QC supervisor
Florence, KY · On-site
Other science degrees, with experience in a pharmaceutical analytical laboratory, will be ... Knowledge of QC analytical techniques is required (for example, HPLC, GC, KF, IR, optical rotation ...
Florence, KY · On-site
Other science degrees, with experience in a pharmaceutical analytical laboratory, will be ... Knowledge of QC analytical techniques is required (for example, HPLC, GC, KF, IR, optical rotation ...
Florence, KY · On-site
Other science degrees, with experience in a pharmaceutical analytical laboratory, will be ... Knowledge of QC analytical techniques is required (for example, HPLC, GC, KF, IR, optical rotation ...
North Salt Lake, UT · On-site
$30 - $36/hr
... pharmaceuticals, nutraceuticals, or food and beverage industries. This is a contract position ... Responsibilities Of The QC Chemist * Prepare, collect, and analyze samples using standard ...
North Salt Lake, UT · On-site
$30 - $36/hr
... pharmaceuticals, nutraceuticals, or food and beverage industries. This is a contract position ... Responsibilities Of The QC Chemist * Prepare, collect, and analyze samples using standard ...
Minimum of 4 years of relevant laboratory experience in a GMP pharmaceutical or biopharmaceutical manufacturing environment. * Strong background in analytical testing within a QC chemistry setting.
Quick apply
Minimum of 4 years of relevant laboratory experience in a GMP pharmaceutical or biopharmaceutical manufacturing environment. * Strong background in analytical testing within a QC chemistry setting.
Newark, NJ · On-site
$25 - $33.75/hr
Job title: Quality Control Analyst Location: New Jersey, Duration: Longterm Job Summary A QC ... Pharmaceutical industry or laboratory experience is preferred. For more information, please reach ...
Quick apply
Newark, NJ · On-site
$25 - $33.75/hr
Job title: Quality Control Analyst Location: New Jersey, Duration: Longterm Job Summary A QC ... Pharmaceutical industry or laboratory experience is preferred. For more information, please reach ...
Be Seen First
El Paso, TX · On-site
$26/hr
Minimum 2 years of experience in a Chemistry lab in a Pharmaceutical environment. If you think this QC Specialist position is a good fit for you, please reach out to me - feel free to call, e-mail ...
Quick apply
Be Seen First
El Paso, TX · On-site
$26/hr
Minimum 2 years of experience in a Chemistry lab in a Pharmaceutical environment. If you think this QC Specialist position is a good fit for you, please reach out to me - feel free to call, e-mail ...
Cleveland, OH · On-site
$60K - $80K/yr
... or pharmaceutical manufacturing. * Knowledge of and experience with Quality Management Systems (QMS) such as 21 CFR 820, ISO13485, or EU IVDR. * Knowledge and experience with current good ...
Cleveland, OH · On-site
$60K - $80K/yr
... or pharmaceutical manufacturing. * Knowledge of and experience with Quality Management Systems (QMS) such as 21 CFR 820, ISO13485, or EU IVDR. * Knowledge and experience with current good ...
Conducts cGMP pharmaceutical testing to ensure regulatory compliance and safety. Assists in method ... Author, review, and revise QC SOPs, test methods, and technical documentation * Develop, validate ...
Conducts cGMP pharmaceutical testing to ensure regulatory compliance and safety. Assists in method ... Author, review, and revise QC SOPs, test methods, and technical documentation * Develop, validate ...
Pearl River, NY · On-site
$55K - $95K/yr
RK Pharma Inc, a vertically integrated pharmaceutical company with our main manufacturing site in Pearl River, NY, is seeking a Quality Control Chemist to work with our growing Quality Teams as we ...
Quick apply
Pearl River, NY · On-site
$55K - $95K/yr
RK Pharma Inc, a vertically integrated pharmaceutical company with our main manufacturing site in Pearl River, NY, is seeking a Quality Control Chemist to work with our growing Quality Teams as we ...
$18.25 - $23.25/hr
... or pharmaceutical manufacturing. * Knowledge of and experience with Quality Management Systems (QMS) such as 21 CFR 820, ISO13485, or EU IVDR. * Knowledge and experience with current good ...
$18.25 - $23.25/hr
... or pharmaceutical manufacturing. * Knowledge of and experience with Quality Management Systems (QMS) such as 21 CFR 820, ISO13485, or EU IVDR. * Knowledge and experience with current good ...
Be Seen First
Irving, TX · On-site
Company Overview Carie Boyd Pharmaceuticals is a national 503B FDA outsourcing registered facility ... other Quality Control duties, as needed Has the decision-making authority for the following : · ...
