$25/hr
Internship, co-op, or academic project experience within medical devices, manufacturing, quality ... Experience working in a regulated industry (Medical Device, Pharmaceutical, Biotechnology, etc.
Quick apply
$25/hr
Internship, co-op, or academic project experience within medical devices, manufacturing, quality ... Experience working in a regulated industry (Medical Device, Pharmaceutical, Biotechnology, etc.
Biotech Co Op information
What is a biotech co op?
Biotech Co Op positions are structured work experiences that allow students to gain hands-on experience in the biotechnology industry while still pursuing their academic studies. These cooperative education programs typically involve alternating periods of classroom learning with paid, practical work at a biotech company. Participants develop valuable skills, enhance their resumes, and often have the opportunity to network with professionals in the field. Biotech Co Ops can lead to job offers after graduation and provide insight into potential career paths within biotechnology.
What types of projects and responsibilities can a biotech co op expect during their placement?
As a Biotech Co-Op, you can expect to participate in a variety of hands-on projects that support ongoing research and development, such as assisting with laboratory experiments, analyzing data, maintaining lab equipment, and documenting results. You will often work closely with scientists, engineers, and other co-ops, gaining exposure to both independent tasks and team-based projects. This role provides a valuable opportunity to develop practical laboratory skills, understand real-world applications of biotechnology, and contribute to meaningful projects that may support product development or process improvements.
What is the difference between Biotech Co Op vs Biotech Intern?
| Aspect | Biotech Co Op | Biotech Intern |
|---|---|---|
| Credentials | Typically enrolled in a related degree program, sometimes with specific coursework | Usually students or recent graduates, often with similar educational backgrounds |
| Work Environment | Full-time or part-time roles within biotech companies, often lasting several months | Temporary positions, often part-time or summer roles in biotech labs or research settings |
| Employer & Industry Usage | Commonly used by biotech firms for ongoing student engagement and talent pipeline | Used by biotech companies to evaluate potential future employees and provide practical experience |
Both Biotech Co Op and Biotech Intern roles provide valuable industry experience for students and recent graduates. Co-ops often involve longer, more integrated work periods, while internships tend to be shorter-term opportunities. Understanding these differences can help candidates choose the best fit for their career development in the biotech industry.
What are the most commonly searched types of Biotech jobs in Puerto Rico?
The most popular types of Biotech jobs in Puerto Rico are:
What are popular job titles related to Biotech Co Op jobs in Puerto Rico?
For Biotech Co Op jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Biotech Co Op jobs in Puerto Rico look for?
The top searched job categories for Biotech Co Op jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Biotech Co Op jobs?
Cities in Puerto Rico with the most Biotech Co Op job openings:
$25/hr
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 27 days ago
Job description
Think the best job opportunities are far away? Think again. Great opportunities are right here in your backyard.
Kelly® Engineering is looking for a Validation Engineering to work at a premier manufacturing client in Añasco, PR.
Let us help you grow at work and discover the next step in your career, all while being a vital part of your community.
Shift : Admin, Monday through Friday. Available weekends, alternate shifts, after-hours activities when needed
Location : On Site | Añasco, Puerto Rico
- Bachelor’s Degree in Engineering or a related technical discipline (required).
- Internship, co-op, or academic project experience within medical devices, manufacturing, quality, or packaging is considered as experience
- Experience working in a regulated industry (Medical Device, Pharmaceutical, Biotechnology, etc.). Experience with tray-sealing processes (required).
- Available for working in ISO Class 7 cleanroom environments and following strict gowning requirements.
- Demonstrate strong documentation, organizational, and communication skills.
- Fluent in English (read, write, speak, and understand).
- Proficient in Microsoft Office (Excel, Word, PowerPoint).
- Thrive in a fast-paced, collaborative manufacturing environment with a strong willingness to learn.
- Preferred Requirements
- At least 4+ years of engineering or manufacturing experience.
- Experience with packaging validation, laboratory testing, or engineering projects.
- Knowledge of FDA QSR, ISO 13485, ISO 9001, GMP, and medical device regulations.
- Exposure to sterile barrier systems and validation methodologies.
- Preferred Requirements
- Supporting packaging validation and testing activities for sterile and non-sterile medical device packaging systems.
- Executing validation protocols, engineering studies, and testing activities in close collaboration with Packaging and Project Engineers.
- Collecting, analyzing, and documenting testing data and validation results.
- Preparing and maintaining technical documentation, including protocols, reports, and test summaries.
- Coordinating with cross-functional teams such as Quality, Operations, Regulatory, and Engineering.
- Supporting troubleshooting, risk assessments, process improvements, and packaging line trials.
- Ensuring compliance with internal procedures and applicable regulatory requirements.
- Opportunity to work in a regulated medical device manufacturing environment.
- Competitive pay rate with room to grow based on experience.
- Collaborate with engineering, quality, and regulatory professionals on impactful validation projects.
- Work for a respected industry leader focused on safety, compliance, and continuous improvement.
- Gain valuable hands-on experience in packaging validation and technical documentation.
- Access to the following benefits:
- Weekly pay (W2)
- Sick, Vacations & Holidays paid*
- Christmas bonus*
- * Must comply with minimum established requirements to qualify.
Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more.
Helping you discover what’s next in your career is what we’re all about, so let’s get to work.
Apply to be Validation Engineering today!
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly® Engineering?
Your engineering skills are in demand, but how do you find the right fit? Easy. At Kelly Engineering, our team creates expert talent solutions to solve the world’s most critical challenges. We connect you with leading organizations where you can collaborate on innovative projects, work with cutting-edge technologies and accelerate your growth. Whether you prefer the variety and flexibility of short-term projects or are looking for a long-term opportunity, we’re here to guide you to the next step in your engineering career.About Kelly
Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.