Stability Coordinator at Sanofi
Virginia, Queensland, Australia -
Full Time


Start Date

Immediate

Expiry Date

29 Apr, 25

Salary

0.0

Posted On

29 Jan, 25

Experience

0 year(s) or above

Remote Job

No

Telecommute

No

Sponsor Visa

No

Skills

Stability Testing, Consumer Healthcare, Dissolution Testing, Chemistry, Analytical Techniques

Industry

Pharmaceuticals

Description

QUALIFICATIONS:

  • Bachelor of Science, Chemistry or related discipline

EXPERIENCE:

  • Analytical laboratory experience performing wet chemical and instrumental techniques within the Consumer Healthcare, OTC, Prescription medicine industries would be advantageous but not essential
  • Experienced user and trouble shooter in analytical techniques (e.g. HPLC, GC, AA, TLC, dissolution testing)
  • Stability testing (or exposure to this) is preferred
  • Working knowledge within GMP & GLP guidelines

SOFT AND TECHNICAL SKILLS:

  • Self-determined individual who is proactive and can work both autonomously and with a team
  • Excellent communication skills- verbal and written
  • Highly organised and ability to prioritise conflicting tasks
  • Report and protocals writing
Responsibilities
  • Routine analysis and stability testing on samples and products in the quality control laboratory ensuring quality and timely generation of results
  • Support the initiation of stability studies, maintain stability equipment, perform stability pulls, coordinate sample preparation, testing, publish periodic stability program status
  • Investigate any out of trends or out of specification results and support in summarizing the results in the stability protocols and reports
  • Ensure all routine scheduled work is completed on a daily basis and to report any required deviations to the schedule to the Head of QC or designate
  • To work from and help to develop Analytical Laboratory Methods and SOP’s, and adhere to Pharmacopoeia’s, regulatory and GLP, GMP Guidelines
  • To plan and coordinate own workload, ensuring all appropriate testing is carried out to GLP guidelines and to Sanofi Consumer Healthcare procedures
  • To check fellow staff members work for accuracy and precision against the appropriate methods, SOP’s and guidelines.
  • May be required to use technical experience to develop methods and procedures
  • May be required to validate technical operations to stringent guidelines
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