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Biotech Manufacturing Associate Jobs in Bayamon, PR

Quality Consulting Group

JT492 - SR. ENGINEER

Juncos, PR · On-site

$102K - $140K/yr

... biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated ... Supervise, coordinate and review work of a small staff of engineers, associates and/or technicians ...

HR Works

Project Coordinator

Guayama, PR · On-site

$80 - $100/hr

Minimum Requirements * Associate Degree in Engineering or related technical field (Bachelor ... biotechnology, or medical device manufacturing is required. * Working knowledge of cGMP and ...

Moriah Engineering

Project Coordinator

Guayama, PR · On-site

$80 - $100/hr

Minimum Requirements * Associate Degree in Engineering or related technical field (Bachelor ... biotechnology, or medical device manufacturing is required. * Working knowledge of cGMP and ...

Ultimate Solutions Corp

Sr Engineer-Packaging

Juncos, PR · On-site

$100 - $125/hr

Work with research, manufacturing, process development, utilities, facilities, quality assurance ... Working knowledge of pharmaceutical/biotech processes * Familiarity with validation processes

Validation & Engineering Group, Inc.

Sr Engineer

Juncos, PR · On-site

$101K - $139K/yr

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Collaborate with Engineering, Validation, Quality Assurance (QA), Manufacturing, and Supply Chain ...

Pinnaql

Sr Engineer

Juncos, PR · On-site

$101K - $139K/yr

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Collaborate with Engineering, Validation, Quality Assurance (QA), Manufacturing, and Supply Chain ...

Ultimate Solutions Corp

Sr Engineer

Juncos, PR · On-site

$125 - $150/hr

Work with research, manufacturing, process development, utilities, facilities, quality assurance ... Working knowledge of pharmaceutical/biotech processes * Familiarity with validation processes

Pinnaql

Sr Engineer

Juncos, PR · On-site

$101K - $139K/yr

... manufacturing, pilot plant or capital projects environment. Applies advanced and diverse ... COMPETENCIES/SKILLS 1. Working knowledge of pharmaceutical/biotech processes 2. Familiarity with ...

Validation & Engineering Group, Inc.

Sr Engineer

Juncos, PR · On-site

$101K - $139K/yr

... manufacturing, pilot plant or capital projects environment. Applies advanced and diverse ... COMPETENCIES/SKILLS 1. Working knowledge of pharmaceutical/biotech processes 2. Familiarity with ...

Veg Group

Sr Engineer

Juncos, PR · On-site

$80 - $100/hr

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Supervise, coordinate and review work of a small staff of engineers, associates and/or technicians ...

Ultimate Solutions

Sr Engineer

Juncos, PR · On-site

$101K - $139K/yr

Work with research, manufacturing, process development, utilities, facilities, quality assurance ... biotech processes • Familiarity with validation processes • Familiarity with documentation in a ...

Ultimate Solutions

Sr Engineer-Packaging

Juncos, PR · On-site

Work with research, manufacturing, process development, utilities, facilities, quality assurance ... biotech processes • Familiarity with validation processes • Familiarity with documentation in a ...

ProQualityNetwork

Senior Engineer-35492

Juncos, PR

$101K - $139K/yr

Manufacturing Equipment and Reliability * Own manufacturing equipment within the CMMS system ... Coordinate and manage the project work of engineers, associates, technicians, contractors, vendors ...

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All JobsBiotech Manufacturing Associate JobsBiotech Manufacturing Associate Jobs in Bayamon, PR

Biotech Manufacturing Associate information

See Bayamon, PR salary details

$11

$18

$30

How much do biotech manufacturing associate jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for biotech manufacturing associate in Bayamon, PR is $18.77, according to ZipRecruiter salary data. Most workers in this role earn between $14.71 and $21.01 per hour, depending on experience, location, and employer.

What is a biotech manufacturing associate?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What are the key skills and qualifications needed to thrive as a biotech manufacturing associate?

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.

What are some common challenges faced by biotech manufacturing associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What job categories do people searching Biotech Manufacturing Associate jobs in Bayamon, PR look for?

The top searched job categories for Biotech Manufacturing Associate jobs in Bayamon, PR are:

What cities near Bayamon, PR are hiring for Biotech Manufacturing Associate jobs?

Cities near Bayamon, PR with the most Biotech Manufacturing Associate job openings:

Biotech Manufacturing Associate jobs near you
Infographic showing various Biotech Manufacturing Associate job openings in Bayamon, PR as of June 2026, with employment types broken down into 89% Full Time, 4% Part Time, 3% Temporary, 3% Contract, and 1% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $39,040 per year, or $18.8 per hour.

JT492 - SR. ENGINEER

Quality Consulting Group, LLC

Juncos, PR • On-site

$125 - $150/hr

Other

Re-posted yesterday

Job description

QUALITY CONSULTING GROUP,a leader inthe pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world‑class manufacturing industry in Puerto Rico & USA

Responsibilities
  • Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment.
  • Applies advanced and diverse engineering principles to the design and implementation of major system modifications, experiments, process and/or capital projects.
  • Develops, organizes, analyzes and presents interpretation of results for operational issues or engineering projects of significant scope and complexity.
  • Complete complex or novel assignments requiring development of new and/or improved engineering techniques and procedures.
  • Develop engineering policies and procedures that affect multiple organizational units.
  • Supervise, coordinate and review work of a small staff of engineers, associates and/or technicians on an ongoing basis as well as on a project basis.
  • Employ advanced engineering techniques and/or modifications of advanced techniques within area of engineering expertise.
  • Apply knowledge of engineering principles and practices outside of area of discipline expertise to broad variety of assignments in related fields.
  • Serves as a peer-recognized engineering technology specialist in at least one area, with overall responsibility for determining methodologies in that area.
  • Application of mature engineering knowledge in planning and conducting projects.
Qualifications
  • Bachelor Degree in Engineering
  • 5 years of Engineering experience
  • Experience managing manufacturing equipment within a Computerized Maintenance Management System (CMMS), including work order approval and closure, preventive maintenance (PM) strategy development, and spare parts management.
  • Knowledge of equipment reliability principles, maintenance optimization, and change control processes.
  • Ability to collaborate effectively with Engineering and cross-functional teams to develop and implement maintenance strategies that improve equipment performance.
  • Experience driving initiatives focused on increasing equipment availability, reducing downtime, and improving system reliability.
  • Proficiency in developing, analyzing, and reporting equipment performance metrics, including availability, downtime, and maintenance effectiveness.
  • Proven experience leading equipment improvement and reliability enhancement projects.
  • Strong technical expertise serving as a Subject Matter Expert (SME) for manufacturing equipment design, maintenance, and compliance activities.
  • Experience troubleshooting manufacturing equipment and supporting root cause investigations.
  • Knowledge of deviation management and experience developing, implementing, and monitoring Corrective and Preventive Actions (CAPAs).
  • Understanding of Good Manufacturing Practices (GMP) and regulatory compliance requirements within a manufacturing environment.
  • Commitment to Environmental, Health, and Safety (EHS) standards and demonstrated ability to promote a safe working environment.
  • Strong analytical, problem‑solving, organizational, and communication skills.
  • Ability to manage multiple priorities and work effectively in a fast‑paced manufacturing environment.

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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