Quality Assurance Senior Associate NS

Quality Oversight Specialist – Night Shift (Onsite)

Schedule: 100% Onsite

Shift: Night shift starting at 6:45 PM

Rotation: Standard 12-hour rotating schedule

Position Overview

This role is responsible for providing quality oversight for large molecule Bulk Drug Substances (BDS), Drug Products (DP), and Finished Products (FP) manufactured at external contract manufacturing facilities. The position plays a key role in ensuring compliance with current Good Manufacturing Practices (cGMP) and supporting manufacturing operations through documentation review, communication, and quality support.

A core responsibility of the role includes translating technical documentation into English, such as batch records, investigations, change controls, and complaint records. The individual will work closely with quality representatives located at contract manufacturing sites. Specific language requirements may apply and will be noted as applicable.

Key Responsibilities

• Review and translate technical documents (batch records, investigations, change controls, complaints) into English
• Provide quality oversight and support to manufacturing activities in a cGMP environment
• Assist production operations with documentation and adherence to established procedures
• Communicate critical information throughout the shift and ensure effective handoff to the incoming shift
• Collaborate with internal teams and on-site quality personnel at contract manufacturing facilities
• Ensure compliance with applicable quality and documentation standards

Required Skills & Experience

• Knowledge of manufacturing processes and facility equipment
• Ability to interpret and apply cGMP principles and quality standards
• Quality assurance or manufacturing experience within the pharmaceutical or medical device industry
• Strong written and verbal communication skills
• Fluency in the required language(s), both written and spoken (as applicable)
• Basic proficiency with Microsoft Word
• Strong attention to detail and ability to follow written procedures
• Team-oriented mindset and effective communication skills

Basic Qualifications

• High School Diploma/GED with 4 years of relevant work experience, or
• Associate’s Degree with 2 years of relevant work experience, or
• Bachelor’s Degree with 6 months of relevant work experience, or
• Master’s Degree

Top Skills Needed

• cGMP and current Good Documentation Practices (cGDP)
• Clear and effective communication
• Ability to follow written procedures and Standard Operating Procedures (SOPs)
• Team collaboration and reliability

Ideal Candidate Will Demonstrate

• Strong communication and teamwork skills
• Ability to follow detailed written instructions
• Willingness and availability to work night shifts and rotating schedules
• Accountability and attention to detail in a regulated environment

If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com

This is a Contract position based out of West Greenwich, RI.

The pay range for this position is $35.00 - $40.00/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)

This is a fully onsite position in West Greenwich,RI.

This position is anticipated to close on May 1, 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.

Salary : $35 - $40