Analytical Scientist

EPM Scientific; South Carolina; Presencial; USD 80.000 - 100.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive salary

Benefits package

Relocation assistance

Opportunities for professional growth

Collaborative work environment

Descripción de la vacante

A pharmaceutical company in South Carolina is looking for an Analytical Scientist to enhance their research and development team. The ideal candidate will have extensive experience in method development, compliance with GMP, and use of HPLC/GC techniques. This position offers a competitive salary, benefits, and opportunities for professional growth within an innovative work environment.

Formación

• Minimum of 4 years of experience in analytical method development in a GMP environment.
• Experience with multiple dosage forms.
• Strong knowledge of GMP regulations and SOP documentation.

Responsabilidades

• Develop and validate analytical methods from scratch.
• Draft and revise SOP documentation for GMP compliance.
• Perform routine and non-routine analysis using analytical techniques.
• Collaborate with teams to support R&D projects.

Conocimientos

Analytical method development

Problem-solving skills

Attention to detail

Communication skills

Educación

Ph.D. or Master's degree in Chemistry or related field

Herramientas

HPLC

UPLC

GC

Empower software

Descripción del empleo

Come join a major player in the pharmaceutical industry! We are committed to excellence and are seeking a highly skilled Analytical Scientist to join our dynamic team.

Job Summary:

The Analytical Scientist will play a crucial role in our research and development efforts, focusing on method development, analytical techniques, and documentation within a GMP (Good Manufacturing Practice) environment. The ideal candidate will have extensive experience in developing methods from scratch, drafting Standard Operating Procedures (SOPs), and utilizing various analytical techniques such as HPLC, UPLC, GC, and Empower, while having worked throughout a variety of dosage forms.

Key Responsibilities:

• Develop and validate analytical methods from scratch to support product development and quality control.
• Draft and revise SOP documentation to ensure compliance with GMP regulations.
• Perform routine and non-routine analysis using HPLC, UPLC, GC, and Empower software.
• Troubleshoot and optimize analytical methods to improve accuracy and efficiency.
• Maintain accurate and detailed records of all analytical activities and results.
• Collaborate with cross-functional teams to support research and development projects.
• Ensure all laboratory activities comply with GMP, GLP (Good Laboratory Practice), and other regulatory requirements.
• Participate in internal and external audits and inspections.
• Stay current with industry trends and advancements in analytical techniques and technologies.

Qualifications:

• Ph.D. or Master's degree in Chemistry, Biochemistry, Analytical Chemistry, or a related field.
• Minimum of 4 years of experience in analytical method development and validation in a GMP environment.
• Experience with multiple dosage forms
• Proficiency in HPLC, UPLC, GC, and Empower software.
• Strong knowledge of GMP regulations and SOP documentation.
• Excellent problem-solving skills and attention to detail.
• Ability to work independently and as part of a team.
• Strong written and verbal communication skills.
• Experience with statistical analysis and data interpretation is a plus.

We offer a competitive salary and benefits package, relocation assistance, opportunities for professional growth and development, and a collaborative and innovative work environment.

EEO Statement: We are an equal opportunities employer and welcome applications from all qualified candidates.