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AbbVie Supervisor-Quality Control (2nd Shift Wed-Sat 4:00p -2:30a) in Worcester, Massachusetts


Quality Control Supervisor oversees a business unit consisting of one of the following disciplines: API Laboratory Operations, Finished Goods Laboratory Operations, Environmental Monitoring, Raw Material/ In-Process Laboratory Operations, Laboratory Support Operations, Laboratory Continuous Improvement/Compliance Operations, Stability, Validation and support Regulatory Submissions.

The Quality Control Supervisor is 2nd Shift, Wednesday to Saturday from 4pm–2:30am .

What You’ll Do

  • Manage, lead, train and develop team to ensure that the department has the appropriate talent and level of performance to meet business objectives.

  • Assist subordinates in problem solving. Identify and resolve people issues without direct supervision.

  • Assure conformance to all government and corporate regulations. Responsible to develop, provide, defend, persuade Corporate/Plant practices with outside organizations. Routinely meet with regulators (FDA & EU) and customers to ensure no interruption in business due to compliance issues.

  • Direct area of responsibility to meet production objectives within planned budgets. Provide input to Supervisor for resources needed to construct budget, updates, and changes in financial plan. Supervise area supplies and equipment within budgeted amounts.

  • Establish and execute plans and commitments consistent to Development, Manufacturing, Customers and Business needs.

  • Provide timely testing or execution of in-process, raw materials, intermediates, API, finished goods, continuous improvement initiatives, QA training, laboratory equipment validation and stability depending on area of responsibility.

  • Apply advanced technical writing skills to prepare project protocol, and final reports to support product registration and/or business needs.

  • Conduct business, interact and negotiate with external contacts and customers to develop positive business relationships.

    What You’ll Have

  • An Associate’s or Bachelor’s Degree in Science related field.

  • Minimum 8+ years of relevant Quality Control Lab, Analytical Testing, HPLC, GMP experience. Previous supervisory or team lead experience preferred.

  • Demonstrated experience with high level of technical skill in technical lab operations and good understanding of related business.

  • Knowledge in Product Quality, Quality Control Lab Operation and Regulatory requirements is required.

  • Ability to work independently and make operational and business decisions to meet operational goals and business needs.

  • Experienced in developing team and managing the budget.

  • Skilled in interacting and establishing a positive interaction with internal and external customers.

  • Shows broad understanding of the issues relevant to technical/science and business.

  • Strong creative problem solving and analytical skills.

    What You’ll Receive

  • Comprehensive Healthcare: Medical, Vision, Dental, FSA, HSA

  • Financial Well-being, Planning & Stability: 401(k) with company match and Annual Retirement Contribution Plan

  • AbbVie Vitality: Health & Wellness programs including Employee Assistance Program (EAP), Health Advocate, Global Well-Being Programs

  • Generous Paid Time Off include, Company Holidays, Vacation, Parental and Caregiver Leave

  • Community Outreach Programs and company match of charitable contributions

  • Perks include AbbVie Product Shop, Employee Loyalty Program, Tuition Assistance, Adoption and Surrogacy Assistance, Mothers at Work and Milk Stork to list a few

At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity and affirmative action employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. If you would like to view a copy of the company’s affirmative action plan or policy statement, please email