Manage, supervise, and administer the implementation of the project-specific QA/QC Plan and QA/QC staff. Reports to: Project Manager or Project Executive Essential Duties & Responsibilities*
Manage, supervise, and administer the implementation of the project-specific QA/QC Plan and QA/QC staff. Reports to: Project Manager or Project Executive Essential Duties & Responsibilities*
Manage, supervise, and administer the implementation of the project-specific QA/QC Plan and QA/QC staff. Reports to: Project Manager or Project Executive Essential Duties & Responsibilities*
Manage, supervise, and administer the implementation of the project-specific QA/QC Plan and QA/QC staff. Reports to: Project Manager or Project Executive Essential Duties & Responsibilities*
QC Analyst
Raleigh, NC · On-site
$60 - $80/hr
The QC Analyst is responsible for evaluating material and product quality by performing various ... pharmaceutical mfg. preferred) Cognitive Requirements * Ability to read and understand military ...
QC Analyst
Raleigh, NC · On-site
$60 - $80/hr
The QC Analyst is responsible for evaluating material and product quality by performing various ... pharmaceutical mfg. preferred) Cognitive Requirements * Ability to read and understand military ...
QC Chemist II
Durham, NC · On-site
Position Summary - The QC Chemist II position performs testing using a variety of analytical ... S with 3-4 years of experience: focus in chemistry, pharmaceutics or related scientific discipline ...
Quick apply
QC Chemist II
Durham, NC · On-site
Position Summary - The QC Chemist II position performs testing using a variety of analytical ... S with 3-4 years of experience: focus in chemistry, pharmaceutics or related scientific discipline ...
QC LCM / Stability Lead
$98K - $138K/yr
QC LCM / Stability Lead Location: Raleigh, NC Salary: $98,000-$138,000/year Schedule: Fully onsite ... Extensive experience with analytical method validation in a cGMP pharmaceutical environment.
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QC LCM / Stability Lead
$98K - $138K/yr
QC LCM / Stability Lead Location: Raleigh, NC Salary: $98,000-$138,000/year Schedule: Fully onsite ... Extensive experience with analytical method validation in a cGMP pharmaceutical environment.
QC Chemist II
Durham, NC · On-site
$60 - $90/hr
Position Summary - The QC Chemist II position performs testing using a variety of analytical ... S with 3-4 years of experience: focus in chemistry, pharmaceutics or related scientific discipline ...
QC Chemist II
Durham, NC · On-site
$60 - $90/hr
Position Summary - The QC Chemist II position performs testing using a variety of analytical ... S with 3-4 years of experience: focus in chemistry, pharmaceutics or related scientific discipline ...
QC Chemist II
Durham, NC · On-site
Position Summary - The QC Chemist II position performs testing using a variety of analytical ... S with 3-4 years of experience: focus in chemistry, pharmaceutics or related scientific discipline ...
QC Chemist II
Durham, NC · On-site
Position Summary - The QC Chemist II position performs testing using a variety of analytical ... S with 3-4 years of experience: focus in chemistry, pharmaceutics or related scientific discipline ...
Sr Manager QC Microbiology
Holly Springs, NC · On-site
$140 - $190/hr
Advanced degree in Microbiology/Molecular Biology/Pharmaceutical Sciences or related. * Leadership in GMP/pharma/biotech/aseptic environment. * Experience leading QC Microbiology and/or environmental ...
Sr Manager QC Microbiology
Holly Springs, NC · On-site
$140 - $190/hr
Advanced degree in Microbiology/Molecular Biology/Pharmaceutical Sciences or related. * Leadership in GMP/pharma/biotech/aseptic environment. * Experience leading QC Microbiology and/or environmental ...
The QC Specialist, Instrumentation works under the direction of senior team members to support ... Thorough understanding of the pharmaceutical/biotech testing. * Proven ability to understand and ...
The QC Specialist, Instrumentation works under the direction of senior team members to support ... Thorough understanding of the pharmaceutical/biotech testing. * Proven ability to understand and ...
Position Overview The QC Specialist, Instrumentation works under the direction of senior team ... Thorough understanding of the pharmaceutical/biotech testing. * Proven ability to understand and ...
Position Overview The QC Specialist, Instrumentation works under the direction of senior team ... Thorough understanding of the pharmaceutical/biotech testing. * Proven ability to understand and ...
Position Overview The QC Specialist, Instrumentation works under the direction of senior team ... Thorough understanding of the pharmaceutical/biotech testing. * Proven ability to understand and ...
