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Internship Quality Assurance Biotech Jobs in Puerto Rico

Pinnaql

Specialist QA

Guaynabo, PR · On-site

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Specialist QA FUNCTIONS - Review and approve product MPs. - Approve process validation protocols ...

Mirus Consulting Group

Specialits QA - 35669

Juncos, PR · On-site

Bachelor's Degree in Science, Engineering, Biotechnology, Chemistry, Biology, Pharmacy, or a related technical field. * Minimum of 4 years of directly related experience in Quality Assurance within a ...

New

Validation & Engineering Group, Inc

PR

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Specialist QA FUNCTIONS - Review and approve product MPs. - Approve process validation protocols ...

New

Pinnaql

Specialist QA

Juncos, PR · On-site

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Specialist QA FUNCTIONS - Review and approve product MPs. - Approve process validation protocols ...

New

MENTOR TECHNICAL GROUP CORP

PR · On-site

... biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, PR, ... Support QA oversight of Site Utilities Systems and Environmental Monitoring results. Coordinate ...

ECHO Consulting Group

Specialist QA

Juncos, PR · On-site

ECHO Consulting Group is a leader in providing solutions for the pharmaceutical, biotechnology ... Represent QA on NPI team. * Lead investigations. * Lead site audits. * Own site quality program ...

Pinnaql

Specialist QA

Juncos, PR · On-site

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Specialist QA * Shift: Non Standard Functions: * Perform On-the-floor Plant Quality Assurance (PQA ...

New

Validation & Engineering Group, Inc

PR

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Specialist QA * Shift: Non Standard Functions: * Perform On-the-floor Plant Quality Assurance (PQA ...

New

Kelly Services

PR

$38/hr

We at Kelly ® Science & Engineering hear you, and we're here for you! We're seeking a Specialist QA to work at a premier biotechnology client in Juncos, PR . Sound good? Take a closer look below.

Pharma Bioserv

Be Seen First

Sr. Quality Assurance Specialist

San Juan, PR · On-site

$60K - $75K/yr

... biotechnology & bio-engineering companies within the regulated industry for over 30 years. Since ... We are looking candidates with experience within regulated environment for a SR. Quality Assurance ...

Danaher

Quality Assurance Specialist II

Fajardo, PR · On-site

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance ...

Danaher

Quality Assurance Specialist II

Fajardo, PR · On-site

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance ...

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All JobsQuality Assurance Biotech JobsInternship Quality Assurance Biotech JobsInternship Quality Assurance Biotech Jobs in Puerto Rico

Internship Quality Assurance Biotech information

What does an internship in quality assurance in biotech involve?

An Internship in Quality Assurance (QA) in the biotech industry typically involves assisting in the development, implementation, and monitoring of quality systems to ensure that products meet regulatory standards and company policies. Interns may help with documentation, conduct audits, participate in inspections, and review procedures for compliance with Good Manufacturing Practices (GMP). This role provides hands-on experience in quality control, process validation, and understanding regulatory requirements that are critical in biotech manufacturing. It's a valuable opportunity to learn about the importance of quality in delivering safe and effective biotechnological products.

What are the key skills and qualifications needed to thrive as an internship quality assurance biotech, and why are they important?

To thrive as an Internship Quality Assurance Biotech, you generally need a background in life sciences or biotechnology, attention to detail, and basic knowledge of quality standards such as GMP or ISO. Familiarity with laboratory information management systems (LIMS), documentation tools, and regulatory databases is often required. Strong analytical thinking, communication, and teamwork skills help interns excel in quality-focused environments. These competencies ensure accurate compliance, effective documentation, and support the integrity of biotechnological research and production processes.

What are some common challenges faced during a quality assurance internship in the biotech industry?

As a Quality Assurance intern in biotech, you may encounter challenges such as understanding complex regulatory requirements, adapting to fast-paced project timelines, and learning to use specialized documentation and quality management systems. Additionally, interns often need to quickly develop a keen attention to detail, as even minor errors can impact compliance and product safety. Collaboration with cross-functional teams, such as R&D and manufacturing, is also key, so strong communication skills are essential for success in this role.

