Packaging Shift Lead (3rd Shift)

Grand River Aseptic Manufacturing; Grand Rapids (MI); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Medical benefits starting day 1

Paid volunteerism starting day 1

PTO 13 days/year

Wellness time off

Paid holidays

Job summary

Grand River Aseptic Manufacturing is seeking a Packaging Lead to oversee packaging activities for parenteral products and lead a small team. You will coordinate with Finishing, QA, and Supervisors to ensure compliant procedures and batch records.

The role requires 1+ years in pharma or FDA-regulated environments, proficiency with Word/Excel/Outlook, and willingness to work off-shifts and weekends. A life sciences degree and leadership experience are preferred.

Qualifications

• 1+ years of experience in pharmaceutical or FDA-regulated industry with CFR and cGMP knowledge.
• Proficient in Word, Excel and Outlook.
• Willingness to work off-shift, weekends, and on-call as needed.
• Associate’s degree preferred; leadership experience welcomed.

Responsibilities

• Lead all packaging activities for parenteral products.
• Coordinate activities with other departments to meet production needs.
• Ensure adequate levels of operating supplies.
• Train staff on safety and packaging procedures.
• Write/revise departmental procedures and batch records.
• Support quality systems and batch record reviews.
• Assist with training of packaging staff and cGMP compliance.
• Maintain housekeeping and documentation standards.
• Assist with maintenance, calibration, and audits as needed.
• Foster a positive team environment and participate in continuous improvement.

Skills

Packaging leadership

cGMP knowledge

Document control

Team training

Problem solving

MS Office

Education

Associate degree in life sciences

Tools

QAD software

Batch records

Job description

Description

Agility, Impact, Methodology. Do you exhibit these values and wish to be around others that do too? Do you thrive in fast-paced environments where agility, adaptability, and high standards go hand in hand? Are you driven to make a meaningful impact, whether through your work, your support of others, or your commitment to your community? Are you motivated by a disciplined, science-based approach that ensures consistent excellence, safety, and integrity in everything you do? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day!

Overview of this Position:

General purpose of this position. Oversee the execution of tasks while leading Labeling and Packaging areas. Achieve goals set by Packaging Supervisor and Area Management. Coordinate applicable training tasks with Finishing Trainer, Quality Assurance, and Supervisors to meet all guidelines of established procedures and cGMP regulations.

Non-Negotiable Requirements:

• 1 or more years of relevant experience in pharmaceutical or FDA regulated industry with a thorough understanding of CFR, cGMP, FDA guidelines and multinational regulatory standards.
• Available for off-shift, weekend, and/or on-call work, as needed.
• Must have proficient computer skills in Microsoft Word, Excel and Outlook.

Preferred Requirements

• Associate’s degree in life sciences or equivalent training and/or experience.
• Previous experience as a line lead or other leadership equivalent role.

Responsibilities Include (but are not limited to):

• Lead all packaging activities for small and/or large volume parenteral liquid drug products.
• Effectively coordinate activities by communicating with other operational departments.
• Ensure adequate levels of operating supplies to meet production needs.
• Train staff on good safety practices and enforce all safety regulations.
• Write and/or revise departmental procedures and batch records as needed for the packaging department.
• Perform necessary QAD functions to support the needs of the department.
• Assist with training employees in packaging departmental procedures, general Finishing procedures and cGMPs.
• Practice good housekeeping techniques.
• Accurately document data and complete batch record reviews as needed.
• Assist in the scheduling and performance of routine maintenance and calibration of production equipment.
• Participate in client communications, including problem solving, schedule development, and project status updates.
• Assist with disciplinary actions for poor performance or conduct of direct reports, as necessary.
• Assist with goal setting and attainment for department and direct reports.
• Foster a positive team environment that promotes productivity and employee satisfaction.
• Actively participate in Continuous Quality and Safety Improvements.
• Support GRAM’s Core Values.
• Support Agency, customer and vendor audits as needed.

Full job description available during formal interview process.

What Sets GRAM Apart from Other Employers:

MEDICAL BENEFITS starting day 1: Blue Cross Blue Shield medical and dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying for 75% of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums!

Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!

PTO: Full-time employees accrue up to 13 days of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!

WELLNESS TIME OFF: Employees earn 1 hour of time off for every 30 hours worked to use how you choose.

PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!

PAY: Depends on Experience and is discussed during the interview process.