Senior Quality Analyst
Guaynabo, PR · On-site
Masters Degree in Science preferred. * Four (4) years of experience in Pharmaceutical/Biotechnology ... and ensure material control until regulatory approval. * Conform to EHS management system ...
Senior Quality Analyst
Guaynabo, PR · On-site
Masters Degree in Science preferred. * Four (4) years of experience in Pharmaceutical/Biotechnology ... and ensure material control until regulatory approval. * Conform to EHS management system ...
... analysis, CAPA, risk assessments, or change control within a Quality Management System ... Life Sciences, Pharmaceuticals and Medical Devices Join our winning team today. Together, we'll ...
... analysis, CAPA, risk assessments, or change control within a Quality Management System ... Life Sciences, Pharmaceuticals and Medical Devices Join our winning team today. Together, we'll ...
... analysis, CAPA, risk assessments, or change control within a Quality Management System. • ... Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner ...
... analysis, CAPA, risk assessments, or change control within a Quality Management System. • ... Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner ...
... cause analysis, CAPA, risk assessments, or change control within a Quality Management System ... Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner ...
... cause analysis, CAPA, risk assessments, or change control within a Quality Management System ... Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner ...
... cause analysis, CAPA, risk assessments, or change control within a Quality Management System ... Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner ...
... cause analysis, CAPA, risk assessments, or change control within a Quality Management System ... Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner ...
... cause analysis, CAPA, risk assessments, or change control within a Quality Management System ... Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner ...
... cause analysis, CAPA, risk assessments, or change control within a Quality Management System ... Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner ...
... analysis, CAPA, risk assessments, or change control within a Quality Management System ... Life Sciences, Pharmaceuticals and Medical Devices Join our winning team today. Together, we'll ...
... analysis, CAPA, risk assessments, or change control within a Quality Management System ... Life Sciences, Pharmaceuticals and Medical Devices Join our winning team today. Together, we'll ...
JT370 - QUALITY ENGINEER II
Humacao, PR · On-site
$72K - $93K/yr
... statistical analysis to assess the cost of and determine the responsibility for products or ... May specialize in the areas of design, incoming material, production control, product evaluation ...
JT370 - QUALITY ENGINEER II
Humacao, PR · On-site
$72K - $93K/yr
... statistical analysis to assess the cost of and determine the responsibility for products or ... May specialize in the areas of design, incoming material, production control, product evaluation ...
PR · On-site
Perform disinfectant and sanitization validation for Microbiology QC Laboratories and manufacturing ... Analyze validation data, investigate deviations, and recommend corrective actions when necessary.
Quick apply
PR · On-site
Perform disinfectant and sanitization validation for Microbiology QC Laboratories and manufacturing ... Analyze validation data, investigate deviations, and recommend corrective actions when necessary.
PR · On-site
Perform disinfectant and sanitization validation for Microbiology QC Laboratories and manufacturing ... Analyze validation data, investigate deviations, and recommend corrective actions when necessary.
Quick apply
PR · On-site
Perform disinfectant and sanitization validation for Microbiology QC Laboratories and manufacturing ... Analyze validation data, investigate deviations, and recommend corrective actions when necessary.
PR · On-site
Perform disinfectant and sanitization validation for Microbiology QC Laboratories and manufacturing ... Analyze validation data, investigate deviations, and recommend corrective actions when necessary.
Quick apply
PR · On-site
Perform disinfectant and sanitization validation for Microbiology QC Laboratories and manufacturing ... Analyze validation data, investigate deviations, and recommend corrective actions when necessary.
PR · On-site
Perform disinfectant and sanitization validation for Microbiology QC Laboratories and manufacturing ... Analyze validation data, investigate deviations, and recommend corrective actions when necessary.
Quick apply
PR · On-site
Perform disinfectant and sanitization validation for Microbiology QC Laboratories and manufacturing ... Analyze validation data, investigate deviations, and recommend corrective actions when necessary.
JT371 - SR QUALITY ENGINEER
Humacao, PR · On-site
$89K - $120K/yr
... statistical analysis to assess the cost of and determine the responsibility for products or ... Quality Systems & Change Control * Regulatory Compliance & Manufacturing Change Management ...
