Quality Assurance Manager

32806 Orlando, Florida Signature Aviation

Posted 1 day ago

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Job Description

We are seeking a highly skilled and detail-oriented Manager, Quality Assurance lead and oversee the QA processes and strategies within our IT department. In this role, you will be responsible for ensuring the delivery of high-quality software and IT systems by establishing robust testing frameworks, managing QA teams, and driving continuous improvement in testing methodologies. The ideal candidate will possess a strong background in QA practices, excellent leadership skills, and a deep understanding of IT systems and software development life cycles.
+ Lead, mentor, and manage a team of QA professionals, fostering a culture of quality and continuous improvement.
+ Define team objectives and ensure alignment with organizational goals.
+ Provide training and development opportunities to enhance team capabilities and skills.
+ Develop and implement a comprehensive QA strategy, ensuring it aligns with the organization's IT and business objectives.
+ Establish and maintain QA standards, processes, and best practices across all IT projects.
+ Select and implement testing tools and frameworks to streamline and automate testing processes.
+ Oversee the creation of test plans, test cases, and test scripts to ensure thorough validation of software and systems.
+ Monitor the effectiveness of testing efforts and make improvements as necessary.
+ Work closely with development, product management, and operations teams to define quality goals and address any issues that arise.
+ Act as the primary point of contact for QA-related matters, ensuring timely communication with stakeholders.
+ Track and manage defects to ensure timely resolution and report on trends and metrics.
+ Develop and enforce processes for identifying, documenting, and addressing software defects.
+ Define key performance indicators (KPIs) for QA efforts and regularly report on progress to leadership.
+ Analyze testing results to provide insights and recommendations for process improvements.
+ Ensure compliance with regulatory and security standards related to IT quality and testing.
+ Identify risks related to software quality and implement mitigation strategies.
**Minimum Education and/or Experience:**
+ Bachelor's degree in Computer Science, Information Technology, or a related field.
+ 5+ years of experience in quality assurance, with at least 2 years in a leadership role.
+ Proven expertise in managing QA processes for software development and IT systems.
+ Proficiency in automated testing tools (e.g., Selenium, TestComplete, JUnit).
+ Knowledge of software development lifecycle (SDLC) and Agile methodologies.
+ Experience with performance testing tools (e.g., JMeter, LoadRunner) is a plus.
+ Certification in quality management or testing (e.g., ISTQB, CSTE, Six Sigma).
+ Experience with cloud-based systems and DevOps environments.
+ Familiarity with continuous integration/continuous deployment (CI/CD) pipelines.
**Additional knowledge and skills:**
+ Exceptional leadership and team management skills.
+ Excellent communication and interpersonal skills, with the ability to influence and inspire others.
+ Comfortable in highly dynamic and frequently ambiguous environments.
+ Strategic thinking and analytical skills.
+ Strong organizational skills with the ability to manage complex and competing priorities.
+ Ability to work collaboratively in a cross-functional team environment.
With more than 225 locations worldwide, Signature Aviation is the largest global network of private aviation terminals, delivering safe, convenient, and elevated experiences to those we serve. As a premier hospitality organization and a certified Great Place to Work, we are committed to redefining private air travel. Our nearly 6,000-strong team of aviation experts and enthusiasts is dedicated to delivering excellence to our guests and communities, and it starts with taking care of our team. Signature provides a variety of benefits, programs, and resources to support our team members' overall well-being and professional development. We proudly volunteer and give back, focusing on elevating the neighborhoods where we operate, empowering the next generation of aviation professionals, and supporting our veterans.
From your health to your financial wellness, there are several benefits for you and your family when joining Signature Aviation.
**Our Benefits:**
+ Medical/prescription drug, dental, and vision Insurance
+ Health Savings Account
+ Flexible Spending Accounts
+ Life Insurance
+ Disability Insurance
+ 401(k)
+ Critical Illness, Hospital Indemnity and Accident Insurance
+ Identity Theft and Legal Services
+ Paid time off
+ Paid Maternity Leave
+ Tuition reimbursement
+ Training and Development
+ Employee Assistance Program (EAP) & Perks
Qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, or other protected characteristics.
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Quality Assurance Technician

32801 Orlando, Florida Coca-Cola Beverages Florida

Posted 26 days ago

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Job Description

Permanent
Coke Florida is looking for a Quality Assurance Technician based out of our Orlando location.

