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Biotech Manufacturing Associate Jobs in Bayamon, PR

Inteldot

Specialist Manufacturing 35529

Juncos, PR · On-site

Biotech and manufacturing experience Responsibilities: * Initiate, revise, and approve ... Associates + 8 years of Manufacturing Operations experience OR High school/GED + 10 years of ...

Inteldot

Specialist Manufacturing 35466

Juncos, PR · On-site

Experience in biotechnology pharmaceutical process support, especially on Drug Substance processes ... Associates + 8 years of Manufacturing Operations experience OR High school/GED + 10 years of ...

Weil Group, Inc.

Specialist Manufacturing

Juncos, PR · On-site

... Biotech and manufacturing experience SUMMARY With minimal supervision, support the execution of ... Associates + 8 years of Manufacturing Operations experience OR -High school/GED + 10 years of ...

Cencora

Specialist Manufacturing

Juncos, PR

... or Associate's degree and 10 years of Manufacturing Operations experience or High school diploma ... Experience in biotechnology pharmaceutical process support, especially on Drug Substance processes ...

Amgen

Manufacturing Process Technician

Juncos, PR · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Associate's degree Or High school/GED + 1 year of Manufacturing work or military experience ...

ProQualityNetwork

Senior Engineer 35570

Juncos, PR · On-site

$101K - $139K/yr

Provide technical guidance to engineers, technicians, and engineering associates. * Coordinate ... Pharmaceutical and biotechnology manufacturing processes. * Medical device manufacturing processes.

ProQualityNetwork

Senior Engineer- 35392

Juncos, PR

$101K - $139K/yr

Provide technical leadership and guidance to engineers, associates, and technicians on both daily ... Working knowledge of pharmaceutical or biotechnology manufacturing processes. * Experience working ...

ProQualityNetwork

Senior Engineer 35449

Juncos, PR · On-site

$101K - $139K/yr

Provide technical guidance to engineers, technicians, and engineering associates. * Coordinate ... Pharmaceutical and biotechnology manufacturing processes. * Medical device manufacturing processes.

Weil Group, Inc

EHS Associate

Juncos, PR · On-site

EHS Associate for Capital Projects will provide technical Environmental, Health & Safety (EH&S ... biotechnology, or manufacturing facilities preferred. • Knowledge and experience in: oProcess ...

Weil Group, Inc.

EHS Associate

Juncos, PR · On-site

EHS Associate for Capital Projects will provide technical Environmental, Health & Safety (EH&S ... biotechnology, or manufacturing facilities preferred. • Knowledge and experience in: oProcess ...

Quality Consulting Group

JT333 - 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 ...

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

Biotech Manufacturing Associate information

See Bayamon, PR salary details

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How much do biotech manufacturing associate jobs pay per hour?

As of Jul 28, 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 are Biotech Manufacturing Associates?

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 jobs can I get with an associate's degree in biotechnology?

Biotech Manufacturing Associates are common roles for those with an associate's degree in biotechnology, involving tasks such as preparing and operating laboratory equipment, following strict safety protocols, and documenting processes. Other positions include quality control technician, laboratory technician, and production operator, often requiring knowledge of GMP standards and familiarity with lab tools and procedures.

What does a biotech associate do?

A biotech manufacturing associate is responsible for performing tasks related to the production of biotechnological products, such as preparing equipment, following manufacturing protocols, and ensuring quality control. They often work in laboratory or cleanroom environments, using tools like bioreactors and adhering to safety and regulatory standards. Strong attention to detail and knowledge of GMP (Good Manufacturing Practice) are essential for this role.

What does a biotech manufacturing associate do?

A biotech manufacturing associate is responsible for producing, processing, and packaging biological products in a manufacturing environment. They operate equipment, follow strict safety and quality protocols, and document production activities to ensure compliance with regulatory standards. The role often requires attention to detail, knowledge of GMP practices, and the ability to work in a team setting.

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 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.

How much does a manufacturing associate make at KBI Biopharma?

A Biotech Manufacturing Associate at KBI Biopharma typically earns between $50,000 and $70,000 annually, depending on experience and location. The role involves working in a regulated environment, often requiring knowledge of GMP protocols and bioprocessing equipment.

What are the key skills and qualifications needed to thrive as a Biotech Manufacturing Associate, and why are they important?

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 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.
Senior Manufacturing Engineer

Senior Manufacturing Engineer

BioPharma Consulting JAD Group

Juncos, PR • On-site

$88K - $121K/yr

Contractor

Posted 7 days ago

Job description

The Sr. Engineer independently leads and executes complex engineering activities related to process optimization, troubleshooting, system/facility modifications, and capital projects within manufacturing, operations, pilot plant, or engineering environments. This role applies advanced engineering principles, develops technical solutions, directs project execution, and provides expert guidance on methodologies, validation, and documentation in a highly regulated pharmaceutical/biotech setting.

Key Responsibilities

  • Lead complex or novel engineering assignments requiring development of new or improved techniques and procedures.
  • Develop engineering policies and procedures impacting multiple organizational units.
  • Supervise, coordinate, and review work from engineers, associates, and technicians on both ongoing and project‑based tasks.
  • Apply advanced engineering techniques and adapt specialized methods to diverse assignments.
  • Utilize engineering knowledge beyond core discipline to support cross‑functional initiatives.
  • Serve as a peer‑recognized subject matter expert (SME) in at least one engineering technology area.
  • Plan and conduct engineering projects using mature technical judgment and scientific methodology.
  • Develop technical solutions to complex problems requiring creativity, innovation, and engineering expertise.
  • Collaborate with Research, Manufacturing, Process Development, Utilities, Facilities, Quality Assurance, and Validation to define requirements for major system or facility modifications.
  • Partner with Project Managers to deliver engineering projects within schedule, budget, and quality expectations.
  • Coordinate external consultants, architects, and engineering firms in developing standard design documentation.
  • Develop departmental or multi‑disciplinary project budgets and manage cost controls for assigned areas.

Skills

  • Working knowledge of pharmaceutical/biotech manufacturing processes.
  • Familiarity with validation processes, protocol execution, and documentation in regulated environments.
  • Ability to interpret and apply GLP, GMP, GDP and engineering science to production systems.
  • Ability to operate specialized laboratory and engineering equipment.
  • Technical report writing and verbal communication skills.
  • Comprehensive understanding of validation requirements for new equipment installations.
  • Ability to manage multiple projects simultaneously and determine when additional internal/external resources are required.
  • Ability to manage contractors, vendors, and cross‑functional teams.
  • Working knowledge of financial analysis tools and project cost development.
  • Ability to develop schedules, manage change, and ensure completion and follow‑up of engineering tasks.

Requirements

Required Education

  • Doctorate in Engineering, OR
  • Master’s degree + 2 years of engineering experience, OR
  • Bachelor’s degree in Engineering + 4 years of engineering experience

Preferred Qualifications

  • Experience with packaging equipment.
  • Experience in design of new equipment or processes.
  • Engineering project experience (capital projects, system modifications, facility upgrades).
  • Strong knowledge of validation (equipment, process, CSV).
  • Experience in medical device or pharmaceutical manufacturing environments.
  • Bilingual (English/Spanish)

Benefits

  • 8-month contract with possible extension
  • Administrative Shift