(Contract) Process Engineer

Job Description: I s Kymanox the right fit for you? You want to make a difference and have an impact… You enjoy having an influence in your day-to-day work… You are motivated by working alongside a team filled with subject matter experts who will help you learn and grow… You wake up every day and do what you do … because patients deserve better.

If this sounds like you, you’ve come to the right place. The Senior Process Engineer will join our CMC & Pharmaceutical Sciences team and lead the design, development, and optimization of manufacturing processes for pharmaceutical products, including both drug substance and drug product processes for multiple modalities of drug products.

T his role requires expertise in process engineering principles, regulatory compliance, quality assurance, and technical leadership. The successful candidate will drive process improvements while collaborating with cross-functional teams including Quality, Operations, and Regulatory Affairs. In addition to support from a direct, functional manager, work will also be done under the guidance of a senior Kymanox engineer and/or senior project manager.

Responsibilities

Develop technical documentation for drug substance and drug product manufacturing across multiple product modalities (e.g., small molecule, biologics, gene therapies) including SOPs, CMC regulatory filings, manufacturing records, technical reports, process validation and technology transfer documents. Design and develop manufacturing processes from concept through commercial implementation, utilizing industry best practices and regulatory guidelines (FDA, ICH, and other applicable standards).

Lead root cause analysis and implement continuous improvement initiatives to enhance process efficiency, reduce costs, and improve product quality and yield. Create and maintain comprehensive process documentation including process flow diagrams, risk assessments, standard operating procedures (SOPs), batch records, and validation protocols.

Plan, execute, and oversee process validation studies (IQ/OQ/PQ) and technology transfer activities; ensure full regulatory compliance throughout the validation lifecycle. Evaluate and select manufacturing equipment, conduct vendor assessments, and oversee equipment installation, qualification, and integration into production workflows.

Ensure all processes comply with cGMP, FDA regulations, and company quality systems; support regulatory submissions and maintain audit readiness. Partner with Quality, Operations, Product Development, Regulatory Affairs, and Supply Chain teams to ensure seamless process execution and continuous improvement Educational Background: The ideal candidate will have an advanced degree (e.

g., Master of Science, Master of Engineering) in a science-related field such as Biomedical Engineering, Mechanical Engineering, or Chemical Engineering. Experience: 10+ years of experience in the pharmaceutical or combination products industry. Demonstrated expertise in drug substance and drug product process development, process optimization, and continuous improvement methodologies.

Strong knowledge of cGMP regulations, FDA guidance documents, and quality systems Excellent technical writing and documentation skills. Ability to independently support development of technical documentation such as SOPs, batch records, validation protocols, technical reports, and CMC-related content. Strong problem-solving abilities with proven analytical thinking.

Effective communication and interpersonal skills with ability to work across departments Experience with MS Office products (Outlook, Excel, PowerPoint, Word) strongly preferred. Desired Aptitude and Skill Set: Detail-oriented Strong organizational skills and verbal/written communication skills Highly motivated self-starter with a sense of ownership and willingness to learn Thrive in a fast-paced, growing, and dynamic work environment Ability to form partnerships with internal stakeholders Seasoned soft skills (i.

e., high EQ) Technology savvy Travel: Up to 10% travel is possible for support at tradeshows, conferences, and related events. A passport is required for this job. About Kymanox: Join Kymanox – a life sciences professional services company dedicated to life sciences who has successfully delivered over 4000 projects across 20+ countries.

Become a member of a dynamic, fulfilling team that helps a broad range of life science products get to market more quickly, more affordably, and with the highest quality and safety standards possible in today’s biotechnology, pharmaceutical, medical device, and combination product industries. With a reputation of providing unparalleled professional services and our highly collaborative team of engineering, compliance, and project management experts, Kymanox provides an outstanding opportunity for learning and career advancement.

Kymanox encourages team members, especially new graduates, and young professionals, to work on a variety of projects to gain increased learnings in Kymanox’s service offerings and the life science industry as a whole. Kymanox is looking for motivated individuals who want to solve problems in the life science industries while doing the work they love and helping get modern medicines that enhance and save patient lives to market.

Kymanox provides professional services related to engineering, compliance, and project management. We service clients ranging from Fortune 100 companies to virtual start-up companies. The company was founded in 2004 and has been growing steadily since its inception. Our corporate HQ is based in Research Triangle Park, NC.

To learn more about our company, please visit our website: Life Science Solutions | Kymanox Kymanox is an equal-opportunity employer and works diligently to protect the rights of job seekers by following all local, state, and federal laws as well as best Human Resource (HR) practices in the Life Science industry.