Upstream Manufacturing Supervisor - Kelly Services
Oklahoma City, OK 73102
About the Job
Upstream Supervisor (cGMP)
Oklahoma City, OK
The Upstream Manufacturing Supervisor will be responsible for overseeing the cell culture and upstream processing operations. As an integral part of our manufacturing leadership team, you will be instrumental in driving the production of top-tier biopharmaceutical products and lead a team of employees directly or indirectly during production processes.
Job Responsibilities
Upstream knowledge and experience with the following:
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly’s Human Resource Knowledge Center.Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Oklahoma City, OK
The Upstream Manufacturing Supervisor will be responsible for overseeing the cell culture and upstream processing operations. As an integral part of our manufacturing leadership team, you will be instrumental in driving the production of top-tier biopharmaceutical products and lead a team of employees directly or indirectly during production processes.
Job Responsibilities
Upstream knowledge and experience with the following:
- Oversee and supervise GMP manufacturing processes for cell culture-based production, ensuring strict compliance with established protocols and regulatory standards.
- Lead routine tasks such as media preparation, cell inoculation, bioreactor operation, and harvest operations, ensuring meticulous execution and adherence to quality parameters.
- Foster collaboration with cross-functional teams, including Quality Control and Quality Assurance, to uphold product quality and regulatory compliance.
- Spearhead troubleshooting efforts and resolution of process deviations, conducting root cause analyses and implementing corrective measures to optimize manufacturing efficiency.
- Maintain comprehensive documentation of all manufacturing activities in accordance with GMP standards, ensuring the accuracy and completeness of batch records and related documentation.
- Play a pivotal role in technology transfer activities, leveraging expertise in cell culture processes to contribute to process enhancement initiatives.
- Facilitate the training and development of junior team members, actively participating in the formulation of standard operating procedures SOPs pertaining to cell culture manufacturing. Ensure the upkeep of equipment and work areas in accordance with safety protocols and guidelines, fostering a culture of safety and compliance.
- Continuous flow centrifuges
- Homogenization and depth filtration operations
- Single-Use temperature controlled mixing systems
- Bulk fill and aseptic handling techniques
- Responsible for leading daily manufacturing activities, which will include training and supporting performance evaluations.
- Develop, write, and review Standard Operating Procedures, Compounding Records, and Batch Records.
- Ensure team execution of NetSuite functionality for batch material traceability.
- Responsible for review of executed production records for proper GDP and execution of production records.
- Support deviation and CAPA resolution with SME and quality teams.
- Provide input and support to MSAT/PD during development and scale up activities as necessary.
- Support equipment calibration and preventative maintenance as part of the equipment control program.
- Communicate safety policies and goals and ensure team members adhere to facility safety policies.
- BS or MS from an accredited college or university with major coursework in a Scientific or Engineering discipline.
- Experience working in a GMP manufacturing environment is essential.
- The ideal candidate should possess over 6 years of relevant experience, demonstrating a strong proficiency in cell culture techniques and a track record of ensuring adherence to quality standards.
- Requires a strong background in cGMP principles and Quality Management Systems.
- Night Shift-11pm-7am
- Direct Hire Opportunity!
- Flexible to work overtime/weekends as needed
- Benefits Package
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly
Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly’s Human Resource Knowledge Center.Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Source : Kelly Services