Packaging Supervisor

Nova Biomedical Corporation; Waltham (MA); On-site; USD 66,000 - 75,000; Full time

Benefits offered by this job

Hybrid work arrangements

Competitive 401k

Bonus Program

Generous PTO and paid holidays

Tuition reimbursement

Job summary

Nova Biomedical seeks a Packaging Supervisor for the Reagent Manufacturing packaging team in our Waltham, MA facility. You will manage the daily packaging schedules, coordinate with cross-functional teams, and drive on-time delivery while maintaining quality and safety standards.

The role requires 3+ years in packaging/manufacturing, supervisory experience, GMP familiarity, and knowledge of SAP or Master Control. We offer a hybrid work setup, competitive benefits, and opportunities for growth.

Qualifications

• Minimum 3 years in Packaging/Assembly or similar environment.
• Minimum 3 years in a supervisory role in manufacturing or similar environment.
• Minimum 3 years in a GMP environment.
• Minimum 3 years in a regulated safety environment (OSHA).
• Minimum 3 years in a QSR environment.

Responsibilities

• Manage daily packaging schedules on assigned shift to meet demand for finished goods.
• Coordinate with shift supervisors to ensure smooth transitions between shifts.
• Collaborate with Scheduling, R&D, Engineering and Purchasing to meet demand while ensuring quality and on-time delivery.
• Oversee safety, training, coaching, and performance appraisals; enforce Nova policies.

Skills

Packaging supervision

Manufacturing leadership

GMP familiarity

OSHA safety knowledge

QSR knowledge

SAP or MRP experience

Master Control familiarity

FDA/audit experience

NCMR/MRB processes

Lean manufacturing

Tools

SAP

Master Control

Job description

Nova Biomedical One Global Brand One Vision Together under one name Advanced Instruments and Nova Biomedical are now united under one brand Nova Biomedical marking a major milestone in our journey to deliver greater value to our customers By combining our strengths were accelerating innovation supporting critical workflows and delivering world class service across the biopharmaceutical and clinical markets

Job Summary

This individual has shift responsibility for day to day activities of Packaging within Reagent Manufacturing This includes overseeing scheduling of all packaging activities such as calibrator packs external standards and miscellaneous reagents Controls as well as Auto QC products for Nova core and OEM products Short term goals are to deliver products to customers on time with high quality and minimal scrap Long term goals include continuous improvement of packaging operation personnel and processes utilizing resources such as R&D Planning Purchasing QAQC and Consumable Manufacturing Engineering

Responsibilities

• Manage the daily packaging schedules on assigned shift to deliver product on a timely basis so that demand for Finished Goods is met
• This may include pilot requests from R&D and Consumable Manufacturing EngineeringCoordinate with other shift supervisors to ensure delivery of products and smooth and effective transition between shifts
• Work closely with Master Scheduling R&D Manufacturing Engineering and Purchasing to meet demand of customers by ensuring quality and on time delivery of raw materialsuppliesEnsure adequate training of Packaging personnel overtime control reducing scraps labor utilization improving workflow efficiency and cost reduction
• Oversee all safety aspects of Packaging on shiftParticipates in Reagent waste managementInterviews hires trains develops coaches motivates and evaluates staffConduct performance appraisals for employees reporting to this position address resolution of employee issues and enforce Nova policiesEnsure all Packaging equipment is adequately maintained and qualified for daily usageMonitor and control product scrap and create defect awarenessReview as needed of Device History Records DHRs prior to submitting to QCPerform other duties as assigned

Experience Requirements

• Minimum 3 years experience in an AssemblyPackaging or comparable environment is required
• Minimum 3 years experience in a supervisory role in manufacturing or comparable environment is required
• Minimum 3 years experience in a GMP environment
• Minimum 3 years experience in a regulated safety environment OSHA safety standards
• Minimum 3 years experience in a Quality System Regulations QSR
• Working knowledge of SAP or similar MRP system is desired
• Working knowledge of Master Control or similar system is desired
• FDA TUV and customer audit experience is a plus
• Basic Knowledge of Non Conforming Material Report NCMR and Material Review Board MRB process
• Lean Manufacturing knowledge is a plus

Physical Requirements and Working Conditions

Must be able to perform tasks that may involve extended periods of standing sitting pushing pulling lifting bending kneeling reaching twisting turning climbing steps and carrying up to 25 pounds numerous timeshours a dayRequire repetitive use of armswristhands while setting upworking with equipmentraw material throughout the dayWill require use of Personal Protective Equipment PPE and may include but not limited to safety glasses safety shoes lab coat bouffantbeard guard gloves hearing protection face shield nuisance mask bump capMust have good handeye coordination and visual acuityMust be able to distinguish colors

Why Work for Nova Biomedical

• Flexible Medical Dental & Vision Coverage
• Competitive 401k company match
• Bonus Program
• Generous PTO and paid holidays
• Generous Tuition reimbursement
• Hybrid and flexible work arrangements
• Professional development engagement and events
• Company marketplace for lunch and snacks in our Norwood MA Billerica MA and Westbrook ME offices
• Company subsidized cafeteria in our Waltham MA office

Work Location

Work Location Mondays Fridays 7 am 330 pm On site

Targeted Salary Range

66000 75000 annually Nova Biomedical believes in transparency and integrity throughout all we do including compensation The provided salary range for this role represents the expected base salary or hourly rate for this opening Actual compensation will be commensurate with the candidates experience and may vary based on individual factors such as location skills and education

About the Company

At Nova Biomedical were not just building instruments were powering breakthroughs that improve lives Our smart science driven solutions are trusted in over 100 countries to speed drug development and enhance patient care Our integration brings together more than 70 years of scientific excellence with Novas cutting edge innovation forming a powerhouse of precision purpose and possibility With FDA registered ISO certified manufacturing more than 125 FDA approvals and industry trusted diagnostics were setting new standards in quality and reliability Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic IVD instrumentation dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences With headquarters in Norwood and Waltham Massachusetts and a global team of nearly 2000 employees were building a collaborative empowered culture grounded in shared values Customer Centricity Ingenuity Ownership & Accountability Collaboration and Integrity Working at Nova Biomedical means joining a mission driven organization where your contributions matter Whether youre in engineering science manufacturing or support youll be part of a team that values innovation invests in your growth and is committed to making a real world impact on global health

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EEO Statement

Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce As a part of our commitment to a diverse and inclusive workforce Nova Biomedical will continue to take steps to assure that recruitment hiring assignment promotion compensation and all other personnel decisions are made and administered without regard to race religion color national origin citizenship sex sexual orientation gender identity gender expression veteran status age mental or physical disability genetic information or any other protected class

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