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Pharmaceutical Biologist Jobs in Puerto Rico (NOW HIRING)

MMR Consulting

PR · On-site

The ideal candidate will possess strong pharmaceutical project leadership experience within biotech, sterile manufacturing, fill-finish, API, or biologics environments and will serve as a key liaison ...

MMR Consulting

PR · On-site

The ideal candidate will possess strong pharmaceutical project leadership experience within biotech, sterile manufacturing, fill-finish, API, or biologics environments and will serve as a key liaison ...

MMR Consulting

PR · On-site

The ideal candidate will possess strong pharmaceutical project leadership experience within biotech, sterile manufacturing, fill-finish, API, or biologics environments and will serve as a key liaison ...

FITS LLC

Sr. Quality Engineer

Carolina, PR · On-site

$90 - $130/hr

GMP pharmaceutical or biologics manufacturing environments, including Facilities, Utilities, Maintenance, and Engineering (FUME) systems. * Commissioning, qualification, validation, and engineering ...

Becton, Dickinson and Company

Scientist III

Cayey, PR · On-site

Bachelor of Science degree in Biology, Microbiology, Biochemistry, Chemistry or other related field Experience: * 5 years' experience in the medical device or pharmaceutical industry. * Prior ...

Becton, Dickinson and Company

Scientist III

Cayey, PR · On-site

Bachelor of Science degree in Biology, Microbiology, Biochemistry, Chemistry or other related field Experience: * 5 years' experience in the medical device or pharmaceutical industry. * Prior ...

Becton, Dickinson and Company

Scientist II

Cayey, PR · On-site

Bachelor of Science degree in Biology, Microbiology, Biochemistry, Chemistry or other related field Experience: * 3 years' experience in the medical device or pharmaceutical industry. * Prior ...

BD Mexico

Scientist III

Cayey, PR · On-site

$90 - $120/hr

Bachelor of Science degree in Biology, Microbiology, Biochemistry, Chemistry or other related field Experience * 5 years' experience in the medical device or pharmaceutical industry. * Prior ...

Becton, Dickinson and Company

Scientist II

Cayey, PR · On-site

Bachelor of Science degree in Biology, Microbiology, Biochemistry, Chemistry or other related field Experience: * 3 years' experience in the medical device or pharmaceutical industry. * Prior ...

Becton, Dickinson and Company

Scientist II

Cayey, PR · On-site

Bachelor of Science degree in Biology, Microbiology, Biochemistry, Chemistry or other related field Experience: * 3 years' experience in the medical device or pharmaceutical industry. * Prior ...

Legalpmpartners

Cleaning Validation Specialist

Caguas, PR · On-site

$65 - $95/hr

Bachelor's Degree in Engineering, Chemistry, Biology, Microbiology, Pharmaceutical Sciences, Life Sciences, or related discipline. * Equivalent combination of education and relevant pharmaceutical ...

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All JobsPharmaceutical Biologist JobsPharmaceutical Biologist Jobs in Puerto Rico

Pharmaceutical Biologist information

What is a pharmaceutical biologist?

A Pharmaceutical Biologist studies biological systems to develop and improve pharmaceutical drugs. They analyze the effects of compounds on living organisms, conduct laboratory experiments, and collaborate with chemists and pharmacologists. Their work helps in drug discovery, safety testing, and regulatory approval. This role is crucial in creating effective and safe medications for medical use.

What does a pharmaceutical biologist do?

A typical day for a Pharmaceutical Biologist involves designing and conducting laboratory experiments to test drug compounds, analyzing biological data, and documenting results for regulatory purposes. You’ll often collaborate with chemists, pharmacologists, and other scientists to exchange insights and refine experimental approaches. Depending on your organization, you might split your time between hands-on lab work, data interpretation, and meetings to discuss project progress. The role can also require staying current with scientific literature and contributing to regulatory submissions or technical reports. If you enjoy a balance of research, analysis, and team collaboration, this position offers a dynamic and intellectually rewarding work environment.

What are the key skills and qualifications needed to thrive as a pharmaceutical biologist?

To succeed as a Pharmaceutical Biologist, you need a strong background in biology, chemistry, and pharmacology, often supported by an advanced degree in biological sciences or a related field. Experience with laboratory technologies such as high-performance liquid chromatography (HPLC), mass spectrometry, and familiarity with Good Laboratory Practices (GLP) or regulatory certifications is highly valued. Critical thinking, keen attention to detail, and effective teamwork and communication skills help professionals excel in collaborative research environments. These skills are vital for conducting accurate research, ensuring compliance with industry standards, and contributing to the development of safe and effective pharmaceuticals.

