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Job Title: Deviation Writer
Job Description
A Global Pharmaceutical Manufacturer is seeking a Quality Investigator for Aseptic Production Investigations. The individual will perform investigations specifically pertaining to the Aseptic Core and its processes. Responsibilities include conducting historical searches, reviewing videos, interviewing colleagues, and reviewing supporting documentation (batch records, technical assessments, SOPs, etc.). The information will be housed in a proprietary system used daily.
Hard Skills
This is a contract position with a duration of 6 Month(s).
Work Environment
Normal M-F opportunity, 1st shift. The role is cross-functional within an office space as well as partnering with production on the floors.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
Job Description
A Global Pharmaceutical Manufacturer is seeking a Quality Investigator for Aseptic Production Investigations. The individual will perform investigations specifically pertaining to the Aseptic Core and its processes. Responsibilities include conducting historical searches, reviewing videos, interviewing colleagues, and reviewing supporting documentation (batch records, technical assessments, SOPs, etc.). The information will be housed in a proprietary system used daily.
Hard Skills
- Previous pharmaceutical experience in a GMP commercial setting
- 2+ years of experience in Aseptic Manufacturing in a pharmaceutical environment
- Conducting the investigative process, CAPA, Root Cause Analysis
- Exposure to systematic problem solving, root cause analysis, technical writing
- Process improvement
- Continuous improvement efforts
This is a contract position with a duration of 6 Month(s).
Work Environment
Normal M-F opportunity, 1st shift. The role is cross-functional within an office space as well as partnering with production on the floors.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
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