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**Job Title:** Quality Assurance Manager

**Location:** Miami, FL (Local candidates only, or ability to relocate on own)

**Schedule:** Monday–Friday, First Shift

**Salary Range:** $120,000 – $150,000 per year

Summary

A fully onsite **Quality Assurance Manager** role is available for an experienced professional to lead and oversee all aspects of quality assurance within a pharmaceutical manufacturing environment. The ideal candidate will ensure compliance with regulatory standards, maintain robust quality systems, and drive continuous improvement initiatives to support product quality and operational excellence.

Key Responsibilities

+ Oversee and maintain company **quality systems** to ensure compliance with regulatory and internal standards.

+ Lead, train, and develop QA staff while promoting a culture of quality and continuous improvement.

+ Participate in management meetings to align quality initiatives with business goals.

+ Host and support **FDA inspections** and **GMP audits** .

+ Review and approve **batch records, deviations, CAPAs, change controls, and validation protocols** .

+ Supervise the development and maintenance of **product and raw material specifications** .

+ Review and analyze quality data to identify trends, root causes, and opportunities for corrective action.

+ Coordinate and implement **internal quality audits** and track follow-up actions.

+ Manage **customer complaints** , ensuring timely investigation and resolution.

+ Support **international documentation and registration** for products.

+ Collaborate with cross-functional teams to ensure consistent quality standards throughout production and packaging.

+ Recommend and implement **corrective and preventive actions (CAPAs)** to maintain product quality and compliance.

Qualifications

+ Bachelor’s degree in a scientific discipline (Biology, Chemistry, Microbiology, Pharmacy, Engineering, etc.) or equivalent combination of education and experience.

+ Minimum **10 years of experience** in the **pharmaceutical industry** , specifically with **solid oral dosage forms** .

+ In-depth knowledge of **cGMPs** , **FDA regulations** , and **FDA Guidance** .

+ Proven leadership experience with the ability to mentor and develop high-performing teams.

+ Strong organizational skills and the ability to manage multiple projects simultaneously.

+ Excellent communication, analytical, and problem-solving abilities.

+ Proficient in documentation management and computer systems used in regulated environments.

+ Ability to work effectively under pressure and meet tight deadlines.

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (https://www.mykelly.com/help-support-working-with-kelly-us/#Benefits) for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly ® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly’s Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.