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Contract Pharmaceutical Quality Control Jobs (NOW HIRING)

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-$40 per hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

Socket.dev

Pharmaceutical QA Director

Tustin, CA · On-site

$180 - $260/hr

Demonstrated expertise in departmental leadership, quality control, microbiology quality assurance, and process quality assurance within a pharmaceutical manufacturing environment. * Strong knowledge ...

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 ...

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Contract Pharmaceutical Quality Control information

What is contract pharmaceutical quality control?

Contract Pharmaceutical Quality Control refers to the process where pharmaceutical companies outsource the testing and analysis of their products to third-party laboratories or service providers. These contract labs ensure that drug products meet regulatory standards for safety, efficacy, and quality before they reach the market. Services often include analytical testing, microbiological testing, method development, and stability studies. By outsourcing this work, companies can access specialized expertise and equipment, streamline operations, and maintain compliance with global regulations.

What are the key skills and qualifications needed to thrive as a contract pharmaceutical quality control specialist?

To thrive as a Contract Pharmaceutical Quality Control specialist, you need a strong background in chemistry, biology, or a related field, with experience in laboratory testing and quality assurance processes. Familiarity with analytical instruments such as HPLC, GC, and LIMS, as well as knowledge of regulatory standards like GMP and relevant certifications, is typically required. Attention to detail, problem-solving abilities, and strong communication skills are essential for accurate testing and effective collaboration. These skills and qualities ensure product safety, regulatory compliance, and the reliability of pharmaceutical products in a highly regulated industry.

What are some common challenges faced in a contract pharmaceutical quality control role and how can they be effectively managed?

In a Contract Pharmaceutical Quality Control role, professionals often navigate challenges such as tight project deadlines, varying client expectations, and strict regulatory requirements. Managing these challenges effectively involves clear communication with clients, thorough documentation, and staying updated with industry standards like GMP and FDA guidelines. Team collaboration is key, as projects typically involve coordination with analytical chemists, quality assurance specialists, and production staff. Adaptability and attention to detail are essential for ensuring both compliance and client satisfaction in a fast-paced, contract-based environment.

What is the difference between Contract Pharmaceutical Quality Control vs Contract Pharmaceutical Quality Assurance?

AspectContract Pharmaceutical Quality ControlContract Pharmaceutical Quality Assurance
Primary FocusTesting and analyzing drug samples to ensure quality and complianceDeveloping, implementing, and maintaining quality systems and procedures
Work EnvironmentLaboratories, testing facilities, manufacturing sitesOffice settings, quality management departments, regulatory agencies
Required CredentialsDegree in pharmacy, chemistry, or related field; certifications in lab testingDegree in pharmacy, chemistry, or related field; certifications in quality systems
Industry UsageUsed by pharmaceutical companies during product testing phasesUsed for ensuring overall quality compliance and regulatory adherence

Contract Pharmaceutical Quality Control focuses on testing and analyzing pharmaceutical products to verify quality, while Contract Pharmaceutical Quality Assurance emphasizes establishing and maintaining quality systems to ensure compliance. Both roles are essential in the pharmaceutical industry but serve different functions within the quality management process.

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Contract Pharmaceutical Quality Control jobs near you
Infographic showing various Contract Pharmaceutical Quality Control job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution.

Quality Control Chemist I

Riverview, FL • On-site

Piramal Pharma Limited
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Full-time

This job post has expired today. Applications are no longer accepted.

Job description

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Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Quality Control Chemist I

Job Description

Piramal Pharma Solutions' HPAPI Research and Manufacturing facility (Ash Stevens, LLC), located in Riverview, Michigan, is seeking a qualified Quality Control Chemist I to join our Quality Control team. The Quality Control Chemist II is responsible for providing analytical chemistry support for the facility.
To perform this position successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required:
Shall adhere to all applicable regulatory requirements, including FDA, EPA, OSHA, and related safety, health and environmental procedures, policies and practices.
Consistent support and practice of all Piramal Pharma Solutions mission, vision, and values.
Identify and protect the original technical information as part of the company property.

Key responsibilities.

  • Support manufacturing operations through the testing of raw materials and starting materials as required to meet production timelines.
  • Perform cleaning verifications on multi-use equipment using approved methods.
  • Test reference standards and stability samples.
  • Document sample preparation, equipment set-up, and test results in laboratory notebooks or other appropriate test record forms. Verify data with second quality team member as required. Maintain all records as required to maintain compliance.
  • As required, test intermediates and final products to meet production timelines/client requirements.
  • Assist in the revision of documentation as required.
  • Participate in quality unit projects, including but not limited to supplier certification, methods development, methods validation and training of both quality unit members as appropriate.
  • Provide support in the maintenance and calibration of laboratory analytical instrumentation.
  • Assist in the maintenance of the QC laboratory through routine housekeeping, as well as keeping personal bench area and desk organized.
  • As required, perform routine testing on the water system (DI, ice, potable, and QC water), and prepare reports as needed.

Experience/Education.

  • Bachelor's degree in Chemistry or Biochemistry or equivalent.
  • One (1) year of experience in pharmaceutical quality control or equivalent is preferred
  • Familiarity with analytical testing and instrumentation.

Job Competencies.

  • Excellent organizational and planning skills.
  • Strong written, verbal, and interpersonal communication skills.
  • High attention to detail.
  • Demonstrated strong analytical skills, and the ability to work independently against multiple deadlines.

Job Conditions.

The physical demands and work environment described here are representative of those that must be met by a team member to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Physical Demands:
    • Frequent lifting, bending, stooping, squatting, pushing and pulling can be expected.
    • Long periods of standing and walking can be expected in this position.
    • This position may require long periods of sitting, typing, computer entry or looking at a computer.
  • Work Environment:
    • Piramal Pharma Solutions is engaged in the business of pharmaceutical research and contract pharmaceutical manufacturing. As such, all PPS staff work in or nearby either chemical/pharmaceutical research or chemical/pharmaceutical manufacturing equipment and processes.
    • Potential limited exposure to hazardous chemicals.
    • Personal protective equipment including safety glasses, lab coats, gloves, specialized clothing including laboratory uniform and appropriate shoes may be required in areas associated with this position.

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