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Sample Management Scientist Jobs in Florida (NOW HIRING)

Demonstrated experience with stability study set-up, sample management, protocol execution, sample ... Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, Microbiology, Chemical ...

Manage the collection and processing of clinical samples, ensuring compliance with ethical ... data science). Certification and Licensing: * not applicable Experience: * Extensive prior ...

Quality Lead

Miami, FL · On-site

$90 - $130/hr

Demonstrated experience with stability study set-up, sample management, protocol execution, sample ... Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, Microbiology, Chemical ...

Posted today

Quality Lead

Miami, FL · On-site

$90 - $130/hr

Demonstrated experience with stability study set-up, sample management, protocol execution, sample ... Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, Microbiology, Chemical ...

Manage the collection and processing of clinical samples, ensuring compliance with ethical ... data science). Certification and Licensing: * not applicable Experience: * Extensive prior ...

Quality Lead

Miami, FL · On-site

$90K - $100K/hr

Demonstrated experience with stability study set-up, sample management, protocol execution, sample ... Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, Microbiology, Chemical ...

Field Scientist

Sarasota, FL · On-site

$72K - $94K/yr

Conduct environmental site investigations, assessments and surveys to sample, measure and analyze ... management, and site planning and permitting. Terracon is a 100 percent employee-owned ...

Field Scientist

Sarasota, FL · On-site

$72K - $94K/yr

Conduct environmental site investigations, assessments and surveys to sample, measure and analyze ... Report any safety issues or concerns to management. * Understand and practice quality acumen.

Field Scientist

Fort Lauderdale, FL · On-site

$71K - $94K/yr

Conduct environmental site investigations, assessments and surveys to sample, measure and analyze ... management, and site planning and permitting. Terracon is a 100 percent employee-owned ...

Field Scientist

Fort Lauderdale, FL · On-site

$71K - $93K/yr

Conduct environmental site investigations, assessments and surveys to sample, measure and analyze ... Report any safety issues or concerns to management. * Understand and practice quality acumen.

$74K/yr

... of Personnel Management (OPM) Qualification Standards for General Schedule Professional and ... water samples (primarily stream water, soil leachate, and precipitation); using equipment and ...

... scientific data collection and data and/or sample management, preferably directly with in-water sea turtle surveys and/or research, including vessel operation; (2) the ability and desire to work as ...

$74K/yr

... of Personnel Management (OPM) Qualification Standards for General Schedule Professional and ... water samples (primarily stream water, soil leachate, and precipitation); using equipment and ...

$74K/yr

... of Personnel Management (OPM) Qualification Standards for General Schedule Professional and ... water samples (primarily stream water, soil leachate, and precipitation); using equipment and ...

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Showing results 1-20

Sample Management Scientist information

What is a sample management scientist?

Sample Management Scientists are professionals responsible for overseeing the collection, storage, tracking, and distribution of biological or chemical samples in laboratories or research facilities. They ensure that samples are handled according to strict protocols to maintain their integrity and traceability. Their work supports research, drug discovery, clinical trials, and other scientific processes by maintaining high standards for sample quality and data accuracy. Sample Management Scientists often use specialized software and follow rigorous documentation procedures to comply with regulatory requirements.

What are some common challenges faced by sample management scientists in maintaining sample integrity throughout the research process?

Sample Management Scientists often encounter challenges such as preventing sample contamination, ensuring proper labeling and documentation, and maintaining optimal storage conditions. These responsibilities require meticulous attention to detail and strict adherence to protocols in order to guarantee the reliability of research results. Additionally, coordinating with research teams and adapting to evolving project requirements can be demanding, but these challenges also offer opportunities for developing problem-solving skills and process improvements.

What are the key skills and qualifications needed to thrive as a sample management scientist, and why are they important?

To thrive as a Sample Management Scientist, you need a background in laboratory science, strong organizational abilities, and often a degree in chemistry, biology, or a related field. Familiarity with Laboratory Information Management Systems (LIMS), sample tracking software, and regulatory compliance standards is typical. Attention to detail, problem-solving skills, and effective communication help ensure accurate sample handling and collaboration with research teams. These competencies are crucial for maintaining data integrity, meeting project timelines, and supporting reliable scientific results.

What is the difference between Sample Management Scientist vs Laboratory Technician?

AspectSample Management ScientistLaboratory Technician
Required CredentialsBachelor's degree in life sciences or related field; experience in sample handlingAssociate's degree or certification; basic laboratory training
Work EnvironmentResearch labs, pharmaceutical companies, biotech firmsClinical labs, research facilities, manufacturing plants
Employer & Industry UsageUsed in research, development, and quality control sectorsCommon in clinical testing, sample processing, and routine lab tasks

The Sample Management Scientist focuses on overseeing the proper handling, storage, and documentation of samples in research and development settings. In contrast, the Laboratory Technician performs routine testing and sample preparation tasks. While both roles require laboratory experience, the Scientist typically has more specialized knowledge in sample lifecycle management, making them more involved in data integrity and sample tracking systems.

