Top 14 Chemists Jobs in Charlotte, Nc

Quality Control Analyst
Glenmark Pharmaceuticals Inc. —Monroe, NC
- Full-time
- Bachelor of Science
- Mid-level
Research and Development Associate
PAVCO —Charlotte, NC
- Full-time
- Mid-level
- High school diploma or GED
- Math
- Profit sharing
- Paid holidays
Quick Apply
Sr. Principal Chemist
Eli Lilly —Concord, NC
- $115,500 - $169,400 a year
- Full-time
- Continuous improvement
- Mentoring
- Senior level
- Health insurance
- Dental insurance
Applications Scientist
Biotage —Charlotte, NC
- Hybrid work
- Management
- Up to 50% travel
- English
Senior Research and Development Position
PAVCO —Charlotte, NC
- Full-time
- English
- Mid-level
- Continuous improvement
- Profit sharing
- Paid holidays
Quick Apply
Assoc Analytical Chemist
MKS Inc. —Rock Hill, SC
- Full-time
- Bachelor of Science
- Engineering
- Ability to lift 50 pounds
Quick Apply
12d
QC Lab Chemist 3rd Shift (Aug '26)
InChem —Rock Hill, SC
- 8 hour shift
- Ability to walk for extended periods
- Bachelor of Science
- Mid-level
Quick Apply
10d
Senior Scientist
National Gypsum Services Co. —Charlotte, NC
- $114,528 - $143,160 a year
- Online Application
- Pass drug screening
- Doctor of Philosophy
- Travel
- Wellness program
- Paid holidays
Quick Apply
Analytical-Lab-Technician
Prime Beverage Group LLC —Concord, NC
- $22 - $23 an hour
- Full-time
- Mid-level
- Analysis skills
- Continuous improvement
Quick Apply
Postdoctoral Associate-Synthetic organic/medicinal chemistry
Wake Forest University - North Carolina —Charlotte, NC
- $75,000 - $110,000 a year
- Full-time
- Doctoral degree
- University
- Doctor of Philosophy
- Relocation assistance
- Health insurance
Quick Apply
Quality Assurance Chemist
Goulston —Monroe, NC
- Full-time
- Bachelor of Science
- No experience needed
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Senior Product Development Mgr- Digital Inkjet
Dept_PhysLoc —Fort Mill, SC
- Full-time
- 5 years
- Master's degree
- Bachelor's degree
- Paid holidays
- Dental insurance
Quick Apply

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Quality Control Analyst

Glenmark Pharmaceuticals Inc. -
Monroe, NC

Apply Now

Job Details

Full-time

Qualifications

Bachelor of Science
Mid-level

Full Job Description

Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading player in the discovery of new molecules – both New Chemical Entities (NCE's) and New Biological Entities (NBEs'), with eight molecules in various stages of clinical development. Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US generics business, with plans to move into the innovative market as well. The USA subsidiary also markets APIs to regulated and semi-regulated countries.

POSITION SUMMARY:

This position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe manufacturing facility, reporting to the QC Manager. Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain compliance to data integrity and cGMP in QC lab in line with standards prescribed by USFDA. Perform IOQ/Calibration for instruments in QC lab at Monroe with guidance of CQA. Execute and complete procedures and systems for RM, PM, FD and in process testing in QC lab. Provide information, data for evaluation and execution of stability study as per Quality and regulatory requirement. Timely complete testing and ensure compliance during analytical TT and AMV performed in QC lab. Able to be a qualified trainer for QC related systems and SOP’s and responsible that personnel are appropriately trained.

OVERALL JOB RESPONSIBILITIES:

Be cost effective and vigilant of laboratory reagents, glassware, etcetera to ensure department is within the Revenue and Capex Budget as per spent analysis project.
Provide feedback to management with laboratory standard hours for financial prudence in resource planning, allocation and manpower to ensure within approved budgets while building best in class quality processes and systems at site.
Execute and maintain quality system controls to ensure no critical and major market complaints.
Take appropriate steps to reduce wastages and losses in the analysis process and build improved efficiency
Perform day to day activities for the chemical laboratory which shall include testing of in- process, RM, PM and FP samples, Swab sample and Tech Transfer (as applicable).
Ensuring compliance to systems and procedures throughout product lifecycle.
Communicate with Supervisor and/or report any preparations or data that may result in an Incidence & OOS.
Ensure that the QC Laboratory is in a ready state of compliance for internal and external audits.
Execute technology transfer of analytical methods for new products. Execute cleaning validation of new products.
Assist in the monitoring of changes in the monographs Pharmacopoeia requirements, Regulatory agencies recommendations and implement the same in QC Lab.
Apply CAPA for Lab failures in OOS.
Prepare in timely fashion updating and revision of SOP, specification, STP and any other documents
Assist in timely completion of Tech Transfer of Finished products.
Ensure training of QC staff
Perform the Tracking System Deployment for Stability Samples/ Process Validation Samples etc.
Perform the Training Tracking Tool/Software for QUALITY Assurance and Quality Control.

Education :

B.Sc. in Chemistry with concentration in Biochemistry

Experience:

1-3 years in the field of Pharmaceutical (manufacturing facility).
Background in the functional areas of Quality Control in Stability, Finished Goods and some Raw Materials with a some experience in R&D.

Extensive knowledge in general laboratory equipment including but not limited to: HPLC, UV-Vis and FTIR.

Knowledge and Skills :

Knowledge of cGMP, Validations and Qualifications, regulatory guidelines, US Pharmacopoeias, Internal auditing, Handling of regulatory Inspections, well acquainted with QMS, well versed with Change control/deviations and market compliant management system.

Skills in coordination of calibration and preventative maintenance services, including but not limited to: setting up vendor contracts, processing quotes, generating purchasing orders and handling vendor invoices.

Technical writing skills to generate SOPs and serve as the Subject Matter Expert.

Began training under Six Sigma and Project Management.

Support the Management to organize and maintain the QC team, good communications skills, front runner, and GMP trainer.

Other requirements (licenses, certifications, specialized training)

Will be an added advantage if the individual has dealt with multiple audits personally.

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Refine Your Search

chemists jobs in charlotte, nc

Quality Control Analyst

Research and Development Associate

Sr. Principal Chemist

Applications Scientist

Senior Research and Development Position

Assoc Analytical Chemist

QC Lab Chemist 3rd Shift (Aug '26)

Senior Scientist

Analytical-Lab-Technician

Postdoctoral Associate-Synthetic organic/medicinal chemistry

Quality Assurance Chemist

Senior Product Development Mgr- Digital Inkjet

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