QC Analyst
| Dyddiad hysbysebu: | 09 Hydref 2025 |
|---|---|
| Cyflog: | Heb ei nodi |
| Gwybodaeth ychwanegol am y cyflog: | Competitive |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 08 Tachwedd 2025 |
| Lleoliad: | Dartford, Kent |
| Gweithio o bell: | Ar y safle yn unig |
| Cwmni: | Catalent |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | 0091129 |
Crynodeb
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) committed to helping people live better, healthier lives. We partner with pharmaceutical, biotech, and consumer health companies to support product development, launch, and full life-cycle supply. With over 40 global sites and thousands of scientists and technicians, Catalent delivers billions of doses of life-enhancing and life-saving treatments annually.
Join Catalent Pharma Solutions in Dartford, where we lead the industry in high-potent, high-value API micronization. Supplying around 40 micronized products to customers worldwide, we are committed to continuous improvement and people development, ensuring our team thrives.
We are looking for a Quality Control Analyst to support analytical testing and compliance within our QC laboratory.
Shift Patterns
Early: 6:00 AM – 2:00 PM (Monday–Friday)
Late: 1:30 PM – 10:00 PM (Thursday), 1:30 PM – 7:00 PM (Friday)
Night: 9:00 PM – 7:00 AM (Monday–Wednesday), 9:00 PM – 6:30 AM (Thursday)
The Role:
Conduct particle size analysis (laser diffraction), cleaning verification (HPLC), and FTIR/Raman identification testing.
Perform method development, validation, troubleshooting, and technology transfer activities.
Execute differential scanning calorimetry (DSC) and pharmacopoeia analyses as required.
Carry out environmental monitoring and periodic microbiological testing.
Ensure all documentation is accurate, clear, and cGMP-compliant.
Prepare analytical test methods and reports, including Laboratory Investigations, Statements of Results, and Certificates of Analysis.
Review, approve, and report on data generated for QC release.
The Candidate:
Degree in Scientific, Biotech, or related field (or equivalent industry experience).
Strong experience in HPLC/Empower software (highly desirable).
IT proficiency (Microsoft Office: Word, Excel, PowerPoint).
Previous experience in analytical investigations (preferred)
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Join Catalent Pharma Solutions in Dartford, where we lead the industry in high-potent, high-value API micronization. Supplying around 40 micronized products to customers worldwide, we are committed to continuous improvement and people development, ensuring our team thrives.
We are looking for a Quality Control Analyst to support analytical testing and compliance within our QC laboratory.
Shift Patterns
Early: 6:00 AM – 2:00 PM (Monday–Friday)
Late: 1:30 PM – 10:00 PM (Thursday), 1:30 PM – 7:00 PM (Friday)
Night: 9:00 PM – 7:00 AM (Monday–Wednesday), 9:00 PM – 6:30 AM (Thursday)
The Role:
Conduct particle size analysis (laser diffraction), cleaning verification (HPLC), and FTIR/Raman identification testing.
Perform method development, validation, troubleshooting, and technology transfer activities.
Execute differential scanning calorimetry (DSC) and pharmacopoeia analyses as required.
Carry out environmental monitoring and periodic microbiological testing.
Ensure all documentation is accurate, clear, and cGMP-compliant.
Prepare analytical test methods and reports, including Laboratory Investigations, Statements of Results, and Certificates of Analysis.
Review, approve, and report on data generated for QC release.
The Candidate:
Degree in Scientific, Biotech, or related field (or equivalent industry experience).
Strong experience in HPLC/Empower software (highly desirable).
IT proficiency (Microsoft Office: Word, Excel, PowerPoint).
Previous experience in analytical investigations (preferred)
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
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