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 OTS Specialist executes routine technical support activities for GMP Manufacturing Operations across multi-product, Manufacturing, Fill, and Finish CDMO facilities. Activities include cross-functional deviation investigations, CAPAs, AIs, targeted innovations, audit support, and overall plant performance. Support is for all local GRAM sites and the position works closely with Quality as well as Operations, Continuous Improvement, Engineering, MSAT, and Project Management to support site objectives. This is an on-site role. Must be able to work an on-call schedule for technical supports and site deviation analysis, as needed.
Non-Negotiable Requirements:
- Bachelor’s degree in life sciences, engineering, or equivalent training and/or experience is necessary.
- Entry level experience (0-3 years) in pharmaceutical manufacturing.
- Must have proficient computer skills in Microsoft Word, Excel and Outlook.
Preferred Requirements:
- Previous experience in a CMO and sterile filling, manufacturing, and/or fill finish environment is preferred.
- Strong aptitude in root cause analysis, technical writing and CAPA in a GMP environment; LEAN/six-sigma experience is a plus.
Responsibilities Include (but are not limited to):
- Work closely with respective team members from Operations, Engineering, Maintenance, Project Management and Quality to ensure all documentation (and respective data) is gathered in an expeditious manner for timely completion of deviation investigations.
- Ensure appropriate risk analysis, root cause and corrective action tools and identification is used for all deviation investigations.
- Author and revise site procedures in a timely manner to address CAPA and corrective actions for deviation investigation and/or site continuous improvement projects.
- Assess, evaluate, and provide immediate corrective actions for GMP discrepancies and intra batch process monitoring, analysis, and reporting.
- Serve as first line of defense for all operations excursions, GMP lifecycle management of execution level process data, providing for unit operation (i.e., formulation, manufacturing, sterile filling, inspection/labeling).
- Support strategic plans for process and plant improvements to increase efficiency and manage costs.
- Effective cross-functional collaboration with Quality, Continuous Improvement, MSAT, AMAs, MPEs, SCM, Operations Supervision, and Management.
- Assist engineering and validation with implementation, commissioning, and validation of clean room spaces and process equipment as well as inspection and packaging process equipment.
- Take corrective action by thinking creatively and problem solving to develop innovative solutions based on sound scientific analysis.
- Initiate revisions to cGMP procedures, and master batch records as applicable.
- Initiate daily, weekly, and monthly site quality metrics and trend reviews.
- Assist in the review and approval of Validation documents and site change controls.
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!
Skills Required
- Bachelor's degree in life sciences, engineering, or equivalent training/experience
- Entry-level experience (0-3 years) in pharmaceutical manufacturing
- Proficient computer skills in Microsoft Word, Excel, and Outlook
- On-site work availability and ability to work on-call for technical support and deviation analysis
- Previous experience in a CMO and sterile filling, manufacturing, and/or fill-finish environment
- Aptitude in root cause analysis, technical writing, and CAPA in a GMP environment; LEAN/Six-Sigma experience a plus
What We Do
Grand River Aseptic Manufacturing (GRAM) is a leading pharmaceutical contract development and manufacturing organization (CDMO) specializing in aseptic fill-finish services for biologics, small molecules, and vaccines, offering capabilities for liquid and lyophilized vials, syringes, and cartridges.
