QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... assurance within injection molding or plastics manufacturing. * Strong knowledge of ISO standards ...
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... assurance within injection molding or plastics manufacturing. * Strong knowledge of ISO standards ...
JT021 - QUALITY MANAGER
Fajardo, PR · On-site
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... The Quality Manager is responsible for leading all Quality Assurance (QA) and Quality Control (QC) ...
JT021 - QUALITY MANAGER
Fajardo, PR · On-site
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... The Quality Manager is responsible for leading all Quality Assurance (QA) and Quality Control (QC) ...
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Manage QA lists, spreadsheets, and databases required to support business operations. * Participate ...
Quick apply
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Manage QA lists, spreadsheets, and databases required to support business operations. * Participate ...
JT563 - SR QUALITY ENGINEER
Juncos, PR · On-site
$86K - $117K/yr
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance ...
JT563 - SR QUALITY ENGINEER
Juncos, PR · On-site
$86K - $117K/yr
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance ...
As a world leader in life science engineering and technical solutions, MTG ensures compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in ...
As a world leader in life science engineering and technical solutions, MTG ensures compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in ...
CQV Specialist - Upstream Process Equipment & Downstream Biotech Process Equipment
Juncos, PR · On-site
... biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto ... Collaborate with cross-functional teams including Engineering, Operations, and QA/QC to ensure ...
CQV Specialist - Upstream Process Equipment & Downstream Biotech Process Equipment
Juncos, PR · On-site
... biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto ... Collaborate with cross-functional teams including Engineering, Operations, and QA/QC to ensure ...
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Owns or performs QA approval for DQMS Quality Event records (Quality Incident, Deviation, CAPA ...
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Owns or performs QA approval for DQMS Quality Event records (Quality Incident, Deviation, CAPA ...
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
JT570 - SR ENGINEER
Juncos, PR · On-site
$102K - $140K/yr
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... Work with research, manufacturing, process development, utilities, facilities, quality assurance ...
JT570 - SR ENGINEER
Juncos, PR · On-site
$102K - $140K/yr
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... Work with research, manufacturing, process development, utilities, facilities, quality assurance ...
JT289 - IT PROJECT SPECIALIST
Salinas, PR · On-site
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... Test applications in QA environments to ensure proper functionality. * Learn and quickly adapt to ...
JT289 - IT PROJECT SPECIALIST
Salinas, PR · On-site
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... Test applications in QA environments to ensure proper functionality. * Learn and quickly adapt to ...
JT449 - SR ENGINEER
Juncos, PR · On-site
$102K - $140K/yr
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... Work with research, manufacturing, process development, utilities, facilities, quality assurance ...
JT449 - SR ENGINEER
Juncos, PR · On-site
$102K - $140K/yr
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... Work with research, manufacturing, process development, utilities, facilities, quality assurance ...
JT544 - ENGINEER
Juncos, PR · On-site
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... facilities, quality assurance and/or validation departments in developing requirements and ...
JT544 - ENGINEER
Juncos, PR · On-site
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... facilities, quality assurance and/or validation departments in developing requirements and ...
Deviations Owner
Juncos, PR · On-site
... biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto ... Coordinate with production, QA/QC, and project teams to evaluate deviations, determine root cause ...
Deviations Owner
Juncos, PR · On-site
... biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto ... Coordinate with production, QA/QC, and project teams to evaluate deviations, determine root cause ...
$17/hr
... one of out top biotechnology industry client at the East area of PR. With us, it's all about ... Collaborate with Supply Chain Procurement, QA, Dispensing, Receiving, Shipping, and Packaging teams ...
Quick apply
$17/hr
... one of out top biotechnology industry client at the East area of PR. With us, it's all about ... Collaborate with Supply Chain Procurement, QA, Dispensing, Receiving, Shipping, and Packaging teams ...
Preferred Qualifications: * 3+ years related work experience (manufacturing, process development, or quality assurance) in Biotech or pharmaceutical industry with progressively increasing ...
Preferred Qualifications: * 3+ years related work experience (manufacturing, process development, or quality assurance) in Biotech or pharmaceutical industry with progressively increasing ...
PR · On-site
Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning, Qualification ... Collaborate with Quality Assurance, Engineering, Manufacturing, Automation, and Regulatory teams to ...
PR · On-site
Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning, Qualification ... Collaborate with Quality Assurance, Engineering, Manufacturing, Automation, and Regulatory teams to ...
PR · On-site
Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning, Qualification ... Collaborate with Quality Assurance, Engineering, Manufacturing, Automation, and Regulatory teams to ...
Quick apply
PR · On-site
Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning, Qualification ... Collaborate with Quality Assurance, Engineering, Manufacturing, Automation, and Regulatory teams to ...
