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Gmp Manager Jobs in Riviera Beach, FL (NOW HIRING)

Alphazyme

Manager, QA Operations

Jupiter, FL · On-site

The Manager, QA Operations is responsible for the implementation of policies and procedures to ... Industry experience in a Good Manufacturing Practice (GMP) environment is preferred * Thorough ...

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See Riviera Beach, FL salary details

$23.9K

$58.2K

$113.4K

How much do gmp manager jobs pay per year?

As of Sep 4, 2026, the average yearly pay for gmp manager in Riviera Beach, FL is $58,186.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,100.00 and $67,000.00 per year, depending on experience, location, and employer.

What is a GMP manager?

GMP Managers are professionals responsible for ensuring that manufacturing processes in industries such as pharmaceuticals, biotechnology, and food production comply with Good Manufacturing Practice (GMP) regulations. They oversee quality control, develop and implement standard operating procedures, and conduct internal audits to maintain regulatory standards. Their role is crucial for ensuring that products are consistently produced and controlled according to quality standards, thereby safeguarding consumer health and safety.

What are some common challenges faced by a GMP manager in maintaining regulatory compliance, and how are they typically addressed?

A GMP Manager often encounters challenges such as keeping up with evolving regulatory standards, ensuring consistent staff training, and managing thorough documentation. To address these, managers implement regular training programs, conduct internal audits to identify gaps, and foster a culture of quality across teams. Staying proactive about changes in regulations and collaborating with cross-functional teams helps ensure ongoing compliance and smooth inspections.

What are the key skills and qualifications needed to thrive as a GMP manager, and why are they important?

To thrive as a GMP Manager, you need in-depth knowledge of Good Manufacturing Practices, quality assurance, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with quality management systems (QMS), audit tools, and relevant certifications such as Six Sigma or ISO standards is typically required. Strong leadership, problem-solving abilities, and effective communication are vital soft skills for managing teams and ensuring adherence to regulations. These skills and qualifications ensure product safety, regulatory compliance, and continuous improvement within manufacturing processes.

What is the difference between Gmp Manager vs Quality Assurance Manager?

AspectGmp ManagerQuality Assurance Manager
CertificationsGMP certifications, Quality Management certificationsISO 9001, Quality Management certifications
Work EnvironmentPharmaceutical, biotech, or medical device manufacturingVarious industries including manufacturing, healthcare, and food
Employer & Industry UsageRegulated industries with strict compliance standardsBroadly used across multiple industries for quality oversight
Primary FocusEnsuring compliance with Good Manufacturing PracticesOverseeing overall quality assurance processes

The Gmp Manager primarily focuses on ensuring compliance with Good Manufacturing Practices in regulated industries like pharmaceuticals and biotech. In contrast, the Quality Assurance Manager oversees broader quality assurance processes across various industries. Both roles require similar certifications and work environments but differ in their specific compliance and quality scope.

What cities near Riviera Beach, FL are hiring for Gmp Manager jobs?

Cities near Riviera Beach, FL with the most Gmp Manager job openings:

Gmp Manager jobs near you

Manager, QA Operations

Alphazyme

Jupiter, FL • On-site

Full-time

Medical, Retirement, PTO

Re-posted 10 days ago

Job description

Who we are:
Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies.
At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitable culture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai's portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market.
Your next role as a Miracle Maker
Maravai LifeSciences is seeking a #MiracleMaker to join our Quality Assurance team as a Manager, QA Operations. The Manager, QA Operations is responsible for the implementation of policies and procedures to ensure adherence to production quality standards and oversight of the Company's electronic ISO 13485:2016 Quality Management System. The Quality Assurance Manager is expected to ensure compliance with operational, statutory, and regulatory requirements in support of the Company's business objectives.
How you will make an impact:
  • Manage Quality Assurance department day to day operations, including implementing training and performance management activities for direct reports
  • Implement and periodically evaluate documentation and policies to ensure continuous compliance to the quality, integrity, and efficiency standards set by the organization, the ISO 13485:2016 standard, and other statutory and regulatory requirements.
  • Collaborate with management to identify and fill documentation and process gaps required to maintain QMS compliance and address CAPAs, NCs, and audit findings
  • Author and maintain quality documentation, oversee timely reviews of all work instructions associated with production and quality control activities
  • Support Quality Control with customer complaints and Out of Specification (OOS) investigations
  • Actively participate on core teams and provide deliverables from QA on quality processes and required documentation practices from production through testing and shipment
  • Implement and track metrics to monitor performance associated with Quality management
  • Identify and implement efficiency improvement initiatives in support of Continuous Improvement
  • Facilitate proactive solutions by collecting and analyzing quality data
  • Manage Internal Audit Program
  • Perform other functions and duties as required

The skills and experience that you will bring:
  • Bachelor's Degree in Life Science, Biology, Chemistry or Pharmaceutical or related discipline
  • 3-5 years of managerial experience in non-academic biotechnology related industry
  • 1-3 years of supervisory experience
  • Proven experience with: ISO 13485 certification, federal regulations 21 CFR 820 and 21 CFR Part 11
  • Industry experience in a Good Manufacturing Practice (GMP) environment is preferred
  • Thorough knowledge of analytical testing industry standards and quality assurance methodologies
  • Excellent communication and presentation skills are required
  • Demonstrated scientific "problem solving" skills, translated into consultative selling process where the "win" is for both the client and the company
  • Ability to participate with others as a member of the team to ensure that demanding and difficult projects are handled smoothly and cooperatively to enhance success of project and maintain strong relationships within all parts of company
  • Proven ability to thrive in a start-up/change oriented environment
  • Great attention to detail and results driven approach
  • Self-starter with ability to organize and prioritize a diverse set of responsibilities to ensure that focus on growth and success of company is achieved
  • Proven coaching, mentoring, team building and leadership skills

#LI-Onsite
The benefits of being a #MiracleMaker:
  • You have the potential to change, improve, and save lives around the world.
  • You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans.
  • We offer comprehensive medical plans and HSA/FSA options.
  • Fertility & family planning assistance.
  • A variety of additional optional benefits and insurance options, including pet insurance.
  • Retirement contributions.
  • Holidays & Paid Time Off.

Benefits may vary by region and employment type and do not apply to temporary employees or contractors. See a comprehensive list of benefits at our Benefits & growth site at https://www.maravai.com/careers/benefits-and-growth/
To view more opportunities to become a #MiracleMaker, visit our career site at https://www.maravai.com/careers/
Alphazyme, a Maravai LifeSciences company, is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
Click here to view Maravai LifeSciences Privacy Notice
HIRING SCAM ALERT
Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that:
  • Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.)
  • Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment.
  • Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment.

If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at taops@maravai.com. If you believe you have been a victim of fraud, you can report this activity at: www.iC3.gov or www.stopfraud.gov.

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