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PROCESSING APPLICATION
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Job Requirements of Bench Scientist:
-
Employment Type:
Contractor
-
Location:
Sanford, NC (Onsite)
Do you meet the requirements for this job?
Bench Scientist
Careers Integrated Resources Inc
Sanford, NC (Onsite)
Contractor
Job Description (Required): In this role, you will:
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.
Here Is What You Need (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.
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
Bonus Points If You Have (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.
Work Location Assignment: On Premise
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.
Open to Fresh Grad
Hard Skills:
1. Lab Exp
2. Degree in Life/Phys sciences
3. Analytical
4. Ishihara Test (color)
Interview Process:
Panel Interview Teams (Camera-on)
If Yes, how many hours of overtime (on average) per week?: As business requires and pre-approved by manager. Work Environment: Onsite What will the resource be working with, or, have exposure to?:
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.
Here Is What You Need (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.
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
Bonus Points If You Have (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.
Work Location Assignment: On Premise
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.
Open to Fresh Grad
Hard Skills:
1. Lab Exp
2. Degree in Life/Phys sciences
3. Analytical
4. Ishihara Test (color)
Interview Process:
Panel Interview Teams (Camera-on)
If Yes, how many hours of overtime (on average) per week?: As business requires and pre-approved by manager. Work Environment: Onsite What will the resource be working with, or, have exposure to?:
N/A
What is the minimum education experience required?: BS with 0 years of experience, Associates with 2 years of experience, High School Diploma with 6 years of experience
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