Perform and summarize improvement opportunities in technical reports, investigations, plant/lab ... Minimum of five (5) years' experience in pharmaceutical manufacturing industry. * Demonstrated ...
Perform and summarize improvement opportunities in technical reports, investigations, plant/lab ... Minimum of five (5) years' experience in pharmaceutical manufacturing industry. * Demonstrated ...
Perform and summarize improvement opportunities in technical reports, investigations, plant/lab ... Minimum of five (5) years' experience in pharmaceutical manufacturing industry. * Demonstrated ...
Quick apply
Perform and summarize improvement opportunities in technical reports, investigations, plant/lab ... Minimum of five (5) years' experience in pharmaceutical manufacturing industry. * Demonstrated ...
Operate within a GxP-adjacent lab environment; understand documentation and traceability ... Experience in pharmaceutical or life sciences manufacturing (GxP awareness, batch process ...
Operate within a GxP-adjacent lab environment; understand documentation and traceability ... Experience in pharmaceutical or life sciences manufacturing (GxP awareness, batch process ...
Specialist Quality Control
Juncos, PR · On-site
Strong understanding of pharmaceutical/biological product testing requirements. * Advanced ... Strong knowledge of quality analytical lab processes, validation, QA, manufacturing, and process ...
Quick apply
Specialist Quality Control
Juncos, PR · On-site
Strong understanding of pharmaceutical/biological product testing requirements. * Advanced ... Strong knowledge of quality analytical lab processes, validation, QA, manufacturing, and process ...
... Lab Management, and will interact on a regular basis with Engineering, Technical Services and ... Background in pharmaceutical products manufacturing environment and in laboratories areas * More ...
... Lab Management, and will interact on a regular basis with Engineering, Technical Services and ... Background in pharmaceutical products manufacturing environment and in laboratories areas * More ...
Sr. Engineer-Process Engineering
San Juan, PR · On-site
$102K - $131K/yr
Perform and summarize improvement opportunities in technical reports, investigations, plant/lab ... Minimum of three (5) years' experience in pharmaceutical manufacturing industry * Demonstrated ...
Sr. Engineer-Process Engineering
San Juan, PR · On-site
$102K - $131K/yr
Perform and summarize improvement opportunities in technical reports, investigations, plant/lab ... Minimum of three (5) years' experience in pharmaceutical manufacturing industry * Demonstrated ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... Minimum of a Master's degree or equivalent experience in Engineering, Pharmaceutical Sciences, or a ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... Minimum of a Master's degree or equivalent experience in Engineering, Pharmaceutical Sciences, or a ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... A minimum of zero (0) to two (2) years of experience in the pharmaceutical or related industry ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... A minimum of zero (0) to two (2) years of experience in the pharmaceutical or related industry ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... A minimum of zero (0) to two (2) years of experience in the pharmaceutical or related industry ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... A minimum of zero (0) to two (2) years of experience in the pharmaceutical or related industry ...
Packaging Supervisor, 3rd Shift
Gurabo, PR · On-site
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... At least two (2) years' experience in the pharmaceutical industry * Knowledge of cGMP's and ...
New
Packaging Supervisor, 3rd Shift
Gurabo, PR · On-site
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... At least two (2) years' experience in the pharmaceutical industry * Knowledge of cGMP's and ...
New
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... Minimum of a Master's degree or equivalent experience in Engineering, Pharmaceutical Sciences, or a ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... Minimum of a Master's degree or equivalent experience in Engineering, Pharmaceutical Sciences, or a ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... Minimum of a Master's degree or equivalent experience in Engineering, Pharmaceutical Sciences, or a ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... Minimum of a Master's degree or equivalent experience in Engineering, Pharmaceutical Sciences, or a ...
Sr Supervisor Ops Investigations
Gurabo, PR · On-site
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... Minimum two (2) years of supervisory experience in related areas within the pharmaceutical ...
Sr Supervisor Ops Investigations
Gurabo, PR · On-site
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... Minimum two (2) years of supervisory experience in related areas within the pharmaceutical ...
Packaging Supervisor, 3rd Shift
Gurabo, PR · On-site
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... At least two (2) years' experience in the pharmaceutical industry * Knowledge of cGMP's and ...
Packaging Supervisor, 3rd Shift
Gurabo, PR · On-site
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... At least two (2) years' experience in the pharmaceutical industry * Knowledge of cGMP's and ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... At least two (2) years' experience in the pharmaceutical industry * Knowledge of cGMP's and ...
New
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... At least two (2) years' experience in the pharmaceutical industry * Knowledge of cGMP's and ...
New
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... Minimum two (2) years of supervisory experience in related areas within the pharmaceutical ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... Minimum two (2) years of supervisory experience in related areas within the pharmaceutical ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... A minimum of zero (0) to two (2) years of experience in the pharmaceutical or related industry ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... A minimum of zero (0) to two (2) years of experience in the pharmaceutical or related industry ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... Minimum two (2) years of supervisory experience in related areas within the pharmaceutical ...
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... Minimum two (2) years of supervisory experience in related areas within the pharmaceutical ...
Site Engineering Lead
Gurabo, PR · On-site
$98K - $130K/yr
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... The pharmaceutical world is going through a period of important technological transformations ...
Site Engineering Lead
Gurabo, PR · On-site
$98K - $130K/yr
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... The pharmaceutical world is going through a period of important technological transformations ...
