Campus Pride Jobs

labeling/packaging engineer.

• north billerica , massachusetts

• posted 9 days ago

job details

summary

• $65 - $70 per hour

• contract

• bachelor degree

• category life, physical, and social science occupations

• reference49578

job details

job summary:

As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!

location: North Billerica, Massachusetts

job type: Contract

salary: $65 - 70 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

We are seeking a highly skilled and detail-oriented Senior Packaging and Labeling Engineer to join our dynamic team. In this role, you will leverage your expertise in quality systems, change management, label lifecycle management, project management, and process improvements to drive compliance, efficiency, and innovation in packaging and labeling. This position requires a strong understanding of regulatory requirements, technical excellence, and the ability to work cross-functionally to support critical business initiatives.

• Quality Systems Oversight:

• Maintain and enhance packaging and labeling quality systems to ensure compliance with FDA, EMA, and related regulations.

• Develop/improve standard operating procedures (SOPs), work instructions, and quality documentation related to packaging and labeling processes with a focus on lifecycle management.

• Change Management:

• Lead and implement change management strategies for packaging and labeling, supporting product lifecycle changes and minimizing operational impact.

• Manage and review label change requests (LCR) to ensure timely, accurate, and compliant label updates.

• Collaborate with regulatory, quality, and manufacturing teams to evaluate and execute changes, supporting a first-time-right approach.

• Project Management:

• Plan, execute, and oversee packaging and labeling projects from concept through implementation, ensuring alignment with product launch timelines and regulatory requirements.

• Develop project scopes, timelines, and resource plans to ensure seamless coordination with cross-functional teams.

• Identify project risks and implement risk mitigation strategies including process improvements, supply chain redundancy, and regulatory compliance.

• Process Improvement:

• Analyze existing packaging and labeling workflows, identify opportunities for process improvements, and implement best practices to increase efficiency and reduce risk.

• Drive continuous improvement initiatives to streamline labeling and packaging processes, enhancing compliance, productivity, and cost-effectiveness.

• Technical Support and Troubleshooting:

• Provide technical expertise and troubleshooting support for packaging and labeling issues, including root cause analysis and corrective action planning.

• Support manufacturing labeling operations including support, issue trending and improvement projects.

• Ensure that all packaging and labeling specifications meet regulatory/process standards.

• Cross-Functional Collaboration:

• Serve as a key liaison between quality assurance, manufacturing, regulatory affairs, manufacturing, and supply chain to align labeling strategies with overall business objectives.

• Support product launches, updates, and regulatory requirements by coordinating with cross-functional teams to achieve timely and compliant product releases.

qualifications:

• Education: Bachelor's degree in Engineering, regulatory affairs, or a related field.

• Experience: Minimum of 5 years of experience in pharmaceutical packaging and labeling, with specific expertise in sterile injectables and medical devices.

• Regulatory Knowledge: Deep understanding of cGMP, FDA, EMA, and USP guidelines relevant to packaging and labeling, and experience filing label artwork changes.

• Technical Skills: Proficiency with quality systems including change control and quality events, proficiency in labeling equipment, label artwork review and compliance.

• Project Management: Demonstrated success in managing multiple projects in parallel.

• Communication and Collaboration: Excellent communication skills with the ability to work effectively across departments and influence stakeholders.

skills: GMP (Good Manufacturing Practice)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

This posting is open for thirty (30) days.

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.