Quick apply
Be Seen First
Irving, TX · On-site
Company Overview Carie Boyd Pharmaceuticals is a national 503B FDA outsourcing registered facility ... other Quality Control duties, as needed Has the decision-making authority for the following : · ...
Saddle Brook, NJ · On-site
Strong understanding of Quality Control in pharmaceutical/biotechnology/biologics industries * Thorough knowledge of market changes and forces that influence the company * Proficient with computer ...
Quick apply
Saddle Brook, NJ · On-site
Strong understanding of Quality Control in pharmaceutical/biotechnology/biologics industries * Thorough knowledge of market changes and forces that influence the company * Proficient with computer ...
Streamwood, IL · On-site
$17 - $21/hr
Previous QA/QC experience in a manufacturing setting, preferably in the food, personal care, pharmaceutical, or related industry. * Strong attention to detail with the ability to find mistakes and ...
Quick apply
Streamwood, IL · On-site
$17 - $21/hr
Previous QA/QC experience in a manufacturing setting, preferably in the food, personal care, pharmaceutical, or related industry. * Strong attention to detail with the ability to find mistakes and ...
$23 - $30.75/hr
Collaborating with innovative pharmacists, healthcare providers, and pharmaceutical manufacturers ... Position Summary The Quality Control Analyst is responsible for supporting microbiological and ...
Quick apply
$23 - $30.75/hr
Collaborating with innovative pharmacists, healthcare providers, and pharmaceutical manufacturers ... Position Summary The Quality Control Analyst is responsible for supporting microbiological and ...
Be Seen First
Camarillo, CA · On-site
$70/hr
On-Site Required: * 5 to 10 years of experience in Quality Control within pharmaceutical, biotech, or CDMO environments. * Previous experience as QC Manager, QC Supervisor, QC Lead, or senior QC ...
Quick apply
Be Seen First
Camarillo, CA · On-site
$70/hr
On-Site Required: * 5 to 10 years of experience in Quality Control within pharmaceutical, biotech, or CDMO environments. * Previous experience as QC Manager, QC Supervisor, QC Lead, or senior QC ...
Portage, IN · On-site
PhD, MS, or BS in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field * 10-15+ years in pharmaceutical/biotech Quality Control or Analytical Sciences * Significant experience ...
Quick apply
Portage, IN · On-site
PhD, MS, or BS in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field * 10-15+ years in pharmaceutical/biotech Quality Control or Analytical Sciences * Significant experience ...
QUALIFICATIONS PhD, MS, or BS in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field 10-15+ years in pharmaceutical/biotech Quality Control or Analytical Sciences Significant ...
QUALIFICATIONS PhD, MS, or BS in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field 10-15+ years in pharmaceutical/biotech Quality Control or Analytical Sciences Significant ...
Houston, TX · On-site
$23 - $30.75/hr
Collaborating with innovative pharmacists, healthcare providers, and pharmaceutical manufacturers ... Position Summary The Quality Control Analyst is responsible for supporting microbiological and ...
Houston, TX · On-site
$23 - $30.75/hr
Collaborating with innovative pharmacists, healthcare providers, and pharmaceutical manufacturers ... Position Summary The Quality Control Analyst is responsible for supporting microbiological and ...
PhD, MS, or BS in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field * 10-15+ years in pharmaceutical/biotech Quality Control or Analytical Sciences * Significant experience ...
PhD, MS, or BS in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field * 10-15+ years in pharmaceutical/biotech Quality Control or Analytical Sciences * Significant experience ...
$23 - $30.75/hr
Collaborating with innovative pharmacists, healthcare providers, and pharmaceutical manufacturers ... Position Summary The Quality Control Analyst is responsible for supporting microbiological and ...
$23 - $30.75/hr
Collaborating with innovative pharmacists, healthcare providers, and pharmaceutical manufacturers ... Position Summary The Quality Control Analyst is responsible for supporting microbiological and ...
Portage, IN · On-site
PhD, MS, or BS in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field * 10-15+ years in pharmaceutical/biotech Quality Control or Analytical Sciences * Significant experience ...
Portage, IN · On-site
PhD, MS, or BS in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field * 10-15+ years in pharmaceutical/biotech Quality Control or Analytical Sciences * Significant experience ...
$27.88 - $32.10
2% of jobs
$32.10 - $36.32
0% of jobs
$36.32 - $40.54
0% of jobs
$40.54 - $44.76
0% of jobs
$44.76 - $48.97
5% of jobs
$48.97 - $53.19
9% of jobs
$55.91 is the 25th percentile. Wages below this are outliers.
