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.
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
