QA Operations Specialist

5 months ago

Louth, United Kingdom Life Science Recruitment Full time

**QA Drug Substance Operations Specialist**

As QA Drug Substance Operations Specialist, you will be responsible for providing online QA oversight to Drug Substance manufacturing operations in Dundalk, Ireland. This is a crucial role within the Quality organisation with responsibility for directly supporting the manufacturing operations team daily, ensuring compliance with cGMP and corporate and local SOPs.

**Organization Description**
My client is a premier provider of biologics services (from discovery to commercialization) with global customers in the biopharmaceutical and healthcare industries. We´re one of the world's top three contract development and manufacturing companies for biopharmaceuticals, we provide our clients with a world-leading open access technology platform. We enable our clients to research, develop and manufacture drugs from the concept phase to commercial manufacturing.

Our mission is to accelerate and transform discovery, development, and manufacturing in the rapidly growing field of biologics to benefit patients worldwide, with sites/offices in China, the US, the EU, Asia, and Israel. My client currently employ over 10,000 people and provide services to more than 200 customers worldwide, including 13 of the top 20 biopharmaceutical companies.

**Department Description**

As QA Drug Substance Operations Specialist, you will be joining an organization where people of all backgrounds and experiences are respected, and where we work together focused on changing lives.

In this role you will be reporting to the QA Drug Substance Operations Group Leader.

**Your Responsibilities**
- In this role, you will provide QA support to technology transfer and commercial manufacturing operations.
- Perform QA review of SOPs, risk assessments, change controls and other documentation, as applicable, associated with Drug Substance manufacturing operations
- Ensure that Drug Substance manufacturing operations are conducted according to appropriate cGMP behaviors and in compliance with SOPs, batch manufacturing records and other cGMP documentation as applicable.
- Liaise with Manufacturing Operations to ensure that all deviations, investigations, and batch manufacturing record reviews are performed, addressed and closed out in a timely manner as defined in SOPs.
- Work with Manufacturing Operations to ensure that all CAPAs, change controls, self-inspection observations, etc. relating to manufacturing operations are addressed and closed out in the required time frame.
- Liaise with manufacturing operations, QA, QC, Engineering, MSAT etc. in supporting daily operations.
- Ensure clear communication on issues and timely escalation as applicable.
- Identify opportunities for continuous improvement.
- Support internal Quality peers to ensure on-time disposition of drug substance material.
- Provide support for the preparation of regulatory submissions and inspection readiness activities.
- Perform onsite quality monitoring of GMP areas.
- Provide support for health authority inspections including responses to inspection observations, monitoring of follow up actions.
- Perform additional duties at the request of direct supervisor.
- Flexibility to take on additional tasks and responsibilities at the discretion of the QA Drug Substance Operations Group Leader.
- Will act as a role model for the QA function and the wider organisation in adherence to the company corporate core values and PROUD culture.
- ** Your Profile**Education**
- A Bachelor’s degree in a technical discipline (e.g., biochemistry, chemistry, engineering) would be an advantage.

**Knowledge/Experience**
Required:
Preferred:
- Experience in the biotechnology and/or pharmaceutical industry within a Quality operations role preferred.
- Experience in performing internal audits is ideal.
- Experience in supporting Technology Transfer projects would be an advantage.
- Demonstrated knowledge of Quality Management System and continuous/process improvement tools.

**Personal skills**
Required:
- Adaptable, able to multi-task and handle tasks with competing priorities effectively to deliver site priorities.
- Demonstrated organisation and collaboration skills with a teamwork mind-set.
- Excellent communication skills (written and oral).
- Proactive attitude with good attention to detail.
- Analytical with demonstrated problem solving & root-cause analysis skills.
- Strong aptitude withability tointerprettechnical documentation.
- Strong knowledge of cGxP requirements and regulations.
- Knowledge of trouble shooting and problem-solving skills, e.g. formal root cause analysis such as Ishikawa diagrams, FMEA etc.
- Demonstrated knowledge of Quality Management System and continuous/process improvement tools.

**For further information, please contact Alan on**
**/ 087 365 7522

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