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Sr Associate
Thousand Oaks, CADescription:
100% onsite, lab-based role at Thousand Oaks. NO RELOCATION CANDIDATES
Analytical Chemistry role is a 100% onsite, lab-based position, supporting the oligonucleotide (oligo) program with a focus on synthetic small molecules. The ideal candidate holds a Master’s degree in Analytical Chemistry (preferred) or a Bachelor’s with 2-3 years of relevant experience, with hands-on expertise in LC, GC, KF, and proficiency in Empower software. Responsibilities include sample testing, impurity standard management, and chromatography support. Local candidates only.
In this role, you will integrate and optimally utilize platform and in-depth product attribute knowledge to advance products and ensure success through pivotal clinical phases to marketing authorization application.
Key Responsibilities:
Qualifications
Basic Qualifications
0+ Years w/ Relevant MS or equivalent 2+ Years w/ Relevant BS or equivalent 4+ Years w/ Relevant AS or equivalent 6+ Years w/ HS
Top 3 Must Have Skill Sets:
1. QC background
2. Experience with HPLC, GC, KF
3. Bachelor's degree with 3 years experience, or master degree in analytical chemistry
4. Preferred to have empower or electronic notebook
Pay Rate $25.00 to $29.00/hr on W2 based on experience.
"This posting is for Contingent Worker, not an FTE"
100% onsite, lab-based role at Thousand Oaks. NO RELOCATION CANDIDATES
Analytical Chemistry role is a 100% onsite, lab-based position, supporting the oligonucleotide (oligo) program with a focus on synthetic small molecules. The ideal candidate holds a Master’s degree in Analytical Chemistry (preferred) or a Bachelor’s with 2-3 years of relevant experience, with hands-on expertise in LC, GC, KF, and proficiency in Empower software. Responsibilities include sample testing, impurity standard management, and chromatography support. Local candidates only.
In this role, you will integrate and optimally utilize platform and in-depth product attribute knowledge to advance products and ensure success through pivotal clinical phases to marketing authorization application.
Key Responsibilities:
- Select suitable methodology and techniques to develop and validate analytical methods for testing synthetic small molecule and/or synthetic oligonucleotides for drug substances and/or drug products.
- Hands-on experience in sample preparation and analysis of synthetic in-process samples, lot release samples, stability samples and drug product formulations using chromatographic and spectroscopic techniques.
- Organize and document analytical data under Good Documentation Practice using an electronic laboratory notebook system.
- Provide and present results to support drug substance and drug product development.
- Transfer analytical methods to contract manufacturing or contract testing labs.
Qualifications
- Bachelor’s degree and 2 years of scientific experience OR
- Master’s degree
- Preferred Qualifications:
- Master’s degree in Analytical Chemistry, Organic Chemistry, Physical, Pharmaceutical, Life Sciences, or Engineering.
- Experience with HPLC, GC, KF and QC experience.
- Experience with operation, maintenance, and troubleshooting of chromatographic and spectroscopic laboratory equipment.
- Experience in laboratory settings within the pharmaceutical or biotech industry.
- Technical aptitude for identification and implementation of novel analytical technologies.
Basic Qualifications
0+ Years w/ Relevant MS or equivalent 2+ Years w/ Relevant BS or equivalent 4+ Years w/ Relevant AS or equivalent 6+ Years w/ HS
Top 3 Must Have Skill Sets:
1. QC background
2. Experience with HPLC, GC, KF
3. Bachelor's degree with 3 years experience, or master degree in analytical chemistry
4. Preferred to have empower or electronic notebook
Pay Rate $25.00 to $29.00/hr on W2 based on experience.
"This posting is for Contingent Worker, not an FTE"