Process Validation Engineer/Specialist III Contin

DescriptionProcess Validation Engineer/Specialist III - Continued Process Verification (CPV) 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 Process Validation Engineer/Specialist III coordinates and lead Continued Process Verification (CPV) activities at GRAM. Generate and execute validation protocols, validation reports, risk assessments, and procedures. Support audits and represent Validation in client interactions. Lead validation projects and guidance in technical decision-making related to CPV responsibilities. These duties include but are not limited to the statistical analysis and evaluation of the status of process validation of commercially marketed product materials and manufacturing processes.

Non-Negotiable Requirements:

Bachelor's degree in Life Sciences or Engineering related field is required. A minimum of 4 years' work experience in a pharma, biopharma, and/or biotech manufacturing environment. Prior experience and working knowledge of Statistical Process Control (SPC) software. Knowledge of relevant PDA guidance and 2011 FDA Guidance for

Industry Process Validation:

General Principles and Practices. Knowledge of cGMPs for Aseptic Processing facilities, pharmaceutical manufacturing processes, clean rooms, utility systems and packaging operations. Proficient computer skills in Microsoft Word, Excel, and Outlook. Responsibilities Include (but are not limited to): Lead continued process verification strategies, policies, and procedures applicable to all manufacturing processes at GRAM. Assure that all validation is performed to conform to cGMP and GRAM requirements. Prepare comprehensive reports, sampling and data collection, and Statistical Process Control (SPC) strategies for CPV. Provide support to internal customers such as Technical Services, Quality Control, Manufacturing, and other users of Validation services. Lead risk assessments, protocols, and reports. Store and maintain data integrity initiatives across multiple media platforms as dictated in regulatory guidelines as well as internal cGDP requirements. Review CPV documentation for accuracy and completeness. Lead CPV specific deviation investigations and implement CAPA based on validation changes. Review change control documents, work orders, and document change requests to assess impact on validated processes and/or systems. Work cross functionally to establish project schedules. Ensure that report completions meet department and company timeline metrics in fast paced environment. Proactively and regularly communicate with project teams to update on validation status. Identify process improvement opportunities for manufacturing and finishing operations. Open to a flexible and fluid work environment. Work on any assignment as directed and provide flexibility to support. Perform all job responsibilities in compliance with applicable regulations, standard operating procedures, and industry practices. Support Agency, customer, and vendor audits as needed. Full job description available during formal interview process. If you meet the required criteria listed above, GRAM welcomes you to apply today! 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!

PAID TIME OFF

You choose how to use this time for your vacation, sick, or mental health needs!

PTO:

Full-time employees accrue up to 104 hours of paid time off per calendar year, with this amount being prorated your first year.

WELLNESS TIME OFF

(WTO): In addition to PTO, employees earn 1 hour of wellness 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! GRAM supports Equal Opportunity Employment