Quality Control Analyst Ii Jobs (NOW HIRING)

The QC Analyst II plays a key role in ensuring the quality and compliance of raw materials, in-process samples, stability samples, and finished products within a GMP-regulated environment. This position performs routine and complex analytical testing, supports method development and optimization, and maintains rigorous documentation to meet regulatory and quality standards. The role actively promotes safe laboratory practices and contributes to continuous improvement across quality control operations.

• Demonstrate a strong commitment to laboratory safety, quality systems, and regulatory compliance in all daily operations.
• Support and promote a culture of safe laboratory practices by strictly following established environmental, health, and safety procedures.
• Perform routine analytical and laboratory testing on raw materials, in-process samples, stability samples, and finished products.
• Execute testing activities in accordance with approved analytical methods, internal quality standards, and applicable regulatory requirements.
• Operate and maintain analytical instruments such as HPLC, Karl Fischer, UV/VIS spectrophotometers, and LCMS systems in a GMP environment.
• Review and verify analytical data for accuracy, completeness, and adherence to established specifications and acceptance criteria.
• Document experimental results clearly and accurately in laboratory records and electronic systems, ensuring data integrity and traceability.
• Contribute to the preparation of technical reports, summaries, and stability assessments based on analytical data and observations.
• Assist in the development, qualification, and optimization of analytical methods, protocols, and laboratory procedures.
• Support the creation, revision, and maintenance of controlled documentation, including standard operating procedures, test methods, and product specifications.
• Collaborate with cross-functional teams to investigate laboratory issues, support troubleshooting activities, and implement corrective and preventive actions.
• Participate in continuous improvement initiatives to enhance laboratory efficiency, data quality, and compliance with cGMP requirements.
• Provide technical guidance, training, and mentorship to laboratory personnel as needed to ensure consistent application of methods and procedures.

• Bachelor’s degree (BS) in chemistry, biology, or a related scientific discipline.
• 2–5 years of experience as a QC analyst or chemist in a GMP or cGMP environment.
• Hands-on experience with analytical testing equipment and methodologies, including High Performance Liquid Chromatography (HPLC).
• Practical experience with LCMS (Liquid Chromatography–Mass Spectrometry) techniques and instrumentation.
• Proficiency in Karl Fischer titration for moisture or water content determination.
• Experience with UV/VIS spectrophotometry and related analytical methods.
• Strong understanding of quality control principles and practices in a regulated laboratory setting.
• Working knowledge of GMP and cGMP requirements and their application to laboratory operations.
• Ability to accurately review, interpret, and verify analytical data for compliance with specifications.
• Strong documentation skills with a focus on accuracy, completeness, and data integrity.
• Ability to follow established test methods, SOPs, and quality procedures with high attention to detail.
• Effective communication skills to interact with cross-functional teams and laboratory colleagues.

• Experience contributing to the development, qualification, and optimization of analytical methods.
• Familiarity with creating, revising, and maintaining controlled documentation such as SOPs, test methods, and specifications.
• Experience participating in laboratory investigations, troubleshooting analytical issues, and supporting root cause analysis.
• Ability to provide technical guidance and on-the-job training to other laboratory personnel.
• Strong organizational and time management skills to handle multiple samples, tests, and priorities in a QC environment.
• Demonstrated commitment to continuous improvement in laboratory processes, data quality, and compliance.

This role operates in a regulated quality control laboratory that adheres to GMP and cGMP standards. The QC Analyst II works primarily on-site, performing hands-on testing with analytical instruments such as HPLC, LCMS, Karl Fischer titrators, and UV/VIS spectrophotometers. The typical work schedule is Monday through Friday from 8:00 a.m. to 5:00 p.m., supporting predictable daytime hours. The environment emphasizes safety, data integrity, and compliance, with established environmental, health, and safety procedures guiding daily activities. Laboratory work involves following standard operating procedures, handling chemicals and samples with appropriate precautions, and collaborating closely with cross-functional teams in a structured, process-driven setting.

This is a Contract position based out of Milford, MA.

The pay range for this position is $37.00 - $38.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Milford,MA.

This position is anticipated to close on Sep 23, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.