Hauppauge, NY · On-site
$75K - $125K/yr
Manage multiple development projects and develop formulations in a timely manner * · Assist in ... Knowledge of CGMPs related to US FDA Manufacturing environments. * Ability to prioritize and ...
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Hauppauge, NY · On-site
$75K - $125K/yr
Manage multiple development projects and develop formulations in a timely manner * · Assist in ... Knowledge of CGMPs related to US FDA Manufacturing environments. * Ability to prioritize and ...
... • Assist in designing method validation or method transfer protocols and establish project ... FDA guidance • Solid understanding and knowledge of general chemistry and separation science.
... • Assist in designing method validation or method transfer protocols and establish project ... FDA guidance • Solid understanding and knowledge of general chemistry and separation science.
... • Assist in designing method validation or method transfer protocols and establish project ... FDA guidance • Ability to utilize Microsoft Excel and Word to perform tasks • Proficiency in ...
... • Assist in designing method validation or method transfer protocols and establish project ... FDA guidance • Ability to utilize Microsoft Excel and Word to perform tasks • Proficiency in ...
... • Assist in designing method validation or method transfer protocols and establish project ... FDA guidance • Ability to utilize Microsoft Excel and Word to perform tasks • Proficiency in ...
... • Assist in designing method validation or method transfer protocols and establish project ... FDA guidance • Ability to utilize Microsoft Excel and Word to perform tasks • Proficiency in ...
Tucker, GA · On-site
As part of a team, assist with developing and testing formulas and processes for new products ... meet FDA food manufacturing guidelines; keep accurate and detailed records on lab work and data ...
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Tucker, GA · On-site
As part of a team, assist with developing and testing formulas and processes for new products ... meet FDA food manufacturing guidelines; keep accurate and detailed records on lab work and data ...
... most recently FDA-approved medication in Alzheimer's Disease. The Clinical Scientist ... Communicate with investigators, coordinators, and study teams about participants * Assist with ...
... most recently FDA-approved medication in Alzheimer's Disease. The Clinical Scientist ... Communicate with investigators, coordinators, and study teams about participants * Assist with ...
... • Assist in designing method validation or method transfer protocols and establish project ... FDA guidance • Ability to utilize Microsoft Excel and Word to perform tasks • Proficiency in ...
... • Assist in designing method validation or method transfer protocols and establish project ... FDA guidance • Ability to utilize Microsoft Excel and Word to perform tasks • Proficiency in ...
... • Assist in designing method validation or method transfer protocols and establish project ... FDA guidance • Ability to utilize Microsoft Excel and Word to perform tasks • Proficiency in ...
... • Assist in designing method validation or method transfer protocols and establish project ... FDA guidance • Ability to utilize Microsoft Excel and Word to perform tasks • Proficiency in ...
Tucker, GA · On-site
As part of a team, assist with developing and testing formulas and processes for new products ... meet FDA food manufacturing guidelines; keep accurate and detailed records on lab work and data ...
Quick apply
Tucker, GA · On-site
As part of a team, assist with developing and testing formulas and processes for new products ... meet FDA food manufacturing guidelines; keep accurate and detailed records on lab work and data ...
Tucker, GA · On-site
As part of a team, assist with developing and testing formulas and processes for new products ... meet FDA food manufacturing guidelines; keep accurate and detailed records on lab work and data ...
Quick apply
Tucker, GA · On-site
As part of a team, assist with developing and testing formulas and processes for new products ... meet FDA food manufacturing guidelines; keep accurate and detailed records on lab work and data ...
Tucker, GA · On-site
As part of a team, assist with developing and testing formulas and processes for new products ... meet FDA food manufacturing guidelines; keep accurate and detailed records on lab work and data ...
Quick apply
Tucker, GA · On-site
As part of a team, assist with developing and testing formulas and processes for new products ... meet FDA food manufacturing guidelines; keep accurate and detailed records on lab work and data ...
Long Beach, CA · On-site
$80K - $90K/yr
... most recently FDA-approved medication in Alzheimer's Disease. The Clinical Scientist ... Communicate with investigators, coordinators, and study teams about participants * Assist with ...
Long Beach, CA · On-site
$80K - $90K/yr
... most recently FDA-approved medication in Alzheimer's Disease. The Clinical Scientist ... Communicate with investigators, coordinators, and study teams about participants * Assist with ...
... most recently FDA-approved medication in Alzheimer's Disease. The Clinical Scientist ... Communicate with investigators, coordinators, and study teams about participants * Assist with ...
Quick apply
... most recently FDA-approved medication in Alzheimer's Disease. The Clinical Scientist ... Communicate with investigators, coordinators, and study teams about participants * Assist with ...
Hialeah, FL · On-site
$20 - $25/hr
This role assists in maintaining adherence to ICH-GCP guidelines, FDA regulations, IRB requirements ... Associate's or Bachelor's degree in Life Sciences, Healthcare Administration, or related field ...
