- Rayong, Rayong, Thailand
- On-site
- Full-time · Manager
- 5+ years
1–10 jobs· newest first
On-site · Full-time · Manager
Hybrid · Full-time · Mid
$226K–$293KFull-time · Director
$226K–$293KDirector

Manager
On-site · Full-time · Senior
$100K–$130KRemote · Full-time
On-site · Full-time · Entry
+10K new in the last hour
Lead a highly engaged pilot plant team to bridge innovation and production, ensuring successful implementation and optimization of HMO manufacturing processes.
You contribute directly to QIAGEN’s production success by applying advanced technical and scientific expertise in microbial fermentation and downstream processing in a regulated production environment.
Leadership role focused on defining and executing purification development strategy for pivotal, commercial, and lifecycle-management biologics programs.
The salary range for this position is: $226,185.00 - $292,710.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package.
Production Engineer
Lead and manage the purification development strategy for pivotal, commercial, and lifecycle-management biologics programs, providing scientific and technical direction across scale-up, validation readiness, technology transfer, and commercial manufacturing support.
The salary range for this position is: $226,185.00 - $292,710.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package.
Lead technical and operational aspects of downstream biologics manufacturing, ensuring GMP compliance and process robustness.
Provide technical leadership and oversight for GMP manufacturing campaigns across upstream and downstream bioprocessing operations.
Responsible for territory growth, expansion of direct sales, and meeting targets for profitable sales volume and margin dollars in the Georgia, Florida and Puerto Rico regions.
The salary range for this role is $100,000 - $130,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay.
The Technician position helps with the preparation of intermediate components (media solutions, working seed stocks and bacterial antigens) and the downstream processing of intermediate components in a vaccine manufacturing environment.
Job Family Group: Sales and Business Development Are you ready to do something remarkable? Ready to collaborate with an incredible team to solve problems that improve people’s lives? Meet Ingevity. At Ingevity, we develop innovations that purify, protect and enhance the world around us. Our products enable oil to flow better, crops to grow fuller, roads to last longer and ensure that the air we all breathe is cleaner. Our people come from all different backgrounds and help reimagine new possibilities daily. We understand there is no challenge too big and no contribution too small. We seek out new ideas for tackling complex problems and celebrate achieving the improbable. We value each person’s unique talents and synergize them to create meaningful impact and sustainable solutions for our customers and our world. Bold. Energetic. Ingenious. Genuine. If these qualities describe you, we’d love for you to join Ingevity! Ingevity is seeking an experienced Pharma / Biopharma Technology Leader to help establish and grow our presence in the pharmaceutical and biopharmaceutical purification market. This is a highly visible, entrepreneurial individual contributor role will be the platform technology leader for our High Putity Liquid Purification platform and will work hand in hand with a commercial leader for the platform to build the book of business. Ingevity is an emerging participant in this market, and this leader will play a critical role in building technical credibility, developing strategic customer relationships, generating application data, and creating new pathways for adoption across pharmaceutical manufacturers, contract development and manufacturing organizations (CDMOs), and purification technology providers. The successful candidate will combine deep expertise in downstream bioprocessing, pharmaceutical purification, filtration, adsorption, or separation technologies with a proven ability to independently develop customer relationships, support qualification programs, and drive commercialization in highly regulated environments. This role is ideal for a technically strong "player-coach" who enjoys building new opportunities from the ground up and is energized by operating in a highly autonomous, market-creation environment. What You'll Do Technical Leadership & Application Development Lead application development and performance evaluation of activated carbon technologies for pharmaceutical and biopharmaceutical purification processes. Design and execute laboratory studies focused on impurity removal, decolorization, endotoxin reduction, host cell protein (HCP) removal, aggregate reduction, and overall process optimization. Generate technical data packages supporting customer evaluations, qualification efforts, and commercialization activities. Assess adsorption performance, filtration performance, process economics, and scale-up considerations across pharmaceutical applications. Serve as the company's technical subject matter expert for pharmaceutical purification and downstream processing applications. Customer & Market Development Build and maintain relationships with pharmaceutical manufacturers, biopharma companies, CDMOs, and purification technology providers. Partner with commercial teams to identify and develop new business opportunities, customer trials, and strategic partnerships. Provide technical leadership during customer evaluations, qualification programs, and implementation projects. Translate customer challenges into practical purification solutions and support the development of differentiated offerings. Represent Ingevity at customer meetings, scientific conferences, industry forums, and technical workshops. Regulatory, Quality & Commercialization Support Drive compliance initiatives related to USP, European Pharmacopoeia, GMP, ICH, and other pharmaceutical quality standards. Support development of pharmaceutical-grade product specifications, technical dossiers, validation documentation, and qualification packages. Collaborate with Quality, Regulatory, Operations, R&D, and Commercial teams to support successful commercialization and scale-up activities. Contribute to strategies involving Drug Master Files (DMFs), extractables and leachables programs, change control requirements, and other qualification activities. Market Intelligence & Strategic Development Monitor trends in bioprocessing, downstream purification, filtration, chromatography, adsorption science, and emerging pharmaceutical manufacturing technologies. Evaluate competitive technologies and identify opportunities for Ingevity to establish market leadership. Help shape the long-term strategy for pharmaceutical purification solutions and market expansion. Required Qualifications Ph.D. in Chemical Engineering, Biochemical Engineering, Bioengineering, Pharmaceutical Sciences, Biochemistry, Analytical Chemistry, or a related field preferred. Master's degree with substantial relevant industry experience will be considered. Minimum 5+ years of relevant industry experience with a Ph.D. or 8+ years with a Master's degree. Hands-on experience in pharmaceutical or biopharmaceutical purification, downstream processing, filtration, adsorption, chromatography, or separation technologies. Strong understanding of pharmaceutical qualification and validation requirements within GMP-regulated environments. Experience interfacing directly with pharmaceutical manufacturers, biopharma organizations, CDMOs, or life sciences technology providers. Demonstrated ability to communicate complex technical concepts to both scientific and commercial audiences. Proven success working independently in highly visible technical roles. Ingevity is a company made up of extraordinary people of every race, religion and background, all worthy of the same dignity. Our differences are one of our great strengths. Join us in building a culture of increasing diversity and respect – a culture where everyone belongs. Ingevity is an Equal Opportunity Employer, Minorities/Women/Veterans/Disabled. Recruiting Agencies: Ingevity does not accept unsolicited resumes and therefore, will not be responsible for any fees associated with unsolicited resumes.