$53.19 - $57.41
13% of jobs
The median wage is $61.32 / hr.
$57.41 - $61.63
22% of jobs
$61.63 - $65.84
21% of jobs
$66.40 is the 75th percentile. Wages above this are outliers.
$65.84 - $70.06
18% of jobs
$70.06 - $74.28
9% of jobs
$27
$60
$74
| Aspect | Quality Control Pharmacist | Quality Assurance Specialist |
|---|---|---|
| Credentials | Pharmacy license, often with GMP or QA certifications | Relevant certifications like CQE or ISO auditor |
| Work Environment | Laboratories, manufacturing plants, pharmaceutical companies | Quality management departments, regulatory agencies |
| Industry Usage | Ensures product quality through testing and analysis | Develops and maintains quality systems and processes |
The main difference is that a Quality Control Pharmacist focuses on testing and verifying pharmaceutical products to meet quality standards, while a Quality Assurance Specialist develops and oversees quality systems to prevent issues. Both roles are essential in pharmaceutical manufacturing but serve different functions within the quality management process.

Full-time
This job post has expired today. Applications are no longer accepted.
7.7
Based on 398 frontline employees who took The Breakroom Quiz
188th of 518 rated manufacturers
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job Description
Summary:
This position will oversee a team responsible for one of three functions: Day shift, Chromatography group, or Wet chemistry group. These groups support raw material release, API (drug substance) release, in-process reaction completion testing and intermediate release, and stability testing in order to support the site’s fast-paced manufacturing needs. A key opportunity in this role will be the development of staff to grow into future roles within the site.
Essential Functions:
Provide day to day leadership to a team of approximately 3-8 analysts by performing the following: leading organizational change; developing and empowering staff; cultivating relationships; putting staff in a position to succeed, meeting their personal career goals while also achieving organizational goals; building effective teams that apply their diverse skills and perspectives to achieve common goals; driving engagement and creating a climate where staff are motivated to do their best.
Revise/review specifications, SOPs, and other documents regarding QC and assay execution.
Train and supervise staff in order to perform QC tasks by ensuring completion of technique-related training, SOPs, OJT, and knowledge assessments, as well as ensuring on-going compliance to training and site SOPs.
Participate in the discrepancy management process.
Drive closure of deviations/ investigations/ CAPA.
Interact with auditors/clients during visits and tours.
Oversee daily activity for the group to ensure quality results
Performance management for direct reports.
Prepare and Assist in the Writing of Procedures (Standard Operating Procedures, Equipment Operating Procedures, Department Procedures, and Laboratory Investigations) accordance with established standard lead times.
Effectively communicate with peers, manufacturing, AD and QC staff, to resolve technical issues and direct activities.
Provide support to site Safety initiatives.
Other job duties as assigned.
Education:
Bachelor’s degree in physical science, preferably in Chemistry. Other science degrees, with experience in a pharmaceutical analytical laboratory, will be considered.
Experience:
Requires a minimum of 5 years’ experience in quality/analytical/pharmaceutical industry or similar experience with a minimum of one year supervisory/ team lead experience within the pharmaceutical industry in a QA/QC leadership role, preferably with a plant manufacturing focus preferred. Knowledge of QC analytical techniques is required (for example, HPLC, GC, KF, IR, optical rotation, etc.), Empower 3 experience for IPC and Chromatography group roles is preferred.
Competencies:
Excellent knowledge and understanding of chemistry and analytical instrumental technologies. Excellent knowledge of qualitative and quantitative chemical analysis. Excellent understanding of quality and regulatory requirements in the pharmaceutical industry, including pharmaceutical GMPs and descriptive organic chemistry. Excellent problem solving skills and logical approach to solving scientific problems. Excellent proficiency with HPLC, GC, LC/MS KF, FTIR, and other wet chemistry methodology. Excellent interpersonal and communication skills (both oral and written). Good presentation skills to present information to customers, clients, and other employees. Good leadership skills. Ability to read, analyze, and interpret technical procedures and governmental regulations. Ability to write standard operating procedures and policy manuals. Ability to apply mathematical operations, to such tasks as determination of test reliability, analysis of variance, and correlation techniques.
Physical Requirements:
Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pound pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. Safety glasses, safety shoes, lab coat, latex or similar gloves, safety apron, organic respirator occasionally.
Get the full story on Breakroom
Sourced by ZipRecruiter
Biotechnology research and development
10,000+ Employees
Waltham, MA, US
1956