JT371 - SR QUALITY ENGINEER
Humacao, PR · On-site
$89K - $120K/yr
... statistical analysis to assess the cost of and determine the responsibility for products or ... Quality Systems & Change Control * Regulatory Compliance & Manufacturing Change Management ...
PR · On-site
$89K - $122K/yr
... control strategy, and pharmaceutical quality systems. * Experience performing statistical analysis ... Functions as a lead scientific / technical resource or as a project leader. FUNCTIONS 1. ...
Quick apply
PR · On-site
$89K - $122K/yr
... control strategy, and pharmaceutical quality systems. * Experience performing statistical analysis ... Functions as a lead scientific / technical resource or as a project leader. FUNCTIONS 1. ...
Sr Sterility Assurance Scientist
$89K - $122K/yr
Medical
Dental
Vision
Life
Retirement
Additionally, ensure compliance to other applicable Contamination Control, Endotoxin, Sterilization ... Familiarity with basic quality tools and techniques. * Analytical and critical thinking skills are ...
Sr Sterility Assurance Scientist
$89K - $122K/yr
Medical
Dental
Vision
Life
Retirement
Additionally, ensure compliance to other applicable Contamination Control, Endotoxin, Sterilization ... Familiarity with basic quality tools and techniques. * Analytical and critical thinking skills are ...
Quality Eng - P2
$59K - $77K/yr
... Scientific, we'll give you the opportunity to harness all that's within you by working in teams of ... May be responsible for creating risk analyses and FMEAs. * Develops Process Monitoring Systems by ...
Quality Eng - P2
$59K - $77K/yr
... Scientific, we'll give you the opportunity to harness all that's within you by working in teams of ... May be responsible for creating risk analyses and FMEAs. * Develops Process Monitoring Systems by ...
Quality Eng - P2
Dorado, PR · On-site
$63K - $81K/yr
... Scientific, we'll give you the opportunity to harness all that's within you by working in teams of ... May be responsible for creating risk analyses and FMEAs. * Develops Process Monitoring Systems by ...
Quality Eng - P2
Dorado, PR · On-site
$63K - $81K/yr
... Scientific, we'll give you the opportunity to harness all that's within you by working in teams of ... May be responsible for creating risk analyses and FMEAs. * Develops Process Monitoring Systems by ...
Quality Eng - P2
$63K - $81K/yr
... Scientific, we'll give you the opportunity to harness all that's within you by working in teams of ... May be responsible for creating risk analyses and FMEAs. * Develops Process Monitoring Systems by ...
Quality Eng - P2
$63K - $81K/yr
... Scientific, we'll give you the opportunity to harness all that's within you by working in teams of ... May be responsible for creating risk analyses and FMEAs. * Develops Process Monitoring Systems by ...
Quality Eng - P2
$59K - $77K/yr
... Scientific, we'll give you the opportunity to harness all that's within you by working in teams of ... May be responsible for creating risk analyses and FMEAs. * Develops Process Monitoring Systems by ...
Quality Eng - P2
$59K - $77K/yr
... Scientific, we'll give you the opportunity to harness all that's within you by working in teams of ... May be responsible for creating risk analyses and FMEAs. * Develops Process Monitoring Systems by ...
Quality Eng - P2
$63K - $81K/yr
... Scientific, we'll give you the opportunity to harness all that's within you by working in teams of ... May be responsible for creating risk analyses and FMEAs. * Develops Process Monitoring Systems by ...
Quality Eng - P2
$63K - $81K/yr
... Scientific, we'll give you the opportunity to harness all that's within you by working in teams of ... May be responsible for creating risk analyses and FMEAs. * Develops Process Monitoring Systems by ...
Quality Control Analytical Scientist information
What does a quality control analytical scientist do?
A Quality Control Analytical Scientist is responsible for testing and analyzing materials, products, and processes to ensure they meet established quality standards and regulatory requirements. They use a variety of laboratory instruments and techniques, such as chromatography and spectroscopy, to evaluate chemical, physical, and biological properties. Their work helps ensure the safety, efficacy, and consistency of products in industries like pharmaceuticals, biotechnology, and manufacturing. Additionally, they document results, troubleshoot issues, and collaborate with other teams to maintain quality throughout the production process.
What are the key skills and qualifications needed to thrive as a quality control analytical scientist?
