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Biotech Manufacturing Associate Jobs in Bayamon, PR

Pinnaql

Scheduler / Planning Engineer

Juncos, PR · On-site

... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...

Amgen

CMC Statistics Assoc Dir

Juncos, PR · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... The statistician will also provide support to clinical and commercial manufacturing sites in the ...

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 ...

BioPharma Consulting JAD Group

Senior Engineer

Juncos, PR · On-site

$100 - $125/hr

Lead troubleshooting of operational issues in manufacturing, pilot plant, utilities, facilities ... Coordinate and supervise the work of engineers, associates, and technicians on both ongoing and ...

ECHO Consulting Group

Sr Engineer

Juncos, PR · On-site

$100 - $125/hr

ECHO Consulting Group is a leader in providing solutions for the pharmaceutical, biotechnology ... Work with research, manufacturing, process development, utilities, facilities, quality assurance ...

Biopharma-Consulting-Jad-Group

Sr. Engineer

Juncos, PR · On-site

$125 - $150/hr

... manufacturing, pilot plant, and capital project environments. This role applies advanced and ... Supervise, coordinate, and review the work of engineers, associates, and technicians on both ...

BioPharma Consulting JAD Group

Sr. Engineer

Juncos, PR · On-site

$150 - $200/hr

... manufacturing, pilot plant, and capital project environments. This role applies advanced and ... Supervise, coordinate, and review the work of engineers, associates, and technicians on both ...

BioPharma Consulting JAD Group

Sr. Engineer

Juncos, PR · On-site

$101K - $139K/yr

... manufacturing, pilot plant, and capital project environments. This role applies advanced and ... Supervise, coordinate, and review the work of engineers, associates, and technicians on both ...

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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 9, 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.

Scheduler / Planning Engineer

Juncos, PR • On-site

Validation & Engineering Group, Inc.
See more jobs at Validation & Engineering Group, Inc.external

Full-time

Re-posted 12 days ago

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company 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:
  • Scheduler / Planning Engineer

Position Summary
The Scheduler / Planning Engineer will support capital projects and technical initiatives within regulated pharmaceutical and biotechnology manufacturing environments by developing, maintaining, and coordinating project schedules and planning activities.
This role requires strong organizational and analytical skills to support schedule development, progress tracking, resource planning, look-ahead activities, and schedule reporting across multiple projects and workstreams.
Key Responsibilities
  • Develop and maintain project schedules supporting capital projects and engineering initiatives.
  • Support schedule planning activities including logic development, milestone tracking, sequencing, and look-ahead planning.
  • Coordinate schedule updates, progress tracking, and schedule reporting activities.
  • Support identification of schedule risks, conflicts, delays, and resource constraints.
  • Assist with tracking project priorities, deliverables, dependencies, and execution timelines.
  • Support resource loading reviews and planning coordination activities.
  • Participate in project meetings and support communication of schedule status, risks, critical activities, and recovery actions.
  • Coordinate with Project Managers, Engineering, contractors, vendors, and project stakeholders to support schedule alignment activities.
  • Support preparation and maintenance of project planning documentation, trackers, reports, and schedule records.
  • Assist with schedule analysis and continuous improvement initiatives related to planning and project execution activities.
  • Ensure planning and scheduling activities are performed in alignment with applicable project procedures and governance expectations

Additional Requirements
Ability to work on-site in the eastern region of Puerto Rico. Must be eligible to complete client-required onboarding, training, and site access requirements. Ability to work effectively within fast-paced and highly regulated environments.
Qualifications & Experience
  • Associate's or Bachelor's degree in Project Management, Construction Management, Engineering, Business Administration, or related field preferred.
  • Minimum of 3 years of experience supporting project scheduling, planning, or project controls activities.
  • Familiarity with schedule development, progress tracking, milestone management, critical path concepts, and planning coordination activities.
  • Experience supporting capital projects, engineering projects, construction activities, manufacturing projects, or technical programs is preferred.
  • Familiarity with scheduling and planning tools such as Primavera P6, MS Project, Planisware, SAP, Smartsheet, or similar systems is preferred. Strong analytical, organizational, and problem-solving skills with attention to detail and the ability to manage multiple priorities.
  • Excellent verbal and written communication skills in both English and Spanish, including reporting, documentation preparation, and coordination with project stakeholders.
  • Ability to support multiple projects and workstreams simultaneously within fast-paced environments.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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