| Company: | JOHNSON&JOHNSON |
|---|---|
| Job Role: | Analyst, Quality Control. |
| Experience: | (1-2 years). |
| Vacancy: | 20+ |
| Qualification: | Bachelors Degree. |
| Salary: | $ 105900/year. |
| Location: | USA. |
| Join us on Telegram | Click Here |
| Apply Mode: | (Online) |
| Deadline: | Not Mentioned |
Johnson & Johnson employees are inspired and united by the philosophy of caring for the world one person at a time. Our corporate philosophy is anchored in the internationally applicable Credo, which emphasizes the importance of caring. Johnson & Johnson's DePuy Synthesis Companies are the largest and most comprehensive orthopedic and neurological companies in the world. DePuy Synthesis is a global leader in technology, devices, services, and programs in the fields of joint reconstruction, trauma, spine, sports medicine, neurology, cranio-maxillofacial, power tools, and biomaterials. Globally, our offerings help advance health and wellbeing through inspired, innovative and high-quality services. For our Trauma / CMF R&D department in our EMEA headquarters (Zuchwil) we are looking for a highly committed.
Description
Janssen Biotech, Inc. is part of the Janssen Pharmaceutical Companies is recruiting for an Analyst, Quality Control in Malvern, PA. At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at www.janssen.com and follow us @JanssenGlobal. Janssen BioPharma, Inc. is part of the Janssen Pharmaceutical Companies.
Do you want to be a part of the change?
The QC Analyst position supports the Quality Control Chemistry and Microbiology laboratories and conducts biochemical, microbiological, and/or general chemical testing of raw materials, in-process or final product samples submitted to the QC laboratories. The position requires analytical testing to be completed in compliance with all applicable procedures, standards and GMP regulations. This position requires high attention to detail, organizational leadership, interpersonal skills, a quality mindset, critical thinking, and technical writing skills. This position will work in a team environment.
Responsibilities:
Perform analytical testing in compliance with applicable GMP regulations while maintaining a safe work environment in compliance with all applicable environmental, health, and safety regulations. Conduct biochemical, microbiological, and/or general chemical testing of raw material/utility, in-process, or final product samples submitted to the QC laboratories.
- Perform peer review of laboratory data
- Use electronic systems (LIMS, MES, LES, Empower, Trackwise, etc.) for execution and documentation of testing
- Maintain Laboratory Housekeeping including sample management, reagent prep, instrument standardization/calibration
- Complete Document Revisions
- Maintain individual training completion in a compliant state and train new laboratory personnel
- Participate in continuous improvement
- Complete CAPAs when required for the Quality Control organization
- Maintain Laboratory in audit ready state and participate in internal and Health Authority inspections
- Execute CAPAs when required for the Quality Control organization
- Provide input to functional laboratory meetings
Qualifications
Required
- Minimum of a Bachelor’s degree in life sciences or a related area
- Minimum of 2 years of proven experience
- Experience with basic laboratory skills and experience/knowledge of analytical methodologies (Spectroscopy, bioburden, endotoxin, pH, etc.)
- Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and ability to identify gaps in processes or systems
- Ability to read and interpret documents such as SOPs, work instructions, test methods and protocols
- Proficient with using Microsoft Office applications (Outlook, Excel, Word, and Powerpoint)
- Second Shift: must have ability to work Monday-Friday 2PM-10PM
- This position is located in Malvern, PA
Preferred
- Knowledge and awareness of compendial (USP, EP, JP, etc.) requirements and standards for QC testing
- Experience with document revision or technical writing
How to Apply Click on the Below link, it will redirect you to source Page and apply there.
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