QC Chemist (Relocate to Hauppauge, NY)

Job Title: QC Chemist (DPI/MDI)

Work Location: Hauppauge, NY

Relocation: The candidate must be willing to relocate to New York (Relocation is negotiable).

About Us:

Join our dynamic team, We are a leader in the pharmaceutical manufacturing and R&D sector. We specialize in delivering high-quality DPI and MDI products and are committed to innovation, excellence, and regulatory compliance.

Role Objective:

The QC Chemist will be responsible for conducting routine and advanced testing, ensuring compliance with cGMP, SOP, and lab safety standards. The ideal candidate will have experience in pharmaceutical manufacturing or R&D, with hands-on experience in method validation, method transfer, and vendor qualifications.

Key Responsibilities:

Testing and Analysis:

• Conduct routine and advanced testing and analysis within the QC department.
• Operate specialized laboratory equipment and conduct specialized testing as required.
• Participate in investigation activities and ensure compliance with data integrity and cGMP practices.
• Ensure all documentation practices are followed accurately and efficiently.

Compliance and Safety:

• Ensure compliance with all good documentation practices and laboratory safety standards.
• Maintain working knowledge of GMP, SOP, and USP standards.

Laboratory Equipment:

• Operate and maintain HPLC, balance, pH meter, UV, and other laboratory instruments.
• Conduct method validation, method transfer, and vendor qualifications.
• Perform analytical tasks including QC partial size and ICPMS.

Additional Duties:

• Participate in continuous improvement initiatives.
• Perform other duties as assigned by the Head of the Department or Section.

Minimum Qualifications:

Education:

• Bachelor’s degree (BS or BA) in physical sciences preferred.
• Master’s (MS) or Doctorate (PhD) is a plus.

Experience:

• Minimum 2 years of experience as a QC Chemist (MUST HAVE).
• Minimum 3 years of in-lab chemist experience (MUST HAVE).
• DPI experience preferred.

Skills:

• Proficient in English, both spoken and written.
• Strong organizational, learning, and teaching skills.
• Ability to understand and analyze complex datasets.
• Working knowledge of Microsoft Office and scientific software.

Industry Knowledge:

• Hands-on experience in pharmaceutical manufacturing or R&D setting.
• Experience with method validation, method transfer, and vendor qualifications.

Working Conditions:

Environment:

• Work in a cGMP laboratory or manufacturing environment.
• Personal protective equipment (PPE) such as uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc., may be required.

Shifts:

• May be assigned on a work-shift basis (Day, Evening, Night).
• Weekend or Holiday work may be requested or required.

Physical Requirements:

• Mobility: Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up to 10 kg may be required.
• PPE: Able to wear appropriate personal protective equipment at all times.
• Desk Work: Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period.

Application Process:

Interested candidates who meet the qualifications and are willing to relocate to New York are encouraged to apply. Please submit your resume and cover letter detailing your relevant experience and qualifications.

Note: No sponsorship is available for this position.

Join our team and contribute to our mission of delivering high-quality pharmaceutical products. Apply today to make a difference!