Analytical Development Analyst (Epping) at Aspen Pharma Group

Description

• Fine Chemicals requires the services of a highly competent ADD Analyst 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 related field.
• A minimum of 2 years’ experience in a pharmaceutical environment
• Experienced in the practical application of analytical test methods, instrumentation software, troubleshooting, and data processing, especially related to chromatography.
• Ability to design and execute method validation experiments.
• Good knowledge and understanding of GLP (Good Laboratory Practice).     
• Must have experience in or knowledge of the API testing environment.
• Technologically proficient working with various software platforms i.e. MS Office, ERP Systems, LIMS

BASIC JOB TASKS INCLUDE BUT NOT LIMITED TO THE FOLLOWING:

• Execute and perform analysis using appropriate equipment and related techniques. This may include stability testing, investigative or confirmatory analysis, reference standard analysis, cleaning sample analysis, or method development trials.
• Perform analytical method development trials and method validation or verification analysis, as directed. This may include the compilation of associated reports.
• Adhere to GLP such as recording of results, reporting OOS events, and ensuring safe use and disposal of materials.
• Ensuring that training requirements are met.
• Ensure tasks are performed according to the training provided.
• Maintenance of GLP in the Laboratory.
• Adhere to all Company OHSE rules and regulations.
• Comply with GMP requirements as outlined by Company SOP’s and written instructions in all tasks and activities.

PERSONAL ATTRIBUTES:

• 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