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Planet Pharma is seeking a Senior Associate Scientist (contract) for the Vaccine Product Development group, within Protein Development and Clinical Manufacturing. The role is lab-based and focuses on executing plate-based analytical methods to measure protein concentration and quality for cell-free protein synthesis materials and intermediates.
The candidate will be the primary operator for lysate ELISA and Bradford assays, support method qualification, manage critical reagents, and apply
Duties:
Independently performs complex laboratory studies, analyzes data, troubleshoots methods and supports development activities.
Client is looking for a highly skilled, motivated, and talented contractor to join the Vaccine Product Development organization as a Senior Associate Scientist (contract) within Protein Development and Clinical Manufacturing.
The contractor will play a key role in executing and maintaining the plate-based analytical methods that measure protein concentration and quality for cell-free protein synthesis raw materials and in-process intermediates. The successful candidate will be the primary operator for the lysate ELISA and Bradford assays, support method qualification and critical reagent management, and apply these methods to process characterization studies.
This position is for a scientific role which will be lab based, and will require excellent scientific judgment, independence, precise and consistent data generation and thorough record keeping.
Skills:
10+ years laboratory experience
Education:
BS in Biology/Chemistry or related field
BS. in Chemistry, Analytical Chemistry, Biochemistry, or related field with minimum 5 years relevant industry experience; MS with minimum 3 years industry experience in Pharma/Biotech industry required.
Strong technical understanding in analytical chemistry and biochemistry. Hands-on proficiency with plate-based immunoassays (ELISA) and colorimetric protein assays (e.g., Bradford, BCA); experience with HPLC, CE-SDS, or Western blotting is a plus.
Experience with method qualification or validation activities, and accurate data analysis and interpretation of experimental results related to process characterization.
Ability to think critically and demonstrate troubleshooting and problem-solving skills.
Maintain accurate records of experimental procedures, results and conclusion in compliance with regulatory guidelines.
Team player, proactive and willing to work in a collaborative team environment.
Scientific creativity and curiosity for applying new technologies to complex analytical challenges; experience with liquid-handler programming (Tecan, Biomek) preferred.
Pay range: 70-90/hr DOE