Scientist/Senior Scientist
- Employer
- EPM Scientific
- Location
- Sisters, OR
- Closing date
- Aug 4, 2021
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Scientist/Sr. Scientist - Analytical Development
Pay: $70,000 - $120,000 + annual bonuses & full benefits package
A rapidly growing CDMO is focusing on creating treatments and preventing illness to support healthier lifestyles. A global leader in the life sciences industry is looking for a Scientist/Sr. Scientist, Analytical Development to join their team. This could be a great opportunity for anyone that focusses on method development.
Responsibilities:
* Support in method validation processes
* Document experiments and results with thorough observations
* Exercise technical discretion in the design
* Implement experiments that contribute to project goals
* Display expertise in technical areas, technical reports, summaries, and protocols
* Plan scientific presentations for clients, colleagues, and management, participate in client discussions
* Act as a mentor for junior chemists in method development and regulatory compliance
Requirements:
* S./M.S. with experience in pharmaceutical formulation development and analytical chemistry
* Experience with pharmaceutical applications such as dissolution, GC, XRPD, HPLC, KF, and particle sizing
* Experience in method development, qualification, and validation
* CMC knowledge and experience in advancing drug product formulations through later stage trials
* High ability to work in a successful, team oriented, and customer focused environment
* Must have excellent written and verbal skills
* Encourage safety and high-quality standards of work performance
Pay: $70,000 - $120,000 + annual bonuses & full benefits package
A rapidly growing CDMO is focusing on creating treatments and preventing illness to support healthier lifestyles. A global leader in the life sciences industry is looking for a Scientist/Sr. Scientist, Analytical Development to join their team. This could be a great opportunity for anyone that focusses on method development.
Responsibilities:
* Support in method validation processes
* Document experiments and results with thorough observations
* Exercise technical discretion in the design
* Implement experiments that contribute to project goals
* Display expertise in technical areas, technical reports, summaries, and protocols
* Plan scientific presentations for clients, colleagues, and management, participate in client discussions
* Act as a mentor for junior chemists in method development and regulatory compliance
Requirements:
* S./M.S. with experience in pharmaceutical formulation development and analytical chemistry
* Experience with pharmaceutical applications such as dissolution, GC, XRPD, HPLC, KF, and particle sizing
* Experience in method development, qualification, and validation
* CMC knowledge and experience in advancing drug product formulations through later stage trials
* High ability to work in a successful, team oriented, and customer focused environment
* Must have excellent written and verbal skills
* Encourage safety and high-quality standards of work performance
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