
• Therapy Area: Other Specialties
• Salary Max: 156500
• Workday Global Grade: 14
• Travel: No
• Compensation: USD 80,500 - USD 156,500 - yearly

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Responsible for implementing and maintaining the effectiveness of the Quality System. Support manufacturing operations in the resolution of events, impact assessment and documentation discrepancies. Provide guidance for product/process impact analysis, perform holistic evaluation of events, review and approve investigations and risk based evaluations in support to routine operations and product disposition.

Responsibilities

• Support routine operations to ensure that all quality goals are met, and all practices and procedures comply with AbbVie policies and applicable regulations for the Quality areas under responsibility. Serve as backup for the QA Manager leading the team and providing support to quality initiatives.
• Ensures investigations of plant events are evaluated in a timely manner; completed thoroughly and documented accurately in the plant CAPA system.
• Performs product impact analyses for plant events and places product on QA hold where appropriate.
• Participates on the Validation Review Board as the Manufacturing Quality Assurance function. Approves standard operating procedures; change management and risk management documents. Ensures all documents are in compliance with Abbvie global procedures and regulatory requirements.
• Approves calibration requests, calibration out of tolerance and preventive maintenance records. Ensures that these documents have appropriate justifications according to product /process limits established. Demonstrates accountability and responsibility of EHS performance and compliance.
• Maintains an effective liaison and cooperative relationship with other Quality areas and Plant departments. Oversees manufacturing operations to ensure practices are in alignment with approved procedures.
• Provide support to the Compliance team during internal and external audits as required.
• Provide guidance for new product introduction activities. Develop risk assessments to support manufacturing activities for new products and ensure material control until regulatory approval.
• Conform to EHS management system requirements and compliance obligations, promote continuous improvement, and consider EHS aspects during the design and change process. Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal, and any other program applicable according to the position duties.

Qualifications

• Bachelors Degree in Biotechnology, Biology, Chemistry or Engineering.
• Masters Degree in Science, preferred.
• Four (4) years of experience in Pharmaceutical/Biotechnology industry in a similar position.
• This position requires knowledge of quality / compliance / Investigations / Risk management as well as regulations and standards affecting biological products.
• Excellent written and spoken communication skills in English and Spanish.
• Knowledge of GMP, safety regulations.
• Quality/compliance management skills.
• Fast paced and adaptable to continuously changing environment. Subject to work with multiple priorities and interruptions and under reasonable pressure due to the nature and function of the area.
• Sound decision making and problems solving skills to assure business unit compliance.
• Strong analytical skills, ability to analyze data and trends and draw conclusions.
• Good mathematics background with an understanding of basic statistical concepts.
• Availability for second (2) and third (3) shift.

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law. 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.

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 employer 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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