Job Description
Our client is looking to fill the role Quality Control Chemist. The Quality Control Chemist conducts intermediate to advanced-level physical and chemical analysis of raw materials, in-process samples, and finished products following established protocols. This role includes mentoring junior staff, performing complex cleaning validations, maintaining sophisticated instrumentation, and ensuring timely delivery of analytical results to meet project deadlines.
Responsibilities: Advanced Technical Analysis - Execute complex testing procedures across all sample categories with expertise in multiple analytical methods and instrumentation platforms
- Conduct advanced troubleshooting and preventive maintenance on laboratory equipment
- Perform comprehensive physical and chemical analysis of materials throughout the manufacturing process to support product release decisions and process validation studies
Instrumentation & Data Management
- Demonstrate mastery of analytical software platforms, including setup of complex testing sequences and advanced data reporting capabilities
- Operate and maintain sophisticated instruments including UV spectrophotometers, FTIR, gas chromatography (GC), high-performance liquid chromatography (HPLC), and ion chromatography (IC) systems
- Execute higher-complexity analytical methods requiring advanced instrument expertise
Cleaning Validation & GMP Compliance
- Independently perform sampling and analysis of complex manufacturing equipment cleaning procedures in full compliance with current Good Manufacturing Practice (cGMP) standards
- Contribute technical expertise to cleaning-related investigations and process improvements
- Support regulatory compliance through rigorous adherence to documentation standards
Quality Systems & Investigations
- Lead investigations of out-of-specification (OOS) results, trending anomalies, and process deviations according to regulatory guidelines
- Collaborate with management on investigation documentation and product impact assessments
- Mentor team members on laboratory investigation and OOS procedures
Method Development & Validation
- Support analytical method validation studies and technology transfer initiatives
- Author, review, and update laboratory testing procedures and standard operating protocols
- Contribute to continuous improvement projects focused on cost reduction and process optimization
Training & Leadership
- Provide technical training and guidance to chemists, laboratory assistants, and temporary personnel
- Support customer and regulatory audit activities, particularly in areas of data integrity and instrumentation documentation
- Conduct peer reviews and quality audits to ensure GMP compliance across laboratory operations
Documentation & Compliance
- Maintain meticulous laboratory notebooks and documentation systems in accordance with cGMP standards and internal procedures
- Perform systematic auditing of laboratory data and testing records
- Demonstrate consistently reliable analytical performance with minimal need for repeat testing or investigations
Required Qualifications:
Education & Experience (Position level determined by combination of education, experience, and demonstrated competencies)
Option 1:
- Bachelor's degree in Chemistry or related scientific discipline
- 0-2 years experience (Chemist I) or 3-5 years experience (Chemist II) in chemistry laboratory, quality control, or research and development within the pharmaceutical industry
Option 2:
- Master's degree in Chemistry or related scientific discipline
- 2-3+ years experience in chemistry laboratory, quality control, or research and development within the pharmaceutical industry
Technical Competencies
- Intermediate to advanced proficiency in laboratory procedures, analytical equipment operation, and instrumentation maintenance
- Strong foundation in safety protocols and laboratory best practices
- Comprehensive understanding of chromatographic methods and analytical problem-solving techniques
- Thorough knowledge of cGMP regulations and data integrity documentation requirements
If you meet the required qualifications and are interested in this role, please apply today.
The Solomon Page Distinction Solomon Page offers a comprehensive benefit program for hourly employees. We pride ourselves on offering medical, dental, 401(k), direct deposit and commuter benefits to our employees, including freelancers - which sets us apart in the industries we serve.
About Solomon Page Founded in 1990, Solomon Page is a specialty niche provider of staffing and executive search solutions across a wide array of functions and industries. The success of Solomon Page reflects an organic growth strategy supported by a highly entrepreneurial culture. Acting as a strategic partner to our clients and candidates, we focus on providing customized solutions and building long-term relationships based on trust, respect, and the consistent delivery of excellent results. For more information and additional opportunities, visit: solomonpage.com and connect with us on Facebook , and LinkedIn .
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Job Tags
Hourly pay, Full time, Temporary work, Freelance,