We are looking for 3rd shift, working 9:00PM - 5:30AM, weekend availability is required.

What You Will Do:

As a Coke Florida Quality Assurance Technician, you will be responsible for conducting qualitative and quantitative testing of beverages, syrups, and rawmaterials throughout the entire production process, ensuring products and packaging meets standards.

Roles and Responsibilities:

  • Responsible for blending syrup batches for multiple flavors, including Carbonated, Non-Carbonated Beverages
  • Receive and store concentrate loads following FEFO/FIFO
  • Complete blind receivers
  • Drive a PIT (Power Industrial Truck/ Forklift) safely to move raw materials
  • Operate a lift table to bring materials to blending area
  • Perform Tank and Blending System CIP (Clean in Place)
  • Perform Water Treatment backwash and Regent
  • Unload High Fructose Corn Syrup from Railcars into Silos
  • General area housekeeping

For this role, you will need:
  • High school diploma or GED required
  • Bachelor's degree in science related field preferred
  • 1-3 years prior production/manufacturing experience or 2+ years relevant lab technician experience.
  • Food/beverage industry experience a plus.
  • Demonstrated attention to detail and accuracy.
  • Strong analytical skills.
  • Ability to read, write, and keep records.
  • Good computer skills including literacy with Excel and Word.
  • Familiarity with lab safety and handling of hazardous materials.
  • Blending experience is a must.

Additional qualifications that will make you successful in this role
  • Bachelor's degree in science related field preferred
  • Food/beverage industry experience a plus
This job description is not an exhaustive list of all functions that the employee may be required to perform, and the employee may be required to perform additional functions. Coke Florida reserves the right to revise the job description at any time and to assign additional duties and responsibilities as needed.

Employment with Coke Florida is at-will. The employee must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations may be made to enable qualified individuals with disabilities to perform essential functions of their job, absent undue hardship.

Coca-Cola Beverages Florida is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state or local protected class.

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Quality Assurance Restoration Technician

34747 Kissimmee, Florida IICRC

Posted 6 days ago

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Job Description

Join The Servpro Family

We pride ourselves on being the best at what we do, our family-oriented culture, long-term growth potential for our employees, and appreciate the value of diversity in the workplace. If you're a motivated, hard-working individual, who values the importance of a job well done, strong customer service experience and a passion for the restoration industry, then we want you on our winning team!

What You'll Do:

Performs setup and monitoring along with job closeout and quality assurance inspections. Has general knowledge of the residential and commercial construction practices along with a strong passion for customer service. You will be following practices and procedures and may be required to use said knowledge to collect and provide prompt accurate data used to measure and monitor the quality of work performed in the field. Performs a variety of tasks. Works under general supervision. A certain degree of creativity and latitude is required. Reports to Operations Manager or equivalent. This is a safety sensitive position.

  • Ensure customer satisfaction
  • Troubleshoot and diagnose problems with setup and operation of drying and cleaning equipment.
  • Provide on-site resolution to observed problems that may include site clean-up, documentation completion and recording of photos, videos and technical information.
  • Effectively communicate with customers and office staff
  • Promptly and accurately complete all required paperwork
  • Perform maintenance on various types of equipment and structures
  • Quality inspections of job site
  • Initiative to train and develop using the company provided resources
  • Keep manager informed of new developments, changes or customer concerns
  • Other tasks (administrative or other) per process or as defined by management team
  • Train entry level employees as required
Job Essentials For Success:
  • #1: Customer Service Oriented
  • Able to clearly and confidently educate customers on our products and services
  • Minimum of 2-year experience in a similar industry
  • Clean 3 Year Driving Record
  • Team player
  • Able to also work well independently
  • Coachable
What We Offer:
  • Company Vehicle and Phone
  • *SPIFF/BONUS INCENTIVES*
  • Paid Holidays
  • Paid Training
  • Health Benefits!
  • Work Life Balance
  • A company that believes your success and growth

This is a safety-sensitive position. Applicants are subject to a background check, must be authorized to work in the United States. Must not have any violent or sexual related felonies.

Benefits:
  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Health insurance
  • Life insurance
  • Vacation time off
  • Referral program
  • Vision insurance
Schedule:
  • 8 hour shift
  • Monday to Friday
  • On call
  • Weekend availability

Compensation: $23.00 - $31.00 per hour

Picture Yourself Here Fulfilling Your Potential.

