Project Manager
Humacao, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...
Project Manager
Humacao, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...
Project Manager
Punta Santiago, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...
Project Manager
Punta Santiago, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...
Project Manager
Juncos, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...
Project Manager
Juncos, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...
Project Manager
Juncos, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...
Project Manager
Juncos, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...
Project Manager
Gurabo, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...
Project Manager
Gurabo, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...
Project Manager
Humacao, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...
Project Manager
Humacao, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...
... biotechnology, or manufacturing environments. • Demonstrated experience supporting cleanroom or controlled environment operations, including environmental controls, contamination control practices ...
... biotechnology, or manufacturing environments. • Demonstrated experience supporting cleanroom or controlled environment operations, including environmental controls, contamination control practices ...
Long-standing experience (Minimum of 5-10 years in regulated life sciences, medical device, pharmaceutical, biotechnology, or manufacturing environments. Demonstrated experience supporting cleanroom ...
Long-standing experience (Minimum of 5-10 years in regulated life sciences, medical device, pharmaceutical, biotechnology, or manufacturing environments. Demonstrated experience supporting cleanroom ...
... biotechnology, or manufacturing environments. * Demonstrated experience supporting cleanroom or controlled environment operations, including environmental controls, contamination control practices ...
... biotechnology, or manufacturing environments. * Demonstrated experience supporting cleanroom or controlled environment operations, including environmental controls, contamination control practices ...
Long-standing experience (Minimum of 5-10 years in regulated life sciences, medical device, pharmaceutical, biotechnology, or manufacturing environments. Demonstrated experience supporting cleanroom ...
Long-standing experience (Minimum of 5-10 years in regulated life sciences, medical device, pharmaceutical, biotechnology, or manufacturing environments. Demonstrated experience supporting cleanroom ...
... biotechnology, or manufacturing environments. • Demonstrated experience supporting cleanroom or controlled environment operations, including environmental controls, contamination control practices ...
... biotechnology, or manufacturing environments. • Demonstrated experience supporting cleanroom or controlled environment operations, including environmental controls, contamination control practices ...
... biotechnology, or manufacturing environments. * Demonstrated experience supporting cleanroom or controlled environment operations, including environmental controls, contamination control practices ...
... biotechnology, or manufacturing environments. * Demonstrated experience supporting cleanroom or controlled environment operations, including environmental controls, contamination control practices ...
EH&S Coordinator
Juncos, PR · On-site
Experience working at biotech campuses. * Knowledge of GMP environments and cleanroom construction safety considerations. * Experience supporting commissioning/startup phases. At Validation ...
EH&S Coordinator
Juncos, PR · On-site
Experience working at biotech campuses. * Knowledge of GMP environments and cleanroom construction safety considerations. * Experience supporting commissioning/startup phases. At Validation ...
EH&S Coordinator
Juncos, PR · On-site
Experience working at biotech campuses. * Knowledge of GMP environments and cleanroom construction safety considerations. * Experience supporting commissioning/startup phases. At Validation ...
EH&S Coordinator
Juncos, PR · On-site
Experience working at biotech campuses. * Knowledge of GMP environments and cleanroom construction safety considerations. * Experience supporting commissioning/startup phases. At Validation ...
JT562 - SR MANUFACTURING ENGINEER
Juncos, PR · On-site
$100 - $125/hr
QUALITY CONSULTING GROUP, a leader inthe pharmaceutical, biotech, medical devices, and ... execution, cleanroom and layout changes, change control updates, and decommissioning--while ...
JT562 - SR MANUFACTURING ENGINEER
Juncos, PR · On-site
$100 - $125/hr
QUALITY CONSULTING GROUP, a leader inthe pharmaceutical, biotech, medical devices, and ... execution, cleanroom and layout changes, change control updates, and decommissioning--while ...
EHSS Coordinator
Punta Santiago, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... cleanroom improvements, equipment installations, commissioning activities, and other regulated ...
EHSS Coordinator
Punta Santiago, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... cleanroom improvements, equipment installations, commissioning activities, and other regulated ...
EHSS Coordinator
Humacao, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... cleanroom improvements, equipment installations, commissioning activities, and other regulated ...
EHSS Coordinator
Humacao, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... cleanroom improvements, equipment installations, commissioning activities, and other regulated ...
EHSS Coordinator
Gurabo, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... cleanroom improvements, equipment installations, commissioning activities, and other regulated ...
EHSS Coordinator
Gurabo, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... cleanroom improvements, equipment installations, commissioning activities, and other regulated ...
EHSS Coordinator
Humacao, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... cleanroom improvements, equipment installations, commissioning activities, and other regulated ...
EHSS Coordinator
Humacao, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... cleanroom improvements, equipment installations, commissioning activities, and other regulated ...
EHSS Coordinator
Humacao, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... cleanroom improvements, equipment installations, commissioning activities, and other regulated ...
EHSS Coordinator
Humacao, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... cleanroom improvements, equipment installations, commissioning activities, and other regulated ...
Biotech Cleanroom information
What is a biotech cleanroom?
A Biotech Cleanroom is a specially designed, controlled environment used in biotechnology labs and manufacturing facilities to minimize contamination from dust, microbes, or other airborne particles. These rooms maintain strict temperature, humidity, and particle count standards to protect sensitive biological samples and processes. Workers in biotech cleanrooms follow rigorous gowning and hygiene protocols, and equipment is regularly sterilized. Cleanrooms are essential in producing pharmaceuticals, medical devices, and other biotech products that require high levels of purity and safety.
What are the key skills and qualifications needed to thrive as a biotech cleanroom technician?
