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Program Biotech Jobs in Puerto Rico (NOW HIRING)

Pinnaql

Validation Specialist

Aibonito, PR · On-site

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... programs . * Support cleanroom and utility qualification activities, including environmental ...

Veg Group

Validation Specialist

Aibonito, PR · On-site

$85 - $120/hr

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... programs . * Support cleanroom and utility qualification activities, including environmental ...

Veg Group

Scheduler / Planning Engineer

Juncos, PR · On-site

$70 - $90/hr

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... or technical programs is preferred. * Familiarity with scheduling and planning tools such as ...

New

Veg Group

Scheduler / Planning Engineer

Humacao, PR · On-site

$70 - $90/hr

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... or technical programs is preferred. * Familiarity with scheduling and planning tools such as ...

New

Pinnaql

Specialist Tech Engineering

Juncos, PR · On-site

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Ensure the maintenance team training program , standard operating procedures and equipment/system ...

Pinnaql

Scheduler / Planning Engineer

Juncos, PR · On-site

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... or technical programs is preferred. * Familiarity with scheduling and planning tools such as ...

Pinnaql

Scheduler / Planning Engineer

Gurabo, PR · On-site

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... or technical programs is preferred. * Familiarity with scheduling and planning tools such as ...

Pinnaql

Scheduler / Planning Engineer

Humacao, PR · On-site

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... or technical programs is preferred. * Familiarity with scheduling and planning tools such as ...

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Showing results 41-60

All JobsProgram Biotech JobsProgram Biotech Jobs in Puerto Rico

Program Biotech information

What is a program biotech?

A Program Biotech is a professional who manages and coordinates biotechnology projects or programs within an organization. They oversee research and development activities, ensure compliance with regulations, manage budgets, and facilitate collaboration between scientists, engineers, and other stakeholders. Their role is crucial in bringing biotech innovations from concept to market by ensuring projects stay on schedule and meet organizational goals.

What are the key skills and qualifications needed to thrive as a program biotech professional?

To excel as a Program Biotech professional, you need a solid background in life sciences, project management, and regulatory knowledge, often supported by an advanced degree in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), project management software, and compliance frameworks like GLP or GMP is common. Strong leadership, problem-solving abilities, and effective communication are crucial soft skills for coordinating multidisciplinary teams. These skills and qualifications are essential to drive innovation, ensure regulatory compliance, and achieve successful outcomes in complex biotech projects.

What are some common challenges faced by program biotech professionals when managing cross-functional teams?

Program Biotech professionals often coordinate projects that involve diverse teams, including research scientists, regulatory specialists, and business development staff. One key challenge is ensuring clear communication and alignment among team members with varying backgrounds and priorities. Additionally, balancing project timelines with regulatory requirements and scientific uncertainties can require strong problem-solving skills. Being proactive in facilitating collaboration and adapting to shifting project goals are essential for success in this role.

What is the difference between Program Biotech vs Laboratory Technician?

AspectProgram BiotechLaboratory Technician
Required CredentialsBiotech degree or certification, specialized trainingAssociate degree or certification in laboratory sciences
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsClinical, research, or industrial labs
Employer & Industry UsageBiotech firms, research institutions, pharma companiesHospitals, research labs, manufacturing plants
Common Search & ComparisonYesNo

Program Biotech professionals focus on research, development, and overseeing biotech projects, often requiring advanced degrees and specialized training. Laboratory Technicians perform routine lab tests and support research or manufacturing processes, typically with an associate degree. While both roles work in lab environments within the biotech and healthcare industries, Program Biotech roles are more research-oriented, whereas Laboratory Technicians handle day-to-day testing and sample analysis.

What job categories do people searching Program Biotech jobs in Puerto Rico look for?

The top searched job categories for Program Biotech jobs in Puerto Rico are:

Program Biotech jobs near you

Validation Specialist

Pinnaql

Aibonito, PR • On-site

Full-time

Posted 19 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:
  • Validation Specialist

Key Responsibilities:
  • Develop, review, and execute Validation Master Plans (VMPs) and validation protocols, including IQ, OQ, and PQ.
  • Validate and qualify equipment, facilities, utilities, cleanrooms, and other systems that may impact medical-device safety and product quality.
  • Establish and maintain validation documentation, including protocols, reports, acceptance criteria, traceability, and stakeholder approvals.
  • Define and document validation roles, responsibilities, training, and competency requirements.
  • Maintain equipment inventories and support calibration, preventive maintenance, and qualification programs.
  • Support cleanroom and utility qualification activities, including environmental monitoring and trending.
  • Perform and document risk assessments, including FMEA, to identify and mitigate risks associated with equipment, processes, and systems.
  • Manage validation-related change controls, deviations, and CAPAs, ensuring appropriate investigation, documentation, and closure.
  • Coordinate with Engineering, Quality, Manufacturing, Facilities, Operations, and other stakeholders to ensure validation activities are completed according to project requirements.
  • Plan and coordinate resources, equipment availability, and required downtime to meet project milestones and schedules.
  • Obtain appropriate stakeholder review and sign-off for validation deliverables.
  • Support ongoing validation controls, including periodic requalification, continued monitoring, data trending, and management review.
  • Ensure validation activities remain compliant with applicable medical-device quality and regulatory requirements.
  • Identify potential compliance gaps and recommend corrective or preventive actions.

Required Qualifications
  • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline.
  • Experience in validation and qualification within the medical device, pharmaceutical, biotechnology, or other regulated manufacturing environment.
  • Hands-on experience with IQ/OQ/PQ protocols and validation documentation.
  • Experience with risk management methodologies, including FMEA.
  • Knowledge of change control, deviations, CAPA, calibration, maintenance, and equipment qualification processes.
  • Experience working with facilities, utilities, cleanrooms, and/or environmental monitoring programs.
  • Strong understanding of Good Manufacturing Practices (GMP) and applicable quality requirements.
  • Strong technical writing, documentation, organizational, and project coordination skills.
  • Ability to work collaboratively with cross-functional teams and manage multiple validation activities simultaneously.

Preferred Qualifications:
  • Experience supporting medical device manufacturing and quality systems.
  • Familiarity with FDA and/or international medical-device regulatory requirements.
  • Experience with validation lifecycle management and periodic requalification programs.
  • Experience with electronic quality management or validation management systems.
  • Knowledge of process validation, computerized systems validation, or equipment automation is a plus.

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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