Manufacturing Systems Specialist at Exelead Inc., USA

Indianapolis, Indiana, United States -

Full Time

Start Date

Immediate

Expiry Date

24 Jan, 26

Salary

116800.0

Posted On

26 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Data Analysis, Batch Record Review, Deviation Investigation, CAPA Project Management, Documentation Control, Audit Support, SAP Transactions, Lean Six Sigma, Attention to Detail, Analytical Skills, Communication Skills, Problem-Solving Skills, Organizational Skills

Industry

Description

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: In this role you will play a critical role in ensuring the efficient and compliant operation of manufacturing systems within the pharmaceutical/biotech industry. Responsibilities include but are not limited to: Collecting and analyzing data to identify trends, performance metrics, and areas for improvement within the manufacturing systems. Reviewing batch records to support product release, ensuring accuracy, compliance, and adherence to quality standards. Investigating and writing deviations, ensuring thorough documentation and timely resolution to maintain product quality and compliance. Completing Corrective and Preventive Action (CAPA) projects and other Continuous Improvement (CI) projects as assigned, driving process enhancements and operational excellence. Controlling the incoming and outgoing documentation to the manufacturing department, ensuring accuracy, completeness, and compliance with regulatory requirements. Providing support to leadership during audits, including preparation, documentation review, and response to audit findings. Completing SAP transactions and reconciling materials and products in a timely and accurate manner, ensuring inventory accuracy and compliance with regulatory standards. Who You Are: Minimum Qualifications: Bachelors Degree in any discipline. 3+ years of experience in a pharmaceutical or biotech company. Preferred Qualifications: Experience in data analysis, batch record review, deviation investigation, and CAPA project management. Experience in controlling documentation, supporting audits, and completing SAP transactions. Lean Six Sigma Green Belt certification. Strong attention to detail, analytical skills, and experience working in a fast-paced, regulated environment. Excellent communication, problem-solving, and organizational skills. Pay Range for this position: $68,700 - $116,800 The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. RSREMD RSREMD RSREMD What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Responsibilities

Ensure the efficient and compliant operation of manufacturing systems within the pharmaceutical/biotech industry. Responsibilities include data analysis, reviewing batch records, investigating deviations, and supporting audits.