QC Lab Technician 1

SGS_JOB_2108

Scientific
 New Jersey
To analyze and / or test under cGMP
raw materials
intermediates and finished products by applying validated or compendia methods.

Contract - 12 Months

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

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