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Manager Biochemistry Jobs in Boca Raton, FL (NOW HIRING)

Tech Tammina LLC

Sr. Project Engineer

Boca Raton, FL · On-site

$93K - $122K/yr

... Biochemical, or Chemical Engineering. * Minimum of 10 years of engineering experience in a cGMP Food/Pharmaceutical/Biological manufacturing environment. Responsibilities * Managing mid-to-large ...

Tech Tammina LLC

Sr. Project Engineer

Boca Raton, FL · On-site

$93K - $122K/yr

... Biochemical, or Chemical Engineering. * Minimum of 10 years of engineering experience in a cGMP Food/Pharmaceutical/Biological manufacturing environment. Responsibilities * Managing mid-to-large ...

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Showing results 1-20

All JobsBiochemistry JobsManager Biochemistry JobsManager Biochemistry Jobs in Boca Raton, FL

Manager Biochemistry information

See Boca Raton, FL salary details

$26.1K

$77.5K

$130.5K

How much do manager biochemistry jobs pay per year?

As of Sep 12, 2026, the average yearly pay for manager biochemistry in Boca Raton, FL is $77,508.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,400.00 and $110,600.00 per year, depending on experience, location, and employer.

What is the difference between Manager Biochemistry vs Laboratory Supervisor?

AspectManager BiochemistryLaboratory Supervisor
CredentialsBachelor’s or Master’s in Biochemistry, relevant certificationsTypically similar credentials, often with additional supervisory certifications
Work EnvironmentResearch labs, clinical labs, pharmaceutical companiesClinical or research laboratory settings, overseeing daily operations
ResponsibilitiesOverseeing biochemistry testing, managing staff, ensuring qualitySupervising lab technicians, coordinating testing procedures, maintaining safety

The main difference is that a Manager Biochemistry focuses on strategic oversight, project management, and team leadership in biochemistry labs, while a Laboratory Supervisor handles daily operational tasks and staff supervision. Both roles require relevant credentials and work in similar environments, but the Manager Biochemistry typically has broader responsibilities and a higher level of decision-making authority.

Is a manager biochemistry a good career?

A manager in biochemistry oversees laboratory operations, research projects, and team management within scientific settings. It is a stable career with opportunities for advancement, requiring strong leadership, scientific expertise, and often a relevant advanced degree. The role offers a combination of scientific and managerial responsibilities, making it suitable for those interested in both research and leadership.

What careers can a Manager Biochemistry lead to?

A Manager Biochemistry can advance to senior leadership roles such as Director of Biochemistry, Laboratory Director, or Research Director, overseeing research teams and laboratory operations. They may also transition into roles in pharmaceutical or biotech companies, regulatory agencies, or pursue specialized expertise in areas like clinical research or quality assurance.

What are popular job titles related to Manager Biochemistry jobs in Boca Raton, FL?

For Manager Biochemistry jobs in Boca Raton, FL, the most frequently searched job titles are:

What job categories do people searching Manager Biochemistry jobs in Boca Raton, FL look for?

The top searched job categories for Manager Biochemistry jobs in Boca Raton, FL are:

Manager Biochemistry jobs near you
Infographic showing various Manager Biochemistry job openings in Boca Raton, FL as of August 2026, with employment types broken down into 85% Full Time, 14% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $77,508 per year, or $37.3 per hour.

Manager, QCA

Plantation, FL • On-site

Goodwin Biotechnology Inc
See more jobs at Goodwin Biotechnology Incexternal

Full-time

Posted 23 days ago

Job description

Description:

Scope of Function: Manages, supervises, and oversees the Quality Control Analytical team with solid technical and scientific experience in the pharmaceutical industry to ensure adherence to established quality standards. Manage Qualification and Validation of Analytical Methods transferred by Protein Characterization Group. Overall responsibility for the Quality Control Analytical functions. Responsible for planning and successful execution of QC testing and tasks. Participate in Internal and external audits and inspections. Ensure compliance with regulatory and corporate requirements. Lead the Investigations for OOS/ABT/OOT. Propose corrective actions to improve compliance with quality specifications.

Requirements:

  Specific Duties: 

· Provide leadership and strategic direction for the Department. 

· Ensure the Analytical Services are maintained in compliance with company and GMP/GLP standards and guidelines.

· Supports and leads the design, development, and qualification/validation of analytical methods intended to assess critical quality attributes of raw materials, drug substances, intermediates, and products.

· Lead the coordination of activities and communication to assure efficient and timely transfer of methods to the Quality Control Group from Process Development.

· Ensure evaluation and testing of GBI products are performed in accordance with regulatory standards, and scientific best practices and are completed on schedule.

· Develop and manage stability program schedules and Quality Control Lab schedules.

· Responsible for generating/reviewing Stability Protocols per ICH guidelines and generating the Summary Reports 

· Review, write and supervise the execution of the input and output reports and SOPs 

· Ensure all the exception documents are closed on time. 

· Provides coaching and mentoring of junior staff to maximize potential and retain key employees.

· Participates in client audits and in other regulatory inspections, and meetings as required.

· Monitor laboratory notebooks to ensure issuance, review, and archival are conducted in a timely manner in accordance with established standards. 


Education and Skills Required: 


Education: 

Bachelor in biological or biochemical sciences or related field. 

Experience: 

Must have at least five years of direct work experience in FDA regulated environment.

Skills: 

· The candidate will be a problem-solver with the ability to exercise sound judgment under challenging circumstances.

· Excellent written and verbal communication skills with the ability to effectively promote intra-and inter-departmental cooperation.

· Knowledge of GMP, ICH, and compendial requirements and their application.

· Strong attention to detail, observation, organizational, and leadership skills.

· Possess strong character with self-confidence and integrity. 

· Time Management skills

· Conflict Resolution.

· Critical Thinking.

· Time Management.

· Priority Management.

· Diversity Awareness.