To thrive as a Biotech Cleanroom Technician, you need knowledge of aseptic techniques, good laboratory practices (GLP), and a background in biology or biotechnology, often with an associate’s or bachelor’s degree. Familiarity with cleanroom protocols, environmental monitoring equipment, and compliance systems like GMP (Good Manufacturing Practice) is typically required. Attention to detail, reliability, and effective communication are critical soft skills for maintaining sterile environments and following strict procedures. These skills ensure product safety, regulatory compliance, and consistent quality in sensitive biotech manufacturing processes.
What are some common challenges faced when working in a biotech cleanroom environment?
One of the main challenges in a biotech cleanroom is maintaining strict adherence to contamination control protocols while performing complex tasks. Employees must follow rigorous gowning procedures, regularly sanitize equipment, and be vigilant about minimizing particle generation. The controlled environment can feel restrictive due to specialized attire and limited personal items, but it's essential for ensuring product quality and safety. Teamwork and clear communication are crucial, as tasks often require coordination with colleagues to maintain workflow efficiency and compliance with regulatory standards.
What is the difference between Biotech Cleanroom vs Laboratory Technician?
| Aspect | Biotech Cleanroom | Laboratory Technician |
|---|---|---|
| Required Credentials | Cleanroom certification, life sciences training | Associate degree or relevant certification, lab safety training |
| Work Environment | Controlled cleanroom environment, strict contamination control | Standard laboratory setting, varied equipment |
| Industry Usage | Biotech manufacturing, pharmaceutical production | Research labs, clinical testing |
Biotech Cleanroom specialists focus on maintaining contamination-free environments for biotech and pharmaceutical manufacturing, requiring specialized cleanroom protocols. Laboratory Technicians support research and testing in general lab settings. While both roles require scientific knowledge, cleanroom roles emphasize contamination control and certification, whereas lab technicians focus on testing and data collection.
What job categories do people searching Biotech Cleanroom jobs in Puerto Rico look for?
The top searched job categories for Biotech Cleanroom jobs in Puerto Rico are:
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:
Position Summary
The Project Manager will lead and support a portfolio of capital projects and strategic initiatives within regulated pharmaceutical and biotechnology manufacturing environments. This role is responsible for managing projects through all phases of execution while ensuring alignment with business objectives, safety requirements, quality expectations, schedule commitments, and budget targets.
Projects may support manufacturing operations, packaging systems, process improvements, facility upgrades, cleanroom improvements, commissioning and qualification activities, operational excellence initiatives, utilities, and other regulated engineering programs.
The role requires strong leadership, technical coordination, and cross-functional collaboration with Engineering, Operations, Quality, Procurement, EHSS, Construction, external contractors, and equipment vendors.
Key Responsibilities
Qualifications & Experience
Additional Requirements
The above statements describe the general nature and level of work performed and do not represent an exhaustive list of responsibilities.
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.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
- Project Manager
Position Summary
The Project Manager will lead and support a portfolio of capital projects and strategic initiatives within regulated pharmaceutical and biotechnology manufacturing environments. This role is responsible for managing projects through all phases of execution while ensuring alignment with business objectives, safety requirements, quality expectations, schedule commitments, and budget targets.
Projects may support manufacturing operations, packaging systems, process improvements, facility upgrades, cleanroom improvements, commissioning and qualification activities, operational excellence initiatives, utilities, and other regulated engineering programs.
The role requires strong leadership, technical coordination, and cross-functional collaboration with Engineering, Operations, Quality, Procurement, EHSS, Construction, external contractors, and equipment vendors.
Key Responsibilities
- Lead overall project delivery, governance, and execution throughout the project lifecycle.
- Develop and maintain project plans, schedules, budgets, forecasts, resource strategies, and risk management plans.
- Coordinate cross-functional teams to ensure projects are delivered safely, on schedule, within budget, and in compliance with applicable GMP and site requirements.
- Handle project financial performance including cost tracking, forecasting, variance analysis, and reporting.
- Support procurement coordination, contractor management, vendor management, and technical alignment activities.
- Lead project meetings and communicate project status, risks, issues, mitigation plans, and key decisions to stakeholders and leadership teams.
- Coordinate project scope changes, project documentation, and project-related change activities as required.
- Prepare and maintain project documentation including schedules, status reports, risk logs, budgets, meeting minutes, action trackers, and project closeout packages.
- Coordinate activities supporting commissioning, qualification, startup, operational readiness, and turnover to operations.
- Support project execution activities in alignment with applicable EHSS requirements and site procedures.
- Identify project risks, resource constraints, and execution challenges while driving timely resolution and escalation when needed.
- Support continuous improvement initiatives related to project execution, compliance, and operational performance.
Qualifications & Experience
- Bachelor's degree in Engineering required.
- Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries.
- Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and regulated operational systems.
- Proven experience managing project scope, schedule, budget, risks, stakeholder communications, and cross-functional coordination.
- Experience supporting projects through design, procurement, construction, commissioning, startup, qualification, and operational handover phases.
- Experience coordinating with engineering firms, contractors, equipment vendors, and internal technical teams.
- Strong understanding of GMP environments, regulated project execution, and quality system expectations.
- Familiarity with project management, scheduling, cost tracking, and reporting tools such as MS Project, SAP, Planisware, Primavera, or similar systems is preferred.
- PMP certification is preferred.
- Excellent verbal and written communication skills in both English and Spanish, including technical writing, documentation preparation, meeting facilitation, and communication of project deliverables.
- Strong leadership, organizational, analytical, and problem-solving skills with the ability to manage multiple priorities and complex project portfolios.
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.
The above statements describe the general nature and level of work performed and do not represent an exhaustive list of responsibilities.
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.
About Pinnaql
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
11 - 50 Employees
Headquarters location
Malvern, PA, US
Year founded
2019