Position Overview The QC Specialist, Instrumentation works under the direction of senior team ... Thorough understanding of the pharmaceutical/biotech testing. * Proven ability to understand and ...
Associate II, Quality Control
Durham, NC · On-site
... of the world's best pharmaceutical, biotechnology and medical companies. As specialists in ... The QC Associate I/II is responsible for supporting key functional, tactical, and operational ...
Associate II, Quality Control
Durham, NC · On-site
... of the world's best pharmaceutical, biotechnology and medical companies. As specialists in ... The QC Associate I/II is responsible for supporting key functional, tactical, and operational ...
... Pharmaceutical, Industrial/Manufacturing, and EV/Battery/Renewables market segment groups (MSG ... Manage, supervise, and administer the implementation of the project-specific QA/QC Plan and QA/QC ...
... Pharmaceutical, Industrial/Manufacturing, and EV/Battery/Renewables market segment groups (MSG ... Manage, supervise, and administer the implementation of the project-specific QA/QC Plan and QA/QC ...
QC Tech II-
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
QC Tech II-
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
QC Tech II
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
QC Tech II
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
QC Tech II
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
QC Tech II
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
QC Tech II
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
QC Tech II
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
QC Tech II
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
QC Tech II
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
QC Analyst / Laboratory Technician
Durham, NC · On-site
$24/hr
Job Title: QC Analyst / Laboratory Technician Location: Durham, NC (100% Onsite) Duration: 12 ... pharmaceutical manufacturing environment. The ideal candidate will have experience in ...
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QC Analyst / Laboratory Technician
Durham, NC · On-site
$24/hr
Job Title: QC Analyst / Laboratory Technician Location: Durham, NC (100% Onsite) Duration: 12 ... pharmaceutical manufacturing environment. The ideal candidate will have experience in ...
Quality Control Travel requirements * N/A Education and Experience * B.A. / B.S. in a Engineering discipline, or equivalent experience preferred * Quality Assurance experience in the pharmaceutical ...
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Quality Control Travel requirements * N/A Education and Experience * B.A. / B.S. in a Engineering discipline, or equivalent experience preferred * Quality Assurance experience in the pharmaceutical ...
Internship Pharmaceutical Quality Control information
What is an internship in pharmaceutical quality control?
An Internship in Pharmaceutical Quality Control is a temporary training position where students or recent graduates gain practical experience in ensuring the quality and safety of pharmaceutical products. Interns typically work in laboratory settings, assisting with sample analysis, documentation, equipment calibration, and compliance with regulatory standards. This role helps interns develop key skills in laboratory techniques, data analysis, and understanding of Good Manufacturing Practices (GMP). It is a valuable opportunity for those considering a career in the pharmaceutical or biotechnology industries.
What are the typical responsibilities of an internship in pharmaceutical quality control?
As a Pharmaceutical Quality Control intern, you can expect to assist with routine laboratory testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with regulatory standards. Responsibilities often include preparing chemical reagents, performing analytical techniques (such as HPLC or spectroscopy) under supervision, recording and analyzing data, and maintaining lab equipment. Interns also learn proper documentation practices and may support investigations of deviations or out-of-specification results. This hands-on experience provides insight into the strict quality standards and teamwork required in the pharmaceutical industry.
What are the key skills and qualifications needed for an internship in pharmaceutical quality control?
To excel in a Pharmaceutical Quality Control internship, you need a solid understanding of chemistry, laboratory procedures, and basic GMP regulations, often gained through relevant coursework or a degree in pharmacy, chemistry, or a related field. Familiarity with analytical instruments like HPLC, GC, and software for data analysis is highly valued. Attention to detail, strong organizational skills, and effective communication set candidates apart in this environment. These skills ensure the accuracy and reliability of product testing, which is critical for maintaining safety, regulatory compliance, and product quality.
What is the difference between Internship Pharmaceutical Quality Control vs Pharmaceutical Quality Control Analyst?
| Aspect | Internship Pharmaceutical Quality Control | Pharmaceutical Quality Control Analyst |
|---|---|---|
| Qualifications | Enrolled in or recent graduate of related degree | Bachelor's degree in pharmacy, chemistry, or related field |
| Work Environment | Training-focused, supervised lab setting | Full-time professional lab environment |
| Responsibilities | Assisting with tests, learning procedures | Performing quality tests, data analysis |
Internship Pharmaceutical Quality Control roles are entry-level positions designed for students or recent graduates to gain industry experience. In contrast, Pharmaceutical Quality Control Analysts are full-time professionals responsible for executing quality tests and ensuring product compliance. The internship provides foundational exposure, while the analyst role involves independent work and responsibility.
