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Temporary Pharmaceutical Quality Control Jobs (NOW HIRING)

Orano

Quality Control Supervisor

Brownsburg, IN · On-site

At least 5 years of experience in pharmaceutical quality control, analytical development, or a related GMP laboratory function. * At least 1 year of experience as a laboratory supervisor, team lead ...

Elanco

Academic Worker - Quality (QA/QC)

Elwood, KS · On-site

This role offers a comprehensive introduction to the pharmaceutical quality environment, providing ... This is a temporary, paid position lasting between 3 to 6 months, depending on site needs.

TekWissen LLC

Quality Control Specialist

Vacaville, CA · On-site

$20 - $26/hr

Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom ... Temporary Assignment Work Type: Onsite Shift: Monday to Friday from 08:00 AM to 04:00 PM Summary:

Alexza

QC Analyst II

Fremont, CA · On-site

$41/hr

Bachelor's Degree in science or related field * 2-5 years relevant experience in a cGMP pharmaceutical QC environment, or at least 1 year with a Master's degree Physical Requirements * Prolonged ...

AbbVie

Manager, Quality Control Laboratory

Waco, TX · On-site

Bachelor's degree with 10 years of pharmaceutical Quality experience (preferably in QC) or an equivalent combination of education and experience Additional Information Applicable only to applicants ...

TPI Staffing, Inc

QC Inspector

Houston, TX

$20/hr

Q A/VI Operator Pay Rate: $20.00 /hour Temp to Hire 9AM - 5:30PM Key Responsibilities: * Perform ... food processing, pharmaceutical, etc. fields) preferred. * Basic knowledge of quality control ...

AbbVie

Manager, Quality Control Laboratory

Waco, TX · On-site

$109K/yr

Bachelor's degree with 10 years of pharmaceutical Quality experience (preferably in QC) or an equivalent combination of education and experience Additional Information Applicable only to applicants ...

AbbVie

Manager, Quality Control Laboratory

Waco, TX · On-site

Bachelor's degree with 10 years of pharmaceutical Quality experience (preferably in QC) or an equivalent combination of education and experience Additional Information Applicable only to applicants ...

Glenmark Pharmaceuticals

Quality Control Analyst

Monroe, NC · On-site

$22.25 - $30/hr

Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading ... This position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe ...

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Temporary Pharmaceutical Quality Control information

What is the difference between Temporary Pharmaceutical Quality Control vs Permanent Pharmaceutical Quality Control?

AspectTemporary Pharmaceutical Quality ControlPermanent Pharmaceutical Quality Control
CredentialsTypically requires a degree in pharmacy, chemistry, or related field; may need certifications like GMP trainingSame as temporary; often requires additional experience or certifications for full-time roles
Work EnvironmentLaboratories, manufacturing sites, quality assurance departmentsSame as temporary; often in similar settings but with more stability
Employment TypeShort-term, contract-based positionsFull-time, permanent roles
Job ResponsibilitiesConduct quality tests, document results, support compliance activitiesSame responsibilities but with increased responsibility and oversight

Temporary Pharmaceutical Quality Control roles provide short-term support in quality testing and compliance, ideal for gaining experience or covering staffing gaps. Permanent roles offer long-term stability, with greater responsibilities and career growth opportunities within the pharmaceutical industry.

What cities are hiring for Temporary Pharmaceutical Quality Control jobs? Cities with the most Temporary Pharmaceutical Quality Control job openings:
What are the most commonly searched types of Pharmaceutical Quality Control jobs? The most popular types of Pharmaceutical Quality Control jobs are:
What states have the most Temporary Pharmaceutical Quality Control jobs? States with the most job openings for Temporary Pharmaceutical Quality Control jobs include:
Temporary Pharmaceutical Quality Control jobs near you

Development Scientist II, Analytical Development and Clinical QC (ADQC)

Alexion Pharmaceuticals

New Haven, CT • On-site

Full-time

Posted 11 days ago

Job description

This is what you will do:
This Development Scientist II will be a key team member in Alexion's External Analytical Development and Quality Control group. This position is responsible for maintaining the highest standard of quality and compliance of external quality control testing (GMP) laboratories. This candidate will be responsible for initiation and ownership of laboratory investigations (LIRs) through strong liaison with external contract laboratories and change controls relevant to ADQC biologic programs. The candidate will ensure timely, compliant, and high-quality delivery for LIR closure to enable the generation of final release CoAs. The role will work closely with internal Quality Assurance, Compliance, Analytical Development and Stability teams to ensure product to patients.
You will be responsible for:
  • Responsible for generating and/or mirroring, reviewing, providing assessments, and driving ownership of LIRs to close out Out-of-Specification (OOS), Out-of-Trend (OOT), and atypical results with structured root cause analysis, impact assessment, and/or corrective/preventive actions (CAPAs).

  • Design investigational testing plans ensuring compliant closure of all testing related investigations within the quality system.

  • Lead and/or facilitate cross-functional meetings with quality assurance to ensure structured investigation alignment.

  • Create plans, track, and present timelines to meet established targets, goals, and objectives.

  • Perform review of analytical data to ensure expected assay performance.

  • Identify opportunities for improvement in systems and make recommendations for effective changes to ensure compliance with cGMP.

  • Strong presentation skills

You will need to have:
  • A successful candidate will have strong mental acuity with high attention to detail and ability to maintain accuracy in documentation and processes.

  • Excellent analytical and problem-solving skills with the ability to conduct risk assessments and root cause analysis.

  • A broad knowledge of Pharmaceutical Quality Assurance, regulatory compliance, and/or quality control inclusive of cGMP, FDA regulations, familiarity with ICH guidelines and EU regulations.

  • Strong proficiency in quality management systems and effective communication skills for interacting with cross-functional teams.

  • Strong proficiency with MS Word, Excel, PowerPoint.

  • Ability to bend, reach and stand, with lifting to 15 pounds and carrying over short distances.

  • Ability to travel up to 10%, if needed.

  • Advanced (M.S. or Ph.D.) degree in Biochemistry, Chemistry or related discipline with 2-5 years (Ph.D.) or 10+ (M.S.) hands on biological analytical development experience in pharmaceutical industry.

We would prefer you to have:
  • Working knowledge in validated documentation systems: Veeva Vault (EQV), LIMS, ValGenesis, Kneat, etc.

  • Knowledge of pharmaceutical/biotechnology manufacturing process

  • Database management /statistical analysis (e.g., JMP, Tableau, SAS) with proficiency in Microsoft SharePoint and/or BOX.

Date Posted
09-Aug-2026
Closing Date
03-Sep-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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