Senior Quality Control Analyst

About the Company

Are you an experienced QC Analyst looking for your next challenge?

Would you like to join an up and coming Pharma start up and develop your leadership skills?

About the Position

I'm seeking an experienced Analyst with at least 6 years of experience in a Life Science manufacturing environment with expertise in HPLC, GC, KF, DRT IR, UV etc. You'll join a site that has just invested heavily in their new Laboratory facilities and have the opportunity to function as a Team Lead at the site.

On offer is a permanent role with progression opportunities, a well as a competitive salary and benefits package.

Key Responsibilities

• Effectively coordinating and leading a team so that productivity, quality, documentation, work schedules, safety and housekeeping are run at maximum efficiency.
• Development, coaching, motivation, and morale of team members through effective teambuilding and use of reward and recognitions systems celebrating team success.
• Ensuring that all team members are trained and have completed training records for all training completed.
• To perform routine and non-routine technical duties, and various support activities as required by the site.
• Involvement in forecasting and scheduling of activities within QC sample management.
• Perform a variety of routine Analytical testing techniques for raw materials and product samples (release and stability) and associated documentation
• Review and approve and trend Analytical Testing data.
• Perform as required analytical method technical transfer, verification and validation.
• Support activities including general lab readiness, audit readiness, laboratory equipment qualification and analytical method technical transfer, verification and validation.
• Be part of a motivated and high performing team.
• Contribute to a continuous improvement environment and bring problem solving and troubleshooting capabilities.
• Demonstrate a commitment to learning and personal development.
• Consistently deliver on specific area Key Performance Indicators.
• Operate to the highest standards of Safety, Quality and Compliance.
• Provide support and subject matter expert knowledge in investigations associated with deviations

Experience/Requirements

• At least 5+ years’ experience in a pharmaceutical industry GMP laboratory
• A Degree in chemistry, biochemistry, biotechnology or a related subject.
• Experience in a leadership capacity is desirable.
• Ability to work independently and meeting established timelines.
• Lean Six Sigma experience preferable.
• Knowledge of cGMPs
• Excellent communication skills both written and verbal

Remuneration Package

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