Analytical Development Supervisor (Epping) at Aspen Pharma Group

Description

• Fine Chemicals requires the services of a highly competent ADD Supervisor for the Analytical Development Department.  To qualify for this position the most suitable candidate must fulfill the following requirements

Requirements

JOB REQUIREMENTS:     

• National Diploma or Bachelor of Science Degree in Analytical Chemistry or equivalent
• A minimum of 5 years experience in a pharmaceutical laboratory with at least 2 years in a leading role.
• Experienced in the practical application of analytical test methods, instrumentation software, troubleshooting, and data processing, especially related to chromatography would be advantageous
• Ability to design and coordinate execution of the method validation experiments
• Knowledge and experience in cleaning validation procedures.
• Understanding of reference standard qualification and inventory management.
• Good knowledge and understanding of GLP (Good Laboratory Practice).     
• Experience in or knowledge of the API testing environment would be an added advantage
• Technologically proficient working with various software platforms i.e., Power BI, MS Office, ERP Systems, LIMS

BASIC JOB TASKS INCLUDE BUT NOT LIMITED TO THE FOLLOWING:

• Deliver comprehensive analytical support to internal and external stakeholders.
• Develop, implement, and maintain the cleaning validation program.
• Manage the qualification and administration of reference standards.
• Maintain rigorous GLP compliance, including meticulous documentation of results, thorough investigation and reporting of Out-of-Specification (OOS) events, and safe handling and disposal of laboratory materials.
• Ensure all personnel meet the required training standards.
• Execute all assigned tasks according to established training protocols.
• Maintain and enforce GLP standards throughout the laboratory.
• Develop and train team members, manage employee performance, and timekeeping, recruitment of staff, and maintain staff discipline in accordance with the company disciplinary SOPs / code of conduct.
• Adhere to all Company Occupational Health, Safety, and Environmental (OHSE) rules and regulations.
• Ensure all activities comply with Good Manufacturing Practice (GMP) requirements as outlined in Company Standard Operating Procedures (SOPs) and written instructions.

PERSONAL ATTRIBUTES (Brief Summary): 

• Strong time management and planning abilities.
• Excellent problem-solving and analytical skills.
• Service-oriented mindset.
• Proven team player, quality-conscious, trustworthy, flexible, and detail-oriented.
• Knowledge of relevant processes and systems.
• Exceptional attention to detail and accuracy.
• Effective written and verbal communication, including report writing and document review.
• Proficiency in operating laboratory equipment and critically evaluating data.
• Availability for after-hours and overtime work as needed.