Description

The role involves conducting analysis of dry product stability and finished product samples in compliance with assigned specifications and analytical methodologies within a GMP laboratory environment. Attention to detail and accuracy in execution are critical. This position requires thorough documentation of results in accordance with cGMP standards and adherence to FDA, EPA, and OSHA regulations.

Company Culture and Environment

We foster a culture of safety, compliance, and quality. Our team prioritizes the integrity of our processes and ensures a collaborative approach to laboratory practices. We value continuous improvement and uphold the highest standards in the pharmaceutical industry.

Career Growth and Development Opportunities

Employees are encouraged to actively participate in method development and validation, as well as engage in customer and regulatory audits, which can enhance their expertise and pave the way for advancement in their careers.

Detailed Benefits and Perks

While specific benefits are not detailed in the provided description, our commitment to safety and quality suggests a supportive workplace aimed at employee well-being and professional growth.

Compensation and Benefits

• Competitive salary based on experience
• Comprehensive health, dental, and vision insurance
• Retirement savings plan options
• Opportunities for career development through training and mentorship
• Generous paid time off policies

Why you should apply for this position today

This position offers a unique opportunity to contribute to the safety and quality of pharmaceutical products. Joining our team means being part of a dedicated group that values precision, compliance, and continuous learning.

Skills

• Strong analytical skills with attention to detail
• Familiarity with cGMP laboratory practices
• Knowledge of FDA, EPA, and OSHA regulations
• Proficiency in interpreting analytical methodologies and USP
• Ability to review and validate analytical results
• Strong communication skills for documentation and reporting

Responsibilities

• Conduct analysis of product stability and finished product samples
• Document results in compliance with cGMP
• Ensure adherence to safety and regulatory standards
• Review results for conformance to established standards
• Perform analytical testing of pharmaceutical products
• Support method development and validation of new methods
• Participate in investigations and CAPA as necessary
• Engage in customer and regulatory audits
• Develop and execute validation protocols for test methods
• Fulfill other laboratory support activities as needed

Qualifications

• Minimum of 3 years of experience in a GMP laboratory setting
• Proven ability to comply with regulatory standards
• Experience in analytical testing within the pharmaceutical industry

Education Requirements

• Bachelor’s degree in a relevant scientific field

Education Requirements Credential Category

• Bachelor’s Degree

Experience Requirements

• A minimum of 3 years of relevant laboratory experience

Why work in Tampa, FL

Tampa offers a vibrant work-life balance with its warm weather, beautiful beaches, and diverse cultural scene. The city is known for its growing tech industry and numerous professional opportunities, making it an excellent location for career development. Enjoy a lively community, an array of recreational activities, and a welcoming atmosphere in the heart of Florida.