At SERVPRO, you can make a positive difference in people's lives each and every day! We're seeking self-motivated, proactive, responsible, and service-oriented teammates to join us in our mission of helping customers in their greatest moments of need by repairing and restoring homes and businesses with an industry-leading level of service. With nearly 2,000 franchises all over the country, finding exciting and rewarding SERVPRO career opportunities near you is easy! We look forward to hearing from you.

All employees of a SERVPRO Franchise are hired by, employed by, and under the sole supervision and control of an independently owned and operated SERVPRO Franchise. SERVPRO Franchise employees are not employed by, jointly employed by, agents of, or under the supervision or control of Servpro Franchisor, LLC, in any manner whatsoever.

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Quality Assurance Manager - Manufacturing

32801 Orlando, Florida $110000 Annually WhatJobs

Posted 7 days ago

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Job Description

full-time
Our client is seeking a dynamic and experienced Quality Assurance Manager to oversee and enhance the quality management systems within their manufacturing operations. This role is critical in ensuring that all products meet stringent quality standards and regulatory requirements. You will be responsible for developing, implementing, and maintaining comprehensive quality assurance programs, including inspection, testing, and process control procedures. Key duties involve leading the QA team, conducting internal audits, investigating quality deviations, and implementing corrective and preventive actions (CAPA). You will also work closely with production, engineering, and R&D teams to drive continuous improvement initiatives and resolve quality-related issues. The ideal candidate will possess a deep understanding of quality management principles (e.g., ISO 9001, Six Sigma, Lean Manufacturing) and extensive experience in a manufacturing QA environment. Strong analytical, problem-solving, and leadership skills are essential. You will be responsible for managing quality documentation, ensuring compliance with industry standards, and reporting on quality performance metrics to senior management. This is a hybrid role, requiring on-site presence at Orlando, Florida, US , for critical team collaboration, process oversight, and direct interaction with production facilities, while also allowing for remote work flexibility for strategic planning and reporting. A Bachelor's degree in Engineering, Quality Management, or a related technical field is required. Advanced certifications such as ASQ Certified Quality Manager (CQM) are highly preferred. A minimum of 7 years of experience in quality assurance, with at least 3 years in a management capacity within the manufacturing sector, is necessary. Excellent communication skills and the ability to influence cross-functional teams are vital for success.
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Senior Pharmaceutical Quality Assurance Specialist

32801 Orlando, Florida $115000 Annually WhatJobs

Posted 7 days ago

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Job Description

full-time
Our client, a globally recognized pharmaceutical company committed to advancing human health, is seeking a highly meticulous and experienced Senior Pharmaceutical Quality Assurance Specialist. This role is crucial in ensuring that all manufactured pharmaceutical products meet stringent quality standards, regulatory requirements, and internal protocols. The ideal candidate will possess a deep understanding of Good Manufacturing Practices (GMP), quality control methodologies, and regulatory affairs within the pharmaceutical industry. This position offers the flexibility of remote work, allowing you to contribute your expertise to our mission of developing life-saving and life-enhancing medications from your home office.

