FINISHING SUPERVISOR 2ND SHIFT- GODFREY

Description

JOB SUMMARY

Supervise multi-finishing operations of parenteral liquid drug products. All activities must comply with cGMP's and regulatory requirements. The position requires employee supervision to ensure products comply with cGMP's, SOP's, and batch record instructions, and also that labor and material standards are met. Ensure that planned production occurs on time to meet the forecasted schedule. The individual must have the requisite technical skills to supervise both manual and automated processes in a pharmaceutical or FDA regulated environment and must have the ability to make informed decisions.

ESSENTIAL DUTIES & RESPONSIBILITIES

• Supervise all Finishing 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 for their corresponding department.
• Assist with training employees in all departmental procedures, product inspection and cGMPs
• Practice good housekeeping techniques
• Accurately document data and complete batch records as needed.
• Assist in the scheduling and performance of routine maintenance of production equipment.
• Participate in client communications, including problem solving, schedule development, and project status updates.
• Define and uphold disciplinary actions for poor performance of direct reports, as necessary.
• Foster a positive team environment that promotes productivity and employee satisfaction
• Actively participate in Continuous Quality and Safety Improvements.
• Support Agency, customer and vendor audits as needed.
• Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices.
• Perform all other tasks, projects, and duties as assigned.

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. Shift differential available for second and third shift!

If you meet the required criteria listed above, GRAM welcomes you to apply today!

Requirements

DESIRED SKILLS & ABILITIES

• Experience in pharmaceutical packaging of regulated products with a thorough understanding of cGMP, FDA guidelines and multinational regulatory standards is preferred.
• Ability to interpret and relate Quality standards.
• Must be detail oriented.
• Strong verbal and written communication skills.
• Knowledgeable of GMP standards and the ability to follow CFR guidelines.
• Computer proficient and familiar with Microsoft applications.
• Excellent time management skills.
• Results oriented and efficient.
• Creative and open-minded who fosters an environment in which sharing of ideas is encouraged.
• Ability to work closely with a diverse team.
• Ability to work well in a cross-functional team environment.

Qualified candidates possess a Bachelor's degree in life sciences or equivalent training and/or experience in a related environment. Minimum of 1-year experience as a qualified inspector of parenteral products preferred. Two to five (2-5) years of relevant experience in pharmaceutical or FDA regulated industry. Available for off-shift and/or on-call work, as needed.