PR · On-site
Salary: Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning ... Collaborate with Quality Assurance, Engineering, Manufacturing, Automation, and Regulatory teams to ...
Quick apply
PR · On-site
Salary: Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning ... Collaborate with Quality Assurance, Engineering, Manufacturing, Automation, and Regulatory teams to ...
PR · On-site
Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning, Qualification ... Collaborate with Quality Assurance, Engineering, Manufacturing, Automation, and Regulatory teams to ...
PR · On-site
Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning, Qualification ... Collaborate with Quality Assurance, Engineering, Manufacturing, Automation, and Regulatory teams to ...
Senior Director, R&D GxP Audit
Juncos, PR · On-site
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... (R&D) Quality organization. This leader is responsible for providing independent assurance that ...
Senior Director, R&D GxP Audit
Juncos, PR · On-site
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... (R&D) Quality organization. This leader is responsible for providing independent assurance that ...
Quality Assurance Biotech information
What is a quality assurance biotech?
A Quality Assurance (QA) Biotech job involves ensuring that biotechnology products meet regulatory and company standards for safety, efficacy, and quality. QA professionals develop and implement quality systems, conduct audits, review documentation, and ensure compliance with Good Manufacturing Practices (GMP) and other regulations. They collaborate with various departments, including manufacturing, R&D, and regulatory affairs, to maintain product integrity. Their role is critical in preventing defects, ensuring consistent processes, and maintaining compliance with industry standards.
What are the key skills and qualifications needed to thrive in quality assurance biotech?
To thrive as a Quality Assurance Biotech, you need a solid understanding of biotechnology processes, quality control methodologies, and regulatory standards such as GMP, often supported by a degree in biology, chemistry, or a related field. Familiarity with laboratory information management systems (LIMS), documentation software, and industry certifications like ASQ or GMP training is highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills are valued soft skills in this role. These abilities ensure precise compliance with regulatory requirements, facilitate collaboration with cross-functional teams, and help maintain the integrity and safety of biotech products.
What are the most common challenges faced by quality assurance professionals in the biotech industry?
Quality Assurance professionals in biotechnology often encounter challenges related to staying up-to-date with evolving regulatory requirements and ensuring that all processes consistently meet strict quality standards. Additionally, managing thorough documentation and collaborating across various departments—such as research, manufacturing, and regulatory affairs—can be complex. Those in the role may also need to respond quickly to deviations or quality events, requiring both proactive problem-solving and excellent organizational skills. However, overcoming these challenges is highly rewarding, as it directly contributes to maintaining the safety and efficacy of biotech products.
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 Quality Assurance Biotech jobs in Puerto Rico look for? The top searched job categories for Quality Assurance Biotech jobs in Puerto Rico are:
- Director Verizon Quality Assurance
- Clinical Research Quality Assurance Manager
- Senior Supplier Quality Assurance
- Internship Gmp Quality Assurance
- Internship Quality Assurance Biotech
- Quality Assurance Complaint Handling
- Remote Pharmaceutical Quality Assurance
- Ai Quality Assurance
- Quality Assurance Regulatory
Temporary
Re-posted 28 days ago
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:
Qualifications:
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.
Responsibilities:
- Quality Lead is responsible for overseeing all aspects of product quality within the injection molding operations.
- Develop, implement, and maintain quality systems (ISO 9001, or customer-specific standards).
Establish and monitor quality control plans, inspection procedures, and testing protocols. - Lead root cause analysis and corrective/preventive actions (CAPA) for nonconformities.
- Ensures compliance with customer specifications, industry standards, and regulatory requirements while driving continuous improvement initiatives.
- Establish and inspect quality control processes and audits.
- Perform inspection of parts and interpret engineering drawings/blueprints.
- Ensure inspections and documentation comply with GMP and quality standards.
- Support quality activities during the assigned shift and provide guidance as needed.
Qualifications:
- Bachelor's degree in quality management, or a related field. (Preferred but no required)
- 3 to 5 years of experience in quality assurance within injection molding or plastics manufacturing.
- Strong knowledge of ISO standards, Validations, PPAP, FMEA, SPC, and GD&T.
- Experience with metrology equipment and statistical analysis tools
- Proficient in the use of measurement tools and verification of their calibration.
- Strong documentation skills.
- Leadership abilities.
- Quality-driven and detail-oriented mindset.
- Proven knowledge in the use of micrometers, calipers, optical comparators, and basic measuring equipment.
- Bilingual (English/Spanish) preferred.
- 1st shift but candidate must be available to work 2nd or 3rd shift if needed.
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.
About Quality Consulting Group
Sourced by ZipRecruiter