Document Control Supervisor (2nd shift)

Grand River Aseptic Manufacturing; Grand Rapids (MI); On-site; USD 70,000 - 90,000; Full time

Job summary

Grand River Aseptic Manufacturing seeks a Document Control Supervisor to lead document management in a cGMP environment. This on-site role requires a Bachelor's degree in Life Sciences and relevant experience in the biotechnology or pharmaceutical industry. The position offers competitive pay and comprehensive benefits, including medical coverage from day one, paid volunteerism, and generous PTO.

Benefits

Medical benefits starting day 1

Paid volunteerism

PTO up to 13 days per year

Wellness time off

10 paid holidays per year

Qualifications

• Bachelor's Degree in Life Sciences and 2 years relevant experience.
• Proficient in Microsoft Office applications.
• Understanding of quality assurance concepts.

Responsibilities

• Lead Document Control Technicians in managing controlled documents.
• Supervise the documentation process and ensure compliance.
• Write and revise Standard Operating Procedures (SOPs).

Skills

Problem Solving

Computer Skills

Quality Assurance Concepts

Education

Bachelor's Degree in Life Sciences

Tools

Microsoft Word

Microsoft Excel

Microsoft Outlook

Job description

Description

Quality, Service, Collaboration, Courage. Do you exhibit these values and wish to be around others that do too? Are you interested in making a difference in your community and the world? Are you looking for a place where you can grow and learn in a diverse, community-minded culture? 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:

The Document Control Supervisor is responsible for leading the GRAM Document Control Technicians in support of cGMP operations, which includes managing and executing the processes associated with the issuance, reconciliation and archival of controlled documents. This position manages, coordinates, and maintains quality and process documentation, procedures, and records to ensure controlled documents are issued, distributed, reconciled, and archived in support of a quality manufacturing operation. This is on-site role.

Non-Negotiable Requirements:

• Bachelor's Degree in Life Sciences and 2 years relevant experience working in the Biotechnology, Pharmaceutical, or relevant comparable industry. Equivalent work experience will be considered.
• Must have proficient computer skills in Microsoft Word, Excel, and Outlook.
• Exhibits a good understanding of general quality assurance concepts and practices.
• Successful history of solving problems of moderate complexity.
• Possess strong computer and Internet skills, including online document management software.

Preferred Requirements:

• Familiar with project management methodology and process.
• Prior leadership experience.

Responsibilities Include (but are not limited to):

• Facilitate the life cycle of master documents (including but not limited to SOPs, Batch Records, Test Methods, Protocols, Reports, Specifications, etc.) by functioning as a document workflow coordinator.
• Supervise the on-site documentation process to ensure proper and continuous document control support.
• Supervise the work of Document Control Technicians assisting in the QA/QC Document Control process.
• Provide hands-on leadership, coaching, and coordination of needed actions with a focus on achieving departmental and organizational goals.
• Write and revise Document Control Standard Operating Procedures (SOP).
• Write, review, and participate in investigations related to Document Control activities.
• Create and oversee the proper and timely issuance, implementation, maintenance, and archival of controlled documentation.
• Ensure controlled document issuance, reconciliation, and archival occurs according to SOPs.
• Support offsite storage activities including sending and retrieving boxes from storage. Manage storage database run reports for retention and metrics.
• Assist in internal and external audit preparation and reconciliation.
• Facilitate the document retention process, managing destruction schedules, and coordinating with offsite records vendor and client.
• Support internal, client, and external regulatory inspections by providing documents from the MasterControl DMS, including offsite searching, electronic and physical retrieval from vendor.

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.

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