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Environmental Conditions
Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Work Schedule
Standard (Mon-Fri)
The AD chemist will function as a key member of the team. You’ll be responsible for providing technical support for all phases of drug development. This includes high-quality analytical and technical support to internal and external customers, ensuring analytical infrastructure supports new product introduction and development activities. The role involves maintaining laboratory GMP/Safety standards, ensuring the AD laboratory is inspection-ready, and actively participating in the improvement of the AD group as a center of excellence.
What will you do?
* Provide analytical support, including method development, validation/qualification, and transfer of methods to clients.
* Prepare, review, update analytical methods and specifications as appropriate.
* Prepare QC handover packages, present training sessions to QC, and support method familiarization and validation.
* Support external audits as appropriate.
* Support innovation in analytical methods and optimize current methods.
* Complete analytical data collection, interpretation, and characterization of compounds with proper documentation.
* Prepare and review change controls, study protocols, project reports, and other relevant documentation.
* Develop scientific and technical knowledge through literature, conferences, and training.
* Ensure project delivery within timelines and meet site’s technical, quality, and safety metrics.
* Perform all duties with care, adhering to quality, regulatory, safety standards, and company policies.
* Candidate should have hands-on experience with HPLC, GC, and basic instruments like FTIR, UV, Balance, pH meters; experience with LC-MS, GC-MS, NMR is a plus.
Quality Responsibilities
* Perform duties accurately, comply with Quality Management System requirements.
* Participate in site’s quality initiatives and adhere to quality standards.
* Maintain GMP standards.
* Read SOPs, Quality Policies, and Procedures relevant to the role.
* Attend training and complete assessments.
* Work in a GMP compliance manner and be inspection-ready.
Behaviours
* Demonstrate valued behaviours.
* Effective communication, facilitation, and presentation skills.
* Leadership, influencing, and negotiating skills.
* Positive attitude, passion, and ability to coach, empower, train, and mentor others.
Seniority level
* Not Applicable
Employment type
* Full-time
Job function
* Quality Assurance, Product Management, and Engineering
* Industries: Pharmaceutical Manufacturing and Biotechnology Research
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