Location : Belvidere, NJ 07823. The QC Analyst is responsible for analyzing and testing raw materials, intermediates, stability samples, and finished products under cGMP guidelines using validated or compendial methods. The role involves performing laboratory analysis with minimal supervision, preparing reagents and standards, calibrating and operating instruments (HPLC, GC, ICP, etc.), and maintaining accurate documentation. The analyst supports product release testing, investigates out-of-specification results, and ensures compliance with safety, quality, and regulatory standards. Candidates should hold a degree in a relevant scientific discipline, have 0-3 years of laboratory experience, and demonstrate knowledge of quality control techniques, GMP, and safety practices. Flexibility to work shifts, overtime, and weekends is required. 0-3 years of lab experience Experience in Microsoft Office (outlook, word, and excel) The schedule may be structured with a required overtime component built in. Candidates must be able to work shifts, weekends, overtime (including coverage) and holidays as required. All candidates, both internal and external, applying for this position understand that overtime may be required and adjusted based on business needs and to ensure continued safe operations. Position content- Key areas of accountability/responsibility Performs analysis in the laboratory with minimal supervision. Prepares standards, mobile phases, and reagents. Calibrates and monitors laboratory equipment (HPLC, GC, ICP, etc.) Analyzes raw materials, intermediates, stability samples and finished products for required tests by various analytical and instrumental methods. Performs calculations, collects and prepares data for evaluation. Keeps supervisor informed of work status Investigation of OOS results under guidance of senior staff Maintains good documentation practices. Job Responsibilities: Performs/Applies knowledge and skills to diverse reactions. Release testing of products per current compendia, regulatory and corporate quality systems, and principles. Display and promote positive safety behaviors at all times; use proper personal protective equipment, appropriate safety tools, equipment and procedures to ensure that self and others go home safe each day; that area and equipment operate at the highest safety levels; that all people in the area (lab techs, quality personnel, maintenance, visitors, contractors, etc.) comply with the safety directives and keep the area neat and clean. Ensures incidents are investigated, reported, and risks are assessed in a timely basis. Acts in such a way that safety awareness & accident prevention are considered in performing all tasks Shows leadership by working to SHEQ standards and encouraging colleagues to work to the same standards. All employees to be aware of and follow all DSM Life Saving Rules. Shows leadership by working to support Customer Commitments and encouraging colleagues to work to the same standards. Supports plant and corporate initiatives as outlined in the manufacturing plan. Skills: To analyze and / or test under cGMP, raw materials, intermediates and finished products by applying validated or compendia methods. Education/Experience: Bachelor's degree in a relevant Scientific discipline preferred, associate's degree required. Broad / General knowledge of quality control techniques and methods. Broad understanding of safety, laboratory hygiene and GMP rules
Job ID: 518606564
Originally Posted on: 4/24/2026
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