Quality Control Scientist

Net2Source (N2S); Sanford (NC); On-site; USD 51,618; Full time

Job summary

A prominent staffing agency is seeking a QC Associate level 2 to conduct various chemical tests and ensure compliance with Good Manufacturing Practices. The role requires a bachelor's degree with minimal experience or relevant experience in analytical techniques. Located in Sanford, NC, this position offers an opportunity to work in the pharmaceutical sector with a pay rate of $37.47/hr. Ideal for recent graduates.

Qualifications

• 0+ years experience required for Bachelor's degree, 4 years for Associate's, or 6 years relevant with high school diploma.
• Technical skills in chemistry laboratory testing are essential.
• Knowledge of Good Manufacturing Practices is required.

Responsibilities

• Perform chemical tests such as water analysis and HPLC.
• Ensure documentation complies with Good Manufacturing Practices.
• Review and revise Standard Operating Procedures.

Skills

Technical skills in chemistry laboratory testing

Communication skills

Organizational skills

Problem-solving skills

Ability to multi-task

Education

Bachelor's degree in a relevant field

Associate's degree

High school diploma with relevant experience

Tools

HPLC

Laboratory instruments for Quality Control

Job description

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