Job Information
Actalent Quality Assurance Senior Associate NS in West Greenwich, Rhode Island
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
Job Type & Location
This is a Contract position based out of West Greenwich, RI.
Pay and Benefits
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)
Workplace Type
This is a fully onsite position in West Greenwich,RI.
Application Deadline
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.