What are the most commonly searched types of Pharmaceutical Quality Control jobs in Raleigh, NC?
The most popular types of Pharmaceutical Quality Control jobs in Raleigh, NC are:
What are popular job titles related to Internship Pharmaceutical Quality Control jobs in Raleigh, NC?
For Internship Pharmaceutical Quality Control jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Internship Pharmaceutical Quality Control jobs in Raleigh, NC look for?
The top searched job categories for Internship Pharmaceutical Quality Control jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Internship Pharmaceutical Quality Control jobs?
Cities near Raleigh, NC with the most Internship Pharmaceutical Quality Control job openings:
Traveling Quality Assurance - Quality Control Manager - MSG - Pharmaceutical
Raleigh, NC • On-site
Full-time
Medical, Dental, Vision, Life
Re-posted 9 days ago
Turner Construction rating
7.5
Based on 69 frontline employees who took The Breakroom Quiz
27th of 80 rated construction
Job description
*** This position is for a full time traveling assignment supporting our Advanced Technology Group on a Biotech project. Previous Biotech/pharma experience is strongly preferred. ***
Position Description: Responsible for planning, coordinating and developing the project-specific Quality Assurance/Quality Control (QA/QC) Plan that incorporates the policies and procedures necessary to deliver the project fully compliant with the contract documents. Manage, supervise, and administer the implementation of the project-specific QA/QC Plan and QA/QC staff.
Reports to: Project Manager or Project Executive
Essential Duties & Responsibilities*:
- Manage the development and implementation of the project-specific QA/QC Plan in coordination with the project team, the owner/architect team and the contract documents.
- Assure that sufficient, qualified specialized staff is assigned to provide the required knowledge and experience to execute the plan.
- Maintain a collaborative working relationship with owners, architects, consultants, subcontractors and vendors to ensure that the project-specific QA/QC Plan delivers a fully compliant project.
- Lead, supervise and develop all Turner QA/QC staff, including providing input on or completing performance appraisals.
- Ensure strict adherence to ethics and compliance requirements at all times.
- Develop a comprehensive working knowledge and understanding of the contract documents (including Turner's contract, plans, specifications and applicable codes).
- Develop engineering procedures, including document control, submissions management, creation and tracking of Requests For Information (RFIs), material samples, documentation and tracking of potential cost changes, documentation and tracking of approved change orders within budgetary requirements.
- Implement project-specific QA/QC Plan in coordination with the project safety plan.
- Understand the project execution plan and coordinate QA/QC procedures at appropriate stages of the work, in line with the project schedule.
- Continually improve strategies and tools to efficiently and effectively document, track and record compliance with the contract documents.
- Execute the project-specific QA/QC Plan in a manner that engages all project staff, subcontractors, vendors and consultants.
- Execute the project-specific QA/QC Plan in a manner that engage all project staff, subcontractors, vendors and consultants.
- Conduct testing and inspections and arrange for third-party testing and inspections. Analyze and report the results.
- Expand the development of the plan as the project progresses as appropriate to expand the project by continually improving procedures.
- Direct removal and replacement of, and document all non-compliant materials and/or workmanship. Document compliance after corrective work is completed prior to starting any subsequent work.
- Research and apply additional QA/QC and Lean procedures to enhance the quality of project delivery.
- Oversight of project close-out and quality reports.
The salary range for this position is estimated to be120,000.00 - 217,000.00 annualized, which represents the company's good faithand reasonable estimate of the range of possible compensation at the time ofposting. Additionally, Turner Construction provides flexible benefits,including medical, dental, and vision coverage, financial benefits such as a401(k) plan, Health Savings Account, Flexible Spending Account, wellnessbenefits, a voluntary legal plan, identity theft, life insurance, short-termand long-term disability coverage.
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About Turner Construction
Sourced by ZipRecruiter
Turner Construction, headquartered in New York, NY, US, is a recognized leader in the construction industry. It was established in 1902 and has since curved its niche as one of the most reputable construction firms. Turner Construction provides a broad range of services like general contracting, construction management, design-build, and consulting. Devoted to environment-friendly building practices, it is considered a pioneer in green building and sustainability efforts. Their top-tier projects include Madison Square Garden, Yankee Stadium, and the United Nations Secretariat Building in New York City. The company's mission is to deliver an exceptional product by relentless commitment to their core principles – teamwork, integrity, commitment, and community.
Industry
Construction
Company size
10,000+ Employees
Headquarters location
New York, NY, US
Year founded
1902