Responsibilities:
  • Develop, implement, and maintain robust quality assurance systems and procedures in compliance with FDA, EMA, and other relevant global regulatory guidelines.
  • Conduct thorough reviews of batch records, validation protocols, and reports to ensure accuracy, completeness, and adherence to specifications.
  • Participate in internal and external audits, inspections, and regulatory submissions, ensuring the company's readiness and compliance.
  • Investigate deviations, out-of-specification (OOS) results, and customer complaints, performing root cause analysis and implementing corrective and preventive actions (CAPAs).
  • Oversee the change control process, assessing the impact of proposed changes on product quality and regulatory compliance.
  • Collaborate with manufacturing, R&D, and regulatory affairs departments to address quality issues and drive continuous improvement.
  • Develop and deliver training programs on GMP and quality systems for relevant personnel.
  • Monitor and analyze quality metrics, identifying trends and recommending improvements to enhance product quality and process efficiency.
  • Stay updated on evolving regulatory requirements and industry best practices in pharmaceutical quality assurance.
  • Manage external vendor quality agreements and conduct vendor audits as needed.
  • Prepare and present quality reports and findings to management and cross-functional teams.
Qualifications:
  • Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field. Master's degree is a plus.
  • Minimum of 6 years of experience in Quality Assurance or Quality Control within the pharmaceutical or biopharmaceutical industry.
  • In-depth knowledge of cGMP regulations (21 CFR Parts 210/211, ICH guidelines).
  • Proven experience with deviation management, CAPA systems, change control, and batch record review.
  • Strong understanding of pharmaceutical manufacturing processes and quality control testing.
  • Excellent analytical, problem-solving, and critical thinking skills.
  • Exceptional attention to detail and accuracy.
  • Strong written and verbal communication skills, with the ability to effectively communicate complex quality concepts.
  • Demonstrated ability to work independently and manage multiple priorities effectively in a remote setting.
  • Experience with electronic quality management systems (eQMS) is desirable.
This is an exceptional opportunity to contribute significantly to the quality and compliance of vital pharmaceutical products while enjoying the flexibility of a remote role. If you are a dedicated QA professional passionate about ensuring patient safety and product integrity, we encourage you to apply.
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Lead Pharmaceutical Quality Assurance Manager

32801 Orlando, Florida $175000 Annually WhatJobs

Posted 7 days ago

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Job Description

full-time
Our client, a leading pharmaceutical company, is seeking an experienced and highly motivated Lead Pharmaceutical Quality Assurance Manager to join our team in Orlando, Florida, US . This role is essential for ensuring that our products meet the highest standards of quality, safety, and efficacy. You will lead a team of QA professionals, oversee the implementation and maintenance of quality management systems, and ensure compliance with all relevant regulatory requirements, including FDA, EMA, and other global health authorities. The ideal candidate will have a deep understanding of pharmaceutical manufacturing processes, GxP regulations, and a strong commitment to quality excellence.

Key Responsibilities:
  • Lead and manage the Pharmaceutical Quality Assurance department, providing strategic direction and oversight.
  • Develop, implement, and maintain a robust Quality Management System (QMS) in compliance with GxP guidelines.
  • Oversee the qualification and validation of manufacturing processes, equipment, and facilities.
  • Manage all aspects of batch record review and product release.
  • Conduct internal audits and support external regulatory inspections and audits by customers.
  • Investigate deviations, CAPAs, and change controls, ensuring timely and effective resolution.
  • Develop and deliver training programs on quality systems and GxP compliance for relevant personnel.
  • Monitor key quality performance indicators (KPIs) and report on quality metrics to senior management.
  • Ensure compliance with all applicable regulatory requirements and industry best practices.
  • Manage supplier quality and conduct audits of contract manufacturers and raw material suppliers.
  • Contribute to the continuous improvement of quality processes and systems.
  • Mentor and develop QA staff, fostering a culture of quality and compliance.
Qualifications:
  • Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
  • Minimum of 10 years of progressive experience in Quality Assurance within the pharmaceutical industry.
  • Minimum of 5 years in a management or supervisory role.
  • Extensive knowledge of GxP regulations (GMP, GCP, GLP) and international pharmaceutical guidelines.
  • Proven experience in developing and implementing QMS, including SOPs, CAPAs, change control, and deviation management.
  • Strong understanding of pharmaceutical manufacturing processes, analytical testing, and stability studies.
  • Experience with regulatory agency inspections (FDA, EMA, etc.).
  • Excellent leadership, project management, and problem-solving skills.
  • Strong written and verbal communication skills, with the ability to effectively interact with all levels of the organization and regulatory agencies.
  • Detail-oriented with a strong commitment to accuracy and compliance.
This hybrid role requires a significant presence in our Orlando, Florida, US office, with flexibility for remote work on approved tasks. We offer a competitive compensation package, comprehensive benefits, and a challenging yet rewarding career path.
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Senior Pharmaceutical Quality Assurance Engineer

