Net2Source (N2S)
Overview
Title:
QC Associate level 2 - Raw Materials/Water Duration:
12+ months (Extendable) Location:
Sanford, NC 27330 Client:
Pharma Pay Rate:
$37.47/hr on W2 Responsibilities
Perform various chemical tests such as water analysis, FTIR, ID, HPLC, and other compendial assays. Write and perform raw material verification protocols and associated reports. Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Minimum Requirements
Applicant must have a bachelor\'s degree with 0+ years of experience; OR an associate\'s degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience Demonstrated technical skills in chemistry laboratory testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Open to Fresh Grad Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Preferred Requirements
Experience with laboratory work, particularly using analytical techniques such as HPLC, pH, Polarimetry, etc. Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Ability to manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedure. Physical/Mental Requirements
Non-existent to minimal travel. Must be able to wear appropriate PPE (e.g., lab coat, safety glasses, non-porous shoes, gloves, etc.) Ability to lift 30 lbs, stand for 2 to 3 hours at a time, sit for 2 to 3 hours at a time, walk long distances and bend to obtain items from lower shelving/cabinets. Intellectual capability to perform complex mathematical problems and perform complex data analysis. Perform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories. Support environmental monitoring/water testing in the QC Raw materials laboratory. Test incoming raw materials per compendial methods. Follow Environment Health and Safety requirements for site and QC laboratories. Support product transfers, new product development, regulatory queries, cost improvement projects, and Drug Product plant support for Cleaning Validation. Operate within established HR policies and basic colleague relations guidelines. Hard Skills
Degree in Life/Phys sciences Analytical Seniority level
Associate Employment type
Contract Job function
Science and Research Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Chemical Manufacturing
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Title:
QC Associate level 2 - Raw Materials/Water Duration:
12+ months (Extendable) Location:
Sanford, NC 27330 Client:
Pharma Pay Rate:
$37.47/hr on W2 Responsibilities
Perform various chemical tests such as water analysis, FTIR, ID, HPLC, and other compendial assays. Write and perform raw material verification protocols and associated reports. Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Minimum Requirements
Applicant must have a bachelor\'s degree with 0+ years of experience; OR an associate\'s degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience Demonstrated technical skills in chemistry laboratory testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Open to Fresh Grad Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Preferred Requirements
Experience with laboratory work, particularly using analytical techniques such as HPLC, pH, Polarimetry, etc. Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Ability to manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedure. Physical/Mental Requirements
Non-existent to minimal travel. Must be able to wear appropriate PPE (e.g., lab coat, safety glasses, non-porous shoes, gloves, etc.) Ability to lift 30 lbs, stand for 2 to 3 hours at a time, sit for 2 to 3 hours at a time, walk long distances and bend to obtain items from lower shelving/cabinets. Intellectual capability to perform complex mathematical problems and perform complex data analysis. Perform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories. Support environmental monitoring/water testing in the QC Raw materials laboratory. Test incoming raw materials per compendial methods. Follow Environment Health and Safety requirements for site and QC laboratories. Support product transfers, new product development, regulatory queries, cost improvement projects, and Drug Product plant support for Cleaning Validation. Operate within established HR policies and basic colleague relations guidelines. Hard Skills
Degree in Life/Phys sciences Analytical Seniority level
Associate Employment type
Contract Job function
Science and Research Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Chemical Manufacturing
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