QA Specialist I - Filling

Grand River Aseptic Manufacturing Inc.; Grand Rapids (MI); On-site; Full time

Benefits offered by this job

Medical, dental, and vision insurance

Paid volunteer time

401(k) with immediate vesting

Paid holidays

Generous time off policies

Job summary

A leading pharmaceutical manufacturer in Grand Rapids is seeking a Quality Assurance Specialist to oversee quality systems in the manufacturing of cGMP drug products. The ideal candidate will have a Bachelor’s degree in Life Sciences and 2-5 years of relevant experience. Responsibilities include providing quality oversight, reviewing batch records, and participating in quality investigations. The company offers comprehensive benefits from day one, including medical, PTO, paid volunteerism, and generous holiday policies.

Qualifications

• 2-5 years of related work experience or equivalent GMP experience.
• Knowledge of quality assurance principles in a manufacturing environment.

Responsibilities

• Provide quality oversight in warehousing and manufacturing.
• Review and approve batch records and controlled documents.
• Participate in quality investigations and cross-functional teams.

Skills

Accuracy in task completion

Proficient in Microsoft Word

Proficient in Microsoft Excel

Proficient in Microsoft Outlook

Education

Bachelor’s degree in Life Sciences or related field

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

The Quality Assurance Specialist supports quality systems as they relate to the manufacturing and testing of cGMP drug products. The Quality Assurance Specialist provides oversight and general support for the manufacturing of aseptic processes, deviation and CAPA systems, batch record review, SOP creation and revision, review of quality documents, and supports the Quality Management System.

Non-Negotiable Requirements

• Bachelor’s degree in Life Sciences or related field, and 2-5 years related work experience. In lieu of a bachelor’s degree, equivalent GMP/related work experience may be considered.
• Ability to complete tasks with accuracy and efficiency.
• Proficient computer skills in Microsoft Word, Excel, and Outlook.

Preferred Requirements

Knowledge of quality assurance principles and procedures in a pharma, biopharma, and/or biotech manufacturing environment.

Responsibilities Include (but are not limited to)

• Provide on the floor Quality oversight within the warehouse and manufacturing areas to support compliance with procedures and manufacturing documentation during operations with minimal guidance.
• Establish and maintain good technique with regards to working in classified areas (including gowning qualification).· Review and approve executed batch records and other associated controlled documents.
• Perform QA review in-process, environmental monitoring test results, and material release for incoming materials.
• Participate in cross functional teams to support quality investigations.
• Perform tasks within the quality systems with an understanding of the correlation between systems, such as the relationship between a deviation and CAPA.

Full job description available during formal interview process.

What Sets GRAM Apart from Other Employers

BENEFITS starting day 1: Medical, prescription, dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying a portion 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!