Regulated Industry QC Professional

We are looking for a Regulated Pharmaceutical Process Lead to join our team at Qrc Group Llc. As a key member of our organization, you will be responsible for leading efforts in designing, implementing, and improving aseptic processes and systems within a regulated pharmaceutical environment.The successful candidate will have a strong background in aseptic...

Required Skills and Qualifications- Bachelor's degree in Science with a minimum of 3 years of experience in QC project management in the pharmaceutical or life sciences industry.- Minimum of 2 years of experience in Microbiology-related field- Certification in Project Management (e.g., PMP, PRINCE2) or equivalent experience.- Strong leadership,...

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About the RoleThe successful candidate will have 8+ years of experience in project management in a regulated pharmaceutical, biotechnology, or medical device industry, with a focus on aseptic areas and FDA submissions. You must have a proven track record of leading projects through FDA submissions.You will develop project timelines, resource allocation...

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At Qrc Group Llc, we are seeking a highly experienced Pharmaceutical Engineering Expert to lead our efforts in aseptic processing and system development. The successful candidate will have a strong background in aseptic processing, FDA product submissions, and validation activities.Key responsibilities include:Developing, implementing, and improving aseptic...

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As a Regulatory Consultant at Qrc Group Llc, you will play a crucial role in ensuring the company's compliance with FDA regulations and guidelines. Your expertise in aseptic manufacturing and FDA product submissions will be invaluable to our team.Your key responsibilities will include providing expert regulatory advice for aseptic manufacturing processes,...

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**Job Summary:**We are seeking a highly skilled Senior Aseptic Processing Engineer to lead our efforts in designing, implementing, and improving aseptic processes and systems within a regulated pharmaceutical environment.The ideal candidate will have expertise in aseptic processing, FDA product submissions, and validation activities. Key responsibilities...

Key ResponsibilitiesLead and manage complex projects related to the development, validation, and commercialization of aseptic pharmaceutical or medical device products.Coordinate and oversee all stages of project execution from design, development, and validation through to FDA submission.Develop project timelines, resource allocation plans, and budgets,...