Quality Control Scientist

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

• Perform various chemical tests such as water analysis, FTIR, , 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.

• 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

• 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.

• 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.

• Degree in Life/Phys sciences
• Analytical

• Associate

• Contract

• Science and Research

• Pharmaceutical Manufacturing, Biotechnology Research, and Chemical Manufacturing