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Job Requirements of Quality Control Analyst - II:
-
Employment Type:
Contractor
-
Location:
Swiftwater, PA (Onsite)
Do you meet the requirements for this job?
Quality Control Analyst - II
Careers Integrated Resources Inc
Swiftwater, PA (Onsite)
Contractor
Job Title: Quality Control Analyst - II
Job Location: Swiftwater, PA 18370
Job Duration: 12+ months (Possibilities of Extension)
Work Shift: Mon – Fri – 8 AM – 5 PM
Job Description Summary:
This position supports the execution of routine testing in the Quality Control Analytical Chemistry laboratory, including chemistry assays associated with Incoming Quality and Raw Materials. This position requires proficiency and understanding of the theory related to processes, assays, and equipment, as well as the ability to identify issues/trends. The candidate filling this position will work to ensure tasks are completed in a timely manner, while strictly adhering to Client policies and procedures and cGMP.
JOB RESPONSIBILITIES:
• Perform QC testing while strictly adhering to Client policies and safety procedures, SOP/SWI, Pharmacopeia, Federal Regulations, cGMP, and required training curricula.
• Perform all scheduled activities defined by laboratory management to meet demands of Production, Method Development, Validation, Independent Demand, and Stability program.
• Maintain safety and compliance of the laboratory work area.
• Perform cleaning of laboratories, equipment, and ancillary areas as required.
• Prepare for and operate QC equipment including pre and post-run setup and maintenance.
• Complete required paperwork and documentation as required.
• Troubleshoot sample discrepancies.
• Perform peer proofing on assays.
• Develop a working knowledge of appropriate compendia and/or regulatory guidance.
• Attend/contribute to scheduled team meetings, department, and safety meetings.
Specific tasks may include:
• Raw material testing (pharmacopeia/wet chemistry assays)
• Water testing (TOC and Conductivity analysis)
• pH testing for media
• Buffer assays (titrations and photometric methods)
• Analytical equipment setup, usage, and maintenance
• Sample preparation and disposal
• Coordination of contract laboratory testing
• Chemical handling required with appropriate PPE provided. Vaccinations and vision examinations may be required based on specific job function.
REQUIREMENTS:
• Bachelor’s degree in Chemistry or equivalent
• 2-4 years of relevant experience in cGMP controlled/pharmaceutical industry.
• Exceptional attention to detail and strong writing skills are crucial.
• The candidate must be able to work in a dynamic team environment with flexible schedule, including potential for weekends/holidays.
#sczr2
Job Location: Swiftwater, PA 18370
Job Duration: 12+ months (Possibilities of Extension)
Work Shift: Mon – Fri – 8 AM – 5 PM
Job Description Summary:
This position supports the execution of routine testing in the Quality Control Analytical Chemistry laboratory, including chemistry assays associated with Incoming Quality and Raw Materials. This position requires proficiency and understanding of the theory related to processes, assays, and equipment, as well as the ability to identify issues/trends. The candidate filling this position will work to ensure tasks are completed in a timely manner, while strictly adhering to Client policies and procedures and cGMP.
JOB RESPONSIBILITIES:
• Perform QC testing while strictly adhering to Client policies and safety procedures, SOP/SWI, Pharmacopeia, Federal Regulations, cGMP, and required training curricula.
• Perform all scheduled activities defined by laboratory management to meet demands of Production, Method Development, Validation, Independent Demand, and Stability program.
• Maintain safety and compliance of the laboratory work area.
• Perform cleaning of laboratories, equipment, and ancillary areas as required.
• Prepare for and operate QC equipment including pre and post-run setup and maintenance.
• Complete required paperwork and documentation as required.
• Troubleshoot sample discrepancies.
• Perform peer proofing on assays.
• Develop a working knowledge of appropriate compendia and/or regulatory guidance.
• Attend/contribute to scheduled team meetings, department, and safety meetings.
Specific tasks may include:
• Raw material testing (pharmacopeia/wet chemistry assays)
• Water testing (TOC and Conductivity analysis)
• pH testing for media
• Buffer assays (titrations and photometric methods)
• Analytical equipment setup, usage, and maintenance
• Sample preparation and disposal
• Coordination of contract laboratory testing
• Chemical handling required with appropriate PPE provided. Vaccinations and vision examinations may be required based on specific job function.
REQUIREMENTS:
• Bachelor’s degree in Chemistry or equivalent
• 2-4 years of relevant experience in cGMP controlled/pharmaceutical industry.
• Exceptional attention to detail and strong writing skills are crucial.
• The candidate must be able to work in a dynamic team environment with flexible schedule, including potential for weekends/holidays.
#sczr2
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