QC Analyst Level 3 - FTC

TN United Kingdom; Hengoed; On-site; GBP 30,000 - 50,000; Full time

Job summary

An established industry player is seeking a dedicated QC Analyst Level 3 to join their dynamic team. This role offers the opportunity to engage in the analysis of materials and products while adhering to strict quality standards. You will be part of a supportive community that values your contributions and encourages your professional growth. With a focus on continuous improvement and a commitment to innovative healthcare solutions, this position is perfect for someone passionate about making a difference in the pharmaceutical field. If you're ready to take your career to the next level, this is the place for you.

Qualifications

• Degree in chemistry or life science preferred, or extensive lab experience.
• Strong analytical skills and attention to detail are essential.

Responsibilities

• Perform analysis of materials according to written procedures.
• Maintain accurate records and follow GXP standards.
• Investigate non-conformities and propose improvements.

Skills

Analytical Skills

Attention to Detail

Problem-Solving

Knowledge of GXP Standards

Education

Degree in Chemistry or Life Science

Job description

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At Norgine, our colleagues dare to be different, try new things, drive to achieve their goals and beyond, and develop themselves and their community.

We call it the 3D career at Norgine, offering you a fully-rounded experience with no limits.

Bring everything about yourself that you're proud of—whether it's your passion for making a difference, focus on others' well-being, or intellectual curiosity—to unleash your potential in a fast-paced environment and supportive community.

In return, you'll gain a sense of belonging, a long-term career with ongoing development and upskilling, and a company that cares about people’s wellness as much as you do.

Because at Norgine, we transform lives with innovative healthcare solutions.

We have an exciting opportunity for a QC Analyst Level 3 to join Norgine. The person holding this position will report to the QC Team Leader.

Main Purpose:

To carry out and record the analysis of materials according to written procedures.

If you want a multi-dimensional 3D career in a leading healthcare organization, join us.

Requirements

Key Responsibilities & Accountabilities:

• The job holder is responsible for carrying out all work in accordance with written procedures, protocols, and processes.
• The job holder must inform the Shift Team Leader - QC of any non-conformities discovered and actively investigate these to establish root causes.
• Maintain accurate, legible written records of work and follow GXP standards at all times.

Main Tasks

• Perform analysis of starting materials, intermediates, and finished products according to written procedures.
• Provide accurate records of work carried out.
• Perform all duties in accordance with GCLP, GMP, and safe working practices.
• Propose improvements to analytical methods or working practices and participate in department and company improvement projects.
• Perform calibration checks as per written procedures.
• Verify calculations on analysis records.
• Carry out additional tasks as needed to meet business and department needs.
• Meet daily and long-term performance objectives.

Relationships:

Coordinate with Operations, Global Technical, Pharmaceutical Development, and Regulatory Affairs departments on various issues and information exchanges.

Skills & Knowledge

Ideally qualified to degree level in chemistry or a life science; however, extensive pharmaceutical analytical laboratory experience and troubleshooting skills may substitute for formal qualifications.

Our benefits may vary by location. Please consult with the Norgine TA representative for more details.

Interested? Learn more about your potential career with Norgine and apply today.