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Quality Control Stability Jobs in Connecticut (NOW HIRING)

QC Manager

Plainville, CT · On-site

$110K - $125K/yr

QC Manager Regular Full-Time Plainville, CT, US 4 days ago Requisition ID: 1441 Salary Range: $110 ... Oversee plan and execution of product validation and stability studies, ensuring accurate data ...

This is a hands-on role for someone who enjoys building high-quality control panels, solving ... quality Why ASG * Growing company with long-term stability * Clean, organized shop environment

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Quality Control Stability information

What is a quality control stability role?

A Quality Control Stability role involves monitoring and evaluating the stability of pharmaceutical products, ensuring they maintain their quality, safety, and efficacy throughout their shelf life. Professionals in this position design and execute stability studies, analyze the results, and document findings according to regulatory requirements. They play a crucial part in ensuring compliance with industry standards and supporting product development and release. This role typically requires expertise in analytical testing, regulatory guidelines, and laboratory practices.

What are some common challenges faced in a quality control stability role, and how can they be addressed?

Professionals in Quality Control Stability often encounter challenges such as managing tight timelines for stability testing, interpreting ambiguous results, and ensuring compliance with evolving regulatory requirements. Effective communication with cross-functional teams—such as R&D, production, and regulatory affairs—is essential to address discrepancies and maintain data integrity. Staying organized, maintaining thorough documentation, and keeping up to date with industry guidelines help mitigate these challenges and ensure smooth workflow.

What are the key skills and qualifications needed to thrive as a quality control stability specialist, and why are they important?

To thrive as a Quality Control Stability specialist, you need a solid background in chemistry or related sciences, experience with stability testing, and typically a bachelor’s degree in a scientific field. Familiarity with laboratory instruments (such as HPLC, GC), stability management systems, and knowledge of regulatory guidelines like ICH are essential. Attention to detail, problem-solving, and strong organizational skills help ensure accurate data analysis and effective reporting. These abilities are crucial for maintaining compliance, product safety, and reliability in pharmaceutical or biotech environments.

What is the difference between Quality Control Stability vs Quality Control Inspector?

AspectQuality Control StabilityQuality Control Inspector
CertificationsOften requires certifications like Six Sigma, ISO auditor, or quality management certificationsTypically requires quality inspection certifications or training
Work EnvironmentFocuses on maintaining process stability in manufacturing or production settingsPerforms inspections on products or materials on the production line
Employer & Industry UsageUsed in manufacturing, aerospace, automotive, and industries emphasizing process consistencyCommon in manufacturing, food production, and assembly lines

Quality Control Stability involves ensuring that manufacturing processes remain consistent over time, emphasizing process control and reduction of variability. In contrast, a Quality Control Inspector primarily conducts inspections to verify product quality at various stages. Both roles are essential in quality management but focus on different aspects of quality assurance.

Is quality control stability a good career choice?

Quality Control Stability is a role focused on maintaining product consistency and compliance through testing and monitoring processes. It often requires attention to detail, knowledge of industry standards, and proficiency with testing tools or software. This career can offer steady employment opportunities in manufacturing, pharmaceuticals, or food industries, with potential for advancement and certification.

Is quality control stability a good career path?

Quality control stability involves ensuring products meet quality standards over time, often requiring attention to detail and knowledge of testing procedures. It can offer steady employment and opportunities for advancement in manufacturing, pharmaceuticals, or food industries, especially for those with relevant certifications or experience. The career can be stable, but growth depends on industry demand and individual skill development.

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

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

What cities in Connecticut are hiring for Quality Control Stability jobs?

Cities in Connecticut with the most Quality Control Stability job openings:

Infographic showing various Quality Control Stability job openings in Connecticut as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

QC Manager

Plainville, CT • On-site

$110K - $125K/yr

Other

Medical, Dental, Vision, Retirement

Posted 12 days ago


Key responsibilities

  • Oversee daily QC operations in Chemistry and Microbiology laboratories, ensuring compliance of testing and operations.

  • Collaborate with other departments to resolve quality-related matters and ensure documentation is accurate and approved.

  • Oversee the planning, execution, and reporting of product validation and stability studies, ensuring regulatory compliance.


Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

QC Manager

Regular Full-Time Plainville, CT, US

4 days ago Requisition ID: 1441

Salary Range: $110,000.00 To $125,000.00 Annually

About ALK

ALK is a forward-thinking allergy company with a long tradition of allergy innovation. ALK is devoted to improving quality of life for people with allergies by developing pharmaceutical products that target the actual cause of allergy. ALK is the world leader in allergy vaccination (immunotherapy) – a unique treatment that induces a protective immune response which reduces and potentially halts the allergic reaction.

Since 1923, we have been working to improve the quality of life for allergy patients by developing products that target the cause of allergy. With over 2,200 employees, and with subsidiaries, production facilities and distributors worldwide, we are in a unique position to further the advancement of allergy treatments. The company is publicly traded on NASDAQ OMX Copenhagen (OMX: ALKB) with global headquarters in Horsholm, Denmark and offices North America.

We are currently looking for a Full-TimeQuality Control Managerto join our teamin our Plainville, CTsite. The QC Manager will work closely with other departments and must be able to collaborate effectively with others to ensure their quality control needs and specifications are met. This is a key position in our organization and the successful candidate must be able to communicate strategies clearly and effectively internally. The ideal candidate will be comfortable working in a fast-paced environment, can manage multiple site-specific projects, and feel comfortable leading when necessary.

Primary Responsibilities:

The primary responsibilities for this position include:

  • Oversee daily QC operations in Chemistry and Microbiology laboratories, ensuring end-to-end compliance of incoming, in-process and routine operations and testing including environmental monitoring, water testing, stability, production, and incoming material release.
  • Collaborate with other departments to resolve quality-related matters.
  • Author, edit, review, and approve documents, including SOPs, work instructions, deviations, CAPAs, change controls, protocols, and environmental monitoring reports.
  • Responsible for QC (Microbiology and Chemistry) administration, scheduling, and budgeting.
  • Ensure compliance with regulatory standards and industry best practices (GxP).
  • Oversee and adhere to global quality metric goals and plant metrics.
  • Requisition and procurement of laboratory supplies related to QC laboratories and production support.
  • Provide ILT (Instructor-Led Training) to QC team members on laboratory documents, including SOPs, WINs, and protocols - ensuring all staff are properly trained and qualified for assigned tasks.
  • Provide support, leadership, and development of QC team members.
  • Oversee plan and execution of product validation and stability studies, ensuring accurate data verification, reporting, and compliance with regulatory requirements.
  • Ensure calibration, maintenance and operation of lab instrumentation, including balances, pH meter, UV/vis spectrophotometer, and other analytical equipment as necessary.
  • Serve as primary subject matter expert during internal and external audits (e.g. FDA, Health Canada, Notified Body, and supplier audits).
  • Foster a culture of quality and continuous improvement within the team and other departments.
  • Other duties as assigned.

Skills and Experience:

  • BS / BA in life sciences, biology, chemistry or related field preferred
  • This position requires minimum 5 years of progressive management experience in a laboratory setting with increasing responsibilities in Pharmaceutical or GMP environment.
  • Knowledge of current Good Manufacturing Practices (cGMP), USP, FDA and ICH guidelines is required.

Why ALK?

At ALK, we believe in providing an environment and culture in which our people can thrive, develop, and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance.

ALK offers:

  • Excellent benefits including medical, dental, and vision
  • 401(k) plan with generous employer contribution
  • 12 company-paid holidays per year

ALK is an Equal Employment Opportunity / Affinde... etc.

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