QC Analyst - Chemistry

Cpl Group; Dublin; Presencial; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

Pfizer in Dublin is seeking a QC Analyst in Chemistry to join the state-of-the-art Grange Castle site on a contingent fixed-term contract on site.

You will be a member of Pfizer's dedicated quality control team, responsible for developing and maintaining quality programs and procedures in line with agency guidelines. Your work will support audits, cross-functional collaboration, and global standards.

Formación

• Third level qualification in Science or Engineering (preferred).
• Strong knowledge of analytical techniques, theoretical and practical.
• Excellent interpersonal and communication skills.
• Detail oriented with quick decision making and good troubleshooting.

Responsabilidades

• Perform analysis of QC samples including raw materials, in-process, intermediates, stability and finished product.
• Adhere to good manufacturing practices and related guidelines.
• Write up and execute analytical method transfer exercises for products being transferred to Grange Castle site.
• Assist in generation and maintenance of quality procedures and reports.
• Facilitate laboratory investigations and support product investigations.
• Analyze wet chemistry and analytical equipment (UV, HPLC, FTIR, KF, iCE, ICP, CE).
• Participate in continuous improvement activities to support Lean/Agile targets.

Conocimientos

Analytical thinking

Quality control

Interpersonal communication

Detail-oriented

Problem-solving

Educación

Bachelor's degree in Science, Engineering or equivalent

Herramientas

UV

HPLC

FTIR

KF

iCE

ICP

CE

Descripción del empleo

Cpl in partnership with our Client Pfizer's are seeking QC Analyst in Chemistry divisions to join the team at their state of the art site in Dublin, Grange Castle for a contingent fixed term contract. This is an on site role.

What You Will Achieve

You will be a member of Pfizer's dedicated and highly effective quality control team. You will be responsible for activities involved in developing and maintaining quality programs, processes and procedures that ensure compliance with established standards and agency guidelines. Your contribution in quality risk management will help us in commitment tracking, interpreting policies, manage site complaints and work directly with operating entities to provide process analyses oversight. Thanks to you, we will be prepared for all upcoming audits and inspections. You will be relied on to ensure that the quality assurance programs and policies are maintained and modified regularly. You will make sure that there are uniform standards worldwide and best practice sharing, which will help in fostering the achievement of company's mission globally.

You will be recognized as a subject matter expert with specialized knowledge and skills in procedures, techniques, tools, materials, and equipment. You will be entrusted with adapting standard methods and procedures by applying your knowledge, prior work experience and requirements. Your business awareness of cross-organizational impact on project delivery will elevate the quality of project deliverables. You will arrive at decisions on which methods and procedures are the best fit for different work situations. You will train others and reinforce behaviours that will help us achieve our goal of providing the best to patients.

How You Will Achieve It:

• Perform analysis of quality control samples including, raw materials, In-process , intermediates, stability and finished product in line with Current Good Manufacturing
• Practices {part of GxP}
• Write up and execute Analytical Method Transfer Exercises for products being transferred to the Grange Castle site, ensuring compliance with site, Pfizer Quality Standards (PQS), International Conference on Harmonization guidance and Filing requirements.
• Adhere to good laboratory practices and housekeeping standards.
• Assist in the generation and maintenance of Quality procedures and reports.
• Facilitate laboratory investigations and support associated product investigation.
• Analyse both wet chemistry and the use of analytical equipment including but not limited to, UV, HPLC, FTIR, KF, iCE, ICP, CE and compendial assays.
• Participate, and seek opportunities, in the areas of Right First Time, Continuous Improvement and unburdening activities to facilitate Lean/Agile implementation.

Qualifications:

• Third level Qualification in Science, Engineering or equivalent is preferred though not essential.
• Strong knowledge of analytical techniques both theoretical and practical
• Excellent interpersonal and communication skills
• Detail oriented, quick at decision making, self-motivated with good trouble shooting andproblem-solving abilities.

Nice-to-Have:

• Experience in quality control in a biotech, pharmaceutical, or bio-pharmaceutical manufacturing environment.
• Some experience working in a QC Laboratory or production environment is preferred through not essential.
• Knowledge of computer applications, including MS Office, Excel, Laboratory Information Management System Access and Track wise

This job description indicates the general nature and level of work expected of the incumbent. It is not designed to cover or contain a comprehensive listing of all activities, duties or responsibilities required of the incumbent. Incumbents may be asked to perform other duties as required.

Candidates who complete the recruitment process and are selected as successful will be offered roles in specific teams within the Chemistry space as QC Analyst depending on their skills, experience, and current vacancy requirements.