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Hialeah, FL · On-site
$20 - $25/hr
This role assists in maintaining adherence to ICH-GCP guidelines, FDA regulations, IRB requirements ... Associate's or Bachelor's degree in Life Sciences, Healthcare Administration, or related field ...
Kenosha, WI · On-site
$110K - $130K/yr
Oversee and mentor the R&D Lab Assistant to ensure efficient lab operations.Maintain an organized ... Ensure adherence to food safety and regulatory standards (FDA, FSMA, GFSI).Salary$110,000 - $130 ...
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Kenosha, WI · On-site
$110K - $130K/yr
Oversee and mentor the R&D Lab Assistant to ensure efficient lab operations.Maintain an organized ... Ensure adherence to food safety and regulatory standards (FDA, FSMA, GFSI).Salary$110,000 - $130 ...
Cambridge, MA · On-site +1
$140K - $160K/yr
... and assist in the authoring and reviewing technical regulatory submission documents ... Knowledge of relevant industry guidance for US and Global products and regulatory guidelines (FDA ...
Cambridge, MA · On-site +1
$140K - $160K/yr
... and assist in the authoring and reviewing technical regulatory submission documents ... Knowledge of relevant industry guidance for US and Global products and regulatory guidelines (FDA ...
Hialeah, FL · On-site
$20 - $25/hr
This role assists in maintaining adherence to ICH-GCP guidelines, FDA regulations, IRB requirements ... Associate's or Bachelor's degree in Life Sciences, Healthcare Administration, or related field ...
Quick apply
Hialeah, FL · On-site
$20 - $25/hr
This role assists in maintaining adherence to ICH-GCP guidelines, FDA regulations, IRB requirements ... Associate's or Bachelor's degree in Life Sciences, Healthcare Administration, or related field ...
Your ability to plan research, contribute to publications, and assist in securing funding will be ... Working knowledge of GCP, ICH, DHHS, OIG and FDA regulations and scientific expertise in the ...
Your ability to plan research, contribute to publications, and assist in securing funding will be ... Working knowledge of GCP, ICH, DHHS, OIG and FDA regulations and scientific expertise in the ...
$43.10 - $64.11/hr
Your ability to plan research, contribute to publications, and assist in securing funding will be ... Working knowledge of GCP, ICH, DHHS, OIG and FDA regulations and scientific expertise in the ...
$43.10 - $64.11/hr
Your ability to plan research, contribute to publications, and assist in securing funding will be ... Working knowledge of GCP, ICH, DHHS, OIG and FDA regulations and scientific expertise in the ...
Austin, TX · On-site
Effectively assist in managing a project from the evaluation phase through the product development ... Knowledge of Design Control requirements as defined by the FDA Quality System guidelines (High ...
Austin, TX · On-site
Effectively assist in managing a project from the evaluation phase through the product development ... Knowledge of Design Control requirements as defined by the FDA Quality System guidelines (High ...
$7.93 - $9.86
2% of jobs
$9.86 - $11.78
4% of jobs
$11.78 - $13.70
11% of jobs
$14.29 is the 25th percentile. Wages below this are outliers.
$13.70 - $15.63
24% of jobs
The median wage is $16.43 / hr.
$15.63 - $17.55
20% of jobs
$19.21 is the 75th percentile. Wages above this are outliers.
$17.55 - $19.47
16% of jobs
$19.47 - $21.39
6% of jobs
$21.39 - $23.32
4% of jobs
$23.32 - $25.24
1% of jobs
$25.24 - $27.16
8% of jobs
$27.16 - $29.09
3% of jobs
$7
$17
$29
$75K - $125K/yr
Full-time
Posted 22 days ago
We are seeking a Senior Formulation Scientist to join our dynamic R&D team, where you’ll play a key role in developing innovative pharmaceutical and nutraceutical products. In this hands-on role, you’ll design formulations, support process improvements, and contribute directly to product development from concept to commercialization. This position offers exposure to oral solid dosage forms. Candidates may specialize in drug formulation or nutraceutical formulation, with the opportunity to grow into broader product development responsibilities.
The Sr. Scientist Formulation is primarily responsible for formulation product development and leading the process development activities from concept through commercialization.
Why Join CPC?
At CPC, you’ll be part of a team that has set the standard in pharmaceutical development and contract manufacturing since 1971, helping bring high-quality OTC, dietary supplement, and prescription products to market faster and safer than ever. We pride ourselves on quality as a core value, innovative problem-solving, and a collaborative culture where everyone plays a role in advancing formulation and manufacturing excellence. CPC offers an inclusive, respectful workplace with opportunities to grow your skills and career while working with cutting-edge technologies and serving leading global brands. With a commitment to employee success, competitive benefits, and a culture built on teamwork and integrity, CPC is a place where your contributions truly make an impact.
Requirements:Responsibilities: Responsibilities include, but are not limited to:
Education and Experience:
Skills, Knowledge, and Abilities:
Supervisory Responsibilities:
Personal Protective Equipment or Attire Required for Position:
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Pharmaceutical and medicine manufacturing
501 - 1,000 Employees
Hauppauge, NY, US
1971
