Quality Control Associate - Raw Materials/Water
Quality Control Associate - Raw Materials/Water
Posted on :
22-08-2025
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1 Vacancy
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Job Description
Position Details:
Our client a world-leading Pharmaceutical Company in Sanford NC is currently looking for a QC Chemist to join their expanding team.
Job Title: QC Chemist / Pharma Industry
Duration: 12 months contract extendable up to 48 months
Location: Sanford NC
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description: (Required):
Our client a world-leading Pharmaceutical Company in Sanford NC is currently looking for a QC Chemist to join their expanding team.
Job Title: QC Chemist / Pharma Industry
Duration: 12 months contract extendable up to 48 months
Location: Sanford NC
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description: (Required):
Quality Control Associate - Raw Materials/Water
Summary:
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 a supervisor and working under their direction
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.
Write Standard Operating Procedures (SOPs) technical reports project plans etc.
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 a supervisor and working under their direction
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.
Write Standard Operating Procedures (SOPs) technical reports project plans etc.
Minimum Qualifications:
Bachelors degree in Life/Physical sciences with 0 years of experience (open to fresh grads) OR;
Associates degree in Life/Physical sciences with a minimum of 4 years of experience OR;
High school diploma or GED with a minimum of 6 years of relevant experience
Demonstrated technical skills in chemistry laboratory testing
Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management retains management interpretation and evaluation
Experience with Ishihara Test (color)
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
Excellent organizational skills and strong ability to multitask
Strong written and verbal communication skills
Bachelors degree in Life/Physical sciences with 0 years of experience (open to fresh grads) OR;
Associates degree in Life/Physical sciences with a minimum of 4 years of experience OR;
High school diploma or GED with a minimum of 6 years of relevant experience
Demonstrated technical skills in chemistry laboratory testing
Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management retains management interpretation and evaluation
Experience with Ishihara Test (color)
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
Excellent organizational skills and strong ability to multitask
Strong written and verbal communication skills
Preferred Qualifications:
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 procedures
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 procedures
Location/Schedule:
This is a fully onsite role in Sanford NC
Flexible schedule - manager will review during interview stage
This is a fully onsite role in Sanford NC
Flexible schedule - manager will review during interview stage
Employment Type
Full-time
Key Skills
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