32801 Orlando, Florida $110000 Annually WhatJobs

Posted 7 days ago

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Job Description

full-time
Our client is looking for a highly skilled Senior Pharmaceutical Quality Assurance Engineer to join their innovative team. This role plays a critical part in ensuring the highest standards of quality and compliance throughout the pharmaceutical product lifecycle. You will be responsible for developing, implementing, and maintaining robust quality assurance systems and processes, including those related to GMP (Good Manufacturing Practices), validation, documentation, and regulatory affairs. Your expertise will be crucial in conducting internal audits, investigating deviations, and implementing corrective and preventive actions (CAPA) to uphold product integrity. This position involves close collaboration with research and development, manufacturing, and regulatory departments to ensure all products meet stringent industry standards and regulatory requirements. You will also be involved in the review and approval of critical documentation, such as batch records, validation protocols, and SOPs. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, analytical testing, and regulatory guidelines (FDA, EMA, etc.). Excellent analytical and problem-solving skills, attention to detail, and the ability to manage multiple projects concurrently are essential. This role requires a proactive approach to identifying potential risks and opportunities for quality improvement. You will contribute significantly to the continuous improvement of our client's quality management system, ensuring the safety and efficacy of pharmaceutical products. This is a hybrid role, requiring some on-site presence in our Orlando, Florida, US facility for critical meetings, audits, and team collaboration, while offering flexibility for remote work on other days.
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Senior Pharmaceutical Quality Assurance Manager

32801 Orlando, Florida $120000 Annually WhatJobs

Posted 7 days ago

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Job Description

full-time
Our client, a leader in the pharmaceutical industry, is seeking a highly experienced Senior Pharmaceutical Quality Assurance Manager to join their team in Orlando, Florida, US . This critical role will be responsible for ensuring that all pharmaceutical products meet stringent quality standards and comply with regulatory requirements. The ideal candidate will possess a deep understanding of cGMP (current Good Manufacturing Practices), quality control processes, and regulatory affairs within the pharmaceutical sector. This position requires strong leadership, analytical skills, and a commitment to maintaining the highest levels of product quality and patient safety.

Responsibilities:
  • Develop, implement, and maintain robust quality management systems (QMS) in accordance with cGMP and other relevant regulatory guidelines (e.g., FDA, EMA).
  • Oversee all aspects of quality assurance, including batch record review, deviation management, change control, CAPA (Corrective and Preventive Actions), and OOS (Out-of-Specification) investigations.
  • Lead and mentor the Quality Assurance team, providing guidance, training, and performance management.
  • Conduct internal audits and participate in external audits (regulatory agencies, customers, partners) to ensure compliance and identify areas for improvement.
  • Review and approve validation protocols and reports for equipment, processes, and analytical methods.
  • Collaborate with manufacturing, R&D, and regulatory affairs departments to ensure product quality throughout the product lifecycle.
  • Monitor key quality metrics and performance indicators, reporting on quality trends and recommending strategic improvements.
  • Ensure that all personnel are adequately trained on quality procedures and cGMP requirements.
  • Manage supplier quality agreements and perform supplier audits to ensure the quality of raw materials and components.
  • Stay abreast of evolving regulatory requirements and industry best practices in pharmaceutical quality assurance.
  • Lead continuous improvement initiatives to enhance the efficiency and effectiveness of the QMS.
  • Manage product quality complaints and investigations.
  • Represent the QA department in cross-functional project teams.
Qualifications:
  • Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field. Ph.D. is a plus.
  • Minimum of 8 years of progressive experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry, with at least 3 years in a management or supervisory role.
  • In-depth knowledge of cGMP, ICH guidelines, and other relevant regulatory standards.
  • Proven experience in managing and implementing QMS components such as deviation handling, change control, CAPA, and batch record review.
  • Strong understanding of pharmaceutical manufacturing processes, quality control testing, and validation principles.
  • Excellent analytical, problem-solving, and decision-making skills.
  • Exceptional leadership, communication, and interpersonal skills.
  • Ability to effectively manage teams and influence cross-functional stakeholders.
  • Experience with regulatory inspections (FDA, EMA) is essential.
  • Proficiency in quality management software and Microsoft Office Suite.
  • Detail-oriented with a strong commitment to quality and compliance.
This is a significant opportunity to contribute to ensuring the safety and efficacy of vital pharmaceutical products.
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Quality Assurance Technician - Night Shift

32801 Orlando, Florida Coca-Cola Beverages Florida

Posted 1 day ago

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Job Description

Permanent
Coke Florida is looking for a Quality Assurance Technician based out of our Orlando location.

We are looking for 3rd shift, working 9:00PM - 5:30AM, weekend availability is required as needed.

