C&Q Specialist
Juncos, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
C&Q Specialist
Juncos, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
C&Q Specialist
Punta Santiago, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
C&Q Specialist
Punta Santiago, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
Document Controller
Juncos, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... This role will perform tasks to support the business areas mainly focused on the development of ...
Document Controller
Juncos, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... This role will perform tasks to support the business areas mainly focused on the development of ...
Document Controller
Barceloneta, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... This role will perform tasks to support the business areas mainly focused on the development of ...
Document Controller
Barceloneta, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... This role will perform tasks to support the business areas mainly focused on the development of ...
C&Q Specialist
Humacao, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
C&Q Specialist
Humacao, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
C&Q Specialist
Punta Santiago, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
C&Q Specialist
Punta Santiago, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
C&Q Specialist
Humacao, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
C&Q Specialist
Humacao, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
C&Q Specialist
Humacao, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
C&Q Specialist
Humacao, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
Document Controller
Juncos, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... This role will perform tasks to support the business areas mainly focused on the development of ...
Document Controller
Juncos, PR · On-site
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... This role will perform tasks to support the business areas mainly focused on the development of ...
C&Q Specialist
Gurabo, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
C&Q Specialist
Gurabo, PR · On-site
... biotechnology manufacturing environments ... This role is responsible for supporting protocol development, field execution activities, equipment ...
... development, and manufacturing initiatives. You will collaborate with technical specialists ... REQUIREMENTS: • 8 years of B2B sales experience in life sciences, biotech, pharmaceutical, or ...
... development, and manufacturing initiatives. You will collaborate with technical specialists ... REQUIREMENTS: • 8 years of B2B sales experience in life sciences, biotech, pharmaceutical, or ...
Sr. Account Manager
Cayey, PR · On-site
... development, and manufacturing initiatives. You will collaborate with technical specialists ... REQUIREMENTS: • 8 years of B2B sales experience in life sciences, biotech, pharmaceutical, or ...
Sr. Account Manager
Cayey, PR · On-site
... development, and manufacturing initiatives. You will collaborate with technical specialists ... REQUIREMENTS: • 8 years of B2B sales experience in life sciences, biotech, pharmaceutical, or ...
Sr Data Scientist
Juncos, PR · On-site
Identify business needs, conduct SWOT analyses, propose analytical approaches, obtain stakeholder ... Collaborate with external vendors and digital partners to support model development, automation ...
Quick apply
Sr Data Scientist
Juncos, PR · On-site
Identify business needs, conduct SWOT analyses, propose analytical approaches, obtain stakeholder ... Collaborate with external vendors and digital partners to support model development, automation ...
Minimum of 5 years of experience supporting utility systems in a pharmaceutical, biotechnology ... development. * Experience preparing executive-level business cases and capital investment proposals.
Minimum of 5 years of experience supporting utility systems in a pharmaceutical, biotechnology ... development. * Experience preparing executive-level business cases and capital investment proposals.
Field Application Specialist
Caguas, PR · On-site
Learn about the Danaher Business System which makes everything possible. The Field Application ... development and implementation of customer products/applications/solutions in alignment with ...
Field Application Specialist
Caguas, PR · On-site
Learn about the Danaher Business System which makes everything possible. The Field Application ... development and implementation of customer products/applications/solutions in alignment with ...
Field Application Specialist
Caguas, PR · On-site +1
Learn about the Danaher Business System which makes everything possible. The Field Application ... development and implementation of customer products/applications/solutions in alignment with ...
Field Application Specialist
Caguas, PR · On-site +1
Learn about the Danaher Business System which makes everything possible. The Field Application ... development and implementation of customer products/applications/solutions in alignment with ...
... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Learn about the Danaher Business System which makes everything possible. The Quality Engineering ...
... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Learn about the Danaher Business System which makes everything possible. The Quality Engineering ...
... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Learn about the Danaher Business System which makes everything possible. The Quality Engineering ...
... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Learn about the Danaher Business System which makes everything possible. The Quality Engineering ...
... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Learn about the Danaher Business System which makes everything possible. The Quality Engineering ...
... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Learn about the Danaher Business System which makes everything possible. The Quality Engineering ...
Engineer - 35626
Juncos, PR · On-site
Collaborate with Manufacturing, Maintenance, Process Development, Utilities, Facilities, Quality ... business needs. Competencies * Technical Problem Solving * Analytical Thinking * Process ...
Engineer - 35626
Juncos, PR · On-site
Collaborate with Manufacturing, Maintenance, Process Development, Utilities, Facilities, Quality ... business needs. Competencies * Technical Problem Solving * Analytical Thinking * Process ...
Intern Biotech Business Development information
What does an intern in biotech business development do?
An Intern in Biotech Business Development supports the growth strategies of biotechnology companies by assisting with market research, identifying partnership opportunities, and helping to analyze industry trends. They may prepare reports, participate in meetings with potential partners, and support the development of business proposals. This role provides hands-on experience in both the science and business aspects of the biotech industry, bridging technical knowledge and commercial strategy.
What are some common responsibilities for an intern in biotech business development?
As an Intern in Biotech Business Development, you'll typically assist with market research, help identify potential partnership opportunities, and support the preparation of presentations or business proposals. You'll often work closely with both scientific and commercial teams to understand new technologies and evaluate their market potential. This role also involves attending team meetings, tracking industry trends, and sometimes participating in outreach to potential collaborators or clients. It's a great way to gain hands-on experience at the intersection of science and business while building valuable professional networks.
