Job Title: Quality/Regulatory Specialist

Job Description

We are seeking a Quality/Regulatory Specialist who will stay current on quality guidelines and industry standards. This role involves providing leadership and management of all quality control personnel, creating and maintaining documentation of quality programs, and managing certifications for exporting and importing goods.

Responsibilities

+ Provide leadership and management of all quality control personnel.

+ Create and maintain documentation of quality programs.

+ Maintain training files and controlled documents.

+ Design, review, and approve controlled documents such as SOPs, work instructions, GMP, and associated forms.

+ Complete all required documentation accurately and in a timely manner.

+ Provide guidance to effectively resolve deviations and out-of-specification results.

+ Manage investigations and corrective actions relating to product quality and communicate trends to management.

+ Provide support for regulatory, certification, and customer quality audits as needed.

+ Perform all other duties as assigned by the supervisor.

Qualifications

+ BS in Sciences, preferred degrees in Biology or Chemistry.

+ Experience working in a food production environment or pharmaceutical (2-5+ years).

+ Experience with the ISO process and working in a regulated environment.

+ Understanding of Quality Control systems.

Work Environment

This is a small, family-oriented company that is in the process of expanding. The work environment is close-knit and collaborative. The company is growing and expanding its plant by 5000 sq ft. The work schedule is Monday through Friday, 7 AM to 4 PM (or 5 PM). Remote work is possible after training.

Pay and Benefits

The pay range for this position is $25.00 – $35.00/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 Ames,IA.

Application Deadline

This position is anticipated to close on Apr 24, 2025.

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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are 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

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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.