*QA Compliance Lead, Facilities and Equipment

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Would you like to be a part of AGC Biologics’ growing success?

We are seeking a highly motivated and experienced QA Compliance Lead to join our team. In this role, you will be responsible for ensuring GMP (Good Manufacturing Practices) compliance for our facilities and equipment. You will play a critical role in ensuring the quality and safety of our products, while ensuring that our operations comply with relevant regulations and standards.

AGC Biologics is a leading global Contract Development and Manufacturing Organization, with a deep commitment to improving life quality by bringing new biopharmaceuticals to market. Because of our dedication to building and empowering our internal teams, AGC Biologics is an innovative leader in the industry with an extensive network of cGMP facilities in the US, Europe and Asia. As such, we deliver a deep expertise, dynamic solutions and technologies, as well as customized services for the scale-up and cGMP manufacturing of protein-based therapeutics and cell and gene therapies. We forge exceptionally strong partnerships with our clients, and we never lose sight of our pledge to deliver a reliable and compliant drug substance supply, Right, On time.

Position Overview:

As the QA Compliance Lead, you will be a vital member of a highly motivated, multidisciplinary team. Your daily responsibilities will include:

  • Develop and implement GMP policies and procedures to ensure compliance with industry standards and regulations
  • Identify and evaluate potential compliance risks, and develop and implement corrective actions to mitigate these risks
  • Maintain up-to-date knowledge of industry regulations and standards, and communicate relevant changes to relevant stakeholders
  • Collaborate with cross-functional teams to ensure that GMP compliance is integrated into all aspects of operations, from design to manufacture
  • Train and educate employees on GMP compliance requirements and best practices

Your Profile:

It is crucial to possess a self-motivated personality with a practical approach to daily tasks, while maintaining a commitment to quality. Our working environment is dynamic and demanding, necessitating the capability to problem-solve, fulfill commitments, and provide a favorable experience for our clients.

Education and Experience:

The ideal candidate should possess the following qualifications

  • A science-based Master's degree or equivalent
  • At least 5 years of experience in a GMP-regulated environment, with a focus on compliance and quality assurance
  • Strong knowledge of GMP regulations and standards, including FDA 21 CFR 210/211
  • Knowledge of Data Integrity principles, and related guidelines such as CFR21 Part 11 and EU GMP Annex 11
  • Excellent communication and interpersonal skills, with the ability to effectively communicate with cross-functional teams and stakeholders
  • Strong problem-solving skills, with the ability to identify and evaluate potential compliance risks and develop effective solutions
  • Ability to work efficiently in a fast-paced, matrix environment
  • Ability to meet deadlines and effectively manage multiple tasks
  • Flexibility to adapt to changing business needs and priorities

At AGC, we serve international clients and English is our company language. As such, professional proficiency in both written and spoken English is a requirement.

About The Department:

You will be joining the Quality Assurance department, consisting of over 80 colleagues, with primary responsibilities in Manufacturing, Raw Materials, Quality Control, and Facilities and Equipment.

The Quality Assurance Facilities and Equipment team is comprised of highly qualified scientists with diverse professional backgrounds and several years of experience in the field of Quality Assurance.

The main objective of the team is to ensure that our production facilities and laboratories comply with current Good Manufacturing Practice (GMP) standards, including EU GMP, 21 CFR, and ICH guidelines at all times.

The team is mainly responsible for the review and approval of quality documentation, including equipment qualifications, IQ, OQ, PQ, environmental monitoring, cleaning validation, deviation handling, and approval of CAPA and change requests.

Applications:

We continuously assess incoming applications and schedule interviews accordingly. To ensure prompt consideration, please submit your application and resume promptly.

The advertisement will be closed once the ideal candidate has been identified.

For additional information regarding the position, feel free to reach out to Volker Jentzsch, Senior Manager of QA Facilities & Equipment, at +45 2294 3062.

Want to keep posted about our growth and to learn more about our company?

We also urge you to follow us on our LinkedIn Company Page and give us a quick Like on Facebook !

AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.

Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing.


Information og data

Denne ledige stilling har jobtypen "Finansmedarbejder", og befinder sig i kategorien "Økonomi og jura".

Arbejdsstedet er beliggende i København

Jobbet er oprettet på vores service den 8.2.2023, men kan have været deaktiveret og genaktiveret igen.

Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Finansmedarbejder
  • København

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