Change Control Specialist

Location:

Allegan, MI, US, 49010

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, ACO®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.

Join us on our One Perrigo journey as we evolve to win in self-care.

Description Overview

Perrigo Company is dedicated to making lives better by bringing Quality, Affordable Self-care products that consumers trust everywhere they are sold. Help us do it.

We are seeking a motivated and detail-oriented Change Control (CC) Specialist to join our Quality team. This role offers a structured career pathway from entry-level to senior-level responsibilities, providing opportunities for professional growth in validation, regulatory compliance, and continuous improvement initiatives.

Scope of the Role

Apply knowledge of change control processes to assess and manage product quality issues.
Collaborate with cross-functional teams to drive compliance and continuous improvement.
Lead or contribute to training initiatives and knowledge sharing across departments.
Independently determine project scope and requirements based on experience level.
Perform data mining, reconciliation, and advanced database searches using tools like SAP and TrackWise.
Create and review technical documentation and validation strategies.

Experience Required

• Bachelor’s degree in a STEM field or equivalent experiance.
• Entry-level candidates with foundational knowledge of change control are encouraged to apply.
• Mid-level professionals should have 2+ years of relevant experience.
• Senior-level candidates should have 5+ years of progressively responsible experience in validation or quality systems.

Technical Skills:

• Proficiency in Microsoft Office, SAP, TrackWise, and data analysis tools.
• Understanding of 21 CFR regulations related to drug manufacturing and validation.
• Strong technical writing and research skills, with increasing complexity at higher levels.

Soft Skills & Competencies:

• Strong problem-solving and decision-making abilities.
• Excellent communication and collaboration skills.
• Ability to manage multiple priorities and adapt to changing deadlines.
• Leadership potential and a proactive mindset for continuous improvement.

Career Path Opportunities:

This role is part of a structured career pathway with opportunities to advance into roles such as:

• Quality Engineer
• Validation Engineer
• Supplier Quality Management (SQM) Professional
• QA/QC Supervisor
• Operations Supervisor
• External Quality Professional

Benefits
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.

Find out more about Total Rewards at Perrigo.

We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here

Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you.

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo