Quality Control Analyst I

Maveris is an IT and cybersecurity services company committed to helping organizations create secure digital solutions to accelerate their mission. We are Veteran-owned and proud to serve customers across the Federal Government and private sector. We have an opening for a full-time, permanent Sr. Quality Control Analyst to join our talented, dynamic team in support of a large Federal Government customer. 

Veterans are encouraged to apply. 

This position is required to be onsite 80% of the time in Hines, IL, Austin, TX, or Martinsburg, WV.

Duties

• Quality Control & Process Improvement: 
• Continuously monitor and assess processes to identify areas for improvement, ensuring best practices are consistently applied. 
• Work with cross-functional teams to develop and implement solutions that enhance operational efficiency and reduce risk. 
• Conduct thorough analysis of current workflows,...

Summary:
The Quality Control Analyst III plays a vital role in ensuring that the highest quality standards are met throughout the development and commercialization phases. This position involves executing both routine and non-routine testing, assisting with method transfers, method validation, and supporting laboratory operations. The analyst will also contribute to data trending, investigations, and laboratory maintenance. This position is critical in supporting continuous operational schedules and upholding regulatory compliance within the Quality Control department.

Responsibilities:

• Perform routine and non-routine analytical and microbiological assays to support raw materials, in-process samples, product release, and stability studies, in adherence to SOPs.
• Support weekend laboratory operations to ensure seamless testing schedules (Analytical, Microbiology, Raw Materials).
• Maintain accurate and up-to-date...

Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Group Leader within the Research Products/ISO department based onsite in our Andover, MA facility.  CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets.  CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years.

Under the general supervision of a group leader, the Quality Control Analyst II will perform various analytical techniques to determine isotopic enrichment, chemical purity,...

Summary:
The Quality Control Analyst III plays a vital role in ensuring that the highest quality standards are met throughout the development and commercialization phases. This position involves executing both routine and non-routine testing, assisting with method transfers, method validation, and supporting laboratory operations. The analyst will also contribute to data trending, investigations, and laboratory maintenance. This position is critical in supporting continuous operational schedules and upholding regulatory compliance within the Quality Control department.

Responsibilities:

• Perform routine and non-routine analytical and microbiological assays to support raw materials, in-process samples, product release, and stability studies, in adherence to SOPs.
• Support weekend laboratory operations to ensure seamless testing schedules (Analytical, Microbiology, Raw Materials).
• Maintain accurate and up-to-date...

Summary:
The Quality Control Analyst III plays a vital role in ensuring that the highest quality standards are met throughout the development and commercialization phases. This position involves executing both routine and non-routine testing, assisting with method transfers, method validation, and supporting laboratory operations. The analyst will also contribute to data trending, investigations, and laboratory maintenance. This position is critical in supporting continuous operational schedules and upholding regulatory compliance within the Quality Control department.

Responsibilities:

• Perform routine and non-routine analytical and microbiological assays to support raw materials, in-process samples, product release, and stability studies, in adherence to SOPs.
• Support weekend laboratory operations to ensure seamless testing schedules (Analytical, Microbiology, Raw Materials).
• Maintain accurate and up-to-date...

Direct Biologics, LLC is a rapidly growing biotechnology company specializing in advanced regenerative medicine therapies. We are currently seeking a highly skilled and motivated Quality Control Analyst to join our team. As a Senior Quality Control Analyst, you will play a crucial role in ensuring the safety, efficacy, and quality of our late-stage product.

In this role, you will be responsible for conducting comprehensive analysis of our product using state-of-the-art laboratory techniques and complex equipment. You will collaborate closely with cross-functional teams including Research and Development, Process Development, Manufacturing, Quality Assurance, and Regulatory Affairs, with attention on compliance with industry standards and regulatory requirements. Your primary focus will be on method transfers and product characterization, additional tasks include stability and release testing.

Primary Role and Responsibilities:

• Perform day-to-day drug...

The Quality Control Lab Analyst performs a wide variety of laboratory tests on raw materials, in process samples, finished products, chemicals, using different equipment.

Schedule is a Rotating Shift of 7am-530pm and 5pm to 330am, 10 hour shifts, 4 day work week

Pay Range is 18-25/hour based on experience

Requirements

ESSENTIAL FUNCTIONS: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requests for reasonable accommodations should be directed to the Human Resources Department.

• Conducts Lab testing such as HPLC, FTIR, UV-Vis, pH, GC, etc
• Perform all routine qualitative and quantitative analyses, from simple to very complex
• Examine critically test results, entry data into the company ERP computer system.
• Performs calibrations and standardizations of the Quality Control Laboratory equipment and methods
...

Founded in 2003, IT Concepts’ core values – customer-centricity, teamwork, driven to deliver, innovation, and integrity – ensure we work together to be the best, realize objectives, and make a positive impact in our communities. We intentionally created and sustain our ITC culture that embraces change, experimentation, continuous learning, and improvement. We bring our design thinking problem-solving approach that challenges assumptions, prioritizes curiosity, and invites complexity to deliver innovative, efficient, and practical solutions. As we continue to grow in the support of our government customers, we are looking for driven and innovative individuals to join our team.