What are the most commonly searched types of Quality Assurance Biotech jobs in Puerto Rico?

The most popular types of Quality Assurance Biotech jobs in Puerto Rico are:

What job categories do people searching Internship Quality Assurance Biotech jobs in Puerto Rico look for?

The top searched job categories for Internship Quality Assurance Biotech jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Internship Quality Assurance Biotech jobs?

Cities in Puerto Rico with the most Internship Quality Assurance Biotech job openings:

Internship Quality Assurance Biotech jobs near you

JT669 - SPECIALIST QA

Quality Consulting Group

Juncos, PR • On-site

Contractor

Posted 2 days ago

New

Job description

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
  • Review, approve, and maintain manufacturing process documentation (MPs) in compliance with cGMP requirements
  • Review, approve, and ensure accuracy, completeness, and traceability of GMP documentation, including protocols, reports, investigations, and quality records
  • Approve process validation protocols and reports, including PPQs and cleaning validation documentation
  • Participate as Quality representative on incident triage teams, ensuring timely and compliant decision-making
  • Review and approve planned incidents, deviations, and nonconformances, ensuring appropriate risk assessment and documentation
  • Approve Environmental Characterization and environmental monitoring reports
  • Release and maintain compliance of sanitary utility systems
  • Represent Quality Assurance on New Product Introduction (NPI) teams
  • Lead and document investigations, root cause analyses, and CAPA development
  • Lead and support site audits, including internal, external, and regulatory inspections
  • Own, maintain, and continuously improve site quality program procedures
  • Serve as QA Manager designee on the local Change Control Review Board (CCRB)
  • Review and approve risk assessments and mitigation strategies
  • Support automation systems, including review of validation and change documentation
  • Support facilities, utilities, and environmental compliance programs

Qualifications:
  • Bachelor's degree in Engineering, Life Sciences, Quality, or a related field.
  • Experience in Quality Assurance within a cGMP/GxP manufacturing environment, preferably in the pharmaceutical or medical device industry.
  • Experience conducting on-the-floor Plant Quality Assurance (PQA) reviews and supporting manufacturing operations.
  • Strong knowledge of cGMP requirements, Quality Systems, manufacturing processes, and documentation practices.
  • Proven experience with deviations, CAPAs, change controls, investigations, and compliance assessments.
  • Experience with batch record review, MES, EBR, SAP, EDMQ, DQMS, TrackWise, and other quality/manufacturing systems.
  • Experience supporting or leading continuous improvement initiatives and projects.
  • Experience assessing changes for potential impact to product quality and ensuring compliance with established procedures.
  • Experience with Computer System Validation (CSV) and/or Computer Systems Quality Assurance (CSA), preferably within medical devices or other regulated industries.
  • Experience with GxP application validation, including Validation Master Plans, Risk Assessments/GxP Assessments, IQ, OQ, PQ, test scripts, and validation summary reports.
  • Proven experience in commissioning and qualification activities.
  • Experience supporting New Product Introduction (NPI) and complex projects involving new products.
  • Strong understanding of manufacturing, distribution, Quality Assurance, Quality Laboratory, and Process Development processes.
  • Experience supporting internal and external audits and regulatory inspections, including serving as a Quality Unit representative.
  • Ability to interact effectively with regulatory agencies and cross-functional teams.
  • Strong leadership, influencing, negotiation, facilitation, and decision-making skills.
  • Excellent organizational skills with the ability to manage multiple assignments and follow projects through completion.
  • Strong analytical skills, including data trending, evaluation, and compliance assessment.
  • Proficiency in Microsoft Word, PowerPoint, Excel, database applications, and other business systems.
  • Excellent written and verbal communication skills in English and Spanish.
  • Ability to work independently while effectively collaborating with all levels of the organization.
  • Strong interpersonal and cross-functional collaboration skills.
  • Non-Standard Shift

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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