Site Engineering Lead
Gurabo, PR · On-site
$98K - $130K/yr
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... The pharmaceutical world is going through a period of important technological transformations ...
Site Engineering Lead
Gurabo, PR · On-site
$98K - $130K/yr
Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... The pharmaceutical world is going through a period of important technological transformations ...
Pharmaceutical Lab information
What is the highest paying job in the pharma industry?
How to become a pharmaceutical lab technician?
What is the highest paid lab technician?
What are the typical career advancement opportunities for someone working in a Pharmaceutical Lab?
Pharmaceutical Lab professionals often start as lab technicians or analysts and can progress to senior scientist or supervisory roles with experience and additional qualifications. Many companies encourage continuing education, offering opportunities to specialize in areas like quality control, regulatory affairs, or method development. Career growth can also involve cross-functional collaboration, leading to roles in research management or project leadership. Advancement is typically performance-based, with a focus on technical expertise, reliability, and effective teamwork.
What is a Pharmaceutical Lab job?
A Pharmaceutical Lab job involves conducting research, testing, and analysis to develop and ensure the safety, quality, and effectiveness of medications. Professionals in this role may work on formulation, stability testing, quality control, or regulatory compliance. They follow strict protocols and use specialized equipment to analyze drug compounds. These jobs are essential for bringing new medications to market and maintaining high standards in pharmaceutical production.
What do pharmaceutical labs do?
What are the key skills and qualifications needed to thrive in the Pharmaceutical Lab position, and why are they important?
Success in a Pharmaceutical Lab role requires a strong background in chemistry, biology, or a related scientific field, with relevant laboratory experience and a bachelor's degree or higher. Familiarity with laboratory equipment, analytical instruments (such as HPLC, GC, or spectrophotometers), Good Laboratory Practice (GLP), and sometimes certifications like CLIA are highly valuable. Attention to detail, strong problem-solving skills, and effective teamwork help individuals excel in this environment. These skills ensure accurate research results, compliance with regulatory standards, and smooth lab operations.
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 26 days ago
Job description
We’re seeking an Principal Scientist to work with one of our top global biopharmaceutical clients in the Carolina, PR area. With us, it’s all about finding the job that’s just right
Principal Scientist – TSMS
Organization Overview:
The TSMS function provides technical expertise and support to Dry Product Operations (DPO) ensuring compliance with cGMP, regulations, company standards and business practices. The primary areas of support include technical expertise for process manufacturing and business process improvements, compliance with business systems, new product introduction, site technical agenda for continuous improvement, process and cleaning validation programs.
Responsibilities:
- Technical leadership - Provide DPO expertise for site capital projects to make sure that established process/equipment design requirements are fulfilled.
- Establish and maintain technical information of the process and unit operations within the manufacturing process.
- Develop and monitor process indicators to identify and address performance issues and identify improvement opportunities.
- Perform troubleshooting and investigation on unexpected issues.
- Own process related deviations, CAPAs and changes. Lead or participate in investigations, problem-solving activities such as root cause analysis, FMEA, problem analysis and in development/implementation of countermeasure for quality events.
- Provide technical expertise for requirements, design, selection, installation, qualification, operation, of process and equipment.
- Perform and summarize improvement opportunities in technical reports, investigations, plant/lab trials, data analysis and process modeling.
- Ensure process complies with current industry regulatory expectations, new regulations, and corporate policies and programs.
- Develop and/or provide technical training to Operators, Process Team members and less experienced and/or new Scientists on DPO process requirements.
- Provide technical support to achieve the reliable and compliant manufacture of oral drug products following the applicable regulations and corporate standards.
- Â Evaluate preventive / corrective actions applying scientific expertise on process, equipment, facilities, computer systems and manufacturing operations.
- Responsible for regulatory submission and active participation in continuous improvement initiatives.
- Provide technical support for the technology transfer of solid dosage products to a commercial facility.Â
-  PhD in Chemical Engineering, Chemistry or scientific related field. Minimum of five (5) years’ experience in pharmaceutical manufacturing industry.Â
- Demonstrated strong technical knowledge in Process and Equipment requirements, specifically those related to Active Pharmaceutical Ingredient and or Spray Dried Dispersion (SDD) and/or Dry Product operations.
- Knowledge of process safety management.
- Bilingual (English/Spanish) with strong written and oral communication skills.
- Excellent communication skills at all levels (with both internal and external resources).
- Strong leadership and organizational skills
- Knowledge in managing multiple project objectives or assignments.
- Technical Writing
- Strong customer service focus
- Computer literate, self-driven, teamwork oriented, problem-solving skills, critical thinking.
- Knowledgeable of cGMP and process safety requirements and experience in conducting activities in a regulated environment.
- Ability to accomplish multiple tasks.
- Influence skill.
- Demonstrated technical leadership skills.
Additional Information:
- Available to work or provide support to a 24/7 operation, if necessary.
- Availability to travel within and outside Puerto Rico and U.S.
- Work as a resource in other strategic areas of the business, based on business needs.
Why Kelly® Engineering?
Your engineering skills are in demand, but how do you find the right fit? Easy. At Kelly Engineering, our team creates expert talent solutions to solve the world’s most critical challenges. We connect you with leading organizations where you can collaborate on innovative projects, work with cutting-edge technologies and accelerate your growth. Whether you prefer the variety and flexibility of short-term projects or are looking for a long-term opportunity, we’re here to guide you to the next step in your engineering career.About Kelly
Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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