Quality Control Chemist

Quality Control Chemist Prinston Laboratories Charlotte, NC Job Details Full-time $50,000 - $60,000 a year 1 day ago Benefits Health savings account Relocation assistance Health insurance Dental insurance 401(k) Flexible spending account Paid time off Employee assistance program Vision insurance 401(k) matching Life insurance Qualifications Gas chromatography Technical documentation Pharmaceutical regulatory compliance GMP Wet chemistry Project management Bachelor's degree Laboratory compliance Laboratory quality control Quality standards in production Chemistry Cross-functional communication

Full Job Description Job Title:

QC Chemist - Location is Charlotte, North Carolina

ABOUT US

Prinston Laboratories is a pharmaceutical company engaged in product development, product registration, manufacturing, marketing and sales of high quality affordable generic prescription products to customers. We deliver and maintain high quality and integrity in all of our products, which are manufactured in world-class cGMP manufacturing facilities. We currently have an immediate opening for a QC Chemist for our facilities at Prinston Laboratories, located in Charlotte, North Carolina.

RESPONSIBILITIES

Quality Control Chemist The QC Chemist will perform analytical analysis of raw materials, Finished Product and Stability samples including active pharmaceutical ingredients and excipients according to compendial and Prinston Laboratories test procedures and follow the Standard Operating Procedures. Duties will include but not be limited to compendial analysis and method verifications / validations of raw materials within the raw material laboratory. Primary Duties and Responsibilities  Set-up, perform, and review routine analytical testing.  Prepare samples for analysis by wet chemistry, titration, PSD, and other required instrumentation.  Coordinate findings with sample data from a variety of analyses, including GC and HPLC analyses.  Perform system maintenance and calibrations to ensure equipment is operating with specified requirements. Ensures all work performed strictly adheres to Company policies, Pharmacopeial requirements, and cGMP regulations.  Proper handling of hazardous waste in compliance with the Company SOP and hazardous waste rules.  Document work in a clear and organized manner.  Follow all safety rules and regulations and conducts periodic safety audits.  Follow all cGMP rules and regulations. Qualification Requirements Qualifications include a Bachelor's Degree in Chemistry or related field with relevant QC experience . Strong knowledge of cGMPs and related compliance regulations and guidance required.  A thorough understanding of analytical method qualification, ability to validate/verify and optimize analytical methods and trouble shoot issues/problems.  In depth knowledge in chemistry principles and compendial methodologies, including regulatory requirements and compendial performance criteria.  Track record of managing complex projects to completion within company expectations for deadline, cost, and overall deliverable.  A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments in the company.  Must have excellent organizational, verbal communication and technical documentation skills.

Job Type:

Full-time Pay:

$50,000.00 - $60,000.00 per year

Benefits:

401(k) 401(k) matching Dental insurance Employee assistance program Flexible spending account Health insurance Health savings account Life insurance Paid time off Relocation assistance Vision insurance

Work Location:

In person