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Job Requirements of Clinical Supply Specialist:
-
Employment Type:
Contractor
-
Location:
West Point, PA (Onsite)
Do you meet the requirements for this job?
Clinical Supply Specialist
Careers Integrated Resources Inc
West Point, PA (Onsite)
Contractor
Job Title: Clinical Supply Specialist
Location: West Point, PA, 19486
Contract: 23+ Months (Possible of extension)
Work Shift: 3 - days onsite – Hybrid role
Job Description Summary:
Our department supports the release of clinical supply to global clinical trials.
Primary duties may include but are not limited to the following:
• Evaluation and disposition of clinical supply materials with the assurance that the materials were produced in conformance to all applicable policies/procedures of our Company and compliance with all governing regulations.
• Coordinate and/or support the preparation of procedures, processes, and quality improvements.
• Completing projects to improve the performance of our processes, including continuous process improvements, and value capture projects that seek to improve yield, reduce cost, or lower our processing cycle times.
• Assists in the coordination of significant quality events including fact finding, investigation support
• Actively using and championing the use of Lean Six Sigma and our company's Production System (MPS) tools, both in problem solving and day-to-day operational activities.
Qualifications/Education:
• Bachelor's Degree or higher in engineering, science, or related discipline.
Required skills and experience:
• Minimum 2 years of experience in the pharmaceutical or equivalent industry, Good Manufacturing Practice (GMP) related field including Technical, Engineering, Quality or Operations.
• Familiarity with batch disposition activities
• Strong problem-solving, and written and oral communication skills
• Ability to manage multiple priorities
• Demonstrated teamwork skills and ability to work independently
• Proficiency in the use and maintenance of Microsoft applications (Excel, Outlook, and/or MS Access, Teams)
• Attention to detail, flexibility and an awareness of production and quality control problems.
Preferred skills and experience:
• Proven ability to work independently and collaborate effectively as part of a team.
• Strong organizational, interactive, and time management skills.
• Computer skills; knowledge and competency in ERP/MES, SAP
Location: West Point, PA, 19486
Contract: 23+ Months (Possible of extension)
Work Shift: 3 - days onsite – Hybrid role
Job Description Summary:
Our department supports the release of clinical supply to global clinical trials.
Primary duties may include but are not limited to the following:
• Evaluation and disposition of clinical supply materials with the assurance that the materials were produced in conformance to all applicable policies/procedures of our Company and compliance with all governing regulations.
• Coordinate and/or support the preparation of procedures, processes, and quality improvements.
• Completing projects to improve the performance of our processes, including continuous process improvements, and value capture projects that seek to improve yield, reduce cost, or lower our processing cycle times.
• Assists in the coordination of significant quality events including fact finding, investigation support
• Actively using and championing the use of Lean Six Sigma and our company's Production System (MPS) tools, both in problem solving and day-to-day operational activities.
Qualifications/Education:
• Bachelor's Degree or higher in engineering, science, or related discipline.
Required skills and experience:
• Minimum 2 years of experience in the pharmaceutical or equivalent industry, Good Manufacturing Practice (GMP) related field including Technical, Engineering, Quality or Operations.
• Familiarity with batch disposition activities
• Strong problem-solving, and written and oral communication skills
• Ability to manage multiple priorities
• Demonstrated teamwork skills and ability to work independently
• Proficiency in the use and maintenance of Microsoft applications (Excel, Outlook, and/or MS Access, Teams)
• Attention to detail, flexibility and an awareness of production and quality control problems.
Preferred skills and experience:
• Proven ability to work independently and collaborate effectively as part of a team.
• Strong organizational, interactive, and time management skills.
• Computer skills; knowledge and competency in ERP/MES, SAP
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