Can you work in pharmaceuticals with a pharmaceutical biologist degree?

A pharmaceutical biologist degree prepares individuals for roles in drug development, research, and quality control within the pharmaceutical industry. Graduates often work in laboratories, conducting experiments and analyzing biological data, sometimes requiring additional certifications or advanced degrees for certain positions.

How much do pharmaceutical biologists make?

Pharmaceutical biologists typically earn a median annual salary of around $70,000 to $90,000, depending on experience, education, and location. Entry-level positions may start lower, while those with advanced degrees or specialized skills can earn higher salaries, especially in research and development environments.

How to become a pharmaceutical biologist?

To become a pharmaceutical biologist, typically a bachelor's degree in biology, biochemistry, or a related field is required, followed by advanced education such as a master's or Ph.D. for research roles. Gaining laboratory experience, understanding drug development processes, and developing skills in molecular biology and pharmacology are also important for this career.

What are popular job titles related to Pharmaceutical Biologist jobs in Puerto Rico?

For Pharmaceutical Biologist jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Biologist jobs in Puerto Rico look for?

The top searched job categories for Pharmaceutical Biologist jobs in Puerto Rico are:

Pharmaceutical Biologist jobs near you
Infographic showing various Pharmaceutical Biologist job openings in Puerto Rico as of August 2026, with employment types broken down into 59% Full Time, and 41% Contract. Highlights an 100% In-person job distribution.

ZL01-120925 - Specialist Quality Control

Validation & Engineering Group, Inc.

Juncos, PR • On-site

Full-time

Re-posted yesterday

Job description

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
  • Specialist Quality Control

SUMMARY
Under general direction, functions as the technical specialist for testing and development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources.
FUNCTIONS
  • Responsible for providing technical guidance, provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise.
  • Resolve technical issues and troubleshoot for assays as necessary
  • Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety.
  • Manage existing and/or develop and implement new programs, processes and methodologies.
  • Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact.
  • Approve lab investigations, Lead audit teams
  • May serve as subject matter expert to develop technical training.
  • May perform routine work in a specific area of responsibility as necessary.
  • Represents the department/organization on various teams, independently responsible for following through on multi-site action items.
  • May interact with regulatory agencies regarding area(s) of responsibility including written responses.
  • May resolve issues with outside resources.
  • Performs special projects as requested by supervisor, May supervise employees as necessary to meet technical requirements.

EDUCATION
  • Doctorate OR
  • Masters + 2 years of directly related experience OR
  • Bachelors + 4 years of directly related experience OR

COMPETENCIES/SKILLS
  • Excellent communication skills, facilitation and presentation skills.
  • Excellent technical writing skills.
  • Strong computer operation skills including work processing, presentation, database and spreadsheet application skills.
  • Excellent project management and organizational skills including the ability to independently understand, follow, implement complex instructions and follow assignments through to completion.
  • Advanced skill in handling multiple responsibilities, tasks and projects simultaneously including ability to shift priorities.
  • Excellent knowledge of and experience with processes involved in quality analytical labs, validation, manufacturing, quality assurance, process development and distribution.
  • Extensive knowledge of all testing including the development and validation of assays and the ability to perform all testing in specific area of responsibility.
  • Knowledge of pharmaceutical processes.
  • Strong knowledge of U.S. regulations and practices pertaining to the testing of pharmaceutical/biological products.
  • Knowledge of basic international regulations and practices pertaining to the testing of pharmaceutical/biological products.
  • Extensive knowledge and application of GMPs/CFRs.
  • Ability to evaluate compliance issues.
  • Skill in evaluating and documenting according to Company and various guidelines.
  • Proficient at maintenance, troubleshooting and operation of equipment in area of expertise.
  • Advanced scientific data analysis and interpretation skills.
  • Advanced skills in solving complex problems.
  • Advanced data trending and evaluation.
  • Strong skill in working independently and to effectively interact with various levels.
  • Ability to interact with regulatory agencies both orally and in writing.
  • Initiate, coordinate and lead cross functional teams.
  • Excellent skill in leading, motivating, influencing, and negotiating.

ATRIBUTES:
  • Scientific Data Analysis.
  • Strong Technical Writing (English and Spanish) mainly focuses.
  • Strong knowledge in Microsoft Excel as a Tool for Data Analysis.
  • Good Communication skills.
  • Project Management.
  • Knowledge in Computer System and Method Validation (Experience preferable).
  • Strong knowledge and experience with quality process management.
  • Basic Knowledge on equipment preventive maintenance and troubleshooting.
  • Agile on prioritization of critical tasks.
  • Ability to develop inspection or qualification protocols in a short timeframe period.
  • Strong negotiation skills.

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