Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and ... In-depth experience of bio-processing unit operations (Cell Culture, Drug Substance Purification)
Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and ... In-depth experience of bio-processing unit operations (Cell Culture, Drug Substance Purification)
Specialist Manufacturing
Juncos, PR · On-site
... Drug Substance Purification) • Knowledge in Root Cause Analysis methodologies (Fishbone, Six ... Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and ...
Specialist Manufacturing
Juncos, PR · On-site
... Drug Substance Purification) • Knowledge in Root Cause Analysis methodologies (Fishbone, Six ... Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and ...
PR · On-site
Educational background in Life Sciences and/or Engineering. * In-depth experience of bio-processing ... Cell Culture, Drug Substance Purification) * Knowledge in Root Cause Analysis methodologies ...
Quick apply
PR · On-site
Educational background in Life Sciences and/or Engineering. * In-depth experience of bio-processing ... Cell Culture, Drug Substance Purification) * Knowledge in Root Cause Analysis methodologies ...
PR · On-site
... development. At present, the Business Analyst under this business unit, shall: * Develop and ... Execute Limited Drug Distribution (LDD) Report testing. * Generate work capacity assessments for ...
Quick apply
PR · On-site
... development. At present, the Business Analyst under this business unit, shall: * Develop and ... Execute Limited Drug Distribution (LDD) Report testing. * Generate work capacity assessments for ...
PR · On-site
... development. At present, the Business Analyst under this business unit, shall: * Develop and ... Execute Limited Drug Distribution (LDD) Report testing. * Generate work capacity assessments for ...
Quick apply
PR · On-site
... development. At present, the Business Analyst under this business unit, shall: * Develop and ... Execute Limited Drug Distribution (LDD) Report testing. * Generate work capacity assessments for ...
Educational background in Life Sciences and/or Engineering. * In-depth experience of bio-processing ... Cell Culture, Drug Substance Purification) * Knowledge in Root Cause Analysis methodologies ...
Quick apply
Educational background in Life Sciences and/or Engineering. * In-depth experience of bio-processing ... Cell Culture, Drug Substance Purification) * Knowledge in Root Cause Analysis methodologies ...
Specialist Manufacturing
Juncos, PR · On-site
The role applies process, operational, and scientific expertise, along with compliance knowledge ... Ability to communicate effectively with manufacturing, process development, engineering, and ...
Quick apply
Specialist Manufacturing
Juncos, PR · On-site
The role applies process, operational, and scientific expertise, along with compliance knowledge ... Ability to communicate effectively with manufacturing, process development, engineering, and ...
Specialist Manufacturing
Juncos, PR · On-site
Preferred Qualifications: • Educational background in Life Sciences and/or Engineering. • In ... Drug Substance Purification) • Knowledge in Root Cause Analysis methodologies (Fishbone, Six ...
Specialist Manufacturing
Juncos, PR · On-site
Preferred Qualifications: • Educational background in Life Sciences and/or Engineering. • In ... Drug Substance Purification) • Knowledge in Root Cause Analysis methodologies (Fishbone, Six ...
Specialist Manufacturing
Juncos, PR · On-site
Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and ... Experience in biotechnology pharmaceutical process support, especially on Drug Substance processes ...
Specialist Manufacturing
Juncos, PR · On-site
Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and ... Experience in biotechnology pharmaceutical process support, especially on Drug Substance processes ...
Associate Customer Service
Arecibo, PR · On-site
$12.50 - $17.25/hr
Career development with an international company where you can grow the career you dream of ... Food and Drug Administration (FDA) regulations, other regulatory requirements, cooperative ...
Associate Customer Service
Arecibo, PR · On-site
$12.50 - $17.25/hr
Career development with an international company where you can grow the career you dream of ... Food and Drug Administration (FDA) regulations, other regulatory requirements, cooperative ...
Associate Customer Service
$12.50 - $17.25/hr
Career development with an international company where you can grow the career you dream of ... Food and Drug Administration (FDA) regulations, other regulatory requirements, cooperative ...
