Stability Analyst
Description✓Stability Analyst
✓Holmes Chapel
✓Competitive Salary + Bonus
✓Permanent Role
✓Are you an enthusiastic and motivated scientist/recent graduate who wants to kickstart your career as a Stability Analyst in the pharmaceutical industry? Then keep reading!
✓The Company:
✓At their state-of-the-art facility, this world-leading CDMO [Contract Development and Manufacturing Organisation] is a hub of scientific ingenuity, dedicated to producing life-changing medications that improve the health and wellbeing of millions
✓Their collaborative and innovative environment offers unparalleled opportunities for growth and development.
✓What You'll Do:
✓As a Stability Analyst you will play an essential role in the Quality Control team.
✓You will:
✓Conduct testing, reporting, and investigation activities in the laboratory to ensure compliant and timely delivery of products.
✓Maintain adherence to GMP, site procedures, HSE, and LEAN standards
✓What We're Looking For:
✓Science degree/HND/NVQ 4 or equivalent
✓Excellent interpersonal skills for effective team communication
✓Self-motivated with the ability to plan and manage workload
✓Desirable Skills:
✓At least 1 year's experience in GMP
✓Strong technical knowledge of Quality Control principles in a GMP environment
✓Understanding of compliance management, analytical chemistry/microbiology, and laboratory instrumentation
✓What Else Do You Need To Know?
✓This is a days-based role [37.5 hours a week] with flexible start/finish times
✓Incredible benefits package that includes: Private Healthcare, 10% Company Pension Contribution, Lifestyle Benefits, and more!
✓What Now?
✓If you are passionate about making a difference, driving innovation, and working in an inspiring environment, submit your up-to-date CV now! We are more than happy to answer any questions and support you wherever possible Show more →
✓Holmes Chapel
✓Competitive Salary + Bonus
✓Permanent Role
✓Are you an enthusiastic and motivated scientist/recent graduate who wants to kickstart your career as a Stability Analyst in the pharmaceutical industry? Then keep reading!
✓The Company:
✓At their state-of-the-art facility, this world-leading CDMO [Contract Development and Manufacturing Organisation] is a hub of scientific ingenuity, dedicated to producing life-changing medications that improve the health and wellbeing of millions
✓Their collaborative and innovative environment offers unparalleled opportunities for growth and development.
✓What You'll Do:
✓As a Stability Analyst you will play an essential role in the Quality Control team.
✓You will:
✓Conduct testing, reporting, and investigation activities in the laboratory to ensure compliant and timely delivery of products.
✓Maintain adherence to GMP, site procedures, HSE, and LEAN standards
✓What We're Looking For:
✓Science degree/HND/NVQ 4 or equivalent
✓Excellent interpersonal skills for effective team communication
✓Self-motivated with the ability to plan and manage workload
✓Desirable Skills:
✓At least 1 year's experience in GMP
✓Strong technical knowledge of Quality Control principles in a GMP environment
✓Understanding of compliance management, analytical chemistry/microbiology, and laboratory instrumentation
✓What Else Do You Need To Know?
✓This is a days-based role [37.5 hours a week] with flexible start/finish times
✓Incredible benefits package that includes: Private Healthcare, 10% Company Pension Contribution, Lifestyle Benefits, and more!
✓What Now?
✓If you are passionate about making a difference, driving innovation, and working in an inspiring environment, submit your up-to-date CV now! We are more than happy to answer any questions and support you wherever possible Show more →