Synergy Bioscience, a contract research organization (CRO), serving the life science industry by providing product development, analytical chemistry, and microbiology testing. We are currently seeking highly qualified R&D scientists with extensive experience in pharmaceutical product development and instrumental analysis and writing technical reports.

Role and Responsibilities:

The successful candidate will be responsible for effectively working on product development aspects, such as formulation, lyophilization, leachable/extractable, test method development/validation, stability studies, and others. They will analyze results, interpret data, and provide both oral updates and written reports in collaboration with the laboratory manager. Adherence to standard operating procedures (SOPs), safety guidelines, and compliance with current Good Manufacturing Practices (cGMP) regulations will be required in this highly regulated work environment. The individual will also ensure that the R&D lab remains a GMP-compliant and safe working environment.

Key responsibilities include:

• Conducting R&D activities using laboratory equipment such as LC-MS, GC-MC, or ICP-OES.
• Writing SOPs, Protocols, and technical reports.
• Following cGMP and GDP work requirements.

Qualifications and Experience:

• Ph. D. degree in chemistry or biochemistry with at least 3 years of experience. Applicants with MSc degree may be considered if they have the right skill sets. 
• Exceptional technical writing and communications skills.
• In-depth knowledge of US FDA regulations and the ICH Guidelines.
• Strong organizational skills.

Skills Required:

• Detail-oriented with the ability to multitask and prioritize tasks to meet deadlines.
• Demonstrated ability to use logic and reasoning to solve problems.
• Self-motivated individual, capable of working both independently and in a team, while maintaining a focus on quality.
• Professional attitude emphasizing teamwork and cooperation.