Chemist II
Salt Lake City, UT · On-site
Description: QC - Chemist first shift: (9 a.m. - 5:30 p.m. M-F - start/end times somewhat flexible) 5 Months (possible extension) Salt Lake City, UT Responsibilities include: * Responsible for ...
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Chemist II
Salt Lake City, UT · On-site
Description: QC - Chemist first shift: (9 a.m. - 5:30 p.m. M-F - start/end times somewhat flexible) 5 Months (possible extension) Salt Lake City, UT Responsibilities include: * Responsible for ...
Chemist I
Salt Lake City, UT · On-site
$30 - $33/hr
Description: 2 QC - Chemist Salt Lake City, UT First shift: (9 a.m. - 5:30 p.m. M-F 4-5 Months with possible extension Responsibilities include: * Responsible for maintaining safety and compliance ...
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Chemist I
Salt Lake City, UT · On-site
$30 - $33/hr
Description: 2 QC - Chemist Salt Lake City, UT First shift: (9 a.m. - 5:30 p.m. M-F 4-5 Months with possible extension Responsibilities include: * Responsible for maintaining safety and compliance ...
Applications & Support Scientist
Lehi, UT · On-site
$95K - $125K/yr
... quality control workflows adapting conventional HPLC methods to the capillary scale to deliver ... Pharma, biopharma, academic research, government or forensic labs, environmental testing, food ...
Quick apply
Applications & Support Scientist
Lehi, UT · On-site
$95K - $125K/yr
... quality control workflows adapting conventional HPLC methods to the capillary scale to deliver ... Pharma, biopharma, academic research, government or forensic labs, environmental testing, food ...
Applications & Support Scientist
$95K - $125K/yr
... and quality control workflows - adapting conventional HPLC methods to the capillary scale to ... Pharma, biopharma, academic research, government or forensic labs, environmental testing, food ...
Applications & Support Scientist
$95K - $125K/yr
... and quality control workflows - adapting conventional HPLC methods to the capillary scale to ... Pharma, biopharma, academic research, government or forensic labs, environmental testing, food ...
Applications & Support Scientist
Lehi, UT · On-site
$95K - $125K/yr
... and quality control workflows - adapting conventional HPLC methods to the capillary scale to ... Pharma, biopharma, academic research, government or forensic labs, environmental testing, food ...
Applications & Support Scientist
Lehi, UT · On-site
$95K - $125K/yr
... and quality control workflows - adapting conventional HPLC methods to the capillary scale to ... Pharma, biopharma, academic research, government or forensic labs, environmental testing, food ...
Quality Control Pharma information
What is quality control in the pharmaceutical industry?
Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.
What are the key skills and qualifications needed to thrive as a quality control professional in the pharmaceutical industry?
To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.
What are some of the common challenges faced by quality control professionals in the pharmaceutical industry?
Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.
What is the difference between Quality Control Pharma vs Quality Assurance Pharma?
| Aspect | Quality Control Pharma | Quality Assurance Pharma |
|---|---|---|
| Primary Focus | Testing and inspecting raw materials, in-process, and finished products for compliance | Developing and maintaining quality systems and processes to prevent defects |
| Certifications | GMP, GLP, relevant laboratory certifications | GMP, ISO 9001, quality management system certifications |
| Work Environment | Laboratories, testing facilities | Quality departments, documentation, audits |
| Common Employer Roles | Pharmaceutical companies, contract labs | Pharmaceutical companies, regulatory agencies |
While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.
Is Quality Control Pharma a good career?
Quality Control Pharma involves testing and inspecting pharmaceutical products to ensure they meet safety and quality standards. It requires attention to detail, knowledge of laboratory techniques, and often involves certifications such as GMP training. The role offers stable employment opportunities in the pharmaceutical industry with potential for career advancement.
What are popular job titles related to Quality Control Pharma jobs in Utah?
For Quality Control Pharma jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Quality Control Pharma jobs in Utah look for?
The top searched job categories for Quality Control Pharma jobs in Utah are:
What cities in Utah are hiring for Quality Control Pharma jobs?
Cities in Utah with the most Quality Control Pharma job openings:
Job description
Description:
QC - Chemist
first shift: (9 a.m. – 5:30 p.m. M-F – start/end times somewhat flexible)
5 Months (possible extension)
first shift: (9 a.m. – 5:30 p.m. M-F – start/end times somewhat flexible)
5 Months (possible extension)
Salt Lake City, UT
Responsibilities include:
• Responsible for maintaining safety and compliance standards in the laboratory and work areas.
• Responsible for testing and analyzing incoming materials, intermediates, finished products, swab samples and other samples of a moderate scope and complexity of activity.
• Responsible for preparing, maintaining and reviewing thorough records, documentation on solutions, sample preparation and investigational/experimental samples.
• Responsible for supporting laboratory investigations into Out of Specification/Out of Trend results or other laboratory events.
• Responsible for performing revisions to documentation such as Standard Operating Procedures, Test Methods and Specifications.
• Responsible for supporting the send-out of materials for contract laboratory testing.
• Responsible for assisting with verification of compendial methods.
• Responsible for assisting with activities associated with the stability program including sampling and statistical analyses.
• Responsible for executing projects of a limited to moderate scope as assigned.
• Responsible for assisting with activities related to the sampling of incoming materials as needed.
• Responsible for the routine operation of the laboratory; washing and cleaning of glassware
• Responsible for receiving activities related to incoming materials and goods for the laboratory
Education/Experience:
• Bachelor’s degree preferably in the sciences
• Prefer 1-2 years’ experience (will consider recent graduates)
• Excellent working knowledge of basic scientific principles and experience managing experiments
• Sharp attention to detail and following safety protocols
• Collaboration and communication skills are essential
Responsibilities include:
• Responsible for maintaining safety and compliance standards in the laboratory and work areas.
• Responsible for testing and analyzing incoming materials, intermediates, finished products, swab samples and other samples of a moderate scope and complexity of activity.
• Responsible for preparing, maintaining and reviewing thorough records, documentation on solutions, sample preparation and investigational/experimental samples.
• Responsible for supporting laboratory investigations into Out of Specification/Out of Trend results or other laboratory events.
• Responsible for performing revisions to documentation such as Standard Operating Procedures, Test Methods and Specifications.
• Responsible for supporting the send-out of materials for contract laboratory testing.
• Responsible for assisting with verification of compendial methods.
• Responsible for assisting with activities associated with the stability program including sampling and statistical analyses.
• Responsible for executing projects of a limited to moderate scope as assigned.
• Responsible for assisting with activities related to the sampling of incoming materials as needed.
• Responsible for the routine operation of the laboratory; washing and cleaning of glassware
• Responsible for receiving activities related to incoming materials and goods for the laboratory
Education/Experience:
• Bachelor’s degree preferably in the sciences
• Prefer 1-2 years’ experience (will consider recent graduates)
• Excellent working knowledge of basic scientific principles and experience managing experiments
• Sharp attention to detail and following safety protocols
• Collaboration and communication skills are essential
About Unicon Pharma
Sourced by ZipRecruiter
Industry
Recruiting and staffing services
Company size
11 - 50 Employees
Headquarters location
Edison, NJ, US
Year founded
2013