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LL01-062425 Jr Chemist

LL01-062425 Jr Chemist

Validation & Engineering Group, IncManati, 091
Hace 14 días
Descripción del trabajo

Department : Field - LL Location : Manati, 091

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Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas : Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a skilled and detail-oriented Chemist with experience in Finished Product Testing or Raw Material Analysis within the Medical Device industry. The successful candidate will play a key role in ensuring the quality and compliance of materials and products, adhering to regulatory requirements and industry standards.

  • Jr Chemist

Key Responsibilities

1. Quality Control & Analysis

  • Perform chemical, physical, and instrumental testing on raw materials, in-process samples, and finished products.
  • Use analytical techniques such as HPLC, GC, FTIR, UV-Vis spectroscopy, and titration to ensure material conformance to specifications.
  • 2. Documentation & Compliance

  • Accurately document all results and findings in compliance with cGMP, ISO 13485, FDA, and other regulatory standards.
  • Prepare and review lab reports, Certificates of Analysis (CoA), and batch records.
  • 3. Method Development & Validation

  • Assist in developing, optimizing, and validating analytical methods for raw materials and finished products.
  • Perform method transfers and support process validation activities.
  • 4. Instrument Calibration & Maintenance

  • Calibrate, maintain, and troubleshoot laboratory instruments to ensure accurate and reliable results.
  • Follow established protocols for preventive maintenance and equipment qualification.
  • 5. Collaboration & Continuous Improvement

  • Work closely with R&D, Quality Assurance, and Production teams to address quality issues and support product development.
  • Participate in investigations of non-conformances and implement corrective / preventive actions.
  • Contribute to process improvements, cost reduction, and efficiency initiatives in the laboratory.
  • 6. Regulatory Support

  • Provide technical support during audits and regulatory inspections.
  • Stay updated on industry standards, guidelines, and regulations affecting raw material and finished product testing.
  • Qualifications : 1. Education

  • Bachelor’s or Master’s degree in Chemistry, Analytical Chemistry, or a related field.
  • 2. Experience

  • Minimum 2 years of experience in a Finished Product Lab or Raw Material Lab in the Medical Device, Pharmaceutical, or related industry.
  • Experience with cGMP, ISO 13485, and FDA regulations.
  • 3. Technical Skills

  • Proficiency in analytical techniques such as HPLC, GC, FTIR, UV-Vis, and wet chemistry methods.
  • Strong knowledge of material characterization and quality control principles.
  • Experience with Laboratory Information Management Systems (LIMS) is a plus.
  • 4. Soft Skills

  • Strong analytical and problem-solving skills.
  • Excellent communication and documentation abilities.
  • Ability to work both independently and as part of a team.
  • START YOUR APPLICATION

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    Jr • Manati, 091

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