What job categories do people searching Sample Management Scientist jobs in Florida look for?

The top searched job categories for Sample Management Scientist jobs in Florida are:

What cities in Florida are hiring for Sample Management Scientist jobs?

Cities in Florida with the most Sample Management Scientist job openings:

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Job description

PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods.
SUMMARY:
The Quality Lead is responsible for leading Quality Control laboratory operations and ensuring analytical testing, stability programs, laboratory documentation, and equipment activities are performed in compliance with cGMP requirements and company procedures. This role provides technical leadership, supports laboratory investigations, maintains audit readiness, and collaborates with cross-functional teams to ensure product quality, regulatory compliance, and continuous improvement of laboratory operations.
Work Schedule: Monday - Friday 8am-5pm
JOB QUALIFICATIONS:
  • Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, Microbiology, Chemical Engineering, or a related scientific discipline, or an equivalent combination of education and relevant experience.
  • Minimum of 5-10 years of progressive analytical laboratory experience in a pharmaceutical, OTC, medical device, or other regulated cGMP environment, with demonstrated responsibility in quality control and laboratory operations.
  • Minimum of 3-5 years of experience in leadership roles and technical experience is preferred.
  • Strong technical knowledge of analytical testing, stability program support, laboratory instrumentation, calibration systems, preventive maintenance coordination, and troubleshooting of routine laboratory equipment.
  • Demonstrated experience with stability study set-up, sample management, protocol execution, sample pull scheduling, data review, and issuance of stability-related documentation and summary reports.
  • Working knowledge of cGMP requirements, good documentation practices, data integrity principles, laboratory investigations, deviation management, OOS/OOT processes, CAPA systems, and audit readiness expectations applicable to pharmaceutical laboratories.
  • Strong analytical, investigative, and organizational skills, with the ability to prioritize multiple activities, manage timelines, and perform effectively with minimal supervision
  • Excellent interpersonal, written, and verbal communication skills, with the ability to collaborate across Quality Control, Quality Assurance, Operations, external laboratories, and service providers.
  • Proficient in Microsoft Office and laboratory software systems, including the ability to maintain secure, accurate, compliant, and inspection-ready records.

POSITION RESPONSIBILITIES:
  • Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, Microbiology, Chemical Engineering, or a related scientific discipline, or an equivalent combination of education and relevant experience.
  • Minimum of 5-10 years of progressive analytical laboratory experience in a pharmaceutical, OTC, medical device, or other regulated cGMP environment, with demonstrated responsibility in quality control and laboratory operations.
  • Minimum of 3-5 years of experience in leadership roles and technical experience is preferred.
  • Strong technical knowledge of analytical testing, stability program support, laboratory instrumentation, calibration systems, preventive maintenance coordination, and troubleshooting of routine laboratory equipment.
  • Demonstrated experience with stability study set-up, sample management, protocol execution, sample pull scheduling, data review, and issuance of stability-related documentation and summary reports.
  • Working knowledge of cGMP requirements, good documentation practices, data integrity principles, laboratory investigations, deviation management, OOS/OOT processes, CAPA systems, and audit readiness expectations applicable to pharmaceutical laboratories.
  • Strong analytical, investigative, and organizational skills, with the ability to prioritize multiple activities, manage timelines, and perform effectively with minimal supervision.
  • Excellent interpersonal, written, and verbal communication skills, with the ability to collaborate across Quality Control, Quality Assurance, Operations, external laboratories, and service providers.
  • Proficient in Microsoft Office and laboratory software systems, including the ability to maintain secure, accurate, compliant, and inspection-ready records.

PHYSICAL REQUIREMENTS:
  • Work safely and follow all OSHA regulations and company safety policies and procedures.
  • Works frequently in a lab environment, handling of chemicals.
  • Employees are required to wear eye protection and lab coats while in the lab area
  • Ability to frequently lift and/or move up to 25 lbs
  • Ability to occasionally lift and/or move up to 35 lbs
  • Ability to regularly stand, sit, and walk to perform tasks

BENEFITS:PLD is a proud equal opportunity employer offering many corporate benefits, including:
  • Medical and Dental Benefits
  • Vision
  • 401K with employer match
  • Group Life Insurance
  • Flex Spending Accounts
  • Paid Time Off and Paid Holidays
  • Tuition Assistance
  • Corporate Discount Program
  • Opportunities to Flourish Within the Company

The EEO statement needs to be included in the detailed description... PL Developments is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
#HP1
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.