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Internship Pharmaceutical Quality Control Jobs (NOW HIRING)

Garonit Pharmaceutical

QC Supervisor

Fairfield, NJ · On-site

Bachelor's degree in Chemistry or a related scientific field. * 2+ years in a supervisory or management role in a pharmaceutical QC lab. * Strong experience with Empower 3, HPLC, GC, and wet ...

Garonit Pharmaceutical

QC Supervisor

Fairfield, NJ

Bachelor's degree in Chemistry or a related scientific field. * 2+ years in a supervisory or management role in a pharmaceutical QC lab. * Strong experience with Empower 3, HPLC, GC, and wet ...

Astrix Inc

QC Analyst II (Chemistry)

Rensselaer, NY · On-site

$30 - $47/hr

Candidates with strong analytical chemistry, chromatography, and pharmaceutical QC laboratory experience are highly encouraged to apply. Key Responsibilities * Perform analytical testing for incoming ...

Cipla

Quality Control (QC) Chemist

Fall River, MA · On-site

$65K - $105K/yr

Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) * Evaluate critical quality attributes (CQA) such as particle ...

Cipla

Quality Control (QC) Chemist

Fall River, MA · On-site

$65K - $105K/yr

Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) * Evaluate critical quality attributes (CQA) such as particle ...

System One Holdings, LLC

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

Cipla

$65K - $105K/yr

What You'll Do Analytical Testing & Expertise Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) Evaluate critical ...

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Internship Pharmaceutical Quality Control information

What are some typical responsibilities for interns 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 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 is the difference between Internship Pharmaceutical Quality Control vs Pharmaceutical Quality Control Analyst?

AspectInternship Pharmaceutical Quality ControlPharmaceutical Quality Control Analyst
QualificationsEnrolled in or recent graduate of related degreeBachelor's degree in pharmacy, chemistry, or related field
Work EnvironmentTraining-focused, supervised lab settingFull-time professional lab environment
ResponsibilitiesAssisting with tests, learning proceduresPerforming 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 key skills and qualifications needed to thrive as an Internship Pharmaceutical Quality Control, and why are they important?

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.
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Internship Pharmaceutical Quality Control jobs near you
Pharmaceutical Quality Control Manager

Pharmaceutical Quality Control Manager

Yoh, A Day & Zimmermann Company

Rosenberg, TX

$105K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 8 days ago

Job description

Yoh Life Sciences is hiring for a Pharmaceutical Quality Control Manager in Houston, TX.  The QC Manager will serve as a scientific liaison in the lab by supporting method development validation and verification of protocols in a regulated pharmaceutical laboratory environment. General responsibilities include analytical testing of raw materials, in-process samples, finished products and  laboratory instrumentation calibration, such as HPLC, GC, CE, ICP, FTIR, TOC, dissolution apparatus within a cGMP environment. This role requires a minimum of 8 years within a quality control or analytical chemistry laboratory.
Title: QC Manager
Duration: Permanent
Pay: $80,000-105,000 DOE
Location: Houston, TX
Shift: M-F 8-5pm
PRIMARY DUTIES AND RESPONSIBILITIES:
  • Write method validation protocols/reports and perform method development/validation/ verification for API and finished drug products. 
  • Familiar with analytical testing of raw materials, in-process samples, finished products, and analytical laboratory instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC, dissolution apparatus, etc.
  • Supervise the daily activities of the pharmaceutical QC laboratory by establishing testing priorities and schedules, and assignments of staff based on company priorities and objectives. 
  • Serves as scientific liaison to other facilities and departments and scientific/quality control member of the Material Review Board.
  • Assists with appropriate review of analytical results of completed raw material, stability samples, and finished product testing. 
  • Reviews and approves laboratory investigations, corrective and preventive actions, change requests, and deviations as necessary.
  • Maintain equipment calibration schedule and ensure that all required calibrations and maintenance are completed in a timely fashion.
  • Author SOP's and assist with the revision process of current procedures.
  • Ensure pharmaceutical laboratory compliance with applicable regulations. 
  • Assist with procedural, cGMP, and safety training of laboratory staff.
  • Assist with preparations for internal and external (including FDA) laboratory audits and inspections.
  • Administers annual laboratory budget and other related duties as required.

REQUIRED SKILLS, ABILITIES, AND QUALIFICATIONS:
  • Bachelor's or higher degree in Chemistry or related discipline.
  • 10+ years of experience in a pharmaceutical QC or Analytical chemistry laboratory.
  • Experience with semi-solid and liquid pharmaceutical environment.  
  • 3+ years of experience in GLP or GMP (preferred) environment.
  • Strong leadership experience, team of 4 or more
  • Strong communication with the ability to build relationships at all levels of the organization.
  • Ability to organize, prioritize, and effectively perform concurrent tasks with minimal supervision.

Estimated Min Rate: $73500.00
Estimated Max Rate: $105000.00
What’s In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:
  • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
  • Health Savings Account (HSA) (for employees working 20+ hours per week)
  • Life & Disability Insurance (for employees working 20+ hours per week)
  • MetLife Voluntary Benefits
  • Employee Assistance Program (EAP)
  • 401K Retirement Savings Plan
  • Direct Deposit & weekly epayroll
  • Referral Bonus Programs
  • Certification and training opportunities

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: https://www.yoh.com/privacy-notice

Company Description

Yoh delivers expertise, methodology, and momentum to keep work moving forward. From strategy to execution, we deliver bold ideas and big results through consulting, staffing, and enterprise solutions. Nearly a century after our founding, Yoh remains STEM-centered, collaborative, and committed to client success. Yoh is a proud member of the Day & Zimmermann family of companies. Visit us at https://www.yoh.com/