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Biotech Quality Control Jobs in Connecticut (NOW HIRING)

LanceSoft Inc

Quality Engineer III

North Haven, CT

$71K - $92K/yr

... biotech companies. Our staff maintains a commitment to excellence by developing lasting and ... Statistical Quality control/statistical process control, design of experiments, failure mode and ...

VIRSCIO, INC.

Histology Lab Manager

New Haven, CT · On-site

Operate, maintain, troubleshoot, and perform quality control activities for histology ... biotechnology, or CRO setting. * Specific competencies * Demonstrated expertise in tissue ...

VIRSCIO, INC.

Histology Lab Manager

New Haven, CT · On-site

Operate, maintain, troubleshoot, and perform quality control activities for histology ... biotechnology, or CRO setting. * Specific competencies * Demonstrated expertise in tissue ...

PSG Global Solutions

Biomarker Scientist

New Haven, CT

$35.50 - $44.50/hr

... biotechnology and medical companies. As specialists in recognising talent we pride ourselves on not ... Perform quality control checks on Flow Cytometers and other Laboratory instruments, reagents, and ...

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Biotech Quality Control information

See Connecticut salary details

$29K

$77.4K

$123.2K

How much do biotech quality control jobs pay per year?

As of Aug 19, 2026, the average yearly pay for biotech quality control in Connecticut is $77,362.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,600.00 and $95,100.00 per year, depending on experience, location, and employer.

What is a biotech quality control?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What does a biotech quality control do?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

What are the key skills and qualifications needed to thrive in biotech quality control?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What are popular job titles related to Biotech Quality Control jobs in Connecticut?

For Biotech Quality Control jobs in Connecticut, the most frequently searched job titles are:

What job categories do people searching Biotech Quality Control jobs in Connecticut look for?

The top searched job categories for Biotech Quality Control jobs in Connecticut are:

Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Connecticut as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $77,362 per year, or $37.2 per hour.

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

BioCT Innovation Commons

New Haven, CT • On-site

$110 - $160/hr

Other

Posted yesterday

New

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 mentalacuity with high attention to detail and ability tomaintainaccuracy 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, regulatorycompliance,and/or quality control inclusive of cGMP, FDA regulations, familiarity with ICH guidelines and EU regulations.

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

  • Strong proficiency with MS Word, Excel, PowerPoint.

  • Ability tobend, reach and stand,withliftingto15poundsand 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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