QA Analyst (2nd Shift)

As a QA Analyst, you will play a crucial role in ensuring quality and compliance through auditing, evaluating materials, and driving continuous improvement efforts. Your contribution will directly impact the success of our customers by maintaining high-quality standards in our facility and production lines.

Responsibilities

• Perform reviews of Production Batch Records to maintain a world-class manufacturing control program.
• Ensure documentation records are accurate and compliant with GDP requirements.
• Ensure compliance with current SOPs, Work Instructions, and test procedures.
• Train personnel to improve compliance with regulatory and quality requirements.
• Provide technical, process direction, and training to manufacturing personnel.
• Utilize interpersonal skills to foster a culture of quality and increase quality awareness.
• Document and investigate deviations and out-of-specification (OOS) situations.
• Proactively update SOPs, Work Instructions, controlled forms, and test methods to support improvements and compliance.
• Ensure product quality specifications and customer standards are met and maintained.
• Complete approvals to run as needed and document quality events for effective decision-making.
• Ensure products meet specifications prior to release and maintain current reference and product standards.
• Utilize data to focus improvement efforts and resolve ongoing quality issues on the floor.
• Document OOS situations, determine root causes, and suggest solutions to prevent recurrence.
• Maintain compliance with current regulatory expectations and practices.
• Implement and maintain standards and processes to eliminate waste throughout the department.
• Apply and utilize lean tools to permanently implement improvements.
• Institutionalize 5-S in all aspects of the department.

• Experience in a GMP manufacturing environment such as pharmaceuticals, medical devices, cosmetics, or food manufacturing.
• Experience reviewing batch records and/or compounding records.
• Bachelor's degree in Chemistry, Biology, or related field.
• GMP, batch record, Quality Assurance within the specified industries.

• Working knowledge of drug manufacturing regulations such as cGMP & 21CFR regulations.
• Experience with investigations and deviations.
• Strong attention to detail.
• Ability to multi-task.
• Strong sense of urgency.
• Strong organizational skills.
• Highly self-motivated with the ability to work independently.
• Confident communicator comfortable with making outbound calls and enforcing policies.

This position requires working the 2nd shift from 2 PM to 10 PM, Monday through Friday, at the Eden Prairie site. You will spend the majority of your time on the manufacturing floor ensuring equipment runs efficiently and the area is properly cleaned. The role also involves desk work for reviewing batch records, writing protocols, and assisting with investigations. Initial training will be conducted on the 1st shift, Monday to Friday from 6 AM to 2 PM for two weeks. There may be opportunities for voluntary overtime on Saturdays and possibly Sundays.

Job Type & Location

This is a Contract to Hire position based out of Eden Prairie, MN.

The pay range for this position is $26.00 - $28.00/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 Eden Prairie,MN.

This position is anticipated to close on Jun 26, 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 without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment 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 the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall 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 applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.