What are the key skills and qualifications needed to thrive as an intern in biotech business development, and why are they important?
To thrive as an Intern in Biotech Business Development, you need a solid background in life sciences or biotechnology, strong analytical skills, and an interest in business strategy, usually supported by relevant coursework or a related degree. Familiarity with CRM platforms, market research tools, and Microsoft Office Suite is often expected. Excellent communication, teamwork, and organizational skills help you build relationships and manage multiple projects effectively. These skills are crucial for identifying business opportunities, supporting partnerships, and contributing to the growth of a biotech organization.
What is the difference between Intern Biotech Business Development vs Intern Biotech Research Assistant?
| Aspect | Intern Biotech Business Development | Intern Biotech Research Assistant |
|---|---|---|
| Primary Focus | Market analysis, partnership development, sales strategies | Laboratory research, data collection, experiment support |
| Required Skills | Business acumen, communication, basic biotech knowledge | Laboratory techniques, data analysis, scientific knowledge |
| Work Environment | Office setting, client meetings, industry events | Laboratory, research facilities, experimental setups |
| Common Employer Types | Biotech companies, startups, pharma firms | Research institutes, biotech labs, universities |
Intern Biotech Business Development roles focus on market strategies and building industry partnerships, requiring business skills and industry knowledge. In contrast, Intern Biotech Research Assistant positions involve laboratory work and scientific research. Both roles are essential in biotech but serve different functions within the industry.
What are the most commonly searched types of Biotech Business Development jobs in Puerto Rico?
The most popular types of Biotech Business Development jobs in Puerto Rico are:
What are popular job titles related to Intern Biotech Business Development jobs in Puerto Rico?
For Intern Biotech Business Development jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Intern Biotech Business Development jobs in Puerto Rico look for?
The top searched job categories for Intern Biotech Business Development jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Intern Biotech Business Development jobs?
Cities in Puerto Rico with the most Intern Biotech Business Development job openings:
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 C&Q Specialist will support commissioning and qualification activities associated with capital projects and technical initiatives within regulated pharmaceutical and biotechnology manufacturing environments.
This role is responsible for supporting protocol development, field execution activities, equipment startup support, commissioning and qualification documentation, and coordination activities associated with regulated systems and operational readiness initiatives.
Projects may support one or more of the following areas: manufacturing systems, process equipment, packaging systems, clean utilities, facilities, cleanroom environments, process improvements, utilities infrastructure, automation-related systems, or other regulated operational systems.
The role requires strong technical documentation skills, field coordination capabilities, and collaboration with Engineering, Operations, Quality, contractors, vendors, and project teams to support compliant project execution activities.
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:
- C&Q Specialist
Position Summary
The C&Q Specialist will support commissioning and qualification activities associated with capital projects and technical initiatives within regulated pharmaceutical and biotechnology manufacturing environments.
This role is responsible for supporting protocol development, field execution activities, equipment startup support, commissioning and qualification documentation, and coordination activities associated with regulated systems and operational readiness initiatives.
Projects may support one or more of the following areas: manufacturing systems, process equipment, packaging systems, clean utilities, facilities, cleanroom environments, process improvements, utilities infrastructure, automation-related systems, or other regulated operational systems.
The role requires strong technical documentation skills, field coordination capabilities, and collaboration with Engineering, Operations, Quality, contractors, vendors, and project teams to support compliant project execution activities.
Key Responsibilities
- Support assigned commissioning and qualification.
- Generate, review, and execute commissioning and qualification protocols and related technical documentation.
- Support field execution activities including commissioning support, verification activities, and operational readiness coordination.
- Participate in FAT & SAT activities, equipment inspections, field walkthroughs, and startup support activities as required.
- Support collection, review, and organization of commissioning and qualification documentation and test records.
- Document test results and execution activities in accordance with applicable GMP and data integrity expectations.
- Support identification, documentation, and follow-up of deviations, punch-list items, corrective actions, and technical observations during execution activities.
- Coordinate with Engineering, Operations, Quality, contractors, vendors, and project teams to support project execution and turnover activities.
- Support scheduling and coordination of field execution activities, testing activities, and resource needs.
- Participate in project meetings and support communication of execution status, technical issues, risks, and action items.
- Support continuous improvement initiatives related to commissioning, qualification, documentation, and operational readiness activities.
- Ensure commissioning and qualification activities are performed in alignment with applicable site procedures, GMP requirements, safety rules, policies and project expectations.
Qualifications & Experience
- Bachelor's degree in Engineering, Science, Business Administration, or related technical field preferred.
- Minimum of 2 years of relevant C&Q, validation, startup, or field execution experience required for candidates with Engineering or Science degrees.
- Candidates with Business Administration or other non-technical degrees should have a minimum of 3 years of relevant experience.
- Experience supporting one or more of the following areas is preferred: manufacturing systems, process equipment, packaging systems, clean utilities, facilities, cleanrooms, automation systems, or regulated operational infrastructure.
- Familiarity with commissioning and qualification documentation, protocol execution, technical field support, and GMP documentation practices.
- Familiarity with GMP regulations, data integrity principles (ALCOA), and regulated documentation practices.
- Familiarity with systems such as Kneat, Bluebeam, TrackWise, CMMS platforms, or similar technical and quality systems is preferred.
- Excellent verbal and written communication skills in both English and Spanish, including technical writing, protocol documentation, and communication of technical deliverables.
- Strong organizational, troubleshooting, analytical, and problem-solving skills with the ability to support multiple priorities and field activities simultaneously.
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