Associate Customer Service
$12.50 - $17.25/hr
Career development with an international company where you can grow the career you dream of ... Food and Drug Administration (FDA) regulations, other regulatory requirements, cooperative ...
Preferred educational background in Life Sciences and/or Engineering. Preferred Qualifications * In ... Drug Substance Purification. * Knowledge of Root Cause Analysis methodologies, including:
Preferred educational background in Life Sciences and/or Engineering. Preferred Qualifications * In ... Drug Substance Purification. * Knowledge of Root Cause Analysis methodologies, including:
Preferred educational background in Life Sciences and/or Engineering. Preferred Qualifications * In ... Drug Substance Purification. * Knowledge of Root Cause Analysis methodologies, including:
Quick apply
Preferred educational background in Life Sciences and/or Engineering. Preferred Qualifications * In ... Drug Substance Purification. * Knowledge of Root Cause Analysis methodologies, including:
Our award-winning culture is collaborative, innovative, and science based. If you have a passion ... Train team members on hands-on tasks to support skill development. * Support investigations and ...
Our award-winning culture is collaborative, innovative, and science based. If you have a passion ... Train team members on hands-on tasks to support skill development. * Support investigations and ...
Technician I, Remote Care
$13.18 - $25.02/hr
Career development with an international company where you can grow the career you dream of. * A ... S. Food and Drug Administration (FDA) regulations, other regulatory requirements. * Adhere to ...
New
Technician I, Remote Care
$13.18 - $25.02/hr
Career development with an international company where you can grow the career you dream of. * A ... S. Food and Drug Administration (FDA) regulations, other regulatory requirements. * Adhere to ...
New
... development, inspection product transfer and inspection operational support of Sterile/Biologics ... Improves inspection processes, technologies and systems to insure compliance with drug quality and ...
Quick apply
... development, inspection product transfer and inspection operational support of Sterile/Biologics ... Improves inspection processes, technologies and systems to insure compliance with drug quality and ...
Responsibilities The Associate Director - Technical Services/Manufacturing Science (TS/MS) Dry ... Performance management and development of staff. * Partner within TS/MS , ENG and across functional ...
Responsibilities The Associate Director - Technical Services/Manufacturing Science (TS/MS) Dry ... Performance management and development of staff. * Partner within TS/MS , ENG and across functional ...
Our award-winning culture is collaborative, innovative, and science based. If you have a passion ... Drug Product Experience * Experience in Pharmaceutical, Medical Device and/or Biotech Manufacturing ...
Our award-winning culture is collaborative, innovative, and science based. If you have a passion ... Drug Product Experience * Experience in Pharmaceutical, Medical Device and/or Biotech Manufacturing ...
Phd Drug Development Scientist information
What does a PhD drug development scientist do?
A PhD Drug Development Scientist is responsible for researching, designing, and conducting experiments to develop new pharmaceutical drugs or improve existing ones. They typically work in laboratories within pharmaceutical companies, biotechnology firms, or academic institutions. Their work involves understanding disease mechanisms, identifying drug targets, optimizing drug candidates, and ensuring safety and efficacy through preclinical and clinical trials. They also analyze data, collaborate with interdisciplinary teams, and comply with regulatory standards throughout the drug development process.
What are the key skills and qualifications needed to thrive as a PhD drug development scientist, and why are they important?
To thrive as a PhD Drug Development Scientist, you need deep expertise in pharmacology, biochemistry, and molecular biology, typically backed by a doctoral degree in a relevant scientific field. Familiarity with laboratory techniques, data analysis software, and regulatory documentation systems is crucial, as are certifications like Good Laboratory Practice (GLP) or Good Clinical Practice (GCP). Strong analytical thinking, meticulous attention to detail, and effective collaboration and communication skills help you navigate complex research and multidisciplinary teams. These skills ensure rigorous scientific discovery, regulatory compliance, and successful advancement of drug candidates from research through clinical development.