To thrive as a Quality Control Analytical Scientist, you need a solid background in chemistry, analytical techniques, and a relevant degree such as a BS or MS in chemistry, biochemistry, or a related field. Proficiency in laboratory instrumentation like HPLC, GC, and spectrophotometry, along with knowledge of GMP/GLP regulations and possible certifications, is typically required. Attention to detail, problem-solving, and effective communication are essential soft skills for accurate data interpretation and teamwork. These skills ensure precise analytical results, regulatory compliance, and the integrity of product quality in regulated industries.
What are some typical challenges faced by quality control analytical scientists when working with new pharmaceutical products?
Quality Control Analytical Scientists often encounter challenges when validating analytical methods for new pharmaceutical products, such as ensuring accuracy, reproducibility, and compliance with strict regulatory standards. They may need to troubleshoot unexpected results, adapt to evolving testing technologies, and coordinate closely with cross-functional teams like R&D and manufacturing to resolve issues swiftly. Attention to detail and strong communication skills are essential in addressing these challenges and ensuring product quality throughout the development and production lifecycle.
What is the difference between Quality Control Analytical Scientist vs Quality Control Chemist?
| Aspect | Quality Control Analytical Scientist | Quality Control Chemist |
|---|---|---|
| Credentials | Bachelor's or Master's in Chemistry, Biochemistry, or related field; relevant certifications | Bachelor's degree in Chemistry or related field; certifications are common but not always required |
| Work Environment | Laboratories within pharmaceutical, biotech, or manufacturing companies | Laboratories in similar industries, often performing routine testing |
| Job Focus | Developing and validating analytical methods, data analysis, ensuring compliance | Performing routine sample testing, preparing reports, and maintaining documentation |
The main difference is that the Quality Control Analytical Scientist typically focuses on method development, validation, and data analysis, while the Quality Control Chemist primarily conducts routine testing and sample analysis. Both roles are essential in quality assurance within manufacturing industries, but the Analytical Scientist often requires a deeper understanding of analytical techniques and method validation processes.
What are popular job titles related to Quality Control Analytical Scientist jobs in Puerto Rico?
For Quality Control Analytical Scientist jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Quality Control Analytical Scientist jobs in Puerto Rico look for?
The top searched job categories for Quality Control Analytical Scientist jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Quality Control Analytical Scientist jobs?
Cities in Puerto Rico with the most Quality Control Analytical Scientist 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:
- Senior Quality Analyst
Qualifications:
- Bachelors degree in Biotechnology, Biology, Chemistry or Engineering. Masters Degree in Science preferred.
- Four (4) years of experience in Pharmaceutical/Biotechnology industry in a similar position.
- This position requires knowledge of quality / compliance /Investigations /Risk management as well as regulations and standards affecting biological products.
- Excellent written and spoken communication skills in English and Spanish.
- Knowledge of GMP, safety regulations.
- Quality/compliance management skills.
- Fast paced and adaptable to continuously changing environment.
- Subject to work with multiple priorities and interruptions and under reasonable pressure due to the nature and function of the area.
Responsibilities:
- * Support routine operations to ensure that all quality goals are met, and all practices and procedures comply with the company policies and applicable regulations for the Quality areas under responsibility.
- Serve as backup for the QA Manager leading the team and providing support to quality initiatives.
- Ensures investigations of plant events are evaluated in a timely manner; completed thoroughly and documented accurately in the plant CAPA system.
- Performs product impact analyses for plant events and places product on QA hold where appropriate.
- Participates on the Validation Review Board as the Manufacturing Quality Assurance function.
- Approves standard operating procedures; change management and risk management documents.
- Ensures all documents are in compliance with the company global procedures and regulatory requirements.
- Approves calibration requests, calibration out of tolerance and preventive maintenance records.
- Ensures that these documents have appropriate justifications according to product /process limits established.
- Demonstrates accountability and responsibility of EHS performance and compliance.
- Maintains an effective liaison and cooperative relationship with other Quality areas and Plant departments.
- Oversees manufacturing operations to ensure practices are in alignment with approved procedures.
- Provide support to the Compliance team during internal and external audits as required.
- Provide guidance for new product introduction activities.
- Develop risk assessments to support manufacturing activities for new products and ensure material control until regulatory approval.
- Conform to EHS management system requirements and compliance obligations, promote continuous improvement, and consider EHS aspects during the design and change process.
- Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal, and any other program applicable according to the position duties.
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