IT Concepts, Inc. (ITC) is seeking an experienced Quality Control Analyst to support a DOD SOCOM opportunity. ITC will provide the Government with program management and services related to emerging technology solutions including Enterprise Architecture...

Overview:
The Analyst IV – Dossier Data Integrity, Quality Control Operations ensures the integrity, completeness, and accuracy of regulatory filings, laboratory data, and reports to maintain the highest standards of quality and compliance. This role supports commercialization efforts through meticulous review and verification of data, ensuring alignment with Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP).

Key Responsibilities:

• Verify the integrity and traceability of regulatory dossier sections by reviewing them against reference methods and reports.
• Review analytical data to ensure accuracy, correct transcription, and completeness of associated references.
• Audit laboratory notebooks, worksheets, logbooks, and electronic data for compliance and accuracy.
• Ensure adherence to approved protocols during analytical method validation, verification, and transfer...

The Quality Control Analyst II plays a key role in ensuring quality and compliance throughout the product lifecycle, from development to commercialization. This position involves executing both routine and complex testing, supporting method transfers, and contributing to laboratory operations. Located primarily in Norton, MA, with occasional responsibilities in Cambridge, MA, the role ensures timely and efficient quality control operations aligned with organizational goals.

Duties & Responsibilities:

• Perform routine and non-routine analytical and microbiological testing for raw materials, in-process samples, product releases, and stability studies per established SOPs.
• Maintain training records and adhere to schedules, ensuring timely completion of assignments and alignment with project timelines.
• Assist in laboratory maintenance, including equipment upkeep, reagent preparation, and inventory management.
...

BioPharma Consulting JAD Group is seeking a Quality Control Analyst II to join our dynamic team MA. The Quality Control Analyst II will be responsible for conducting various analytical tests, maintaining laboratory equipment, and assisting in method development and validation activities, while adhering to Good Manufacturing Practices (GMP).

Key Responsibilities:

• Perform routine and non-routine analytical and/or microbiological assays, with increasing complexity, to support raw materials, in-process samples, product release, and stability studies, following established SOPs
• Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the department's commitment to meeting project timelines and quality metrics
• Assist in the maintenance of laboratory equipment and inventory, including the preparation of reagents...

Direct Biologics, LLC is a rapidly growing biotechnology company specializing in advanced regenerative medicine therapies. We are currently seeking a highly skilled and motivated Quality Control Analyst to join our team. As a Senior Quality Control Analyst, you will play a crucial role in ensuring the safety, efficacy, and quality of our late-stage product.

In this role, you will be responsible for conducting comprehensive analysis of our product using state-of-the-art laboratory techniques and complex equipment. You will collaborate closely with cross-functional teams including Research and Development, Process Development, Manufacturing, Quality Assurance, and Regulatory Affairs, with attention on compliance with industry standards and regulatory requirements. Your primary focus will be on method transfers and product characterization, additional tasks include stability and release testing.

Primary Role and Responsibilities:

• Perform day-to-day drug...

Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst I based onsite in our Andover, MA facility.  CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets.  CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years.

The Quality Control Analyst I (RP/ISO) is responsible for conducting routine analysis of materials including: Raw Materials, in-process and finished formulations under general supervision and in accordance with standard...

Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst I, that will be primarily focused on wet chemistry, based onsite in our Andover, MA facility.  CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets.  CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years.

The Quality Control Analyst I (RP/ISO) is responsible for conducting routine analysis of materials including: Raw materials, in-process and finished formulations under...

We are currently seeking qualified candidates for a Quality Assurance/Quality Control (QA/QC) Analyst in LaBella’s Program Management Services Division at our client’s office in Orange, CT. This position will be in the electric and gas utility industry working on key initiatives for a customer service/information technology project. Ideal candidates will have experience in the strictly government regulated, utility industry in New York state. Applicants with experience in the highly regulated pharmaceutical or medical industry would also be considered. The Program Management Services Division at LaBella provides comprehensive management services for complex projects and multi-year capital programs. Project teams are established to provide a customized mix of business consulting, project management, financial control and monitoring, administrative, and technical support services.

Salary Range: $65,000 - $105,000

The specific salary offered may be...

We are currently seeking qualified candidates for a Quality Assurance/Quality Control (QA/QC) Analyst in LaBella’s Program Management Services Division at our client’s office in Rochester, NY. This position will be in the electric and gas utility industry working on key initiatives for a customer service/information technology project. Ideal candidates will have experience in the strictly government regulated, utility industry in New York state. Applicants with experience in the highly regulated pharmaceutical or medical industry would also be considered. The Program Management Services Division at LaBella provides comprehensive management services for complex projects and multi-year capital programs. Project teams are established to provide a customized mix of business consulting, project management, financial control and monitoring, administrative, and technical support services.

Salary Range: $65,000 - $105,000

The specific salary offered may be...

Cambridge Isotope Laboratories, Inc. has an outstanding opportunity to join our GMP Quality Control team as a Quality Control Analyst I based onsite in our Tewksbury, MA headquarters. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years.

The Quality Control Analyst I is responsible for conducting routine analysis of GMP/ISO materials including: Raw materials, in-process and finished products under general supervision...