Laboratory Analyst Associate 3262706 (Biotechnology)
Job Title: Laboratory Analyst Associate 3262706 (Biotechnology)
Location: Easr of Puerto Rico - 100% Onsite on Administrative Shift
Duration: Approximately 5 months
Open to Residents of Puerto Rico Only
ProQuality Network is seeking two highly skilled professionals for the position of Process Development Sr. Associate Scientist to join our client, a leading biotechnology organization. Selected candidates will represent ProQuality Network with professionalism and excellence, contributing to vital scientific work that directly impacts the quality and safety of medical products.
Summary of Role
The selected individuals will be responsible for developing and executing studies related to primary packaging defects (vials and syringes) for research, equipment characterization, training, and setup of commercial systems. This is a hands-on laboratory-based role requiring technical proficiency, innovation, and collaboration across departments.
Preferred Qualifications
- Proven experience in preparing syringes/vials with cosmetic, particulate, or solution defects for development purposes.
- Skilled in using laboratory equipment such as:
- Micrometer
- Caliper
- Microscope
- Analytical balance
- Creative mindset and strong manual dexterity to develop and replicate defects on glass and polymer surfaces.
- Ability to:
- Introduce or improve defect creation methods in the laboratory.
- Evaluate and classify primary container defects.
- Create documentation based on technical assessments and reports.
- Solid understanding of:
- Aseptic techniques
- Visual Manual Inspection techniques
- 5S and Lean Manufacturing concepts
- Excellent communication and interpersonal skills to support and motivate team activities.
- Demonstrated capability to prioritize multiple tasks in a fast-paced environment.
- Innovative, analytical, and results-driven mindset with a strong team orientation.
Essential Responsibilities
- Design, plan, and perform experiments with minimal supervision.
- Record, organize, and analyze data to support packaging defect-related studies.
- Participate in developing new methods and improve existing lab protocols.
- Evaluate and interpret experimental results to provide clear recommendations.
- Serve as a resource and technical expert in the development of cosmetic defects.
- Collaborate across departments to ensure timely project execution.
- Maintain compliance with cGMPs, internal protocols, and regulatory requirements.
- Author technical reports, regulatory documents, and related publications.
- Represent the department in cross-functional teams and contribute to safety and quality initiatives.
Educational / Software Requirements
- Master’s Degree in Engineering or related scientific discipline with 3+ years of directly related experience
- OR
- Bachelor’s Degree in Engineering or related scientific discipline with 5+ years of directly related experience
Competencies & Skills
- Advanced scientific analysis and troubleshooting
- Laboratory expertise in scientific experimentation and data interpretation
- Strong technical writing, verbal communication, and problem-solving skills
- Proficiency in project management, negotiation, and conflict resolution
- Adaptability to manage change and multitask across priorities
- Fully bilingual in English and Spanish
- Strong knowledge of current Good Manufacturing Practices (cGMPs)
If you are passionate about science and innovation and would like to be a key contributor representing ProQuality Network in a dynamic biotechnology setting, we invite you to apply at the link below with your most updated resume.