What are some common challenges faced by PhD drug development scientists during the transition from discovery to clinical trials?
PhD Drug Development Scientists often encounter challenges when moving a promising compound from the discovery phase to clinical trials, such as ensuring the drug's safety profile, scalability of synthesis, and regulatory compliance. Balancing scientific rigor with tight project timelines requires strong project management and cross-functional collaboration with regulatory, clinical, and manufacturing teams. Additionally, adapting to evolving regulatory requirements and troubleshooting unexpected preclinical results are common hurdles. Overcoming these challenges is crucial for advancing new therapies to patients and offers valuable experience for career growth.
What is the difference between Phd Drug Development Scientist vs Pharmacologist?
| Aspect | Phd Drug Development Scientist | Pharmacologist |
|---|---|---|
| Required Credentials | PhD in Pharmacology, Chemistry, or related field | PhD or MD in Pharmacology or related discipline |
| Work Environment | Research labs, pharmaceutical companies, biotech firms | Research institutions, pharmaceutical companies, healthcare settings |
| Industry Usage | Developing new drugs, conducting preclinical studies | Studying drug effects, mechanisms, and interactions |
| Common Search/Comparison | Yes | Yes |
The Phd Drug Development Scientist focuses on designing and developing new drugs through research and preclinical testing, while the Pharmacologist studies how drugs work in the body, including their effects and interactions. Both roles require advanced degrees and are integral to the pharmaceutical industry, but they differ in their primary focus and daily responsibilities.
What are popular job titles related to Phd Drug Development Scientist jobs in Puerto Rico?
For Phd Drug Development Scientist jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Phd Drug Development Scientist jobs in Puerto Rico look for?
The top searched job categories for Phd Drug Development Scientist jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Phd Drug Development Scientist jobs?
Cities in Puerto Rico with the most Phd Drug Development Scientist job openings:
Contractor
Posted 20 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 to a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
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:
- Support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions.
- Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations.
- May serve as primary production process owner for process support systems and assist with process ownership responsibilities on more complex process systems.
- Own change controls for manufacturing process changes
- Support major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive Actions, authoring process investigation reports, and presenting within regulatory inspections.
- Support Risk Assessments exercises and Microbial assessment evaluations.
- Led commercial campaign readiness and effectively communicate and collaborate with cross function areas.
- Assist in the generation of training materials and assist in providing training on scientific or technical aspects of the process.
- Provide commercial support when needed and assist on the floor troubleshooting.
- Design, coordinate, and support execution of functional tests, water tests, and other runs to challenge process and operations during major changes, or campaign readiness. Generate technical protocols as needed.
- Assist and provide guidance during MBR (Master Batch Record) creation/revisions.
- Perform assessment to support process, automation, or equipment modification or implementation of special projects
- Initiate, revise, and approve standard manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.
- Assess process performance and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities.
- Complete assessments for CAPA applicability requests from other plants/sites
- Complete assessment for new or changes in BOM's (Bill of Materials)
- Serves as a peer-recognized specialist in at least one area, with overall responsibility for determining methodologies in that area.
- Bachelor's degree in Life Sciences, Biology, Chemistry, and/or Engineering.
- In-depth experience of bio-processing unit operations (Cell Culture, Drug Substance Purification)
- Knowledge in Root Cause Analysis methodologies (Fishbone, Six Boxes, Fishbone, 5 Why's, Kepner Tregoe)
- Previous experience in major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive Actions, authoring process investigation reports, and presenting within regulatory inspections.
- Familiar with Lean Manufacturing Practices
- Ability to communicate and collaborate with technical and management staff within manufacturing, process development, and quality.
- Proficiency in GDP (Good Documentation Practices) on a regulated environment
- Knowledge in systems: Trackwise, Spotfire, CDOCS, and process monitoring platforms
- Strong Technical Writing/presentation abilities, and excellent written/verbal communication skills in English and Spanish
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
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