Quality Control Senior Associate

Actalent is looking for Quality Control Senior Associate in Holly Springs, NC.
This local job opportunity with ID 3667457457 is live since 2026-05-08 00:07:44.
Quality Control Senior Associate

This is a fully onsite position with standard hours, requiring up to 5 days per month with shift flexibility. The Quality Control Senior Associate plays a critical role in supporting the QC organization through various laboratory and analytical tasks.

Responsibilities

• Conduct analytical testing in accordance with SOPs to characterize various substances and materials.
• Perform a variety of assays and routine laboratory procedures under minimal supervision and in accordance with SOPs.
• Maintain equipment to uphold laboratory standards.
• Manage samples efficiently, ensuring proper handling and documentation.
• Evaluate data analysis and apply GMP procedures.
• Assist with procurement activities for consumables and critical reagents for lab start-up.
• Operate and maintain HPLC, UPLC, TOC, UV, and other related chemistry bench-top equipment such as OSMO, turbidimeter, pH, and conductivity meters.
• Participate in QC Chemistry testing activities including validation and method transfers.
• Collaborate on Data Integrity Assessments for computerized lab systems.
• Author, revise, and review documents and reports, including SOPs, test methods, safety assessments, trend reports, qualification/validation summary reports, technical reports, method assessments, and technical assessments.
• Ensure successful training and method transfer activities for HPLC, UPLC, TOC, and other related chemistry equipment.
• Own and manage Deviation, CAPA, and Change Control records to support Quality Control.
• Participate in audits, initiatives, and projects that may be interdepartmental or global in scope.
• Support routine activities over weekends and public holidays as required.

Essential Skills

• GMP and analytical testing experience.
• Compendial review capabilities.
• Proficient in authoring, editing, and reviewing documents.
• Problem-solving skills.
• Collaborative skills.

Additional Skills & Qualifications

• High school diploma/GED with 2 years of work experience, OR an Associate's degree with 6 months of work experience, OR a Bachelor's degree.
• Degree in a related scientific field such as Chemistry, Biochemistry, Physics, or Chemical Engineering is preferred.
• 4 years of relevant laboratory experience in a GMP commercial manufacturing environment within the pharmaceutical or biopharmaceutical industry is preferred.
• Strong knowledge of laboratory techniques.
• Proficient in the use of LIMS and LMES/CIMS.
• Knowledge of related regulatory/industry considerations, compliance issues, and/or scientific discovery.
• Strong written and verbal communication skills, including technical writing and presentation.
• Experience with equipment and method validation, verification, and transfer, including the change control process.
• Ability to interact effectively with a variety of communication and working styles and work well in teams.

Work Environment

This position involves day-to-day testing, compendial review, and document authoring, editing, and reviewing in a laboratory setting.

Job Type & Location

This is a Contract position based out of Holly Springs, NC.

Pay and Benefits

The pay range for this position is $40.00 - $43.00/hr. 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)

Workplace Type

This is a fully onsite position in Holly Springs, NC.

Application Deadline

This position is anticipated to close on May 20, 2026.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

Actalent is an equal opportunity employer.

About Actalent

Actalent is a global leader in engineering and sciences services. For more than 40 years, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.

Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

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