Manager, Upstream Process Development, Plasmid DNA
Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products. As part of our business expansion plan, we are building a state-of-the-art facility that specializes in the development and manufacturing of Plasmid DNA. This facility will be equipped with cutting-edge technology and staffed by a team of highly skilled professionals who are dedicated to advancing the field of Plasmid DNA process development and manufacturing. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client challenges.
Because our success depends on our ability to exceed our clients’ expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team.
Position Summary:
This role presents a unique opportunity to establish the foundation and set direction for the facility currently being designed and constructed. The role will be responsible for leading upstream process development activities, staffing the functional area, and building the infrastructure to enable on-time and within budget execution and completion of future client projects. Partnering closely with cross-functional representatives and clients, this role will ensure Plasmid DNA development activities are completed per agreed upon timelines and deliverables.
Location: The Woodlands, TX
Essential Duties and Responsibilities:
- Establish Plasmid DNA upstream laboratories, including selecting equipment, setting up layouts and workflows, and ensuring alignment with industry standards and safety protocols.
- Recruit, train, and lead a team of scientists and associates responsible for upstream development activities. Provide guidance, mentorship, and performance feedback.
- Lead the development efforts to optimize upstream capability. This involves designing experiments, analyzing data, and making recommendations for improvements.
- Facilitate the seamless transfer of developed processes to manufacturing teams, providing detailed documentation, training, and ongoing support.
- Ensure all upstream development activities adhere to applicable regulatory guidance and industry best practices. Compile and/or support the creation of documentation for regulatory submissions.
- Collaborate with cross-functional teams and clients, including Manufacturing, Quality Control, Quality Assurance, Program Management, and Business Development to ensure alignment of upstream development activities with overall company and client objectives.
- Support investigations via equipment troubleshooting and testing to identify root causes.
- Prepare and present concise, sound scientific presentations of study results to the internal and external team for decision making.
- Face-to-face interaction with clients to discuss laboratory capabilities and provide feedback.
- Author technical documents such as laboratory and equipment SOPs (Standard Operating Procedures), batch records, process development reports, and transfer protocols/reports.
- Evaluate new technologies and innovations to improve operational efficiency or expand upstream development capabilities.
- Perform general laboratory duties associated with equipment maintenance and good housekeeping.
- Keep abreast of industry trends, emerging technologies, and best practices in Plasmid DNA development to ensure the company remains competitive and innovative. Present or publish within the industry as appropriate.
Working Conditions:
- This position is required to work in a lab/office setting. The role requires walking, standing, stooping, kneeling, and crouching. The employee must occasionally lift and or move up to 20 pounds independently.
- Initially, remote working conditions transitioning to long term permanent, onsite position; occasional travel.
Qualifications:
- BS, MS or PhD in Biology, Chemical Engineering, Microbiology or Biochemistry with 10+ years for BS, 7+ years for MS and 5+ year for PhD of relevant research and/or industry experience.
- 3-5 years of people leadership or managing people in direct reporting roles or in matrix organizations.
- In-depth understanding of upstream and upstream process development (upstream controllers, tangential flow filtration (TFF) systems, centrifugation, cell lysis and single use technologies).
- Experience with new laboratory start-up and equipment commissioning.
- Hands-on experience in running and developing upstream processes.
- Creative thinker that can identify and efficiently improve processes to address issues and gaps.
- Demonstrate ability to work independently and on cross-functional teams.
- Proven client interactions and project management experience desired.
- Strong attention to detail.
- Effective verbal and written communication skills.
Compensation Range: The base compensation range for this role is between $120,000 and $150,000. However, the actual compensation may vary depending on your experience and qualifications.
Health Benefits and Program: Bionova offers health benefits at a subsidized rate.
Healthcare, Dental, and Vision insurance
Life Insurance and Disability Program: 100% covered by Bionova.
Retirement Plan (401K) Up to 8% of Employer Match
Paid time off up to two weeks
10 days of Holidays and 5 days of Sick Leave
As an equal opportunity employer, Asahi Kasei believes a diverse workforce will provide us with the ability to continuously support the changes in the economy, society, and environment.