Aseptic Qualified Person - Pharmaceutical - South East

Hiring By - Biostaffic

 BioPharma

United Kingdom

Job Highlights

Not Disclosed

Mid-Senior level

Posted 4 months ago
Job details
Are you an experienced professional with a passion for ensuring the integrity and safety of pharmaceutical products? Do you possess expertise in aseptic processing and a deep understanding of regulatory requirements? If so, we invite you to explore an exceptional career opportunity as an Aseptic Qualified Person with our esteemed organisation. Why Choose Us: Pioneering Innovation: Join a company at the forefront of pharmaceutical innovation, where your expertise in aseptic processing will contribute to the development and manufacturing of life-saving medications and treatments. Commitment to Quality: At our organization, quality is our top priority. As a Pharmaceutical Aseptic Qualified Person, you will play a pivotal role in ensuring that our products meet the highest standards of sterility, purity, and efficacy. State-of-the-Art Facilities: Work in modern, state-of-the-art facilities equipped with cutting-edge technologies and stringent aseptic processing protocols to support your role as a guardian of product quality. Professional Growth: We value the professional growth and development of our team members. As a Pharmaceutical Aseptic Qualified Person, you will have access to ongoing training, mentorship, and career advancement opportunities. Collaborative Culture: Join a collaborative and dynamic team environment where your contributions are valued, and your expertise is respected. Collaborate with cross-functional teams to drive continuous improvement and excellence in aseptic processing. Key Responsibilities: Serve as the primary point of contact for aseptic processing activities, providing expertise and guidance on aseptic techniques, procedures, and regulations. Oversee the qualification and validation of aseptic processing equipment, facilities, and procedures to ensure compliance with regulatory standards and industry best practices. Conduct thorough review and approval of aseptic processing documentation, including batch records, SOPs, and validation protocols, to ensure accuracy, completeness, and compliance. Lead investigations into deviations, non-conformances, and sterility assurance issues, implementing effective corrective and preventive actions to mitigate risks and ensure product quality. Stay abreast of emerging trends, regulatory requirements, and best practices in aseptic processing, providing leadership and guidance to internal stakeholders on implementation strategies and continuous improvement initiatives. Qualifications: Pharmaceutical industry, with a comprehensive understanding of regulatory requirements (e.g., FDA, EMA, PIC/S). Proven track record of successful participation in regulatory inspections and audits related to aseptic processing. Strong analytical and problem-solving skills, with the ability to lead and drive complex investigations to resolution. Excellent communication, interpersonal, and leadership skills, with the ability to collaborate effectively across multidisciplinary teams. Join Us in Advancing Healthcare Through Aseptic Excellence! If you are a dedicated professional seeking to make a meaningful impact in pharmaceutical manufacturing and contribute to the delivery of safe and effective medications, we encourage you to apply for the position of Aseptic Qualified Person. Join us in our mission to uphold the highest standards of sterility, quality, and patient safety

Benefits Offered?

  • No

Bonus Offered?

  • No

Travel Required?

  • No

Location:

  • United Kingdom

Experience:

  • Mid-Senior level

Global Experience Needed?

  • No

Specialized Experience Needed?

  • No

Apply before:

  • Apr 17, 2024
Company Overview
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