What You Will Do:

As a Coke Florida Quality Assurance Technician, you will be responsible for conducting qualitative and quantitative testing of beverages, syrups, and rawmaterials throughout the entire production process, ensuring products and packaging meets standards.

Roles and Responsibilities:

  • Responsible for blending syrup batches for multiple flavors, including Carbonated, Non-Carbonated Beverages
  • Receive and store concentrate loads following FEFO/FIFO
  • Complete blind receivers
  • Drive a PIT (Power Industrial Truck/ Forklift) safely to move raw materials
  • Operate a lift table to bring materials to blending area
  • Perform Tank and Blending System CIP (Clean in Place)
  • Perform Water Treatment backwash and Regent
  • Unload High Fructose Corn Syrup from Railcars into Silos
  • General area housekeeping

For this role, you will need:
  • High school diploma or GED required
  • Bachelor's degree in science related field preferred
  • 1-3 years prior production/manufacturing experience or 2+ years relevant lab technician experience.
  • Food/beverage industry experience a plus.
  • Demonstrated attention to detail and accuracy.
  • Strong analytical skills.
  • Ability to read, write, and keep records.
  • Good computer skills including literacy with Excel and Word.
  • Familiarity with lab safety and handling of hazardous materials.
  • Blending experience is a must.

Additional qualifications that will make you successful in this role
  • Bachelor's degree in science related field preferred
  • Food/beverage industry experience a plus
This job description is not an exhaustive list of all functions that the employee may be required to perform, and the employee may be required to perform additional functions. Coke Florida reserves the right to revise the job description at any time and to assign additional duties and responsibilities as needed.

Employment with Coke Florida is at-will. The employee must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations may be made to enable qualified individuals with disabilities to perform essential functions of their job, absent undue hardship.

Coca-Cola Beverages Florida is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state or local protected class.

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Remote Senior Pharmaceutical Quality Assurance Manager

32801 Orlando, Florida $140000 Annually WhatJobs

Posted 7 days ago

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Job Description

full-time
Our client, a dynamic and growing pharmaceutical company, is seeking a highly experienced Senior Pharmaceutical Quality Assurance Manager to join their fully remote team. This critical role is responsible for ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements throughout their lifecycle. The Senior QA Manager will lead the development, implementation, and maintenance of robust quality management systems (QMS) across the organization. Key responsibilities include overseeing batch record reviews, managing deviations and CAPAs, conducting internal and external audits, and ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulations. You will collaborate closely with R&D, manufacturing, regulatory affairs, and other departments to uphold the highest levels of product quality and patient safety. This position is entirely remote, requiring excellent communication, organizational, and time management skills to effectively manage quality operations from any location. The ideal candidate will have a deep understanding of pharmaceutical manufacturing processes, regulatory frameworks (e.g., FDA, EMA), and a proven track record in quality assurance leadership. We are looking for a meticulous and detail-oriented professional with strong analytical and problem-solving abilities, who is committed to driving quality excellence and continuous improvement in a remote-first environment. This is an exceptional opportunity to contribute to the development and delivery of life-saving medications from a location of your choice.
Responsibilities:
  • Develop, implement, and manage the company's Quality Management System (QMS).
  • Ensure compliance with GMP, GLP, and other relevant pharmaceutical regulations.
  • Oversee batch record reviews and release processes.
  • Manage deviation investigations, root cause analysis, and Corrective and Preventive Actions (CAPA).
  • Plan and conduct internal and external quality audits.
  • Collaborate with cross-functional teams to ensure product quality and safety.
  • Review and approve validation protocols and reports.
  • Stay current with regulatory changes and industry best practices.
  • Train personnel on quality assurance principles and procedures.
  • Prepare for and host regulatory inspections.
Qualifications:
  • Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field; Advanced degree preferred.
  • Minimum of 8 years of experience in pharmaceutical quality assurance or quality control.
  • In-depth knowledge of GMP, GLP, ICH guidelines, and regulatory requirements.
  • Proven experience in developing and implementing QMS.
  • Strong experience with deviation management, CAPA, and change control processes.
  • Excellent analytical, problem-solving, and decision-making skills.
  • Exceptional written and verbal communication skills.
  • Demonstrated ability to lead teams and influence stakeholders in a remote setting.
  • Experience with regulatory inspections (FDA, EMA, etc.).
Apply Now
 

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