Job Description
Associate Director, Upstream Process_ Technical Specialist
The External Manufacturing, Associate Director will support a technical team interfacing between our Company and External Partners (EP) in the Biologics Drug substance manufacturing area. This individual will support the platform lead(s) in the execution of technical transfers to and from External Partners through process validation completion and/or provide global technical operations support for continuous commercial manufacturing at an External Partner.
The Specialist (Biologics External Manufacturing) will provide technical support to the platform lead and to the Focused Factory. Key elements of this role include supporting team/partner interactions, proactive analysis of process performance, supporting change management, deviations/investigations, resolution of production issues, regulatory filing support and supporting continuous improvement initiatives with partners. The ideal candidate will be able to travel to domestic partner sites to effectively manage the partnership and associated activities and will also have effective communication skills and tools for remote support to the partnerships/virtual sites. Demonstrated knowledge in more than one pharmaceutical or Biopharmaceutical operation (e.g., manufacturing, technology, validation, engineering, quality, analytical, drug substance unit operations such as cell bank preparations& Characterizations, cell culture/fermentation and Largescale Bioreactor processes).
Primary Activities will include:
- Reports to the platform lead (or delegate) and receives general direction on goals and objectives. Functions independently and provides coordination, communication, and oversight of assigned External Partner technical issues.
- Supports facility start-up and technical transfers and/or provide global technical operations support for continuous commercial manufacturing at an External Partner.
- Provides on-going support to External Partners to resolve manufacturing issues, proactive analysis of process performance and develops plans to meet capacity needs.
- Collaborates with Biologics Quality Operations and others on the Focused Factory to support the product lifecycle.
- Supports validation strategies for new and existing products.
- Provides a 'calibrated' technical review of External Partners’ process change requests, deviations, protocols, and Master Batch Record changes.
- Troubleshoot manufacturing issues and support investigations through scientific problem-solving approaches.
- Understands regulatory requirements and partners with Operations, Quality, and the External Partner to develop more efficient ways to meet these requirements.
- Based on calibrated oversight model, minimizes duplication of efforts between External Partner and our Company’s systems.
- Partners with External Partner to achieve business goals and to establish a common culture that benefits both our Company and the External Partner.
- Ensure the highest Quality, Compliance and Safety standards by participating and complying with our Manufacturing Division Quality Management System (QMS) requirements, including ownership, as relevant.
Education Minimum Requirement:
- Bachelors or Masters or Equivalent in chemical/biochemical engineering, biotechnology, pharmaceutical science, life sciences
Required Experience and Skills:
- Proven experience in highly regulated certified manufacturing plants with a minimum of 12 yrs. experience in the areas of cell banking, Cell Culture manufacturing process, technical transfer, process validation, or have demonstrated experience in these areas.
- Demonstrated experience on scale-up, process design and tech transfer activities in cell culture large scale manufacturing (preferably 10kL and above)
- Design a process according to the facility fit and equipment fit with minimal changes.
- Great understanding and designing of the gassing strategies, simulation studies, designing protocols etc.
- Supporting of commercial process trouble shooting, investigations support
- Designing of a cleaning process, cleaning validations, dirty equipment hold times establishment, clean equipment hold times, establishing the carry over limits in multiproduct manufacturing set up.
- Establishing the media and product intermediate hold times.
- Perfusion technologies
- Establishing the comparability limits, and design a process to be within comparability.
- Support to design and establish Annual Product Quality Reports
- Proven experience in highly regulated certified manufacturing plants.
- Campaign reviews and product life cycle management
- Establishing the CPV limits and ensuring the process compliance within CPV.
Preferred Experience and Skills:
- Experience with High Performance Organizational tools, Well understanding on the manufacturing digitalization, computer system validation requirements, Process Validations/Cleaning Validations.
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Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Hybrid
Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
10/28/2024
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
