QC Analyst - ICC

Cpl Group; Dublin; On-site; EUR 45,000 - 60,000; Part time

Job summary

Cpl Group, in partnership with Pfizer, is seeking a QC Analyst - ICC teams to join their state-of-the-art site in Dublin, Grange Castle on a contingent 11-month fixed-term contract. This is an on-site role.

You will be part of Pfizer’s dedicated QC team, performing analyses on QC samples, maintaining quality procedures, and supporting investigations. A third-level science or engineering qualification and QC lab experience are preferred.

Qualifications

• Third level qualification in Science or Engineering preferred.
• Experience in a QC Laboratory is desirable.
• Experience with analytical techniques (bioassay/potency, ELISA, blotting, flow cytometry, PCR) is a plus.
• Able to communicate clearly and work well in a team.
• Detail oriented with good troubleshooting and problem-solving abilities.

Responsibilities

• Perform QC analyses on materials, in-process tests, and finished products per GMP.
• Adhere to GLP/GMP and housekeeping standards.
• Assist in generating and maintaining quality procedures and reports.
• Support laboratory investigations and product investigations.
• Contribute to Right First Time, Continuous Improvement and 5S initiatives.

Skills

Interpersonal skills

Detail oriented

Decision making

Problem solving

Communication

Education

Bachelor's degree in Science or Engineering

Tools

MS Office

Excel

LIMS

TrackWise

Job description

Cpl in partnership with our Client Pfizer are seeking QC Analyst - ICC teams to join them at their state of the art site in Dublin, Grange Castle for a contingent 11 month 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 on QC samples (raw material, In-process tests, intermediates and finished product) in line with Current Good Manufacturing Practices.
• 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.
• Participate, and seek opportunities, in the areas of Right First Time, Continuous Improvement and 5S.

Qualifications

Must-Have

• Third level Qualification in Science, Engineering or equivalent is preferred though not essential.
• Some experience working in a QC Laboratory.
• Demonstrate proven experience with analytical techniques including bioassay/potency testing, ELISA, blotting, flow cytometry assays, PCR, molecular biology techniques.
• Excellent interpersonal and communication skills.
• Detail oriented, quick at decision making, self-motivated with good trouble shooting and problem-solving abilities.

Nice-to-Have

• Experience in quality control in a biotech, pharmaceutical, or bio-pharmaceutical manufacturing environment.
• Knowledge of computer applications, including MS Office, Excel, Softmax, Laboratory Information Management System (LIMS) and track wise.
• Mammalian cell culture experience
• Aseptic techniques and sampling handling

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. Shift work may be required for this role (extended days).

Additional Detail

• To be considered for this position you need to be legally eligible to work in Ireland.
• Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
• Due to high volume of applications, we will be contacting successful candidates only.
• We do not offer relocation.

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